{"id":10,"date":"2021-03-30T23:43:22","date_gmt":"2021-03-30T21:43:22","guid":{"rendered":"http:\/\/szulc-euphenics.com\/?p=10"},"modified":"2026-07-24T11:55:21","modified_gmt":"2026-07-24T09:55:21","slug":"lista-genow","status":"publish","type":"post","link":"https:\/\/www.szulc-euphenics.com\/?p=10","title":{"rendered":"Lista Gen\u00f3w :"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>DNA$ &#8230;..Kirkegard\u00a0\u00a035<\/strong>.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">genes list:&nbsp;<\/p>\n\n\n\n<ol class=\"wp-block-list\"><li><strong>2700099C18RiK&nbsp;<\/strong>-* NDC80 homolog, kinetochore complex component paeudogene is a protein that in humans is encoded by the 270009C18Rik gene # pseudogene? 2700099C18Rik &#8211; na cromosomie 17 kt\u00f3ry jest jedn\u0105 z 23 par chromosomie u ludzi. Pseudogen &#8211; fragment kwasu deoksyrybonukleinowego, jt\u00f3ry &#8211; mimo podobie\u0144stwa do gen\u00f3w &#8211; nie jest funkcjonalny, tzn. nie koduje bia\u0142ek.&nbsp;<\/li><li><strong>5HTR3A&nbsp;<\/strong>-*<strong>&nbsp;<\/strong># nowszy lek o moduluj\u0105cym wp\u0142ywie na przeka\u017anictwo serotonergiczne &#8211; wortioksetyna 2021-03 # gen nale\u017cacy do rodziny receptoriw serotoninowych &#8211; koduje Receptor 5-HT3 &#8211; receptor serotoninowy 3 &#8211; receptor jonotropiwy sk\u0142adajacy sie z 5 jednostek<\/li><li><strong>A1BG<\/strong>&nbsp;-* # Alpha-1-B glycoprotein is a 54.3 kSa protein in humans that is encoded by the A1BG gene. 21-03<strong>&nbsp;<\/strong># The gene contains 20 distint introns. Transcription produces 15 different mRNAa, 10 alternatively spliced variants and 5 unspliced forms. There are 4 propable alternative promoters, 4 non overlapping alternative last exons and 7 valudated alternative polyadenalation sites. 2021-03 # Alpha-1-B glycoprotein &#8211; first in list Human protein-coding genes lister in the HGNC database &#8230;::<\/li><li><strong>A1CF&nbsp;<\/strong>-* # Function: Mammalian apolipoprotein B mRNA undergoes site-specific C to U deamination, which is mediated by a multi-component enzyme complex containing a minimal core composed of APOBEC1 and a complementation factor encoded by this gene. 2021-03 # APOBEC1 complementation factor is a protein that in humans is encoded by the A1CF gene<strong>.&nbsp;<\/strong><\/li><li><strong>A2M<\/strong>&nbsp;-* # Function The alpha-microglobulin (aM) family of proteins includes protease inhibitators, typified by the human tetrametric alpha-2-macroglobulin (a2M); they belong to the MEROPS proteinase inhibitator family I39, clan IL 2021-03&nbsp;&nbsp;# Entrez 2 2021-01-#&nbsp;&nbsp;alpha-2-Macroglobulin (alfa2M) is a large (720 KDa) plasma protein &#8230;<\/li><li><strong>A2MP1&nbsp;<\/strong>-* # 8 gen na li\u015bcie HGNC ID 2021-03 # Alpha-2-Macroglobulin Pseudogene 1&nbsp;<\/li><li><strong>AAAS&nbsp;<\/strong>-* # nuclear envelope protein &#8211; otoczka j\u0105drowa&nbsp;&nbsp;2021-03 # also known as adracalin 2021-03 # gene provides instruction for making a protein called ALADIN&nbsp;<\/li><li><strong>AADAC<\/strong>&nbsp;-* # Arylacetamide deacetylase is an enzyme that in humans is encoded by the AADAC gene. Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransfere, 2021-03# 17 numer HGNC:17&nbsp;<\/li><li><strong>AADACL3&nbsp;&nbsp;<\/strong>-* # Gene ontology:&nbsp; &nbsp; &nbsp; &nbsp;&nbsp;Molecular function: ? hydrolase activity&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;function:&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;? GO: 0004091 carboxylic ester hydrolase activity&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;Cellular:&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;? integral component of membrane&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;Biological process:&nbsp;&nbsp;metabolism&nbsp;&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;? catabolic proces&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;2021-03 # Arylacetamine deacetylase-like 3 &#8230;21-03 #&nbsp;&nbsp;&#8211; chromosome 1 wiki list &#8211; first gene at list&nbsp;<\/li><li><strong>AADACL4&nbsp;<\/strong>-* # Gene ontology: Molecular function: ? GO: 0004091 carboxylic ester hydrolase ctivity ? hydrolase activity Cellular component ? membrance &#8230; Biological process: catabolic process 2021-03 # Arylacetamide deacetylase-like 4 i sprotein in humans that is encoded by the &#8230; gene &#8211; second gene p-arm na w koljnosci drugu ?&nbsp;<\/li><li><strong>AAVS1 &#8211; Adeno-associated virus integration site 1 &#8211; is a viral integration site that in humans is encoded by the AAVS1 gene located on chromosome 19.<\/strong><\/li><li><strong>AASS-&nbsp;<\/strong>amonoadipate-semidethyse sinthaz<strong>e&nbsp;<\/strong><\/li><li><strong>ABAT &#8211;&nbsp;<\/strong>4-aminobutyrate aminotransferase &#8211; The ABAT gene provides instructions for making the GABA-transaminase enzyme.&nbsp;<\/li><li><strong>ABCA1<\/strong>&nbsp;&#8211; ATP binding cassette subfamily A member 1&nbsp;<\/li><li><strong>ABCA3 &#8211;&nbsp;<\/strong>The ABCA3 gene provides instruction for making a protein involved in surfactant production.&nbsp;<\/li><li><strong>ABCB1 &#8211; Glikoproteina P usuwa obce substancje w tum leki s wnetrza komorek &#8230;Transporter ABC ATP jest wykorzystywana do przemieszczania roznego rodzaju substrator przez blone &#8230;<\/strong><\/li><li><strong>ABCD1 &#8211; Olej ACTN3&nbsp;<\/strong>&#8211; bia\u0142ko in mi\u0119\u015bnie sprinter\u00f3w &#8211;&nbsp;<\/li><li><strong>ABI3 &#8211; cz\u0142onek rodziny gen\u00f3<\/strong>w ABI 3 (ABI3), znany r\u00f3wnie\u017c jako nowa cz\u0105steczka, w tym SH3 (Nesh) to bia\u0142ko, kt\u00f3re u ludzi jest kodowane przez gen ABI3. Kodowane bia\u0142ko hamuje etopowe przerzuty kom\u00f3rek n. oraz migracje komorek.&nbsp;<\/li><li><strong>ABL1 # BRCA1 has been shown to interact with the following proteins &#8230; 2021-03 #&nbsp;&nbsp;(9 chromosom) koduje ludzie bia\u0142ko Abl,&nbsp;<\/strong><\/li><li><strong>ABO<\/strong>&nbsp;# ABO determines the ABO blood group of an individual by modyfying the oligosaccharides on cell surface glycoproteins. The ABO locus encoded three alleles. &#8211; Histo-blood group ABO system transferase is an enzyme with glycosyltransferase activity, which is encoded by the ABO gene in humans.&nbsp;<\/li><li>ACADM &#8211; (acryl-Cornzyme A dehydrogenase, C-4 to C-12 straighy chain) is a gene that provides instruction for making an enzyme called .:: 3- ci ? gen w koljnosci w genotypie?&nbsp;<\/li><li>ACE &#8211; # Gen ACE zwany tez ?genem wytrzyma\u0142o\u015bci jest zwi\u0105zany z wydolno\u015bci\u0105 naszego organizmu2021-01 # &#8211; (ang. Angiotensin-Converting Enzyme &#8211; glimoproteina, enzym z grupa&nbsp;<\/li><li>ACE2 &#8211; Angiotensin-converting enzyme 2 (ACE2) is an enzyme attached to &#8230; ACE2 also serca tea as the entry point into cells for some corona viruses, including &#8230;SARS-CoV-2. &#8230;.ACE2 &#8211; warianty tego genu miga wplywac na podatnisc na infekce koronawirusmai ludzkimi&nbsp;<\/li><li>ACTL8 &#8211; Actin-like 8 is a protein in humans that is wncoded by the ACTL8 gene. It is a protein that is used in making the intercellular architecture of cells.&nbsp;&nbsp;&#8230;<strong>&nbsp;ACTL8 &#8211; Acrin-like 8 is a protein in humans that is encoded by the ACTL8 gene.&nbsp;<\/strong><\/li><li><strong>ACTN2 &#8211; koduje izoforme alfa-aktyniny&nbsp;<\/strong><\/li><li><strong>ACTN3 &#8211; #&nbsp;<\/strong>Badania genetyczne oceniajace predyspozycje do sportow s\u0105 prowadzone w kierunku 4 genow &#8211; ACTN3, ACE 2021-01&nbsp;<strong>&nbsp;# z bible list &#8230; bia\u0142ko in mi\u0119\u015bnie sprintero &#8230;2020-12#&nbsp;<\/strong>wariacja tego genu pomaga cia\u0142u w budowie bia\u0142ka Alpha-actini-3, kt\u00f3re kontroluje prace szybko kurczliwych wlokien miesniowych.&nbsp;<\/li><li><strong>ADA<\/strong>&nbsp;&#8211; #,dostarcza enzymu deaminy adenozyny LimfocytyT B NK, 2020-11 # chorobotw\u00f3rcza mutacja genu ADA &#8211; sanoistnie skorygowana przez komorki pacjentow &#8211; SCID &#8211; wg.&nbsp;&nbsp;?Edycji Gen\u00f3w? Doudny &#8230; Wiki: Adrnosine deaninase (also known as adenosine aminohydrosine, ADA) is an enzyme (EC 3.5.4.4) involved in purine metabolism.&nbsp;<\/li><li><strong>ADAM2<\/strong>&nbsp;&#8211; Disintegrin and metalloproteinase domain-containing protein 2 or Beta-fertilin is an enzyme that in humans is encoded by the ADAM2 gene.&nbsp;<\/li><li><strong>ADAM7<\/strong>&nbsp;&#8211; Sisintegrin and metalloproteinase domain-containing protein 7 is a protein that in humans is encoded by tve ADAM7 gene<strong>&nbsp;<\/strong><\/li><li><strong>ADAMTS1<\/strong>&nbsp;&#8211; A disintegrin and metalloproteine with thrombospindin mortufs 1 &#8211; is an enzyme that in humans is encoded &#8230; Chromosome 21 is both the smallest human autosome 48 baze pairs &#8211; 1,5 percent&nbsp;<\/li><li>ADCY5- # na liscie Bible1EL &#8230;2020-12 # Chromosome 3<\/li><li>ADGRL2 &#8211; (1p31.1): adhesion G protein-coupled receptor L2<strong>&nbsp;<\/strong><\/li><li><strong>ADM2<\/strong>&nbsp;&#8211; is a protein that in humans is encoded by tve ADM2 gene.<\/li><li>ADPRHL2 &#8211; ADP-ribose glycohydrolase 3 (ARH3) is an enzyme that in humans is wncoded by the ADPRH2 gene.&nbsp;<\/li><li>ADCY8 &#8211; (adenylate cyclades 8) which encodes a membrane bound enzyme that catalyze the formation of cyclic AMP &#8230; Cykliczny adenozyno-3?, 5?-monofisforan &#8211; stymuluje wzrist ruchliwo\u015bci plemnik\u00f3w &#8230;.(cAMP) &#8211; organiczny zwiazek chemiczny z grupy nukleotyd\u00f3w,&nbsp;<\/li><li><strong>ADH4 &#8211;&nbsp;<\/strong>koduje dehyrogenaze alkoholiwa<\/li><li>AKT1 &#8211; BRCA1 has been shown to interact with the following proteins: AKT1&nbsp;<\/li><li>AMELY &#8211; Y isoform AMELY is licated on the Y chromosome and encodes a form of amelogenin&nbsp;<\/li><li><strong>AMPD2<\/strong>&nbsp;&#8211; deaminase 2 is an enzyme that in humans is encoded by the AMPD2 gene. High AMPD2 expression levels correlate poor patient outcome&nbsp;<\/li><li>AHCTF1 &#8211; Protein ELYS is protein that in humans is encoded by tve AHCTF1 gene.&nbsp;<\/li><li><strong>AHR &#8211; #Narine &#8211; ksi\u0105\u017cka 2021-01#&nbsp;&nbsp;The aryl hydrocarbon receptor (AhR) is a protein that in himans is encoded byvthe AGR gene. Mikrobiom, mikrobiota &#8211;&nbsp;<\/strong><\/li><li><strong>AIC &#8211; Aicardi syndrome is a protein that in humans is encoded by the AIC gene.&nbsp;<\/strong><\/li><li>AM<strong>FR &#8211; Autocrine motility factor receptor, isiform 2 is protein that in kumaj\u0105 is encoded by the AMFR gene.&nbsp;<\/strong><\/li><li>ARID1A &#8211; AT-rich interactive domain-containing protein 1 A &#8230;<\/li><li>ATR &#8211; Serine\/threonine-protein kinease ATR also known as ataxia&nbsp;<\/li><li>ATXN7L2 &#8211; Ataxin 7-like 2 is a protein in humans that is encoded by the ATXN7L2 gene. Symbol report for ATXN7L2 AHGNC&nbsp;<\/li><li><strong>AZIN2<\/strong>&nbsp;&#8211; Antizyme inhibitor 2 (Azl2) also know as arginine decarboxylase (ADC)&nbsp;<\/li><li>BCL10 -B-cell lymphoma\/leukemia 10 is a protein that in himans is wncoded by the BCL10 gene.&nbsp;<\/li><li><strong>BCL2L15<\/strong>&nbsp;&#8211; Protein Coding &#8211; Chromosome 1 Open Reading Frame 178 &#8211; 1p13&nbsp;<\/li><li>BEX1 &#8211; Protein BEX1 also known as brain-expressed X-linked protein 1 is a protein that in humans is encoded by the BEX1 gene<\/li><li>BEX2 &#8211; chromosome X z, wyst?puje w p\u0142ucafh.&nbsp;<\/li><li><strong>AKT1 -# list most studied genes 2020-10 #&nbsp;&nbsp;<\/strong>The<strong>&nbsp;<\/strong>Serine-Theronine protein kineaze encoded by AKT1 gene is catalictycally inactive in serum-starved primary and immortalized fibribrast. 2020-08&nbsp;<strong>#&nbsp;<\/strong>Elephant man<\/li><li><strong>AKT3 &#8211;&nbsp;<\/strong>encoded enzyme RAC-gamma serine\/the<\/li><li><strong>ALK&nbsp;<\/strong>-# W kolejnych tetsach na myszach i muszkach owocowych ofkryti ze zwiedzeta ktore milay wylaczony gen postasaky szcuplejsze nawet gdy yly karjione dieta s Mcdonalds 2020-10 # # Disease-relevant genes with no reportable alternations 2020-10-08&nbsp;&nbsp;# kontrola uzycia energii przez nasz orgnizm 2020-10-05 # odgrywa znacz\u0105c\u0105 rok\u0119 w przeciwadzia\u0142aniu przyrostowi masy cia\u0142a 2020-09-29 # provides instructions for making a protein called ALK receptor tyrosine kinease, which is part of a family of proteins called receptor tyrosine kineases (RTKs)<\/li><li><strong>ALS2CR2 &#8211;&nbsp;<\/strong>nazwa genu wziela sie stad, ze znajduje sie w locus domniemanego genu zmutowanego &#8230; ALS.<\/li><li><strong>AMBN &#8211; Amekiblastyna (ang. ameliblastin), znana tak\u017ce jako amelina (ang. amelin) &#8211; bia\u0142ko szkliwa.&nbsp;<\/strong><\/li><li><strong>AMELY &#8211; Amelogenin Y isoform &#8211; is a protein that in humans is encoded by the AMELY gene &#8211; Chromosom Y &#8211; obecnosc chromosomu Y wraz z chromosomem C w jadrze komorki determinuje u czlowieka plec meska .::<\/strong><\/li><li><strong>APC&nbsp;&nbsp;# Gen APC znajduje sie na chromosomie 5 w regionie q21 i zawiera 21 eksonow. 2020-11&nbsp;<\/strong># antyknkogen 2020-09-24 #&nbsp;<strong>&nbsp;<\/strong>(Adenomatus Polyposia Coli gruczolakowata polipowato\u015b\u0107 okre\u017cnicy) gen kodujacy u czlowieka bialko APC.&nbsp;<\/li><li><strong>APOBEC3B &#8211; Probable DNA dC-&gt;dU-editing enzyme APOBEC-3B is protein that in humans is encoded by the APOBEC3B gene &#8211; Chromosome 22 is one of the 23 pairs of chromosomes in himan cells. Humans normally have teo copies of chromosome 22 in each cells. Chromosome 22 ia the second smallest human chromosome, spanning about 49 million DNA baze pairs an drepresbting btewenn 1.5 and 2% of the toralDNA in cells.&nbsp;<\/strong><\/li><li><strong>APOE&nbsp;<\/strong>&#8211; # jednak chromosom 19? &#8230; 2020-12 # (3445 citations) apolipoprotein E &#8211; list the top 20 most popular genes, 2020-10-27# # inzybieria tego genu&nbsp;&nbsp;pozwolilaby wyeliminosac jego wiazacy sie z podwyszszonym ryzykoem&nbsp;&nbsp;alzhaimera warinat E4 2020-10-13 # Apolipoproteina E 20<strong>20-10 #&nbsp;&nbsp;<\/strong>chromosom&nbsp;<strong>9&nbsp;<\/strong><\/li><li><strong>APOO &#8211; Apoliproteim O also known as protein FAN121B is a protein that in humans is encoded by the APOO gene. The X chromosome in humans spans more than 153 million base pairs&nbsp;<\/strong>(the building material of DNA) It represents about 800 protein-coding genes ..<\/li><li><strong>APTX &#8211; zwiazany z opisem Q10 &#8211; Arpataxin is a protein that in humans is encoded by the APTX gene.&nbsp;<\/strong><\/li><li><strong>ARG1 &#8211; The human ARG1 gene encodes the protein argainase: Arginaza &#8211; Rogers zauwazy\u0142 ze badacze badajcy kr\u00f3liki mieli nizszy niz normalnie pozion argininy&nbsp;<\/strong><\/li><li><strong>ARMCC6 &#8211; Armadillo repeat containing X-linked 6 is a protein that in humans is encoded bycthe ARMCX6 gene located on the X-chromosome.&nbsp;<\/strong><\/li><li><strong>ARHGAP44- GTPazy Rho bia\u0142ko aktywuj\u0105ce 44 &#8230;Bia\u0142ko Rho &#8211; kluczowe regulatiry cytoszkieletu w przebiegu mitozy i cytokinezy &#8230;.<\/strong><\/li><li><strong>ARID1A &#8211; AT-rich interactive domain-containing protein 1A<\/strong><\/li><li><strong>ARID1B &#8211;&nbsp;<\/strong>AT-rich interactive domain-containing protein 1B<\/li><li><strong>ARID2 &#8211; AT-rich Interactive domain-containing protein 2 &#8211; limfocyty T&nbsp;<\/strong><\/li><li><strong>ARHGAP11B &#8211;&nbsp;<\/strong>powoduje ze komorki macierzyste mozgu moga sie namnazac, co umizliwia powstanei wiekszego mozgu&nbsp;<\/li><li><strong>ASIP # w poszukiwaniu yellow gene 2020-12 #&nbsp;<\/strong>&#8211; melannin pigments &#8211; aguti?<\/li><li><strong>ASXL3<\/strong>&nbsp;&#8211; Additional&nbsp;&nbsp;sex combs lime 3 &#8211; chromosom 18&nbsp;<\/li><li><strong>ATM &#8211; # bia\u0142ko enzymu kodowane jest przez gen ATM w locus 11q22.3. Kinaza ATM fosforyluje szereg bia\u0142ek, odgrywaj\u0105cych rolebw zatrzymaniu cyklu komorkowego, apoptozie i naprawie DNA. # zesp\u00f3\u0142 ataksa-teleangiektazja 2020-10-06 # gene with protein product<\/strong><\/li><li><strong>ATP-aza ATP7B &#8211; (ATP-aza transportuj\u0105ca Cu2+, EC 3.6,3.4) &#8211; enzym b\u0142onowy obecny g\u0142\u00f3wnie w hepatocytach.&nbsp;<\/strong><\/li><li><strong>ATR is activated in respinse to persistent single-stranded DNA, which is a common intermediate formed during SNA damwage detection and repair.&nbsp;<\/strong><\/li><li><strong>ATXN1 &#8211; Ataxin-1 is a DNA-bibding protein which in humans is encoded by the ATXN1 gene.<\/strong><\/li><li><strong>AURKA &#8211; Kinaza Aurora A (AURKA) &#8211; enzym kodowany przez gen AURKA w locus 20q13 (wcze\u015bniej okre\u015blany STK15 albo STK6) nale\u017c\u0105cy do kinaz serynowo-treoninowych.&nbsp;<\/strong><\/li><li><strong>AVIL &#8211; odpowiada za utrzymanie przez komorki prawidlowego ksztaltu i rozmiarow&nbsp;<\/strong><\/li><li><strong>AZI1- Bia\u0142ko 1 indukowane przez 5-azacytyn\u0119&nbsp;<\/strong><\/li><li><strong>AZIN2 &#8211; Antizyme inhibitator 2 (AzI2) also known as arginine decarboxylase (ADC) is an enzyme that in humans is encoded by the AZIN2 gene. Humans have two copies of chromosome 1 as they dobwith all of the autosomes, which are the non-sex chromosomes.&nbsp;<\/strong><\/li><li><strong>B2M &#8211; B2 microglobulin also known as B2M is a component of MHC class I&nbsp;&nbsp;kolecules, MHC class I molecules have ?1, ?2 &#8230; Doudna p.48<\/strong><\/li><li><strong>BAX &#8211; Ekspresja geny BAX jest reguloeana&nbsp;&nbsp;przez bilanz p53&nbsp;<\/strong><\/li><li><strong>BCAS2 gene &#8211; Pre-mRNA-splicing factor SPF27 is a protein that in humans is wngoded by the BCAS2 gene.&nbsp;<\/strong>BCAS2 &#8211; Pre-mRNA-splicing factor SPF27 is a protein that in humans is encoded by the BCAS2 gene&nbsp;<\/li><li>BCL-2 &#8211; heterogenna grupa bia\u0142ek, reguluj\u0105ca uwalnianie cytochromu c i AIF z mitochondrow.<\/li><li><strong>BCL2 &#8211; apaptosis &#8230; Sulston John (2018-04-06 + )&nbsp;<\/strong><\/li><li><strong>BCL2A1- Bcl-2-related protein A1 is a protein that in humans is encoded by ghe BCL2A1 gene<\/strong><\/li><li><strong>BCL2L1 &#8211;&nbsp;<\/strong>is a human gene # d\u0142ugowiczno\u015b\u0107 &#8230;.2021-01<\/li><li><strong>BCL2L2 &#8211; This gene encodes a pro-survival (anti-apoptic) member of thevbcl-2 protein family..<\/strong><\/li><li><strong>BCL3 &#8211; B-cell lymphoma 3-encoded protein&nbsp;<\/strong><\/li><li><strong>BCL6 &#8211; B-cell lymphoma 6 protein is a protein that in humans is encoded by the BCL6 gene&nbsp;<\/strong><\/li><li><strong>BCL9 &#8211; B-cell CLL\/lymphoma 9 protein that in humans is encoded by the BCL9 gene &#8211; ?To co pochodzi ode mnie &#8211; nawet najglubsze i najdluzej, nieudolnie robione ma sens &#8211; to co pochodzi od innych ludzi &#8230; jest tylko przyczyna choroby u smierci &#8211; I) piersze prawo genetyczne ! &#8230; do&nbsp;&nbsp;ksiazki Wery i do telefonu Kniazia &#8230; wszystko mia\u0142o sens !&nbsp;<\/strong><\/li><li><strong>BCL10&nbsp;<\/strong># Like BCL2, BCL3, BCL5, BCL6, BCL7A, and BCL9, it has clinical significance in lymphoma. 2021-03 # &#8211; B-cell lymphoma\/leukemia 10 is a protein that in humans is encided by the BCL10 gene. Entrez 8915<\/li><li><strong>BDNF &#8211;&nbsp;&nbsp;Neurotroficzny czynnik pochodzenia m\u00f3zgowego (BDNF, z ang. brain-derived neurotrophic factor) &#8211; bia\u0142ko wydzielane przez neurony, nale\u017c\u0105ce do rodziny czynnik\u00f3w wzrostu nerw\u00f3w.&nbsp;&nbsp;2020-11 # 2020-11 #&nbsp;&nbsp;<\/strong>jako biomarker w w przebiegu i leczeniu schizy&nbsp;<\/li><li><strong>BIRC2 &#8211; Baculoviral ISP repeat-containing protein 2&nbsp;<\/strong><\/li><li><strong>BRAF is a human gene that encodes a protein called B-Raf.&nbsp;<\/strong><\/li><li><strong>BRCA1- # ludzka gen supresorowy znajduj\u0105cy si\u0119 na d\u0142ugim ramieniu 17 chromosomu w locus 17q21. Jest to bardzo du\u017cy gen &#8211; obejmuje 80 kpz DNA i zawiera 24 egzony. 2021-01 # breas<\/strong>t cancer chromosome17 &#8211; from base pair<\/li><li><strong>BRCA2<\/strong>&#8211; # Bia\u0142ko kodowane przez BRCA2 jest zaanga\u017cowane w napraw\u0119 DNA (napraw\u0119 przez rekombinacj\u0119 uszkodze\u0144 obu nici DNA) 2020-11# chromosome 13 &#8211;&nbsp;&nbsp;bialko &#8211; naprawa DNA&nbsp;<\/li><li><strong>BRAF<\/strong>&nbsp;&#8211; # wracam przy analizie Q10 &#8211; is a human gene that encodes a protein called B-Raf. 2020-11 Sygnalizacja kinaz aktywiwanych mitigenami (MTK signaling)&nbsp;<\/li><li><strong>BRD4 encoded protein bronodomain-cintaining protein 4&nbsp;<\/strong><\/li><li><strong>BRIP1 &#8211; jego mutacje zwiazane sa ze zwiekszeniem&nbsp;&nbsp;ryzyka &#8230; piersi &#8230;.<\/strong><\/li><li><strong>C1orf109 gene &#8211; Chromosome 1 open reading frame 109 is a protein&nbsp;<\/strong><\/li><li><strong>C1QL1 &#8211; 17q21.31 jest to bia\u0142ko wydzielane o dlugosci 258 aminokwas\u00f3w &#8230; Pre-mRNA tego bia\u0142ka podlega edycji RNA<\/strong><\/li><li><strong>C4 &#8211;&nbsp;<\/strong>schizofrenia&nbsp;<\/li><li><strong>C9orf72 &#8211; (chromosome 9 open reading frame 72) is a rotwein which in humans is encoded by the gene C9&#8230;.<\/strong><\/li><li><strong>c-Fos &#8211; kom\u00f3rkowy protoonkogen, nale\u017cacy do gen\u00f3w wczesnej odpowiedzi kom\u00f3rkowej.&nbsp;<\/strong>Koduje<strong>&nbsp;czynnik transjrypcyjny FOS, kt\u00f3ry (podobnie jak pozosta\u0142e bia\u0142ka z rodziny Fos &#8211; FosB, Fra-1 i Fra-2)?zawiera motyw suwaka leucynowego umo\u017cliwiaj\u0105cy im tworzenie z bia\u0142kami z rodziny Jun, a tak\u017ce Maf, Nrl oraz ATF, heterodiner\u00f3w funkcjonuj\u0105cych jakonj\u0105driwy czynnik transkrypcyjny AP-1 (ang. activator protein-1).&nbsp;<\/strong><\/li><li><strong>CABLES1 &#8211; CDK5 and ABL1 enzyme substrate 1 is a protein that in humans is encoded by &#8230; Chromosom 18 &#8211; jeden z 23 parzystych chromosomow cz\u0142owieka. DNA chromosomu 18 liczy oko\u0142o 76 milion\u00f3w par nukleotyd\u00f3w,&nbsp;<\/strong><\/li><li><strong>CABYR &#8211;&nbsp;<\/strong>Calcium-binding tyrosine phosphorylation-regulated protein &#8211; na locus chromosomie 18 &#8211; is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Cgromosome 18 spans about 80 million base pairs (the building material of DNA) and represents about 2.5 percent of the total DNA in cells.<\/li><li><strong>CACHD1 &#8211; Cache domain containing 1 is a protein in humans that is encoded by the CACHD1 gene.&nbsp;<\/strong><\/li><li><strong>CAMTA1 &#8211; Calmodulin-binding &#8230;chromosom 1 &#8211; na ktorym jest ok? 3141 gen\u00f3w ?&nbsp;<\/strong><\/li><li><strong>CARD10 &#8211;&nbsp;<\/strong>Caspase recruitment domain-containing protein 10 is a protein in the CARD-CC protein family that in humans is encoded by the CARD10 gene.&nbsp;<\/li><li><strong>CARD11 &#8211; Caspase &#8211; Entrez 84433<\/strong><\/li><li><strong>CARD14 &#8211; BCL10 has been shown to interact with CARD14 &#8230;.<\/strong><\/li><li><strong>CASP3 &#8211; The protein encoded by this gene is a cysteine-aspartif acid protease that plays a central role in the ececution-phase of cell apoptosis:&nbsp;<\/strong><\/li><li><strong>CASP9 &#8211; (Chr 1:15.49-15.53) Caspase-9 is an enzyme that in humans is encoded by the CASP9 gene.&nbsp;<\/strong><\/li><li><strong>CASZ1 &#8211; (Chr 1:19.64-10.8) &#8211; Outative survival-related protein is a protein that in humans is encoded by the CASZ1 gene.&nbsp;<\/strong><\/li><li><strong>CCR4 &#8211; C-C chemokine receptor type 4 is protein&nbsp;<\/strong><\/li><li><strong>CSDE1 &#8211; Cold shock domain-containing protein E1 is a protein that inn humans is encoded by the CSDE1 gene<\/strong><\/li><li><strong>CBS- B-Syntaza cystationinowa &#8211; enzym katalizujacy reakcj\u0119 porydoksynozale\u017cnego przekszta\u0142cenia homocysteiny i seryny w cystotaine. Bia\u0142ko enzymu ma trzy podjednostki i domene hemowa. Reakcja katalowana przez CBS &#8230; chromosom 21 najmniejszy z ludzkich chromosomow &#8211; 225 genow i 59 pseudogenow ..<\/strong><\/li><li><strong>CCDC144A &#8211; bia\u0142ko 144a skr\u0119conych helis zawieraj\u0105cycdomen\u0119 &#8230;<\/strong><\/li><li><strong>CCDC40 &#8211; Ten gen koduje bia\u0142ko nieb\u0119dne do funkcjonowania rz\u0119sek ruchliwych &#8230;<\/strong><\/li><li><strong>CCDC47 &#8211; funkcja tego bialka jest nienza ale zaproponowano ze bierze udoAl w homostazoe jonow wapnoa &#8230;<\/strong><\/li><li><strong>CCDC57 &#8211; Bia\u0142ko 57 zawiearj\u0105ce domen\u0119 coiled-coil jest bia\u0142kiem, kt\u00f3re u ludzi jest kodowane przez gen &#8230;jw.&nbsp;<\/strong><\/li><li><strong>CCL1 &#8211; Chmokine (C-C motif) ligand 1 (CCL1) is alao known as small inducible cutokine A1 and I-309 in humans. CCL1 is a small&nbsp;&nbsp;glycoprotein that belongs to the CC chemikine family. Ligand &#8211; atom czasteczka lub anion w zwi\u0105zkach kompleksowych, kt\u00f3ry jest przylacoNy bezposrednio do atomu centralnego lub katoonu centralnego&#8230;<\/strong><\/li><li><strong>CCL2 &#8211; The chemokine (C-C motif) ligand 2 .:..<\/strong><\/li><li><strong>CCL21 (ang. Chemokine (C-C motif) ligand 21) &#8211; bia\u0142ko, niewielka cytokina &#8230;.<\/strong><\/li><li><strong>CCL22 ( C-C motif chemiokine 22) &#8211;&nbsp;<\/strong><\/li><li><strong>CCL3 &#8211; Chemokine (CC motif) ligand 3 &#8211; Gene ID: 6348&nbsp;<\/strong><\/li><li><strong>CCL4 &#8211; Geny chemokin &#8230;<\/strong><\/li><li><strong>CCL5 &#8211; (ang. C-C motif chemokine ligand 5), inna nazwa, RANTES (ang. Regulated on Activation, Normal T-cell&nbsp;<\/strong><\/li><li><strong>CCL6 &#8211; Gene type &#8211; protein coding &#8211; 20 305<\/strong><\/li><li><strong>CCL7 &#8211; is a small cytokine known as a chemiokine&nbsp;<\/strong><\/li><li><strong>CCL8 &#8211; Chemokine (C-C motif) ligand 8 (CCL8), also known as monicyte chemoattrqctant protein 2 (MCP2), is a protein that in humans is encoded by the CCl8 gene. The CCL8 protein is produced as a precursor containing 109 amino acids, which is cleaved to produce mature CCL8 containing 75 amino acids.&nbsp;<\/strong><\/li><li><strong>CCL9 &#8211;&nbsp;<\/strong>Chemokine (C-C motif) ligand 9 (CCL9) is a small cytokine belonging to the CC chemokine family. It is also called macrophafe inflammatory&nbsp;<\/li><li><strong>CCND1 &#8211; Cell cycle&nbsp;<\/strong><\/li><li><strong>CCNE1 &#8211; gene&nbsp;<\/strong>encoded in humans a protein G1\/S-specific cyclin-E1<\/li><li><strong>CCR5&nbsp;<\/strong>&#8211; # W trwaj\u0105cych badaniach klinicznych stwierdzono, \u017ce nukleazy z domen\u0105 palca cynkowego mog\u0105 zaburza\u0107 aktuwno\u015b\u0107 genu CCR5 ludzkich limfocyty T typu CD4+, co mo\u017ce mie\u0107 zastosowanie w leczeniu AIDS. 2021-01 # C-C chemokine receptor type 5, also known as CCR5 or CD125, is a protein on the surface of white blood cells &#8230; 2029-11# Receptor C-C chemokin typu 5, CCR5, CD195 &#8211; bia\u0142ko kodowane u ludzi przez gen CCR5. CCR5 jest jednym z receptor\u00f3w beta-chemokin, podobnym do receptor\u00f3w sprz\u0119\u017conych z bia\u0142kami G, i jak one b\u0119d\u0105cymi integralnym bia\u0142kiem b\u0142onowym osadzonym w niej motywem siedmiu alfa helis. U ludzi gen CCR5 jest po\u0142o\u017cony na kr\u00f3tkim (p) ramieniu chromosomu 3 w pizycji 21. &#8230; wiki 2020-11 # mutacja w tym receptorze zwieksza tez ryzyko zakazenia gorzaczka zachdniego Nilu 2020-10 # mutacja w genie kodujacyn receptor CCR5 czyni osoby mniej podatnyni na zakazenie HIV 2020-10-02 # Receptor C-C chemokin typu 5, CCR5, CD195 &#8211; bia\u0142ko kodowane u ludzi przez gen CCR5. Artyku\u0142 Bartnik &#8211; osoby poznawione obu kopii tego genu uwa\u017cane s\u0105 za odporne na zaka\u017cenie wirusem HIV.<\/li><li><strong>CD4&nbsp;<\/strong>&#8211; (ang. cluster of differentiin 4, synonimy: Leu-3, L3T4, T4) &#8211; glimoproteina&nbsp;<\/li><li><strong>CDH9 &#8211; A 2009 pair of genome-wide association studies found an association between autism &#8230;.<\/strong><\/li><li><strong>CDH10 &#8211; and six single-nucleotide polymorphism in an intergenic region between CDH10 &#8230; This genes encode neuronal cell-adhesion molecules, implicating these molecules in the mechanism of autism.&nbsp;<\/strong><\/li><li><strong>CDH13 &#8211;&nbsp;<\/strong>bialka adhezyjne&nbsp;<\/li><li><strong>CDKN1A &#8211; p21, WAF1 (tak\u017ce inhibitor kinaz zale\u017cnych od cyklin lub bia\u0142ko oddzia\u0142uj\u0105ce z CDK 1) &#8211; bia\u0142ko, kt\u00f3re u cz\u0142owieka kodowane jest przez gen CDKN1A, zlokalizowany na chromosomie 6 (6p21.2) Bia\u0142ko p21 jest silnym&nbsp;<\/strong>inhibitorem kinaz zale\u017cnych od cyklin &#8230;.<\/li><li><strong>CDKN1B &#8211;&nbsp;<\/strong>Cyclin-dependednt kinease inhabitor 1B is an enzyme inhabitor that in humans is encoded by this gene?&nbsp;<\/li><li><strong>CDKN2A &#8211;&nbsp;<\/strong>Cykl kom\u00f3rkowy (geny supresorowe)&nbsp;<\/li><li>CD<strong>KN2B &#8211;&nbsp;<\/strong>Cyclin-dependent kinease 4 inhabitor B&nbsp;<\/li><li>CDC42 &#8211; Pozosta\u0142e sygnalizacje<\/li><li><strong>CDK12 &#8211; niedawno zidentyfikowany gen, ktory kontroluje ekspresje genow niezbednyfh w procesie naprawy DNA.<\/strong><\/li><li><strong>CDX2 &#8211;&nbsp;<\/strong>powoduje upo\u015bledzenie roznicownaia sie komorek progenitorowych<strong>&nbsp;<\/strong><\/li><li><strong>CEBPB &#8211; CCAAT\/enhancer-binding protein beta &#8230;.<\/strong><\/li><li><strong>CETP &#8211; linked to exceptional longevity &#8230;<\/strong><\/li><li><strong>CFI &#8211; F1 &#8211; Complement factor I &#8211; Gen dla czynnika I i ludzi zlokaliowany jest na chromosome 4 &#8230;<\/strong><\/li><li><strong>CFTR&nbsp;<\/strong># Opr\u00f3c tego we wspomnianym genie cz\u0119stochowa dochodzi do in tvn delecjo, a tak\u017ce do zamiany aminokwas\u00f3w in inne lub przedecz es who pojawiania si\u0119 koronowo STOP (mustacje cz\u0119ste zw\u0142aszcza u \u017byd\u00f3w Aszkenazyjskich) &#8211; Genesis X w. 3 2021-01&nbsp;<strong># delecje trzech liter kodu genetycznego w genie CFTR skytkuj\u0105 powstaniem bia\u0142ka pozbawionego waznego aninokwasy &#8211; (ang. cystic fibrosis transmembrane conductance regulator, regulator przewodnictwa) &#8211; bia\u0142ko tworz\u0105ce kana\u0142 chlorkowy w b\u0142onie kom\u00f3rkowej, &#8230; 2020-11 #&nbsp;<\/strong>mukowiscydoza<\/li><li><strong>CHD1 &#8211; Chromatin (other)&nbsp;<\/strong><\/li><li><strong>CHD2 &#8211; Chromodomain-helicase-DNA-binding protein 2&nbsp;<\/strong><\/li><li><strong>CHD4 &#8211; Chromodomain-helicase-DNA-binding protein 4&nbsp;<\/strong><\/li><li><strong>CHD5 &#8211; (Chr 1:6.1-6.18 Mb)&nbsp;<\/strong><\/li><li><strong>CHEK1 &#8211; checkpoint kinease 1 &#8230; serine\/threonine &#8230;.<\/strong><\/li><li><strong>ChEK2 &#8211;&nbsp;<\/strong>ludzki gen koduj\u0105cy bia\u0142ko ChEK2, b\u0119d\u0105ce kinaz\u0105 efektorow\u0105 zaanga\u017cowan\u0105 w napraw\u0119 DNA.&nbsp;<\/li><li><strong>CLIC4 &#8211; Chloride intercelliral chanel 4 is a eukaryotic gene&nbsp;<\/strong><\/li><li><strong>CLUH &#8211; Skupione mitochondriami (cluA\/CLU1) homolog&nbsp;<\/strong><\/li><li><strong>CLOCK &#8211; CarcadiannLocomotor Output Cycles Kaput) or Clock is a gene encoding a basic hic-loop-helix-PAS transcryptions factor that is beliwved to affect both the pesisywwnand perod orf cardian rhythms<\/strong><\/li><li><strong>CLSPN &#8211; protein &#8230; Xenopus claspin is an essential upstream regulator of checkpoint kinease 1&nbsp;<\/strong><\/li><li><strong>CLTA &#8211; Douda: ?zdecydowalismy z Martinem, \u017ce zaprogramujemy CRISPER do wziecia na cel ludzkiegk genu CLTA kodujacego lekki lancuch A klatryny odgrywajevg pena role w procesie endocytozy w ktorej komorki wchlaniaja skladniki odzywvze i hormony.<\/strong><\/li><li><strong>CMPK &#8211; UMP-CMP kinease is enzyme that &#8230;uridine monophosphate (UMP\/cytidine monophosphate&nbsp;<\/strong><\/li><li><strong>CNTNAP2 &#8211; Contain-associated protein-like 2 &#8211; Tourette syndrome &#8211; Obajtek ? 2021-03-08 &#8230;.<\/strong><\/li><li><strong>COL1A1 # Facebook Function: Collagen is a protein that strengthens and supports many tissues in the body, including cartilage, bone, tendon, skin and the white part of the eye (sclera). 2021-03# Collagen, type I&nbsp;&nbsp;&#8211; artykuul geny i golf &#8230; w facebooku moim &#8211; kolagen bialko&nbsp;<\/strong><\/li><li><strong>COL1A2 &#8211; Function: Collagen alpha-2(I) \u017celatyna &#8211; bia\u0142ko uzyskieane z gotowania ko\u015bci i sk\u00f3r &#8230;<\/strong><\/li><li><strong>COL5A1 &#8211; # Elboe tendinopathy is a common pathology of the upper extremity that impacts both athletes and&nbsp;&nbsp;workwrs ?Influence of genetic factors &#8230;? 2021-01 # Collagen alpha-1(V) chain is a protein that in humans is encoded by the COL5A1 gene. This gene encoded an alpha chain for one of the low abundance finrillar collagens.&nbsp;<\/strong><\/li><li><strong>COL11A1 &#8211; Collagen alpha-1 (XI) chain is a protein that in humans is encoded by the COL11A1 gene&nbsp;<\/strong><\/li><li><strong>COMT &#8211; # A marker (rs4680) in the COMT gene also known as the warrior\/strategist gene, may influence a person?a ability to maintain focus and emotional control while&nbsp;&nbsp;under stresa. In regatdsnto gold this may be the difference between laying up on a Par 5, or risk going for a green fir a posaible eagle putt 2021-01-14 # Catechol-O-methyltransferase is one several enzymes that degradate catcholamines&#8230; katechilaminy 2020-10 #&nbsp;&nbsp;<\/strong>rozklada domanie<strong>&#8211;&nbsp;<\/strong>methylt<\/li><li><strong>COQ6 &#8211;&nbsp;<\/strong>Coenzyme Q6 monoodygenase is a protein that in humans is encoded by the COQ6 gene. The protein encoded by this gene belongs to the ubiH\/COQ6 family. It is evolutionarly conserved monoodygenase required for the biosynthesies of coenzyme Q10 (or uniquinone), which is an essential component of the mitochindrial electron transport chain, and one of the most potent lipophilic antioxidants implicated in the protection of cell dameg by reactive oxygen species. Ubichinon, kornzym Q10 &#8211; organiczny zwi\u0105zek chemiczny z grupy chinon\u00f3w, wystepuj\u0105cy w mitochondriach kom\u00f3rek ro\u015blinnych i zwierz\u0119cych. Po przy\u0142\u0105czeniu elektron\u00f3w swobodnie porusza si\u0119 w wenw\u0119trznej b\u0142onie mitochondrialnej umo\u017cliwiaj\u0105c transport elektron\u00f3w mi\u0119dzy komplekasami bia\u0142ek \u0142a\u0144cucha oddechowego, kt\u00f3re wbudowane s\u0105 w wewn\u0119trzn\u0105 b\u0142on\u0119 mitochondrialn\u0105.&nbsp;<\/li><li><strong>CREB &#8211; is a cellular transcription factor&nbsp;<\/strong><\/li><li><strong>CREBBP &#8211;&nbsp;<\/strong>CREB-bibding protein, also known as CREBBP or CBP, is a protein that in humans is encoded by th eCREBBP gene. 2020-11 # CREBP Acetylotanferazy histon?w chronatyny&nbsp;<\/li><li><strong>CRH &#8211; Corticotropin-relasing hormone (CRH) &#8230;. is a peptide hormone involved in the stress response&#8230;.<\/strong><\/li><li><strong>CRHR1 &#8211; Corticotropin-releasing hotmone receptor 1 is a protein &#8230;<\/strong><\/li><li><strong>CRKL &#8211;&nbsp;<\/strong>This gene encodes a protein kinease containing SH2 and SH3 (src homology) domains which has been shown to activate RAD and JUN kinease signaling pathways&nbsp;<\/li><li><strong>CTDNEP1 &#8211; CTD koperta j\u0105drowego fosfatazy 1 &#8230; CTD nuclear envelope phosophate 1&nbsp;<\/strong><\/li><li><strong>CTLA-4 (<\/strong>ang. cytotoxic T cell antigen 4, tak\u017ce: CD152, cluater of differention 152, inne synonimy: CELIAC3, GRD4, GSE, IDDM12) &#8230; link z horoby Hashimoto z ksiazki Narine&#8230;.<\/li><li><strong>CTNNB1 &#8211;&nbsp;<\/strong>Sygnalizacja wnt\/B-katenina (geny supresorowe) &#8211; driga do Lichenia +R2 stacja BP ryba i kawa z karmelem &#8211; na skutery &#8230;.2020-09-01&nbsp;<\/li><li><strong>CTNND2 &#8211; teraz badacze z Uniwersytetu Johna Hopkinsa mowia ze u 13 dziewczat wykryli kilkanasciebwaznych dla autyzmu genow w tym naistotniehszy CTNND2&nbsp;<\/strong><\/li><li><strong>CYP1A2 &#8211; koduje bia\u0142ka z rodziny cytochromu p450, kt\u00f3re metabolizuj\u0105 sk\u0142adniki od\u017cywcze i leki. Jednym z najlepiej rozpoznawanych substrat\u00f3w CYP1A2 jest kofeina. Polimorfizm pojedynczego nukleotydu (SNP) w obrebie CYP1A2 (rs762551) wp\u0142ywa na szybko\u015b\u0107 metabolizmu kofeiny przez uk\u0142ad enzymatyczny cytochromu P450. Wykrycie polimorfizmu warunkije zmniejson\u0105 wydajno\u015b\u00e7 procesu enzymatycznego, a tym samym wilniejsze rozk\u0142adanie kofeiny &#8230;<\/strong><\/li><li><strong>CYP27A1 &#8211; is a gene encoding a cytochromu P450 oxidase, and is common known as sterole 27-hydroxylase. (poszukiwa\u0142em baracuda &#8211; ryba &#8230;.<\/strong><\/li><li><strong>CYP2E1<\/strong>&nbsp;&#8211; upijanie sie &#8211; oraz mutacja -?serotonina -nauroprzekazmik &#8211; nastroj&nbsp;<\/li><li><strong>CXCL8 &#8211; Interlukina 8 (IL-8), &#8230; najsilniejszy czynnik chemitajtyczny u cz\u0142owieka.&nbsp;<\/strong><\/li><li><strong>CXCR4 &#8211;&nbsp;<\/strong># Doudna WHIM &#8211; jeste dzidziczna w sposob dominujacy 2020-11 # Doudna zasp\u00f3\u0142 WHIM rzadkie schorzenie: warts, hypogammaglobulinemia, infections, myelojathexis &#8230;. # Polityka ?Te uniarkowan\u0105 optymistyczn\u0105 histori\u0119 wypada zako\u0144czy\u00e7 informacja o tum, \u017ce CCR5 jest recptorem, za pomoc\u0105 kt\u00f3rego do kom\u00f3rki wnika tylko jeden typ wirusa HIV. Zar\u00f3wno pacjent z Berlina, jak i Londynu byli w\u0142asnie nim zaka\u017ceni. Musz\u0105 przyjmowa\u0107 lek blokuj\u0105cy inny receptor CXCR4 &#8230; 2020-11 # ?kiedy wy\u0142\u0105czyli\u015bmy CXR4 sposowodowobtl powstanie stresu oksydacyjnego 2020-10-05 # jest niezbedny komorkom macierzystym bia\u0142aczki do przetrwania<\/li><li><strong>CXCL12 &#8211; The steomal cell-derived factor 1 SDF &#8230; poszukiwalem ?gene siliencing?<\/strong><\/li><li><strong>CZIB &#8211; encodes the protein CXXC&nbsp;<\/strong><\/li><li><strong>DBC2 &#8211; Deleted in breast cancer 2 &#8211;&nbsp;<\/strong>Naukowcy z Cold Spring Harbor Laboratory i z University of Washington odkryli nowy gen supresorowy now. jtory jest nieobecny lub niekatuwny w ok 60% z r. piers.&nbsp;<\/li><li><strong>DBH &#8211; Dopamine beta-hydroxylase &#8230; Dopamine beta-hydroxylase catalizes the conversion of dopamine to norepinephrine &#8230;..tkwi doslownie na szczycie grupy krwi &#8230;<\/strong><\/li><li><strong>DBT &#8211; (Chr 1:100.18-109.25)&nbsp;<\/strong><\/li><li><strong>DCKRE1B &#8211; DNA cross-link repair 1B protein<\/strong><\/li><li><strong>DDX3Y &#8211; ATP-dependent RNA helicase DDX3Y is an enzyme that in humans is encoded by the DDX3Y gene: DEAD box proteins&#8230;&nbsp;<\/strong><\/li><li><strong>DEPDC1 &#8211; encoding protein DEP domain containing 1 &#8211; HGNC: 22949&nbsp;<\/strong><\/li><li><strong>DEL17P13.1 &#8211; Chroosome 17p13.1 deletion sundrome is a protein in humans that js encoded &#8230;.<\/strong><\/li><li><strong>DENN1B &#8211; is a human gene, located on chromosome 1. The gene is hypothesued by Danish scientists &#8230; to be related to asthma.&nbsp;<\/strong><\/li><li><strong>DENND11 &#8211; Genetic variation newsy assiciated with tusk for childhood asthma &#8230;2andMe<\/strong><\/li><li><strong>DEP domain containing 1 is a protein in humans thta is encoded by the DEPDC1 gene<\/strong><\/li><li><strong>DHH &#8211; Desert hedgehog, also Desert hedgehog homolog or Dhh, is a protein encoded by the DHH gene, and is a member of the hedgehog signaling patway.&nbsp;<\/strong><\/li><li><strong>DIABLO &#8211; on chromosome 12 &#8211; mitochondrial protein&nbsp;<\/strong><\/li><li><strong>DIRAS3- GTO-binding Di-Ras3 &#8230; the gene is a member of the Ras superfamily and is expresswd in normal ovariannand breast wpithelial cells&nbsp;<\/strong><\/li><li><strong>DLK1 &#8211; Protein delta homolog 1 is a protein that in humans is encoded by the DLK1 gene.&nbsp;&nbsp;Ostatnie badania wykaza\u0142y, \u017ce gen homologu 1 typu delta jest niezbedny do aktuwacji i regeneracji mezenchymalnych komorek macierzystych<\/strong><\/li><li><strong>DMD &#8211; # DMD gene encoding the dystrophin protein &#8230; cicerona 2.3 megabases (bp &#8211; base pair) dystrofia mi\u0119\u015bniowa Duchenne muskularny dystrophy ? 2021-01#&nbsp;&nbsp;&nbsp;<\/strong>najdluzszy ludzki gen Dystrofina &#8211; 2,4 mln par zasad &#8211; 11 055- odcinki kodujace<\/li><li><strong>DNASE2 &#8211; Deoxyribonuclease II, lysosomal is a protein that in humans is encoded by the DNASE2 gene.&nbsp;<\/strong><\/li><li><strong>DNMT3A<\/strong>&nbsp;&#8211; Epigentyka<\/li><li><strong>DOCK2 &#8211; (Dedicatir of cytokinesis 2)&nbsp;<\/strong>lub konserwatywne poglasy&nbsp;<\/li><li><strong>DOCK3 &#8211; index ?The Gene? Siddhartha Mukherjee&#8230;Dedicator of cytokinesis 3), also known as MoCA&nbsp;<\/strong><\/li><li><strong>DPH1 &#8211; Bia\u0142ko biosyntezy diftamidu 1 jest bia\u0142kiem, kt\u00f3re u ludzi jest kodowane przez gen DPH1.&nbsp;&nbsp;Diphthamide Biosynthesis 1&nbsp;<\/strong><\/li><li><strong>DPH5 &#8211; Diphthine synthase is an enzyme that in humans is encoded &#8230;<\/strong><\/li><li><strong>DRD1 &#8211; Dopamine receptor D1, is a protein that in humans is encoded by the DRD1 gene &#8230; hybrydyzacja northern ang. northen blot&nbsp;<\/strong><\/li><li><strong>DRD2 &#8211; bierz udIal w przekazywanih sygnalow w obrwboe ata czolowego&nbsp;<\/strong><\/li><li><strong>DRD3 &#8211; This gene encodes the D3 subtupe of the dopamine receptor. The D3 subtupe inhibits adenylyl cyckease through inhibitory G-proteins.<\/strong><\/li><li><strong>DRD4 # mutation in this gene &#8211; disfunction autonomic nerouv system 2021-03 # &#8211; The dopamine receptor D4 is a dopamine D2-like D2-like G protein-coupled receptor encoded by the DRD4 gene on chromosome 11&#8230;&nbsp;&nbsp;2020-11# DR4D &#8211;&nbsp;<\/strong>koduje powstawianie receptor\u00f3w dopaminowych -liberalne l<\/li><li><strong>DRD5 &#8211; D5 rceptor is a subtype of the dopamine receptor that has a 10-fold higher affinity for dopamine than D1 subtype.&nbsp;<\/strong><\/li><li><strong>DTDST &#8211; Dysplazja diastroficzna (ang. diastrophic dysplasia, DD, DTD) &#8211; choroba genetyczna o dziedziczeniu autosomlanum recesywnym, spowodowana mutacj\u0105 w genie DTDST w licus 5q32-q33.1 koduj\u0105cym transporter jon\u00f3w siarczanowych SLC26A2. Mutacje w tym samym genie powoduja achondrogenez\u0119 typu 1B (ONIM#600972) &#8230;<\/strong><\/li><li><strong>DUP17Q12 &#8211; Chromosome 17q12 duplication syndrome is a protein in humans that is encoded by the DUP17Q12 gene<\/strong><\/li><li><strong>DVL1 &#8211; (Chr 1:1.34-1.35) Segment polarity protein dishevelled homolog DVL-1 is a protein that in humans is encoded by the DVL1 gene.&nbsp;<\/strong><\/li><li><strong>EDAR<\/strong>&nbsp;&#8211; development ecodermal tissues<\/li><li><strong>EGFR &#8211;&nbsp;<\/strong># (3410 citations top 20 popular genes 2020-10-27&nbsp;<strong># according Kerpedjiev, the top-10 most-studied genes 2020-10 #<\/strong>&nbsp;7p11.2 2020-01-03&nbsp;<strong>#&nbsp;&nbsp;<\/strong>Sygnalizacja receptorowych kinaz &#8230;RTK<\/li><li><strong>ELMO1 &#8211; # ELMO1 is located on chromosome&nbsp;&nbsp;number seven &#8230; 2020-11#&nbsp;<\/strong>Engulfment and cell motility protein 1<strong>&nbsp;<\/strong><\/li><li><strong>ELMO2 &#8211; Engulfment an dcell motility protein 2&nbsp;<\/strong><\/li><li><strong>ELMO3 &#8211; Chr. 16 q22.1&nbsp;<\/strong><\/li><li><strong>ENAM &#8211;&nbsp;<\/strong>Enamelina &#8211; bia\u0142ko wchodz\u0105ce w sk\u0142ad szkliwa.&nbsp;<\/li><li><strong>ENO1 &#8211; ( Chr 1:8.86-8.88) &#8211; Alfa-enolaza, enolaza 1 &#8211; enzym zaanga\u017cowany&nbsp;<\/strong>w glikoloz\u0119 ulegaj\u0105cy ekspresji w wi\u0119kszo\u015bci tkanek, jeden z izoenzym\u00f3w enolazy. Jest homodimerem 2 podjednostek alfa. Zwi\u0105zek z Nyc-bibding protein-1 Gen koduj\u0105cy to bia\u0142ko, ENO1, koduje r\u00f3wnie\u017c bia\u0142ko zwane MBP1 (Myc-binding protein-1), odpowiedzialne z down-regulacj\u0119 aktywno\u015bci protoonkogenu c-myc. Alfa-enolaza stanowi d\u0142u\u017csz\u0105 form\u0119, mierz\u0105c\u0105 48 kDa, zlokalizowan\u0105 w cytoplazmie i j\u0105srze, podczas gdy kr\u00f3tsza MBP1 o masie 37 kDa spotykana jest g\u0142\u00f3wnie w j\u0105drze. Znaczenie kliniczne: Alfa-enolaza zidentyfikowana zosta\u0142a jako autoantygenem w encefalopatii Hashimoto. Pojedyncze badania identyfikowa\u0142y tak\u017ce enolaz\u0119b1 jako autoantygen zwi\u0105zany z ci\u0119\u017ck\u0105 astm\u0105 oraz domniemany cel antyendotelialnych przeciwcia\u0142 spitykanych w chorobie Beh\u00e7eta. Redukcja ekspresji enzymu w nab\u0142onku rig\u00f3wki stwierdzona zosta\u0142a u ludzi choruj\u0105cych na sto\u017cej rog\u00f3wki.&nbsp;<\/li><li><strong>EP300 &#8211;&nbsp;<\/strong>chromosome 22 (human)&nbsp;<\/li><li><strong>EPHA2 &#8211; (Chr 1:16.12-16.16) EPH receptor A2 (ephrin type-A receptor 2) is a protein that in humans is encoded by the EPHA2 gene.&nbsp;<\/strong><\/li><li><strong>EPOR &#8211; wytwarza czerowne krwinki z Bible1EL*&nbsp;<\/strong><\/li><li><strong>EPS15 &#8211; Epidermal growth factor receptor substrate 15&nbsp;<\/strong><\/li><li><strong>ErbB-1, also named epidermal growth factor receptor (EGFR)&nbsp;<\/strong><\/li><li><strong>ERBB2 &#8211; # Receptor turosine-protein kinease erbB-2, also known as CD340 2020-11 #&nbsp;<\/strong>kinazy &#8230;<\/li><li>ErbB-3, also named HER3<\/li><li>ErbB-4, also named HER4 &#8211; Receptor tyrosine-protein kinease erbB-4 is an enzyme that in humans is encoded by the ERBB4 gene.&nbsp;<\/li><li><strong>ERG &#8211; (ETS-related gene)&nbsp;<\/strong>is an oncogene. &#8211; devil?&nbsp;<\/li><li><strong>ESPIN &#8211; (Chr 1:6.42-6.46) Espin, also known as autosomal recessive deafness type 36 protein or ectoplasmic specialization protein, is a protein that in himans is encoded by the ESpN gene.&nbsp;<\/strong><\/li><li><strong>ESR1 &#8211; estrogen receptor alpha (ERa), also known as NR3A1&nbsp;<\/strong><\/li><li><strong>ETFDH &#8211; # This shortening of neurotransmiter can be rektorem by riboflavin, carnitine, or Coenzyme q10 suplementa 2021-02# zwi\u0105zany z&nbsp;&nbsp;Coenzyme Q10 &#8211; Elektron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial is an enzyme that in&nbsp;&nbsp;himans is encoded by the ETFDH gene. This&nbsp;<\/strong>gene encodes a component of the electron-transfer system in mitochindria and is essential for electron transfer from a number of mitochindrial flavin-cintaining dehydrogenes to the main respiratory chain.&nbsp;<\/li><li><strong>ETV1 &#8211; gen kodujacy bia\u0142ko<\/strong><\/li><li><strong>EVI5 &#8211; Ecotrolic viral integration site 5 protein homolog &#8230;<\/strong><\/li><li><strong>EXTL1 &#8211; Exostosin-kike 1 is a protein that in humans is encoded by the &#8230; This gene is a member of the multiple exostoses (EXT) family of glycosyltranferases,&nbsp;<\/strong><\/li><li><strong>EXTL2 &#8211; Exostosin-like 2 is a protein that in humans is encoded by the &#8230; siarczan heparanu &#8230;<\/strong><\/li><li><strong>EZH2&nbsp;<\/strong>Enhancer of zeste homolog 2<\/li><li><strong>EZR &#8211; Ezryna (cytowilina, vilin-2; symbile: EZR, CVL i VIL2) &#8211; bia\u0142ko wyst\u0119puj\u0105ce w ludzkim organizmie &#8230;<\/strong><\/li><li><strong>F2 &#8211; Protombina &#8211; jedno z bia\u0142ek osocza ktore bior\u0105 udzia\u0142 w procesie krzepni\u0119cia krwi &#8211; Enel &#8211; Badania gentyczne dla sportowc\u00f3w &#8230;<\/strong><\/li><li><strong>F5 &#8211; Mutacja w genie F5 (mutacja leiden czynnika v). Enel&nbsp;<\/strong><\/li><li><strong>F8<\/strong>&nbsp;&#8211; gene &#8211; # Czynnik VIII, czynnik antyhemofilowy, 2021-01 # Factor VIII (FVIII) is anto -hemophilic factor (AHG) Defects in this gene results in hemophilia A, a recesaive X-linked coagulation disorder. 2021-01 # factor&nbsp;<\/li><li><strong>F9 &#8211; # Czynnik IX (czynnik Christmasa) (EC 3.4.21.22) coagulation factor IX &#8211; Symbil report for F9 Report HGNC data for F9 Approved symbol F9 &#8230; gene with protein product&nbsp;<\/strong><\/li><li><strong>F10 &#8211; Factor X, also known by the eponym pod nazw\u0105 czynnika Stuarta-Power, jest enzymem (EC 3.4.21.6) kaskady krzepni\u0119cia. Jest to endopeptydaza serynowa (grupa proteaz S1, klan PA). Syntetyzowany jest w w\u0105trobie, a do jego syntezy potrzbna jest witamina K.&nbsp;&nbsp;<\/strong><\/li><li><strong>FAAH &#8211;&nbsp;<\/strong># Fatty acid amide hydrolase or FASH&nbsp;<strong>&nbsp;<\/strong>anadamid &#8211; molekula blogosci &#8211; enzym &#8211; matabolizm<\/li><li><strong>FAF2 &#8211;&nbsp;<\/strong>ten gen zwi\u0119ksza ryzyko alkoholowej marskosci watroby&nbsp;<\/li><li><strong>FAH &#8211; Niedob\u00f3r hydrolasy funaryloacetoictanu jest sporowdowany mutacj\u0105 genu FAH (15q23-q25)&nbsp;<\/strong><\/li><li><strong>FAM46B &#8211; protein FAM46B also known as family with sequence similarity 46 member B is a protein that in humans is encoded by the FAM46B gene:&nbsp;<\/strong><\/li><li><strong>FAM46c &#8211;<\/strong>&nbsp;gene of the species macaca namestina<\/li><li><strong>FAM76A &#8211; In Homo saliens, tge FAM76A gene produces 9 differwnt mRNAs, 7 of which are alternatively spliced and 2 of which are unspliced. Of the alternatively spliced mRNAs, isoform 1 is the longest variant of the gene and is the subject of this article.&nbsp;<\/strong><\/li><li><strong>FASH &#8211; anandamid &#8211; molekula blogosci&nbsp;<\/strong><\/li><li><strong>FBN2 &#8211; Zes\u00f3\u0142 Bealsa, przyczyn\u0105 choroby jest mutacja w genie FBN2 na chromosomie 5q23. Choroba ta wymaga r\u00f3\u017cnicowania z zespo\u0142em Narfana; fenotypy tych dw\u00f3ch schorze\u0144 nak\u0142adaj\u0105 sie na siebie &#8230;<\/strong><\/li><li><strong>FBXO2 &#8211; (Chr 1:11.64-11.66) F-box only protein 2&nbsp;<\/strong><\/li><li><strong>FBXW7 &#8211;&nbsp;<\/strong>Translacja bialek&nbsp;<\/li><li><strong>FECH &#8211; ma swijblocus na chromosomie 18&nbsp;<\/strong><\/li><li><strong>FGFR1 &#8211;&nbsp;<\/strong>fibroblast growth factor receptor 1 The protein encoded by this gene is a member of the fibroblast growth factor receptir (FGFR) family&#8230;<\/li><li><strong>FGFR2 &#8211; # Fibroblast growth factor &#8230;. 2020-11 #&nbsp;<\/strong>Fibrobla<strong>FOXA1 &#8211;&nbsp;<\/strong>Forkhear box protein A1 (FOXA1),&nbsp;<\/li><li><strong>FITN2 &#8211; Fat storage-inclueing transmembrane protein 2 is a protein &#8230;.Chromosom 20 jest jednym z najmniejszych ludzkich chromosomow &#8230;.<\/strong><\/li><li><strong>FMR1 &#8211; mutacja w genie FMR1, odkrytym w 1991 i zlokalizowanym na chromosomie X (d\u0142ugie rami\u0119, pozycja 27.3, mi\u0119dzy 147 911 951 a 147 951 125 par\u0105 zasad) Jest to mutacja dynamiczna &#8211; polega na powielaniu segmentu genu o sekwencji trzech nukleotydow CGG. 65-200 powt\u00f3rze\u0144 to tzw. premutacja, najcz\u0119\u015bciej nie daj\u0105ca objaw\u00f3w chorobowych, ale maj\u0105ca tendencj\u0119 do wyd\u0142u\u017cania si\u0119? w kolejnych pokoleniach. ? twarz na &#8230; instagram &#8230;<\/strong><\/li><li><strong>FNBP1L &#8211; Formin-binding protein 1-like is a protein that in humans is encoded by the FNBP1L gene. The protein encoded by this gene binds to both CDC42 and N-WASP.&nbsp;<\/strong><\/li><li><strong>FOSB &#8211; Protein fosB, also known as FosB and G0\/G1 switch regulatory protein 3 (G0S3), is a protein that in humans is encoded by the FBJ murine osteosarcoma viral oncogene homolog B (FOSB) gene. role in addiction ? &#8230;.<\/strong><\/li><li><strong>FOXD1 &#8211; zwi\u0119ksza ryzyko poronienia&nbsp;<\/strong><\/li><li><strong>FOXO3 &#8211; Genetic variation in FOXO3 has been shown to be associated with healthspan and longevitu in himans. It is found in most centenarians carowa a variaty and longevitu in humans.&nbsp;<\/strong><\/li><li><strong>FOXP2 &#8211;&nbsp;<\/strong>expressed inter alia in braun &#8211; gen gramatyki<\/li><li><strong>FPGT &#8211; Fucose -1-phosphate guanylyltransferase is an enzyme that in himans is encoded by the FPGT gene.&nbsp;<\/strong><\/li><li><strong>FRAP # Kinaza mTOR, tzw. ssaczy cel repamycyny 2020-11 # &#8211; korujacy bialko mToR<\/strong><\/li><li><strong>FTO &#8211; # certain alleles of the FTO gene appear to be corelated with obesity of Humans 2020-11 # Fat mass and obesity-associated protein&nbsp;<\/strong><\/li><li><strong>FucM&nbsp;<\/strong>&#8211; FUOM Chromosom 10&nbsp;<\/li><li><strong>FUBP1 &#8211; Far upstream element-binding protein 1 &#8211; is a protein that in humans is encoded by the FUBP1 gene.&nbsp;<\/strong><\/li><li><strong>FUT4 &#8211; Fucosyltransferase 4 (alpha (1,3) fucosyltransferase, myeloid-specific), przy czytaniu o Heroeswirusach (\u0142ac. Herpesviridae, od gr. herpeton &#8211; pe\u0142za\u0107) &#8211; rodzina dsDNA wirus\u00f3w&nbsp;<\/strong><\/li><li><strong>FXN &#8211; Frataxim &#8211; is a protein that in humans is encoded by tve FXN gene &#8211; zwiazany z opisem q10 &#8211; utlenianie (oksydacja) &#8211; reakcja chemiczna, w kt\u00f3rej atom przechodzi z ni\u017cszego stopnia utkeniania na wy\u017cszy, co jest r\u00f3wnoznaczne z oddaniem elektron\u00f3w.&nbsp;<\/strong><\/li><li><strong>FZD1 &#8211; Frizzled-1 is a protein that in humans is encoded by the FZD1 gene&nbsp;<\/strong><\/li><li><strong>FZD2 &#8211; is a protein that in humans is encoded by the FZD2 gene&nbsp;<\/strong><\/li><li><strong>FZD3 &#8211; Friszked-3 is a protein that in humans is encoded by the FZD3 gene<\/strong><\/li><li><strong>FZD4 &#8211; Frizzled-4 is a protein that in humans is encoded by the FZD4 gene &#8211; Chr 11: 86.95-86.96 Mb<\/strong><\/li><li><strong>FZD5 &#8211; Frizzled-5 is a protein that in humans is encoded by the FZD4 gene &#8211; Chr 2:207.76-207.77 Mb<\/strong><\/li><li><strong>FZR1 &#8211; Fizzy-related protein homolog, also known hCDH1, is protein that in humans is encoded by the FZR1 gene<\/strong><\/li><li><strong>G3BP1 &#8211; Ras GTPase-activating protein-binding protein 1 is an enzyme that in humans is encoded by the G3BP1 gene<\/strong><\/li><li><strong>GADD45A &#8211; Growth arrest and DNA-damge-inducible protein&#8230; ncreased following stresfull growth arrest conditions and treatment with DNA-damaging agents (mytagenes)&nbsp;<\/strong><\/li><li><strong>GALE &#8211; UDP-glucose 4-epinerase .. The enzyme UDO-glucose 4-epinerase&nbsp;<\/strong><\/li><li><strong>GAP43 &#8211; paralemmin protein family (akcja PALM gene- palma biurkiem)&nbsp;<\/strong><\/li><li><strong>Gar &#8211; zapewnia odpornosc na antybiotyki aminoglikolzydowe<\/strong><\/li><li><strong>GAPDH &#8211; referencyjny gen ?&nbsp;<\/strong><\/li><li><strong>GAPDHS &#8211; Gluceraldehyde-3-phospohate dehydrogenase, spermatogenic &#8230;. is an ezyme &#8211;&nbsp;<\/strong><\/li><li><strong>GATA3 &#8211;&nbsp;<\/strong>jest czynnikiem transkrypcyjnym, ktory u ludzi jest kodowany przez gen GATA3. Badania na modleadh zwierzecych i ludizach wksasuja, ze kontroluje on ekspresje szerokieho zakresu genow waznych biologivznje i klinicznie.&nbsp;<\/li><li><strong>Gag &#8211;&nbsp;<\/strong>retrotranspozon<strong>&nbsp;<\/strong><\/li><li><strong>GBA &#8211; ?-Glucocerebrosidase &#8230; enzyme Gaucher disease?&nbsp;<\/strong><\/li><li><strong>GBP1 -Guanylane bibding protein expression is included by interferon &#8230;<\/strong><\/li><li><strong>GBP2 &#8211; Function: Interferona are cytokines that have antiviral effects and inhabit tumor cell proliferation.&nbsp;<\/strong><\/li><li><strong>GBP5 &#8211; Guanylate binding protein 5 is a protein in humans that is encoded by the GBp5 gene.&nbsp;<\/strong><\/li><li><strong>GFAP &#8211; Kwa\u015bne bia\u0142ko w\u0142\u00f3kienkowe (GFAP z ang. Glial fibrially acidic protein) &#8211; bia\u0142ko filament\u00f3w po\u015brednich, wyst\u0119puj\u0105ce w kom\u00f3rkach glejowych, m.in. w astrocytach, ale r\u00f3wnie\u017c w innych typach kom\u00f3rek, takich jak kom\u00f3rki Leydiga j\u0105dra &#8230; Chromosom 17 &#8211; jeden z 23 parzystych chromosom\u00f3w cz\u0142owieka. DNA chromosomu 17 liczy ponad 81 milion\u00f3w par nukleotyd\u00f3w,&nbsp;<\/strong><\/li><li><strong>GH1 &#8211; Growth hormone 1 somatropin &#8230;.<\/strong><\/li><li><strong>GJB3 &#8211; This gee si&nbsp;&nbsp;amember of th econnexin gene family.&nbsp;<\/strong><\/li><li><strong>GLMN &#8211; This gene encodes a phosphorylated protein that is a member of a Skp1-Cullin-F-box-like complex.&nbsp;<\/strong><\/li><li><strong>GNL2 &#8211; Nucleolar GTP-binding protein 2 is a protein that in humans is encoded by the GNL2 gene.&nbsp;<\/strong><\/li><li><strong>GNRH1 &#8211; odpowiedzialny za produkcj\u0119 ganadoliberyny, znajduje si\u0119 na chromosomie 8. Ganadoliberyna, luliberyna, GnRH (od ang. gonadotropin-releasing &#8230;<\/strong><\/li><li><strong>Gpr49\/Lgr5 &#8211; Marker genowy dojrzalych komorek macierzystych&nbsp;<\/strong><\/li><li><strong>GRB2 &#8211;&nbsp;<\/strong>in 1992, Joseph Schlessinger, a biochemiest at the Yale Univeristy School of Medicine in New Heven, Connecticut, showed &#8230;.&nbsp;<\/li><li><strong>GRB10 &#8211;&nbsp;<\/strong>Growth factor receptor-bound protein 10 also known as insulin receptor-binding protein Grb-IR is a protein that in himans is encoded by the GRB10 gene.&nbsp;<\/li><li><strong>GRIA1&nbsp;<\/strong>&#8211; wmieszany w naklanianie do poszukiwania narkotyku<\/li><li><strong>GSTM1&nbsp;&nbsp;# Function: Cytosolic and membrane-bound forms of glutathione S-transferase are encoded by two distinct supergene families. The mu class of enzymes functions in the detoxification of electrophilic compunds, including carcinogenes, therapeutic drugs, environmental toxins, &#8211; warianty tego genu moga zmiania\u00e7 nasz\u0105 podatno\u015b\u0107 na tomsyny &#8230; a nawt leki .::<\/strong><\/li><li><strong>H19 &#8211; is a gene for a ling noncodibg RNA,&nbsp;<\/strong>found in humans and elsewhere. H19 has a role in the negative regulation (or limiting) of body weight and cell proliferation. Ma\u0142gorzata Wilkowska &#8211; dietetyczka pisze ze H19 nale\u017cy do gen\u00f3w stanowi\u0105cych oko\u0142o 1% wszystkich, dziedziczone sa wylacznie od ojaca lub matki?&nbsp;<\/li><li><strong>HAO2 &#8211; This gene is one of three related genes that have 2-hydroxyacid oxidase activity.&nbsp;<\/strong><\/li><li><strong>HAUS1 &#8211; HAUS augmin-like complex subunit 1 is a protein that in humans is encoded by the &#8230;.<\/strong><\/li><li><strong>HBA1 &#8211; Hemoglobin, alpha 1 , also known as HBA1, is a hemoglobin protein that in humans is encoded by the HBA1 gene<\/strong><\/li><li><strong>HBB&nbsp;<\/strong>&#8211; ?wykorzystali CRISPER do namierzania i przecinania zmutowanwgo genu kodujacego beta-globone co katqlizowalo zmiane blednej litery A w pozycji 17 &#8230;..zdrowa osoba mila w poz. 17 lieter T a u chorej w tym samym miejscu znajdowala sie litera A 2021-01 # Sickle cell &#8211; film Human Nature 2020-12 # Chromosome 11 Doudna 2020-11 # Anemia sierpiwatokrwinkowa (badanie genu HBB) Genesis Centra Genetyki Medycznej&nbsp;&nbsp;# Beta globin # poslugujac sie metod\u0105 CRISPR\/Cas9, naprawili wadliwy ge HBB, zapobiegaj\u0105c beta-talasemii<\/li><li><strong>HD<\/strong>&nbsp;&#8211; The huntingtin gene, also called the HTT or HD (Huntington disease) gene, is the IT15 &#8230;<\/li><li>HDAC1 &#8211; Histone acetylation and deacetylatoon, catalized by multisubunit complex, play a key role in the regulation of eukaryotic gene expression.&nbsp;<\/li><li>HDAC2 &#8211; Ksiazka: ?Wiecej niz DNA ?&#8230; + Internet copy: Aktualne badania koncentrowa\u0142y si\u0119 na zastosowaniu terapii HDI depresji po badaniach dotycz\u0105cych pacjent\u00f3w z depresj\u0105 w \u015brodku epizodu depresyjnego stwierdzono zwi\u0119kszon\u0105 ekspresj\u0119 HDAC2 i HDAC5&nbsp;<a href=\"https:\/\/pl.qwe.wiki\/wiki\/MRNA\">mRNA<\/a>&nbsp;w por\u00f3wnaniu do grupy kontrolnej i pacjent\u00f3w w remisji.<\/li><li><strong>HDEC2 &#8211;&nbsp;<\/strong>ponadprzecietna wytrzymalosc i odpornosc na brak snu&nbsp;<\/li><li><strong>HERC2 &#8211; (ang. hect domain and RCC1-like domain-containing protein) &#8230; ludzki gen regiluj\u0105cy ekspresje geny OCA2.&nbsp;<\/strong><\/li><li><strong>HES3 &#8211; Hes family bHLH transcription factor 3 is a protein that in himans is encoded by the HES3 gene. Gene ontology &#8230;<\/strong><\/li><li><strong>HEXA &#8211; Hexosaminidase A (alpha polipeptyde), also known as HEXA is an enzyme ..Tay Sachs disease &#8230;. from \u015amiech ma po matce? Zimmera book<\/strong><\/li><li><strong>HEXB &#8211; Beta-hexosaminidase subunit beta &#8230;<\/strong><\/li><li><strong>HDHD2 &#8211;&nbsp;<\/strong>Haloacid dehalogenenaae-like hydrolase domain-containing protein 2 is an enzyme that in humans is encoded by the HDHD2 gene<\/li><li><strong>HES3 &#8211; (Chr 1:6.24-6.25) Hes family bHLH transcription factor 3 is a protein that in humans is encoded by the HES3 gene.&nbsp;<\/strong><\/li><li><strong>HFE &#8211; Human homeostatic iron regulator proteinHMGA1 &#8211; przy poszukiwaniu&nbsp;&nbsp;Sulforobus &#8211; organizmow zyjacych w temperaturach ok 80 stopni C &#8230; High-mobility group protein HMG-I\/HMG-Y is a protein that in humans is encoded by the HMGA1 gene &#8230;<\/strong><\/li><li><strong>HGMA2 &#8211; wykryto pierwszy powszechnej gen wzrostu po raz pierwszy naukowy om uda lo sie zidebtyfikowac jeden z wieku genow powszechnej wplywajaych na wzrost &#8230;.<\/strong><\/li><li><strong>HLA-B &#8211;&nbsp;<\/strong>is part of a family of genes called the human leukocyte antigen (HLA)&nbsp;<\/li><li><strong>HLA-A&nbsp;<\/strong># przy poszukiwaniu ?Ricky &amp;Morty genes &#8211; The HLA-A gene is located on the short atm of chromosome 6 and encodes the larger, ?-chain, constituted of HLA-A. 2021-02 # belongs to the HLA class I heavy chain paraligues.&nbsp;<\/li><li><strong>HLA-DRA &#8211; HLA class II histocompatibility antigen, DR alpha chain is a protein that in humans is encoded HLA-DRA gene.&nbsp;<\/strong><\/li><li><strong>HLA-DRB1 # Podatni\u015b\u00e7 na stwardnienie rozsiane jest silnie uwarunowana czynnikami geetycznymi.. W latach 1972-1975 naukowcy odkryli, \u017ce wariant antygenu leukocytu ludzkiego (HLA-DRB1) zwieksza nawet czyerokrotnej prawdopodobienstwo zachorowania. 2021-01 # &#8211; (2340 citations top 20) major histomopatibitlity &#8211; HLA class II histocompatibility antigen,&nbsp;<\/strong><\/li><li><strong>HLA-E &#8211;&nbsp;<\/strong>znaczenie polimorfizmu HLA-E w odpowiedzi immunologicznej&nbsp;<\/li><li><strong>HMGCL &#8211; The HMGCL protein plays an essential role in breaking down dietary proteins and fats for energy.&nbsp;<\/strong><\/li><li><strong>HP1BP3 &#8211; (Chr 1:20.74-29.79) Heterochromatin protein 1, binding protein 3 is a protein that in humans is encoded by the HO1BP3 gene. It has been identified as a novel subtype of the linker histone H1, involved in the structure of heterochromatin Modem organisms Model organism have been used in the study of HP1bP3 function.&nbsp;<\/strong><\/li><li><strong>HRC &#8211; Sarcoplasmic reticulum histirine-rich calcium-binding protein is a protein that in humans is encoded by the HRC gene. Hard Rock Caffe &#8211; powiazane z haslem hrc w wiki &#8211; sic!&nbsp;<\/strong><\/li><li><strong>HSPA1A &#8211; Heat shock 70 kDa protein 1, also trener Hsp72, is a protein that in humans is encoded by the HSPA1A gene. Effects of sauna anthony on stres-related genes. Heat stresa indycza the expression of genes encoding heat-shock proteins and immune respinse mediators.&nbsp;<\/strong><\/li><li><strong>HTT &#8211;&nbsp;<\/strong># te same trzy litery kodu powtarzaja sie zbyt wiele razy 2020-11 #<strong>&nbsp;Na przyk\u0142ad gen&nbsp;<\/strong><em>HTT&nbsp;&nbsp;<\/em>koduje bia\u0142ko nazwane hutingtyn\u0105, a jego mutacja powoduje chorob\u0119 Hutingtona.&nbsp;<strong>IDH1 &#8211; # badanie wykonywane metoda PCR i sekwencjonownai 2020-10 # metabolizm&nbsp;&nbsp;&#8230; skopiowano &#8211; IT15 &#8211; #&nbsp;<\/strong>Doudna &#8211; zmutowana kopia genu HTT praktycznie gwarantuje poczatek otepienia starczego 2020-1<strong>1 #&nbsp;<\/strong>Huntington Disease&nbsp;&nbsp;(HTT gene)&nbsp;<\/li><li><strong>HTR1A &#8211; The serotonin 1A recwptor (or 5-HT1A receptor) is a subtype of serotonin receptor, or 5-HT receptor, that binds serotonin, also known as 5-HT, a neurotransmiter.&nbsp;<\/strong><\/li><li><strong>HTR1B &#8211; 5-hydroxytryptamine receptor 1B also known as the &#8230;.<\/strong><\/li><li><strong>HTR2A &#8211;&nbsp;<\/strong># receptor serotoninowy 2A &#8211; bia\u0142ko transb\u0142onkowe kodowane u cz\u0142owieka genem HTR2A w chromosomie 13&nbsp;<strong>&nbsp;2021-01# The 5-HT2A receptors is cided by the HTR2A gene.&nbsp;<\/strong><\/li><li><strong>HTR2B &#8211; 5-Hydroxytryptamine receptor 2B (5-HT2B) also known as serotonin receptor 2B is a protein that in humans is encoded by the HTR2B gene.&nbsp;<\/strong><\/li><li><strong>HTR2C &#8211; The 5-HT2C receptor is a subtupe of 5-HT receptor that bibds the endrigenus neurotransmiter seritonin &#8230;.<\/strong><\/li><li><strong>IDH2&nbsp;<\/strong>&#8211; Isocitrate dehydrogenase [NADO], mitochondial is an enzyme that in humans is encoded by the IDH2 gene.&nbsp;<\/li><li><strong>lEPOR-<\/strong>&nbsp;(Chr 19:11.38-11.38 Mb) 2020-10 # wytwarza czerw. krwinki<\/li><li><strong>IL22RA1 &#8211; (Chr 1:24.12-24.14) Interkeukin 22 receptor, alpha 1 is a protein that in humans is encoded&nbsp;&nbsp;by the IL22RA1 gene. Function: The protein encoded by this gene belongs to the class II cytokine receptor family, and has been show&nbsp;&nbsp;to be a receptor for interleukin 22 (IL22).&nbsp;<\/strong><\/li><li><strong>IL-6 &#8211; # Facebook first wpis genes &#8230;. is an interleukin that acts as both a pro-inflammatory cytokine and an anti-inflammatory myokine 2021-01-&nbsp;<\/strong># According Kerpedjiev, the top-10 most-studied genes no 8&nbsp;&nbsp;2020-10 #&nbsp;&nbsp;zlokalizowany jest na chromosomie 7p21&nbsp;<\/li><li><strong>IL2RA &#8211; koduje bia\u0142ko CD25&nbsp;&nbsp;&#8211; chromosom 10 &#8211; w poszukiwaniu Maorys\u00f3w &#8230;.jako link z Netflix?a &#8230;&nbsp;<\/strong><\/li><li><strong>IL7R-Interleukin-7 ..:Interleukiny IL &#8211; grupa cytokines biota a udzialy w prices ach umladung odpornosciowego i krwiitwirczych &#8230;<\/strong><\/li><li><strong>IGF2 &#8211; Insulin-like growth factor 2 (IGF-2) is one of three protein hormones that share structural similarity to insulin. Hongerwinter ?&nbsp;<\/strong><\/li><li><strong>IHH &#8211; Indian hedgehog homolog (Drosophila), also known as IHH, is a protein which in humans is encoded by the IHH gene.&nbsp;<\/strong><\/li><li><strong>INS &#8211; The preproinsulin precursor of insulin is encoded by the INS gene, .::.<\/strong><\/li><li><strong>IRS1 &#8211; Insulin receptor substrate Zakopane wpis instagram Relax &#8230;.<\/strong><\/li><li><strong>JAK2<\/strong>&nbsp;&#8211; This gene product is a protein tyrosine kinease involved in a specific subject of cytosine receptor signaling pathways.<strong>&nbsp;<\/strong><\/li><li><strong>JARID1A &#8211; KDM5A gene<\/strong><\/li><li><strong>KCNA5 &#8211; potasu bramkowane napieciem kanaly &#8230;<\/strong><\/li><li><strong>KCNK18 &#8211; migrena&nbsp;<\/strong><\/li><li><strong>KDR &#8211; Kinase insert domain receptor (KDR, a tupe IV receptor tyrisine kinease) also known as vascular endothelial growth factor receptor 2 (VEGFR-2) is a VEGF receptor. KDR is the himan gene encoding it. Gen kdr pochodz\u0105cy od danio pregowanego koduje receptor vascular endotheliel growth factor-2. Zmiany mutogenne w tym genie zosta\u0142y indukowane przeznnukleazy z mitywem palc\u00f3w cynkowych przez badaczy pochodz\u0105cych z UsA. Zaugerowali oni, \u017ce technologia nukeaz z motywem palc\u00f3w cynkowych umo\u017cliwia utworzenie w prosty sposob lucznych generacji zmutowanych alleli; nie opiera si\u0119 na istniej\u0105cych specyficznych liniach zarodkowych i ma zastosownaie do innych kr\u0119gowc\u00f3w, zw\u0142aszcza tych, kt\u00f3rych zarodki s\u0105 \u0142atwo dost\u0119pne;&nbsp;<\/strong><\/li><li><strong>KEAP1 &#8211; encoded Kelch-like ECH-associated protein 1&nbsp;<\/strong><\/li><li><strong>KDM5C &#8211; Lysine-specific demethylase 5C&nbsp;<\/strong><\/li><li><strong>KIAA0930 &#8211;&nbsp;<\/strong>is a protein that in humans is encoded by the KIAA0930 gene&nbsp;<\/li><li><strong>KIF1B &#8211; (chr 1:10.21-10.38)&nbsp;<\/strong><\/li><li><strong>KITLG &#8211; SCF &#8211; stem cell factor 2020-11 # encodes the ligand of theb tyrosine-kinease encoded byvthe KIT locus.&nbsp;<\/strong><\/li><li><strong>KL<\/strong>&nbsp;&#8211; Klotho &#8211; bialko i enzym opozniajacy starzenie&nbsp;<\/li><li><strong>KLF1 &#8211; Krueppel-like&nbsp;<\/strong><\/li><li><strong>KRAS&nbsp;<\/strong>&#8211; the KRAS gene provides instruction for making a protein called K-Ras that is prat of a signaling pathway known as the RAS\/MAPK patway.<strong>&nbsp;<\/strong><\/li><li><strong>LAMA1 &#8211; Laminin subunit alpha-1 is a protein that in himans is encoded by the LAMA1 gene&nbsp;<\/strong><\/li><li><strong>LAMA2 &#8211; Laminin subunit alpha-2 is a protein that in humans is wncoded by the LAMA2 gene &#8230;Laminin an extracellular matrix protein, is a major component of the bazememnt membrane.&nbsp;<\/strong><\/li><li><strong>LAMC1 &#8211; Laminin subunit gamma-1 is a protein that in humans is encoded by the LAMC1 gene &#8230;<\/strong><\/li><li><strong>LEPR &#8211;&nbsp;<\/strong>tworzy bialko LEP-R bedace receptorem leptyny &#8211; grubasowej<\/li><li><strong>LFNG &#8211; Lunatic Fringle &#8211; unusual &#8230;<\/strong><\/li><li><strong>LGALS1 &#8211; Galectin-1&nbsp;<\/strong>is a protein that in humans is encod<strong>ed by the LGALS1 gene (link my\u015blowy z ?Biochemia Harpera &#8230;)&nbsp;<\/strong><\/li><li><strong>LOC100132287 &#8211; # Identifiers Aliases &#8230; External IDs, Species, Entrez, Ensembl, n\/a &#8211; not applicable &#8211; nie dotyczy 2021-03 # encoded uncharacterized LOC100132287 protein &#8230;.Chromosome 1 is the desigantion for the largest rhuman chromosome.&nbsp;<\/strong><\/li><li><strong>LOC6451166 &#8211; Lymphocyte-specific protein 1 pseudo gene is a protein that in humans is encoded by the &#8230;.<\/strong><\/li><li><strong>LOX &#8211; Kysyl oxidase &#8211; Lizyna niezbedna przy budowie baialek wchlania wapn poprawia koncentarcje umywloswa -2020-11-18 start czytania ?Edycja genow? Doudna J. 06:05<\/strong><\/li><li><strong>LPHN3 &#8211; gen koduj\u0105cy latrofilin\u0119 3 (LPHN3) jest zaangazowany w rozwij zespolu napodbudliwosci psychoruchowej z deficytem uwagi (ADHD)&nbsp;<\/strong><\/li><li><strong>LRIF1 &#8211; Ligand-dependent nuclear receptor-interacting factor 1&nbsp;<\/strong><\/li><li><strong>LRP5 -# u czesci osob majacy mutacje jest taka gestosc ze wrecz uniemizliwia zlama ie 2020-10 -15 #&nbsp;&nbsp;<\/strong>mutacja genu reguluje gestosc mineralna kosci<strong>&nbsp;<\/strong><\/li><li><strong>LRP8 &#8211; odgrywa istotn\u0105 role w metabolizmie ?z\u0142ego? cholesterolu LDL&#8230;.<\/strong><\/li><li><strong>LRRK2 &#8211; # W 2004 r. dr Zimprich wras z zespolem odkryl inny, dominujacy gen o nazwie LRRk2, ktory odpowiada za ?sporadyczna? forme choroby Parkinsona 2020-10-08 #&nbsp;&nbsp;ten gen koduje enzym kineazy &#8211; bogaty&nbsp;<\/strong>w leucyn\u0119 powtarzalna kinaza 2, znana rowniz jako dardain i PARK8<strong>&nbsp;&#8211; # pucie kawy zmniejsza ryzyko choroby Parkinsona mawet u isib genetycznie predysponowanych 2020-10 # substancja aminokwasowa w tym enzymie zwiazana jest z rozwojem choroby Parkinsona&nbsp;<\/strong><\/li><li><strong>LYPLAL1 gene &#8211; Lysophospholipase-like 1 is a protein &#8230;.<\/strong><\/li><li><strong>MAOA- # Anerykanscy naukowcy odkryli gen odpowiadajacy za szczescie #&nbsp;<\/strong>gen wojowniczosci &#8211; koduje izoenzym oksydaze<strong>&nbsp;<\/strong>&#8211; odpowiada za rozklad neuroprzekaznikow&#8230; dopaminy seritoniny tyraminy adrenaliny<strong>&nbsp;<\/strong><\/li><li><strong>MAP2K1 &#8211;&nbsp;<\/strong>The protein encoded by this gene is a member of the dual specificity protein kinease family, which acts as a mitigen-activated protein (MAP) kinease:&nbsp;<\/li><li><strong>MAP2K4<\/strong>&nbsp;&#8211; Dual-specificity mitogen-activated protein kinease kinease 4&nbsp;<\/li><li><strong>MAP3K1<\/strong>&nbsp;&#8211; Mitogen-activated protein kinease kinease kinease 1&nbsp;<\/li><li><strong>MAPK1 &#8211;&nbsp;<\/strong>Mitogrn-activated protein kinease 1, also known as MAPK1, p42MAPK, and ERK2, is an enzyme that in humans is encoded by the MAPK1 gene<\/li><li><strong>MaPKAPK2 &#8211; MAP kinease-activated protein kinase 2 is an enzyme &#8230;<\/strong><\/li><li><strong>MARCHF1&nbsp;<\/strong>&#8211; gen ktorego nazwe zmieniono gdyz w excelu zmienial nazwe na ?1-mar?<\/li><li><strong>MC1R &#8211; # Naukowcy zidentyfikowli gen m\u0142odo\u015bci Odnalezienie sposobu na zachowanie m\u0142odo\u015bci jest od wiek\u00f3w po\u017c\u0105dane przez cz\u0142owieka. Niekt\u00f3re analizy przemawiaj\u0105 za tum ze wiek cz\u0142owieka oceniany na podstaiwe jego wygl\u0105du mo\u017ce odzwierciedlac og\u00f3lne zdrowie, a nawet ryzyko \u015bmierci. 2021-03&nbsp;&nbsp;# melanokortyna &#8211; rude 2020-12 #&nbsp;<\/strong>mutacja tego genu mo\u017ce mie\u0107 zwi\u0105zek z tym, \u017ce osoby posiadaj\u0105ce rudy kolor w\u0142os\u00f3w mog\u0105 wygl\u0105da\u0107 statystycznie o 2 lata m\u0142odziej ni\u017c w rzeczywisto\u015bci. Naukowcy potwierdzaj\u0105, \u017ce pierwsza cz\u0119\u015b\u0107 kodu DNA zdaje si\u0119 mie\u0107 wp\u0142yw na to, w jaki sposob ludzie sie starzej\u0105. (melanokortyna-1 receptor wp\u0142ywaj\u0105cy na produkcj\u0119 melaniny &#8230;<\/li><li><strong>MC3R &#8211; Melanocortin receptor 3 is a protein that in himans is encoded by the MC3R gene<\/strong><\/li><li><strong>MC4R &#8211; Melanocortin 4 receptor is a melanocortin receptor #&nbsp;<\/strong>MC4R<strong>&nbsp;&#8211;&nbsp;<\/strong>wytwarza hormon syto\u015bci<\/li><li><strong>MC1R<\/strong>&nbsp;&#8211; melanokortyna &#8211; rude<strong>&nbsp;<\/strong><\/li><li><strong>MCAT &#8211; chromosome 22 &#8211; Malontyl CoA-acryl<\/strong><\/li><li><strong>MCl1 &#8211; regulacja apaptozy&nbsp;<\/strong><\/li><li><strong>MCPH1 &#8211; zespil chinskich badaczy dodak do genomu embrionow malp ludzkich wariant tego genu &#8230; gen bierze udizal w rozwoju mozgu&nbsp;<\/strong><\/li><li><strong>MDM2 &#8211;&nbsp;<\/strong>Mouse double minute 2 homolog (MD2M) also known as E3 ubiquitin-protein&nbsp;<\/li><li><strong>MED12&nbsp;&nbsp;&#8211; Mediator of RNA &#8211; X chromosome&nbsp;<\/strong><\/li><li><strong>MEFV &#8211; Mediterranean fever is a human gene that provides instruction for making a protein called pyrin&nbsp;<\/strong><\/li><li><strong>MEG3 &#8211; (maternally expressed 3) is a maternally expressed, inprinted long non-coding RNA gene. IG-DMR?&nbsp;<\/strong><\/li><li><strong>MET<\/strong>&nbsp;&#8211; tyrosine kinease<strong>&nbsp;<\/strong><\/li><li><strong>MFAP2 &#8211; (Chr 1:16.97-16.98) Microfibrillar-associated protein 2&nbsp;<\/strong><\/li><li><strong>MFN2 &#8211; (Chr 1:11.98-12.01) &#8211; Mitofusin-2&nbsp;<\/strong><\/li><li><strong>MFNG &#8211; Beta-1,3-N-acetylglucosaminyltransferase manic fringle is .::.<\/strong><\/li><li><strong>MIB2 &#8211; (Chr 1:1.62-1.63) first ?&nbsp;&nbsp;<\/strong><\/li><li><strong>MITF &#8211; # box jellyfish &#8230; essential for creating melanin 2921-03 # Microphthalmia-associated transcription factor&nbsp;<\/strong><\/li><li><strong>MMEL1 &#8211; (Chr 1:2.59-2.63) second genes ? in HGP&nbsp;<\/strong><\/li><li><strong>MLH<\/strong>1 &#8211; # MLH1 (hMLH1, MutL homolog 1) &#8211; ludzki &#8230; 2020-11 # located on chromosome 3. #&nbsp;<strong>MLH1 &#8211; gen ten oraz jemu podobne ma kluczowe znaczenie dla zdolosci p53 do zapobiegania rozwojowi r. &#8230;<\/strong><\/li><li><strong>MLH2 &#8211;&nbsp;<\/strong><\/li><li><strong>MLL &#8211;&nbsp;<\/strong>Metykotrqnsferasy histon\u00f3w chromatyny<strong>&nbsp;<\/strong><\/li><li><strong>MLL2<\/strong>&nbsp;&#8211; KMT2D<\/li><li><strong>MML3<\/strong>&nbsp;&#8211; KMT2C gene<strong>&nbsp;<\/strong><\/li><li><strong>MMAA &#8211; Rey &#8230; egzamin Methylmalonic acidura tupe A protein, mitochondrial also known as MMAA is a protein &#8230;.Ontogeneza rozwij od pocz\u0119cia do \u015bmierci &#8230;.<\/strong><\/li><li><strong>MSH<\/strong>&nbsp;&#8211; Integralno\u015b\u0107 genomu<strong>&nbsp;<\/strong><\/li><li><strong>MSH2 &#8211; jeden z 6 genow zwi\u0105zanych z zespo\u0142em Lyncha &#8230; szuka\u0142em genu zwi\u0105zanego ze szczeka Habsburska &#8230;.<\/strong><\/li><li><strong>MSTN &#8211; koduje&nbsp;&nbsp;bia\u0142ko odpowiedzilane w organizmie za ograniczenie rozwoju miesni ? przy wylaczonym tym genie miesnie zaczynaja przyrastac szybciej &#8230;<\/strong><\/li><li><strong>MTFR1L &#8211;&nbsp;<\/strong>Chr 1:25.82-25.83)&nbsp;<\/li><li><strong>MTHFR &#8211; # mutacje genow kodujacych MTHFR powodujace niedob\u00f3r kwasu lewomefiowego zostaly powiazane z predyspozycjami m.in. do chroby niedokrwiennej serca kwas foliowy pelni istotna role w syntezie DNA &#8230;.<\/strong>&#8211; (Chr 1:11.79-11.81) Reduktaza metylenotetrahydrofolianu (ang. methylenettrahydrofolate reductase, MTHFR) &#8211; enzym (EC 1.5.1.20) katalizuj\u0105cy reakcj\u0119 redukcji 5,10-metylenotetrahydrifolianu do 5-metylotetrahudrofolianu 2020-10 # wariant C677T\/A12986c &#8211; badanie waruantu C677T&#8230; genu &#8230; zalecane jest dla kobiet w ciasy kwas foliowy ..:<\/li><li><strong>MTOR &#8211; The mechanistic target of rap amy in (mTOR), biotechnologia.pl &#8211; ?Nowi odkryte biala kotwicz?ce kompleksowa TSC&#8230;.<\/strong><\/li><li><strong>MTR&nbsp;<\/strong>&#8211; # Methionine synthase, coded bt MTR gene is a methyltransferase enzyme which uses the MeB12 and rection tyle 2 to transfer a methyl group from 5-methyltetrahydrifolate to homocysteine &#8230; Witamina B12 produkowana jest g\u0142\u00f3wnie przez bakterie \u017cyj\u0105ce w uk\u0142adzie pokarmowym zwierz\u0105t. U cz\u0142owieka powstaje w symbiozie z bakteriami uk\u0142adu pokarmowego. 2020-11 # Metylotransferaza homocysteinowa (5-methyltetrahydrofolate-homocysteine methyltransferase, MTR, EC 2.1.1.13) to enzym katalizuj\u0105cy ko\u0144cowy etap biosyntezy metiininy.&nbsp;<\/li><li><strong>MTRR &#8211; # to enzym katalizuj\u0105cy reakcj\u0119 metylacji kofaktora enzymu syntazy metionowej, kt\u00f3rym jest kobalamina. Donorem grupy metylowej jest S-adenozylometionina (SAM) 2020-11 # Redukacja syntezy metioninowej (ang. methionine synthase reductase, EC 1.16.1.8) to enzym katalizuj\u0105cy reakcj\u0119 metylacji kofaktora enzymu &#8230;.&nbsp;<\/strong><\/li><li><strong>MUL1 &#8211; (Chr 1 20.5-20.51)&nbsp;<\/strong><\/li><li><strong>MUTYH &#8211; (E. coli MutY homolog) &#8211;&nbsp;<\/strong>gen koduj\u0105cy glikozylaz\u0119 DNA zaanga\u017cowan\u0105 w proces naprawy uszkodze\u0144 oksydacyjnych DNA. Ten tup naprawy okre\u015bla si\u0119 jako naprawe przez wycinanie zasady. Bia\u0142ko MUTH lokalizuje sie w j\u0105drze kom\u00f3rkowym i mitochondriach. Gen MUTYH znajduje sie w licus 1p34.3-31.1.<\/li><li><strong>MYC &#8211;&nbsp;<\/strong>inne czynniki transkrypcyjne&nbsp;<\/li><li><strong>MYD88<\/strong>&nbsp;&#8211; Sygnalizacja NF-kB<\/li><li><strong>MYH7 &#8211; jeden z genow koduj\u0105cych bia\u0142ka buduj\u0105ce serce&nbsp;<\/strong><\/li><li><strong>NBEAL2 &#8211;&nbsp;<\/strong>jest dysfunkcyjnym w zespole szarych p\u0142ytyek&nbsp;<\/li><li>NBPF3 &#8211; (chr 1:21.43-21.49)&nbsp;<\/li><li>NCK1 &#8211; Cytoplasmic protein NCK1 is a protein that in humans is encoded by the NCK1 gene. (Dock means dreadlocks-ortholog)&nbsp;<\/li><li><strong>NELFB<\/strong>&nbsp;&#8211; Cofactor of BRCA1 also known as COBRA1, is a human gene that encodes NELF-B&nbsp;<\/li><li>NF1 &#8211; NF1 jest du\u017cym genem, zawieraj\u0105cym ponad 350 kpz i 60 ekson\u00f3w. DNA genu NF1 podlega tjankowo zr\u00f3\u017cnicowanej alternatywnej transkrypcji. 2020-12# Sygnalizacja kinaz aktywowanych mitogenami (MAPK signalizing) (geny supresorowe) 2020-08-26 # uzalezniene alkoholowe<strong>&nbsp;<\/strong><\/li><li><strong>NFE2L2- Nuclear factor erythroid&nbsp;<\/strong><\/li><li><strong>NFKBIA &#8211; gene provides instruction fir making one piece (the alpha subunit) of the IKK protein complex&#8230;<\/strong><\/li><li><strong>NIPBL &#8211; oko\u0142o po\u0142owa przypadk\u00f3w zespo\u0142u Cornelli de Lange (CdLS1) jest spowodowana mutacj\u0105 w po\u0142o\u017conym na chromosomie 5 genie NIPBL, kt\u00f3ry koduje bia\u0142ko wchodz\u0105ce w sk\u0142ad kohezyny &#8211; kompleksu \u0142\u0105cz\u0105cego siostrzane chromatydy podczas mitozy.<\/strong><\/li><li><strong>NKX21 &#8211; # NKX2-1 &#8211; this gene encodes a protein initially identified as a thyroid-specific transcription factor. 2020-10 # homebox protein<\/strong><\/li><li><strong>NKX3.1 &#8211;&nbsp;<\/strong>Homebox protein Nkx-3.1<\/li><li><strong>NOD2 &#8211; (nucleotide-bibding oligomerization domain containing 2) znane tak\u017ce jako caspase receuitment domain family, member 15 (CARD15)) &#8211; bia\u0142ko odgrywaj\u0105ce role w regulacjibuk\u0142adu odporno\u015bciowego.&nbsp;<\/strong><\/li><li><strong>NOL9 (Chr 1:6.52-6.65) &#8211; Nucleolar protein 9&nbsp;<\/strong><\/li><li><strong>NOTCH1<\/strong>&nbsp;&#8211; Sygnalizacja Notch<\/li><li>NOTCH2 &#8211; Notch Receptor 2&nbsp;<\/li><li>NOTH3 &#8211; bia\u0142ko receptorowe odgrywa ono rol\u0119 w utrzymaniu i rozwoju kom?rek mi\u0119\u015bni g\u0142adkich. U cz\u0142owieka locus genu NOTCh3&nbsp;<\/li><li><strong>NPC1 &#8211; Niemann-Pick disease, type C1 (NPC1) is a disease of a membrane protein that mediates intercellilar cholesterol trafficking in mammals. Chromosom 18 &#8211; jeden z 23 parzystych chromosom\u00f3w cz\u0142owieka. DNA chromosomu 18 liczy oko\u0142o 76 milion\u00f3w par nukleotyd\u00f3w,&nbsp;<\/strong><\/li><li><strong>NRAS &#8211;&nbsp;<\/strong>The NRAS gene provides instruction for making a protein called N-Ras that is involved primary in regulation cell dicision.&nbsp;<\/li><li><strong>NSD1&nbsp;<\/strong>Sotos syndrome<\/li><li><strong>NSD3<\/strong>&nbsp;WHSC1L1 gene<strong>&nbsp;<\/strong><\/li><li><strong>NR3CI &#8211;&nbsp;<\/strong>koduje receptor glukokortykoidowy wychwytujacy hormon stresu (kortyzol)&nbsp;<\/li><li><strong>OCA1 &#8211; ten gen znajduje sie pomiedzy pasemkiem czwartrym a pasmie pierwszyma pasemkiem pierwszym w pasmie drugim, na dlugin ranieniu chromosomu jedenastego&nbsp;<\/strong><\/li><li><strong>OCA2 # Kozmik found the jellyfish version of human gene called Oca2 (ang. oculocutaneous albinism II) ludzki gen w locus 15q11.2-q12&nbsp;&nbsp;odpowiedzialny za dostawe substrat\u00f3w do tyrozynazy w biosyntezie melatoniny. Ma silny wp\u0142yw na kolor oczu. Jego ekspresj\u0119 reguluje gen HERC2.&nbsp;<\/strong><\/li><li><strong>OLFR151&nbsp;<\/strong>&#8211; gen kodujacy powstawanie receptorow OLFR151<\/li><li><strong>OPN3 &#8211; Opsin-3 also known as encephalopsin or panopsin is a protein that, in humans, is encoded by the OPN3 gene. Przy poszukiwaniu Netthusaleh-like proteins are a family of G protein-coupled receptors found in insects that play a role in aging and reproduction.&nbsp;<\/strong><\/li><li><strong>OPN4 &#8211;&nbsp;<\/strong>koduje \u015bwiat\u0142oczu\u0142y pigment obecny w fotoreceptorach&nbsp;<\/li><li><strong>OR10G9 &#8211; Olfactory receptor 10G9 is a protein that in humans is encoded by the OR10G9 gene. Olfactory receptors interact with odprant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell.&nbsp;<\/strong><\/li><li><strong>OTC<\/strong>&nbsp;&#8211; # Hiperamonemia &#8211; zaburzenie metaboliczne charakteryzuj\u0105ce sie zwi\u0119kszonym ponad dopuszczalny poziom st\u0119\u017ceniem amoniaku w surowicy krwi. 2021-01 # Ornithine &#8230;enzyme &#8230; Gelsinger Jesse ?&nbsp;<\/li><li><strong>P21 &#8211; # Cyin-dependent kinease inhibitor 1, &#8230; P21 is a cell cycke inhibitor &#8230;. 2020-11 # to pojedynczy gen, kt\u00f3ry mo\u017ce odgrywa\u0107 g\u0142\u00f3wn\u0105 role w procesie starzejia sie&nbsp;<\/strong><\/li><li><strong>P53 &#8211; Bia\u0142ko p53 &#8211; czynnik transkrypcyjny o w\u0142a\u015bciwo\u015bciach supresora nowotworowego. Bia\u0142ko p53 jest zaanga\u017cowane w regulacj\u0119 wielu proces\u00f3w kom\u00f3rkowych, a w szczeg\u00f3lno\u015bci aktywacji naprawy DNA lub indukcji apoptozy w odpowiedzi na uszkodzenia DNA.&nbsp;<\/strong><\/li><li><strong>PALM &#8211; Paralemmin is protein that in humans is encided by the PALM gene. Chromosom 19 &#8211; jeden z 23 parzystych chromosom\u00f3w cz\u0142owieka. DNA chromosomu 19 liczy ponad 63 miliony par nukleotyd\u00f3w, co stanowi oko\u0142o 2-5% materia\u0142u genetycznego ludzkiej kom\u00f3rki.&nbsp;<\/strong><\/li><li><strong>PARK7 &#8211; (Chr 1:7.95 -7.99) Protein deglycase &#8230;<\/strong><\/li><li><strong>PAX3 &#8211; The PAX3 (paired box gene 3) gene encodes a member of the paired box or PAX family of transcription factors. The PAX family consists of nin\u0119 human (PAX1-PAX9) and nin\u0119 mouse (Pax1-Pax9) member arranged into four subfamilies.&nbsp;<\/strong><\/li><li><strong>PBRM1 &#8211;&nbsp;<\/strong>Protein polybromo-<\/li><li><strong>PCK1 &#8211; from index Harper? Biochemistry PEPCK This&nbsp;<\/strong>enzyme is a main control point fir the regulation of gluconeogenesis&nbsp;<\/li><li><strong>PCSK9&nbsp;<\/strong>&#8211; #PCSK9 has a medical importance because it acts in lipoprotein homeostasis&nbsp;&nbsp;?DNA The story of the Genetic Revolution? James D. Watson 2021-03&nbsp;&nbsp;# delecja tego genu zmnisza pozion chilestrolu LDL020-10-13 # chrom. 1 &#8211; Cholesterol<\/li><li><strong>PDG-FRA &#8211;&nbsp;<\/strong>surafce<strong>&nbsp;<\/strong><\/li><li><strong>PDSS2 &#8211; u ludzi posiadajacych mutacje tego genu komorki slabiej radza sobie z rozkladem kofeiny&nbsp;<\/strong><\/li><li><strong>PER3 &#8211;&nbsp;<\/strong>protein Period3 &#8211; wczesbe zasypianeie&nbsp;<\/li><li><strong>PICALM &#8211; certain alleles of this gene have been &#8230; Alzheimer?s&nbsp;<\/strong><\/li><li><strong>PIK3CA &#8211;&nbsp;<\/strong>Sygnalizacja PI3K<\/li><li>P<strong>IK3R1 &#8211;&nbsp;<\/strong>Phosophoinositide?3-Kinease Regulatory Submit 1. A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e. the hunan chromosomes 1-22) in which a trait manifests in heterozygotes.<\/li><li>PINK1 &#8211; (Chr 1:20.63-20.65)PTRN-induced kinease 1 is a mitochondrial serine\/threonine-protein kinease encoded by the PINK1 gene<\/li><li>PBFOX1 &#8211; nizsze ilosci RBFOX1 w mizgu wydaja sie byc zwuazane ze zwiejszonym amyloidem i globalnym spadkiem funkcjibpiznawvzych w ciaguvzycia<\/li><li>PHKA2 &#8211; Phosphorylase b kinase regulatory subunit alpha, liver isiform is an enzyme that in humans is wncoded by the PHKA2 gene. Bioinformatyka &#8211; Python &#8211; interdyscyplinarna dIedzina \u0142\u0105cz\u0105ca nauki biologiczne i informatyczne.&nbsp;<\/li><li>PHOX2B &#8211; ludzki gen zlokalizowany na chromosomie 4 w locus 4p12. homeotyczny gen &#8211; scilicet kontroluja rozwoj morfogiczny poszczegolnych czesci ciala w poczatkowych stadiach rozwoju zarodkowego &#8230;<\/li><li>PLPP3 &#8211; Fosfohydrolaza fosforanowo-lipidowa 3 &#8211; Instagram 5C_DNA &#8211; pierwszy gen &#8211; link z ?komputer DNA?&nbsp;<\/li><li>PMP22 &#8211; Bia\u0142ko stanowi\u0105ce sk\u0142adnik mieliny zbitej, stanowi\u0105cej 2-5% wszystkich bia\u0142ek mieliny.&nbsp;<\/li><li>PR11-267C16.1 &#8211; Uncharacterized LOC100287225 is a protein that in humans is encoded by the RP11-267C16.1 gene.<\/li><li><strong>PRDX1<\/strong>&nbsp;&#8211; Peroxiredoxin-1 &#8211; is a protein that in humans is encoded by the PRDX1 gene. This gene encodes a member of the peroxiredoxin family of antooxidqnt enzymes, which reduce hydrogen peroxide and alkyl hudroperoxides.&nbsp;<\/li><li><strong>PRDX2<\/strong>&nbsp;&#8211; Peroxiredoxin-2 is a protein that in humans is encoded by the &#8230;. gene&nbsp;<\/li><li>PRNP &#8211; odkrycie geny PRanP u czlowieka i naligicznych genow (Prn-p) u wiekszosci zwierzat wyzszych przyniosko wniosek ze kodowane przez ten gen bialko jest niezbeden w funkcjinownaiu niepoznanych jeszcze fizjologicznych procesow u tych organizmow.&nbsp;<\/li><li>PRPF4 &#8211; U4\/U2 small nuclear ribonucleoprotein Prp4 is protein that in humans is encided by tve PRPF4 gene<\/li><li><strong>PRPF40B<\/strong>&nbsp;&#8211; Pre-mRNA-processing factor 40 homolog B is a protein that in humans that is encoded by the PRPF40B gene<\/li><li>PTCH1 &#8211; Protein patched homolog 1 is a proteinnthat is the member of the patched family and in humans is encoded by the PTCH1 gene &#8230;&nbsp;<a href=\"http:\/\/en.wikipedia.org\/\">en.wikipedia.org<\/a>&nbsp;List of unusual biological names ?Patched?&nbsp;<\/li><li>P<strong>TEN- # (ang. phosphatase and tensin homolog deleted on chromosome ten, MMAC1 &#8230; 2020-11 # # ta sama grupa naukowcow w 1997 roku prowadzona przez dr Michaela Wingleta zidentyfikowali jeden z innych genow supresorowych 2020-10 po# (and. phosphate and tensin #&nbsp;<\/strong>Stgnalizacja PI3K (geny supresorowe)&nbsp;<\/li><li><strong>PTGS1 &#8211; COX-1 &#8211; Cyclooxygenase 1&nbsp;&nbsp;VOLTREN Diclofenacum diethylammonium &#8230;. Diklofenak&nbsp;<\/strong><\/li><li><strong>PTGS2 &#8211; Prostagladin-endoperoxide synthase 2 (prostaglandyn G\/H synthase and cyclooxygenase) (The HUGO official symbol is PTGS2; HGNC ID, HGNC:9605), also known as cyclooxygenase-2 or COX-2, is an enzyme that in humans encoded by the PTGS2 gene.&nbsp;<\/strong><\/li><li><strong>RAC1 &#8211; ras-related C3 botulinum toxin substrate 1&nbsp;<\/strong><\/li><li><strong>RAC2 &#8211;&nbsp;<\/strong>ras-related C3 botulinum toxin substrate 2&nbsp;<\/li><li><strong>RAD51 # is a eukaryotic gene 2021-01 # &#8211; gen bed\u0105cy homologiem prokariotycznego genu RecA. 2020-12 # &#8211; &#8230;Podobne strukturalne bia\u0142ka zosta\u0142y zgrupowane w rodzinie bia\u0142e RAd51, zaanga\u017cowanych w mechanizm naprawy DNA<\/strong><\/li><li><strong>RAG1 &#8211; z Filmu Netflix &#8211; Eli &#8211; Recombinatiin acrivating gene 1 also known as RAG-1 is a protein that in humans is encoded by the RAG1 gene. The RAG1 and RAG2 genes are largely conserved in humans. 55.99 % and 55.98% of the encoded &#8230; immun esystem &#8230;<\/strong><\/li><li><strong>RAG2 &#8211; Recombination activating gene 2 protein (also known as RAG-2) is a lymphocyte-specific protein&nbsp;<\/strong><\/li><li><strong>RAS &#8211;&nbsp;<\/strong>A family of genes that make proteins involved in cell signaling pathways that control cell growth and cell death.&nbsp;<\/li><li><strong>RASGRP1 &#8211; dyenina jest bialkiwm motorycznym, ktorego zadanie polega na transportowaniu organelii wewnatrz komorek<\/strong><\/li><li><strong>RELN &#8211; Reelina (relina) &#8211; bia\u0142ko<\/strong>&nbsp;wyst\u0119puj\u0105ce g\u0142wnie w m\u00f3zgu&#8230; w m\u00f3zgu doros\u0142ym moduluje plastyczno\u015b\u00e7 synaptyczn\u0105 poprzez indukcj\u0119 i utrzymanie d\u0142gotrwa\u0142ego wzmocnienia synaptycznego.&nbsp;<\/li><li><strong>RB1 # (pRb, Rb) &#8211; bia\u0142ko kodowane przez gen supresorowy RB1.&nbsp;<\/strong># Antyonkogen, inaczej gen supresorowy &#8211; gen dzia\u0142ajacy hamujaco na procesy proluferacji kom?rkoweh 2020-10 #&nbsp;<strong>&#8211; gen&nbsp;<\/strong>suoresorowy &#8211; dzialajacy jak strzelec wyborowy &#8211; wykrywa zdradliwa konorke i zabija<\/li><li><strong>RBBp8 &#8211; koduje bia\u0142ko CtIP&nbsp;<\/strong><\/li><li><strong>RBFOX1 &#8211;&nbsp;<\/strong>Fox-1 homolog A, also known as ataxin 2-binding protein 1 &#8230;<\/li><li><strong>RCC2 (Chr 1:17.41 -17.44) &#8211; Protein RCC2 also known as telophase disk &#8230;<\/strong><\/li><li><strong>RECQL &#8211; ATP-dependent DNA helicase Q1 is an enzyme &#8230;.<\/strong><\/li><li><strong>RET &#8211; (<\/strong>Multiple Endocrine Neoplasia And Medullary Tyroid Carcinoma1, Hirschsprung Disease)&nbsp;<\/li><li><strong>RFNG &#8211; Beta-1,3-N- list of unusual&nbsp;<\/strong><\/li><li><strong>RHD &#8211; Rh blood group, D antigen also known as Rh polypeptide 1 (RhPI) or cluster of different ikm 240D (CD240D) is a protein that in humans is encoded by the RHD gene.&nbsp;<\/strong><\/li><li><strong>RHCE &#8211; Blood group Rh(CE) polypeptide is a protein that in humans is encoded by the RHCE gene.&nbsp;<\/strong><\/li><li><strong>RHAG &#8211; Rh-associated glycoproteins (RHAG) is an ammonia transporter protein that in humans is encoded by the RHAG gene.&nbsp;<\/strong><\/li><li><strong>RHBG &#8211; Rh family, B glycoproteins, also known as RHBG, is an ammonia transporter protein which in humans is encoded&nbsp;<\/strong><\/li><li><strong>RHCG &#8211; Rh family, C glycoproteins, also known as RHCG, is a protein that in humans is encoded &#8230;<\/strong><\/li><li><strong>RPE65 &#8211;&nbsp;<\/strong>Leber congenial amaurosis<\/li><li>ROBO1 &#8211; Roundabout homolog 1 &#8211;&nbsp;<\/li><li>ROBO2- Roundabout homolog 2&nbsp;<\/li><li><strong>RPE65 &#8211; Film Unnatural Selection (TV series) Unnatural Slection October 2019 r. Joe Egender &#8211; (chr 1: 68.43-68.35) Retinal pigment epithelium-specific 65 kDa protein, also known as retinold isomerohydrolase, is an enzyme of the vertebrate visual&nbsp;<\/strong><\/li><li><strong>RPS4X &#8211; 40S ribosomel protein S4, X isoform is a protein that in humans is encoded by the RPS4X gene.&nbsp;<\/strong><\/li><li><strong>RPS4Y1 # na chromosomie Y &#8230; from father to son? 2021-03#&nbsp;&nbsp;&#8211; 40S ribosimal protein S4, Y isoform 1 is a protein that in humans is encoded by the ROS4Y1 gene<\/strong><\/li><li><strong>RPS4Y2 &#8211; Ribosomal protein S4, Y-linked 2 also known as RPS4Y2 is a protein which in humans is encoded by the RPS4Y2 gene which resudes on the Y chromosome&#8230;<\/strong><\/li><li><strong>RS4702 &#8211;&nbsp;<\/strong>umo\u017cliwia koronawirusowi szybk\u0105 replikacj\u0119<\/li><li><strong>RUNX1<\/strong>&nbsp;&#8211; Runt-related transcription factor 1 also known as acute myeloid leukemia 1 protein or core-binding factor subundit alpha-2 is a protein that in humans is encoded by the&nbsp;&nbsp;RUNX1 gene.<\/li><li>RUNX3 &#8211; (Chr 1:24.9 &#8211; 24.97 &#8230; Runt-related transcription factor 3 is a protein that in humans is encoded by the RUNX3 gene.&nbsp;<\/li><li>SCN9A &#8211; odpowiada za czesciowa lub calkowita redukcje odczuwania bolu &#8230;&nbsp;<\/li><li>SCT &#8211; Secretin is a hormine that regulates water homeostasis throughout the body and influences the environment of the duodeum byvregulating secretions in the stomach, pancreas, and luver.&nbsp;<\/li><li>SDHB &#8211; (Chr 1:17.02-17.05) &#8211; Succinate dehydrogenase &#8230;<\/li><li>SEMA3A &#8211; Semaphorin-3A&nbsp;<\/li><li>SEMA3E &#8211; semaphorin 3E&nbsp;<\/li><li><strong>SEPT3<\/strong>&nbsp;&#8211; Neuronal-specific swptin-3 is a protein that in humans is encoded by the SEPT3 gene<\/li><li><strong>SEPT-5&nbsp;<\/strong>&#8211; is a protein that in humans is encoded by the SEPT5 gene.&nbsp;<\/li><li>SERPINA1 &#8211; Alfa1-antytrypsyna (alfa1-antytrypsyna, A1AT) &#8211; bia\u0142ko osocza krwi (frakcji alaf1-globulin), b\u0119d\u0105ce jednym z najsilniejszych kr\u0105\u017c\u0105cych inhibitor\u00f3w proteaz serynowych (serpin).&nbsp;<\/li><li><strong>SERPINA3 &#8211; Alpha 1-antichymotrypsin is an alpha globulin glycoprotein that is a number of the serpin superfamily.<\/strong><\/li><li><strong>SERPINC1 &#8211; Antithrombin &#8211; is a small protein mecule &#8211; HGNC &#8230; Osrodek Nowoczesnej Diagnostyki &#8230; Krakowski Szpital &#8230; Jana Pawla Ii&nbsp;<\/strong><\/li><li><strong>SF3A1<\/strong>&nbsp;&#8211; Splicing factor 3 submit 1 is a protein that in himans is encoded by the SF3A1 gene.&nbsp;<\/li><li>SF3B1 &#8211; Splicing factor 3B subunit 1 is a protein that in humans is encoded by the SF3B1 gene.&nbsp;<\/li><li><strong>SFRS7<\/strong>&nbsp;&#8211; Serine\/arginine-rich splicing factor 7 (SRSF7) also known as splicing factor, arginine\/serine-rich 7 (SFRS7) or splicing factor 9G8 &#8230;<\/li><li><strong>SH2D3C &#8211; SH2 domain containing 3C ..:<\/strong><\/li><li><strong>SHBG # Sex hormone-binding globulin (SHBG) or sex steroid-binding globulin(SSBG) is a glycoprotein that binds to androgensband wstrogens Androgeny &#8211; hormony p\u0142ciowe &#8230; 2021-03 # &#8211; st\u0119\u017cenie SHBG jest obni\u017cone m.in. w zespole policystycznych jajnik\u00f3w.&nbsp;<\/strong><\/li><li><strong>SHC1 &#8211; SHC-tranforming protein 1 &#8230;.<\/strong><\/li><li><strong>SHH &#8211;&nbsp;<\/strong>Homolog sonic hedghog &#8211; jedno z trzech bia\u0142ek z rodziny HH wyst\u0119puj\u0105ce w genach kr\u0119gowc\u00f3w. Nazwa tego bia\u0142ka pochodzi od bohatera gier komupterowych i wideo firmy Sega, niebieskiego je\u017ca Sonica&nbsp;<\/li><li><strong>SHOX2 &#8211; im wyzsza jego ekspresja tym girsze rokowania gleiaka<\/strong><\/li><li><strong>SIRT1 &#8211; # A 2015 GWAS study in Han Chinese women positively identified two varianta region near SIRT and LHOO with a genome-wide significant assiciatoon. 2020-11# encoded protein Sirtun 1, also onown as NAD-dependent deacetylase sirtuin-1&nbsp;<\/strong><\/li><li><strong>SIRT6 &#8211; Sirtuin 6 (SIRT6 or Sirt6) os a stresa responsove protein deacetylase and mono-ADL&nbsp;<\/strong><\/li><li><strong>SLC13A5 &#8211; Indy gene &#8211; Solute carrier family 13 (sodium-dependent citrate transporter), member 5 also known as the Na+\/citrate cotransporter or mlndy is a protein that in humans is encoded by the SKC13A5 gene.&nbsp;<\/strong><\/li><li><strong>SLC24A5 &#8211; # Wykryto dwie odmiany r\u00f3\u017cni\u0105ce si\u0119 jedn\u0105 zasad\u0105, jedna wersja wyst\u0119puje u Europejczyk\u00f3w, a deuga jest typowa dla czarnosk\u00f3rych mieszkanscow Afeyki 2020-12 #,Danio &#8211; gen czesciowo odpowiedzialny za kolor sk\u00f3ry czlowieka (w pietnastym chromosomie)&nbsp;<\/strong><\/li><li><strong>SLC2A2 &#8211; Glucose transporter 2 (GLUT2) also known as solute carrier family 2&nbsp;<\/strong><\/li><li><strong>SLC39A1 &#8211; Zinc transporter ZIP1 is a protein that in humans is encoded by the SLC39A1 gene. The protein ZIP1 is responsible for the active transport of zinc into prostate cells. In many prostate cancers SLC39A1 is silienced causing prostate cancer cells to be low in zinc.&nbsp;<\/strong><\/li><li><strong>SLC50A1 &#8211; Sugar transporter SWEET1&nbsp;<\/strong><\/li><li><strong>SLC6A3 &#8211; # second gene in Instagram 2021-01# dat1? the dopamine transporter ia a membrane-spanning protein &#8230;<\/strong><\/li><li><strong>SLC6A4<\/strong>&nbsp;&#8211; # &#8230;&nbsp;&nbsp;<strong>&#8230;.5-HTTLPR (ang. seritonin-transporter-linked polymorphic region) &#8211; obszar polimorficzny zlokalizowany w obr\u0119bie genu SKC6A4 koduj\u0105cego transporter serotoniny.&nbsp;<\/strong>The serotonin transporter (SERT or 5-HTT) also known as the sodium-dependent &#8230; 2021-01#&nbsp;&nbsp;gen koduj\u0105cy transporter seritonint&nbsp;<\/li><li><strong>SLC6A8 &#8211; bia\u0142ko kodowane przez ten gen jest bia\u0142kiem b\u0142ony kom\u00f3rkowej, kreatyny &#8230; kreatyna wplywa na zdolnosc tegeneracji naszyhc wlokien miesniowych oraz gojenie sie ran.&nbsp;<\/strong><\/li><li><strong>SLC6A20<\/strong>&nbsp;&#8211; chromosom 3 &#8211; artyku\u0142 TVP info o korelacji genow w zwiazku z podatniscia oraz przebiegiem COViD 19<\/li><li><strong>SMCP<\/strong>&nbsp;&#8211; Sperm mitochondrial-associated cysteine-rich protein is a protein that in humans is encoded by the SmCP gene.<\/li><li>SMO &#8211; Smoothend is a protein in humans is encoded by the SMO gene.&nbsp;<\/li><li>SOD1 &#8211; Superoxide dismutase [Cu-Zn] also known as superoxide dismutase 1 or SOF1 is an enzyme that in humans is encoded by the SOD1 gene, located on chromosome 21. apoptosis &#8230;<\/li><li>SORL1 &#8211; bia\u0142ko transportowe SORL1 &#8211; siedmioosobowa rodzina austriacka leczona przez wiele lat w Klinice Neurologii Szpitala Ogolnego w Linzu&nbsp;<\/li><li>SOX9 &#8211; Transcription factor SOX-9 is a protein that in humans is encoded by the SOX9 gene<\/li><li>SOX10 &#8211; Transcription factor SOX-10 &#8211; Chr 22:37.97<\/li><li>SL<strong>C6A4 &#8211;&nbsp;<\/strong>gen<strong>&nbsp;<\/strong>encoded protein seritonina&nbsp;<\/li><li>SLIT2 &#8211; Slit homolog 2 protein&nbsp;<\/li><li><strong>SMAD2<\/strong>&nbsp;&#8211; Stgnalizacja TGF-? (geny supresorowe)&nbsp;<\/li><li><strong>SMAD4 &#8211;<\/strong>&nbsp;This gene encodes a member of the Smad family of signal transduction proteins.&nbsp;<\/li><li><strong>SMARCA1 &#8211; Kompleks SWI\/SNF<\/strong><\/li><li><strong>SMARCA4 &#8211; # ludzki gen&nbsp;<\/strong>kodujacy bialko AtPazy SMARCA4. Gen SMARCA4 znajduje sie w kocus 19p13.3 2020-10 # Transcripcion activator BRG1&nbsp;<\/li><li><strong>SMG7<\/strong>&nbsp;&#8211; Protein SMG7 is a protein that in humans is encoded by tge SMG7 gene.&nbsp;<\/li><li>SMN1 &#8211; is a telomeric copy of the gene encoding SMN protein &#8230;spinal musczn antropy<\/li><li>SMN2 &#8211; bia\u0142ko SMN jest produkowane nie tylko przez SMN1, lecz tak\u017ce przez drugi, bli\u017aniaczo podobny gen &#8211; SMN2. Od liczby kopii SMN2 zale\u017cy nasilenie objaw\u00f3w klinicznych SMA. W rdzeniowym zaniku mi\u0119\u015bni, spowodowanym delecj\u0105 SMN1, gen SMN2 jest jedynym \u017ar\u00f3d\u0142em bia\u0142ka SMN (inspiracja Netflix)&nbsp;<\/li><li>SMYD3 &#8211; lysine &#8211; jej niedob\u00f3r skutkuje objawami zm\u0119czenia i rozdraznienia, powoduje anemie &#8230;<\/li><li>SOX-2 &#8211; czynniki transkrypcyjne<\/li><li><strong>SPG23 &#8211; Spastic paraplegia 23 (SPG autosomal recessive)?is a 25cM gene locus at 1q24-q32. HSP heredity spastic paralegia &#8230;<\/strong><\/li><li><strong>SPOP # Speckle-type POZ protein 2021-02 # &#8211;&nbsp;<\/strong>Translation\/protein homeostatis\/ubiquitition<\/li><li><strong>SPRED1 &#8211; Sprouty-related, &#8230; has seven coding exons &#8230;<\/strong><\/li><li><strong>SPRR1A &#8211; Cornifin-A is a protein that in humans is encoded by the SPRar1A gene. W poszukiwaniu najkr\u00f3tszego genu (Chr 1:152.99-152.99 Mb<\/strong><\/li><li><strong>SPRR1B &#8211; Cornifin-B is a protein that in humans is encoded by the SPRT1B gene (Chr 1: 153.03 -153.03 Mb&nbsp;<\/strong><\/li><li><strong>SPRR2A &#8211; Small proline-ruch protein 2A&nbsp;<\/strong><\/li><li><strong>SPRR2B &#8211; brak opisu w wikipedii &#8230; Small proline-rich protein 2B Homo sapiens (Human) Cross-linked envelope protein of keratinocytes.&nbsp;<\/strong><\/li><li><strong>SPRR2C &#8211; Small proline-rich protein 2C, pseudogene<\/strong><\/li><li><strong>SPRY (Chr 1:9.29-9.37) SPRY domain-containing SOCS box protein 1 is a protein that in humans is encoded by the &#8230;<\/strong><\/li><li><strong>SFRS2 &#8211;&nbsp;<\/strong>Splicing factor, arginine\/serine-rich 2&nbsp;<\/li><li><strong>SLITRK6&nbsp;<\/strong>&#8211; homosexuality &#8211; ekspresja tego genu w miedzynizgowiu<\/li><li><strong>SMAD2 &#8211;&nbsp;<\/strong>Matki przeciw decplentaetic&nbsp;<\/li><li><strong>SMAD4<\/strong>&#8211; Serine\/arginine-rich splicing factor 1<\/li><li><strong>SFRS2 &#8211;&nbsp;<\/strong>Splicing factor, arginine\/serinne-rich 2 is a protein that in himans is encoded by the SFRS2 gene<\/li><li><strong>SPRTN &#8211; Spartan (SPRTN) is a protein that in humans is encoded by the SPRTN gene. It is involved in DNA repair.&nbsp;<\/strong><\/li><li><strong>STK11 &#8211;&nbsp;<\/strong>Serine\/threonine kinease 11 (STK11) also known as liver kinease B1 (LKB1) or reneal carcioma antigen NY-REN-19 is a protein kinease that in humans is encoded by the STK11 gene.&nbsp;<\/li><li><strong>SRY&nbsp;<\/strong>&#8211;&nbsp;&nbsp;# gen SRY &#8211; gen znajduj\u0105cy si\u0119 na chromosomie Y, koduj\u0105cy bia\u0142ko czynnik determinuj\u0105cy rozw\u00f3j j\u0105dra (TDF, ang. test\u00f3w-determinuje factor ), inicjuj\u0105cy p\u0142e\u0107 m\u0119sk\u0105. W 1992 r. MKOL wprowadzil krzepisz who ktorego sportiest z genen STY nie moge starogard jako kobiety 2021-01 #&nbsp;&nbsp;&nbsp;(ang. sex-determininh regionY), 2020-10 # SRY &#8211; determine maleness responsible &#8230; # male sex &#8211; w chromosomie Y zawierajacym 58 milionow par zasad (58mbp) i zawiera 78 genow &#8211; 0 38 calkowitej zawaetosci DNA<\/li><li><strong>STK11 &#8211; Serine\/threonine kinease 11 (STK11) ludzki antyonkogen w locus 19p13.3, koduj\u0105cy bia\u0142ko kinazy treoninowo-serynowej (EC 2.7.11.1) .<\/strong><\/li><li><strong>TAAR1 gene &#8211; Trace amine-associated receptor 1 (TAAR1) is a trac\u0119 anime-associated receptor protein&nbsp;<\/strong><\/li><li><strong>TARBP1 &#8211; Probable methyltransferase TARBP1 &#8211; is an enzyme that in humans is encoded by the TARBP1 gene.&nbsp;<\/strong><\/li><li><strong>TAS1R3 &#8211; Taste receptor tupe 1 member 3&nbsp;<\/strong><\/li><li><strong>TAS2R38 # (Chr 7 : 141.97-141.97 Mb) 2020-10&nbsp;&nbsp;<\/strong>&#8211; # propylotiouracyl 2020-10-09 # odpowiedzialny za recepcje smaku gorzkiego<\/li><li><strong>TBCE &#8211; Tubulin-specific chaperone E is a protein . The TBCE gene is either deleted or mutated in Sanjad-Sakati Stndrome &#8230;<\/strong><\/li><li><strong>TERT&nbsp;<\/strong>&#8211; Proces starzenia si\u0119 powinien zosta\u00e7 uznany za chorob\u0119. art. SPider?sWeb 2020-09-28 # Telomere stability 2020-09?21 #&nbsp;<strong>&#8211;&nbsp;<\/strong>BioViva &#8211; dluzsze telimery Elizabeth Parish &#8211; terapia abty age&nbsp;<\/li><li><strong>TET2 &#8211; Tet&nbsp;<\/strong>methylocytosine dixygenase 2&nbsp;<\/li><li><strong>TG &#8211; koduj\u0105cy tyreoglobulin\u0119<\/strong><\/li><li><strong>TGFBI # Odkryto zwi\u0105zek mi\u0119dzy oty\u0142o\u015bci\u0105 a infekcjami sk\u00f3ry &#8230; biotechnologia.pl &#8230; School of Pharnaceutical Science na Ximen University &#8230; opublikowano w ?Science Translational Medicine? ujawniaj\u0105 mwchanizmy \u0142\u0105cz\u0105ce oty\u0142o\u015b\u0107 i infekcje sk\u00f3ry &#8230;?Oty\u0142o\u015b\u0107 wi\u0105\u017ce si\u0119 ze zwi\u0119szonym ryzykiem infekcji sk\u00f3ry, ale nie jest jasne, w jaki sposob os\u0142abia nasz uk\u0142ad odporno\u015bciowy.&nbsp;&nbsp;Odkryli\u015bmy, \u017ce kiedy myszy s\u0105 karmione diet\u0105 wysokot\u0142uszczow\u0105 i staj\u0105 si\u0119&nbsp;&nbsp;oty\u0142e, adipocyty sk\u00f3ry ulegaj\u0105 powi\u0119kszeniu i trac\u0105 zdolno\u015b\u00e7 do walki z inwazj\u0105 bakterii podczas infekcji sk\u00f3ry &#8211; wyja\u015bnia dr Ling-juan Zang ze School of Pharmaceutical Science na Ximen University. Jak si\u0119 okaza\u0142o zwi\u0119kszona liczba dojrza\u0142ych&nbsp;<\/strong>adipocyt\u00f3w (kom\u00f3rek t\u0142uszczowych) zwi\u0119ksza sygnalizacj\u0119 TGF?, co z kolei zmniejsza liczb\u0119 kom\u00f4rek progenitorowych adipocyt\u00f3w sk\u00f3ry, kt\u00f3re wytwarzaj\u0105 peptyd przeciwdrobnoustrojowy zwany katelicydyn\u0105. Jego brak sprawia \u017ce nask\u00f3rek jest podatny na infekcje Staphylococcus aureus&#8230;&nbsp;<strong>&#8230;? &#8211; Transfforming growth factor, beta-inducted, 68kDa, also known as TGFBI,&nbsp;<\/strong><\/li><li><strong>TGFBR2<\/strong>&nbsp;&#8211; transforming growth factor beta receptor 2&nbsp;<\/li><li><strong>THBS3 &#8211; Thrombospondin-3 (TSP3) is a protein that in humans is encoded by the THBS3 gene.&nbsp;<\/strong><\/li><li><strong>TJP1 &#8211; ZO-1 &#8211; szczep Escherichia coli Nissle 1917 reguluje ekspresj\u0119 genu ZO-1, co skutkuje stabilizacj\u0105 po\u0142\u0105cze\u0144 \u015bcis\u0142ych mi\u0119dzy enterocytami i zwi\u0119ksza szczekno\u015b\u00e7 bariery jelitowej.&nbsp;<\/strong><\/li><li><strong>TLR1 &#8211; is a member of the troll-like receptor family&nbsp;<\/strong><\/li><li><strong>TLR9 &#8211; Toll-like receptor 9 is a protein that in humans is encoded by the &#8230; prebiotyki, probiotyki, farmabiotyki &#8211; ekspresja genow &#8230;Nau<\/strong>kowcy analizowali te\u017c alterantywn\u0105 strategi\u0119 wzmocnienia odpowiedzi odporno\u015bciowej, mianowicie oddzia\u0142ywanie z receptorami troll-like (TLR), uczestnicz\u0105cymi we wrodzonej odpowiedzi odporno\u015bciowej. Uda\u0142o si\u0119 z powodzeniem zmodyfikowa\u00e7 genetycznie adenowirus onkologiczny w taki spos\u00f3b, aby stymulowa\u0142 receptor TLR9 na kom\u00f3rkach dendrytycznych i wywo\u0142ywa\u0142 aktywacj\u0119 limfocyt\u00f3w T. Bardziej dalekosi\u0119\u017cnym celem b\u0119dzie wytworzenie metodami in\u017cynierii genetycznej ?superwirusa? do leczenia chor\u00f3b nowotworowych.&nbsp;<\/li><li><strong>TMEM63A &#8211; Transmembrane protein 63A is a protein that in himans is encoded by the TMEM63A gene. The matur\u0119 human protein is approxumaly 92.1 kilodaltons<\/strong><\/li><li><strong>TMEM81 &#8211; Transmembrane Protein 81 or TamEM81 is a protein that in humans is encoded by the TMEM81 gene.&nbsp;<\/strong><\/li><li><strong>TMEM201 &#8211; ( Chr 1.9) is a protein transmemebrane protein 201&nbsp;<\/strong><\/li><li><strong>TMEM9 &#8211; Transmembrane protein 9 is a proyein thta in humans is encoded by the TMEM9 gene&nbsp;<\/strong><\/li><li><strong>TMORRSS2&nbsp;<\/strong>&#8211; gen kodyjact enzym potrzbny wirusowi do zkazania &#8211; COVID-19&nbsp;<\/li><li><strong>TNFSF18 &#8211; Tumor necrosis factor ligand superfamily member 18 is a protein that in humans is encoded by the TNFS18 gene<\/strong><\/li><li><strong>TNF &#8211; (6) &#8211; zostal&nbsp;<\/strong>sklonowany w 1985 r. cytokina&nbsp;<\/li><li><strong>TNN &#8211; tenscin N &#8211; brak opisu na wikipedii 2021-02 &#8230;charakterization of a nobel member of the tenscin family that meditates neurotransmiter repulsion from hippocampal explants &#8230;.&nbsp;<\/strong><\/li><li><strong>TNNT2 &#8211; Cardiac muscle troponin T (cTnT) is a protein that in humans is encoded by the TNNT2 gene<\/strong><\/li><li><strong>TOR1A &#8211;&nbsp;<\/strong>ludzkie bia\u0142ko dodowane przez gen TOR1A (DYT1) w locus 9q34. Bia\u0142ko to nale\u017cy do rodziny ATapas zwi\u0105zanych z r\u00f3\u017cnymi aktywno\u015bciami kom\u00f3rkowymi (ATPases Associated with diverse cellural Activities),&nbsp;<\/li><li><strong>TOR1AIP<\/strong>&nbsp;&#8211; Torsin-1A-interacting protein 1 is a protein that in humans is encoded by the TOR1AIP1 gene. It?s deletion from mouse hepatocytes lends to defected very-low density lipoprotein secretion and causes non-alcoholic fatty liver disease &#8230;<\/li><li><strong>TP53 &#8211; koduje bialko p53 TRPC2 &#8211;&nbsp;<\/strong>wspiera rozpoznawanie feromonow # bialko &#8211; p53 &#8211; # Genome integrity 2020-09-21 # Guardian of the genome&nbsp;<\/li><li><strong>TO53BP2<\/strong>&nbsp;&#8211; Apoptosis-stimulating of p53 protein 2 (ASPP2) also known as Bcl2a1-binding&nbsp;<\/li><li><strong>TPA &#8211; koduj\u0105cy tkanowy aktywator plazminogenu #&nbsp;&nbsp;<\/strong>TPA &#8211; Tkankowy aktywator plazminogenu (ang. tissue plasminogen activator, PLAT, tPA) ..<\/li><li><strong>TRE-CTC1-5 &#8211; is a protein that in humans is encoded by the TRE-CTC1-5 gene&nbsp;<\/strong><\/li><li><strong>TRP &#8211;&nbsp;&nbsp;( 1q31) &#8211; trp operin &#8230;<\/strong><\/li><li><strong>TSC1 # Hamaratynw &#8211; bia\u0142ko cz\u0142owieka kodowane przez gen TSac1 w locus 9q34. 2020-11#-&nbsp;<\/strong>Sygnalizacja mTOR (geny supresorowe)&nbsp;<\/li><li><strong>TSC2 &#8211; TSC2 cz\u0142owieka odpowiada genowi Tsc2 u zwierz\u0105t 2020-12 #&nbsp;<\/strong>Tuberous Sclerosis Complex 2 (TSC2), also known as Tuberin, is a pritein&nbsp;<\/li><li>TSHZ3 &#8211; pojedynczy gen decyduje o wrodzonej umiej\u0119tno\u015bci oddychania i sprawia ze dziecko robi pierwszy wdech &#8230;<\/li><li>TTN -2- # Titin is a giant protein, greater than 1 ?m in length, (mikrometr 1 milionowa metra) Tytyna (konektyna) &#8211; d\u0142ugie, w\u0142\u00f4kniste bia\u0142ko mi\u0119\u015bni poprzecznie pr\u0105\u017ckowanych u kr\u0119gowc\u00f3w, \u0142\u0105czy filiametry # TTN &#8211; Titin also known as connectin, is a protein a giant protein &#8230;2020-11&nbsp; &nbsp;&nbsp;# TTN (najd\u0142u\u017csza sekwencja koduj\u0105ca w ludzkim organizmoe piczaca poand 240 kilopar zasad, gen koduj\u0105cy bia\u0142ko tytun\u0119) 2020-10 # gen kodujacy Tytyne &#8211; bialko 3 najczesciej wystepujace<\/li><li><strong>TYR &#8211; # mutacje genu TYR prowadz\u0105 do niedoboru tyronazy i powoduja albinizm typu I, schorzenie genetyczne zwi\u0105zane z blad\u0105 sk\u00f3r\u0105 pozbawion\u0105 pigmentacji i czerwonym zabarwieniem oczu 2021-03 social media 2021-03 #Tyrozynaza &#8211; produkowanie melaniny In humans the tyrosinase enzyme is encoded by the TYR gene 21-03#&nbsp;&nbsp;powsta\u0142y przesz\u0142o p\u00f3\u0142 miliarda lat temu, jest szeroko rozpowszechniony w\u015br\u00f3d zwierz\u0105t, ro\u015blin&nbsp;&nbsp;i grzyb\u00f3w. Umo\u017cliwia wytwarzanie bia\u0142ka zwanego tyrozyn\u0105, bior\u0105cego udzia\u0142 w syntezie melatoniny, waznego barwnika.. U ludzi mutacje genu TYR prowadz\u0105 do niedoboru tyronazyny i powoduj\u0105 albinizm typu I, schorzenie genetyczne zwi\u0105zane z zaburzeniami widzenia&nbsp;<\/strong><\/li><li><strong>U2AF1 &#8211; Sp<\/strong>licing factor U2AF 35 kDa subunit is a protein that in humans is encoded by the U2AF1 gene<\/li><li>U2<strong>AF2 &#8211;&nbsp;<\/strong>Splicing factor U2AF 65 kDa subunit&nbsp;<\/li><li><strong>UAP1 &#8211; UDP-N-ascetylhexosamine pyrophosphorylase is an enzyme that in humans is encoded by the UAP1 gene&nbsp;<\/strong><\/li><li><strong>UBC &#8211; encoded a protein Polyubiquitin-c&nbsp;<\/strong><\/li><li><strong>UBE3A &#8211; is gene therapy ready to treat some forms of autism? Allyson Berent UTX &#8211; Demetylazy histon?w chromatyny&nbsp;<\/strong><\/li><li><strong>UBR4 &#8211; (Chr 1: 19) E3 ubiqutin-protein ligase enzyme&nbsp;<\/strong><\/li><li><strong>USF1 &#8211; This gene encodes a member of the basic helix-loop-helix leucine zipper family and can &#8230;.<\/strong><\/li><li><strong>USH2A &#8211; Usherin is a protein that in himans is encoded by the USH2A gene. Laminina &#8211; bia\u0142ko &#8230; sk\u0142adnik b\u0142ony podstawowej &#8230;.&nbsp;<\/strong><\/li><li><strong>USP48 &#8211; (Chr 1:21 ) &#8211; encoded enzyme Ubiqutin carboxyl &#8230;<\/strong><\/li><li><strong>UTX &#8211; chromosom 10 utx to istotny komponent systemu kontroli transjrypcji<\/strong><\/li><li><strong>UTY &#8211; Histone demethylase UTY is &#8230;&nbsp;<\/strong><\/li><li><strong>V1aR&nbsp;&nbsp;&#8211;&nbsp;<\/strong># je\u015bli gen produkuje du\u017ce ilo\u015bci wazopresyny &#8211; nornini g\u00f3rskie zmieni\u0142y sie z \u0142ajdakow w czu\u0142ych partneriw 2021-01#&nbsp;<strong>wplywa na produkcje hormonu wiernosci wazooresyny<\/strong><\/li><li><strong>VDR &#8211; wp\u0142yw polimorfizmi\u00f3w genu VDR n aoty\u0142o\u015b\u0107, zmiany metaboliczne, zaburzenia masy kostnej &#8230;<\/strong><\/li><li><strong>VEGFA &#8211;&nbsp;<\/strong>czynnik wzrostu \u015br\u00f3db\u0142onka naczyniowego,&nbsp;<\/li><li><strong>VEGF &#8211; Czynnik wzrostu \u015br\u00f3db\u0142onka naczyniowego, VEGF (z ang. vascular endothelial growth factor) &#8211; czynnik wzrostu bior\u0105cy udzia\u0142 w tworzeniu sieci naczy\u0144 krwiono\u015bnych zaarodka oraz w angiogenezie.&nbsp;<\/strong><\/li><li><strong>VHL &#8211; # bia\u0142ko VHL, pVHL &#8211; znajdujacy si\u0119 na chromosomie 3. 2020-11 # Bia\u0142ko von Hipa-Lindaua,&nbsp;<\/strong><\/li><li><strong>VPS13D &#8211; ( Chr 1.12)&nbsp;<\/strong><\/li><li><strong>Vacar protein sorting-assiciated protein 13D is a protei&nbsp;&nbsp;that in humans is encoded by the &#8230;&nbsp;<\/strong><\/li><li><strong>VPS35 &#8211; gen ten ma wplyw na chorobe Parkinsona Amarican Jurnal of Human Genetics<\/strong><\/li><li><strong>VPS45 &#8211; Vesicles mediated protein sorting plays &#8230;.<\/strong><\/li><li><strong>VPS72 &#8211; Vacular protein sorting&nbsp;<\/strong><\/li><li><strong>VWF &#8211; Czynnik von Willebranda, VWF (z ang. von Willebrand factor) &#8211; niezb\u0119dny sk\u0142adnik krwi bior\u0105cy udzia\u0142 w&nbsp;<br>procesie jej krzepni\u0119cia, du\u017ca glikoproteina zbudowana z kilku podjednostek kodowanych przez gen po\u0142o\u017cony na chromosomie 12.&nbsp;<\/strong><\/li><li><strong>Wrap53 &#8211; wytwarza moleku\u0142\u0119 ?antysens RNA?, ktora jest potrzbnea do produkcji bialka p53<\/strong><\/li><li><strong>WWP1 &#8211;&nbsp;<\/strong>WW-domain containg proteins are founds in all eukariontes&nbsp;<\/li><li><strong>ZRSR2 &#8211;&nbsp;<\/strong>U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa &#8230;<\/li><li><strong>XBP1 &#8211; X-box binding protein 1&nbsp;<\/strong><\/li><li><strong>Xq28<\/strong>&nbsp;&#8211; sexual orientation &#8211; pederastian<\/li><li><strong>YY1AP1 &#8211; YY1-associated protein 1&nbsp;<\/strong><\/li><li><strong>ZBED6 &#8211; Zinc finger, BED-type containing 6 is a protein that in himans is encoded by the ZBED6 gene<\/strong><\/li><li><strong>Zbtb7 &#8211; Pokemon &#8211; zinc finger stranger name &#8230;.<\/strong><\/li><li><strong>ZC3H11A &#8211; Zinc finger CCCH domain-containing protein 11A is a protein that in humans is encoded by the ZC3H11A gene<\/strong><\/li><li><strong>ZFHX3 &#8211; Zinc finger homebox protein 3 is a protein that in humans is encoded by the ZFHX3 gene.&nbsp;<\/strong><\/li><li><strong>ZFY &#8211;&nbsp;<\/strong># This gene encodes a zinc finger-containing protein &#8230;.2021-01 #&nbsp;<strong>Zinc finger Y-chromosomal protein is a protein that in humans is encoded by the ZFY gene of the Chromosome Y&nbsp;<\/strong><\/li><li><strong>ZNF157 &#8211; Chr X &#8211; This gene product is a likely zinc finger family transcription factor.&nbsp;<\/strong><\/li><li><strong>ZNF236 &#8211; Zinc finger protein 236 is a protein that in humans is encoded by the ZNF236<\/strong><\/li><li><strong>ZNF341<\/strong>&nbsp;&#8211; zinc finger protein 341&nbsp;<\/li><li>ZNF436 &#8211; ( Chr 1: 23.26 &#8211; 23.37 ) Zinc finger protein 436 is a protein that in humans is encoded by the ZNF436 gene.&nbsp;&nbsp;&nbsp;#&nbsp;&nbsp; &nbsp; &nbsp;<\/li><li>ZNF521 &#8211; Zinc finger protein 521 is a protein that in humans is encoded by the ZNF521 gene. Gene with protein product&nbsp;&nbsp;HGNC: 24605&nbsp;<\/li><li>ZNF532 &#8211; Zinc finger protein 532 is a protein that in humans is encoded by the ZNF532 gene.&nbsp;<\/li><li>ZNF544 &#8211; zinc finger protein 544 Homo sapiens<\/li><li>ZNF648 &#8211; Zinc finger protein 648 is a protein that in humans is encoded by the ZNF648 gene.&nbsp;<\/li><li>ZNF687 &#8211; Zinc finger protein 687 is a zinc finger protein ..\/ palec cynkowy, motyw palca cynkowego (ang. zinc finger domain) &#8211; rodzaj domeny bia\u0142kowej wyst\u0119puj\u0105cej w bia\u0142kach wi\u0105\u017c\u0105cych DNA&nbsp;<\/li><li>ZNF695 &#8211; Zinc finger protein 695 is a protein that in humans is encoded by the ZNF695 gene. Entrez&nbsp;&nbsp;57116&nbsp;<\/li><li>ZZNF880 &#8211; Zinc finger protein 880 os a protein that in humans is encoded by the ZNF880 gene<\/li><li>ZYX &#8211; # Focal adhesions are actin-rich structures that enable cells to adhere to the extracellular matrix and at which protein complexes involved in signal transduction assemble. 2020-12 # Zyxin is a protein that in himans is encoded by ZYX gene<\/li><li>XRCC6 &#8211; Ku70 os a protein that, in humans, is encoded by the XRCC6 gene &#8211; chromosome 22<\/li><li><\/li><\/ol>\n\n\n\n<ol class=\"wp-block-list\"><li>aaaa<\/li><li>aaaa<\/li><\/ol>\n\n\n\n<ol class=\"wp-block-list\"><li><\/li><\/ol>\n\n\n\n<p class=\"wp-block-paragraph\">#&nbsp;<\/p>\n\n\n\n<ol class=\"wp-block-list\"><li>..<\/li><li><strong>MECP2- X<\/strong>&nbsp;chromosome<\/li><li><\/li><\/ol>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>SRY-&nbsp;<\/strong>gene determine maleness<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>SRY-&nbsp;<\/strong>gene determine maleness<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">SV40 &#8211; simian virus<strong>&nbsp;<\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>MICE:&nbsp;<\/strong><strong>Gt(ROSA)26Sor &#8211; This gene produces a long non-coding RNA(incRNS) that is under the control of a constitutibe prompter. -3-ci naczesciej ciattions<\/strong><strong>&nbsp;&nbsp;<\/strong>Wys\u0142ane z iPhone&#8217;a<\/p>\n","protected":false},"excerpt":{"rendered":"<div class=\"mh-excerpt\"><p>DNA$ &#8230;..Kirkegard\u00a0\u00a035. genes list:&nbsp; 2700099C18RiK&nbsp;-* NDC80 homolog, kinetochore complex component paeudogene is a protein that in humans is encoded by the 270009C18Rik gene # pseudogene? 2700099C18Rik &#8211; na cromosomie 17 kt\u00f3ry jest jedn\u0105 z 23 par chromosomie u ludzi. Pseudogen &#8211; fragment kwasu deoksyrybonukleinowego, <a class=\"mh-excerpt-more\" href=\"https:\/\/www.szulc-euphenics.com\/?p=10\" title=\"Lista Gen\u00f3w :\">[&#8230;]<\/a><\/p>\n<\/div>","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-10","post","type-post","status-publish","format-standard","category-bez-kategorii"],"_links":{"self":[{"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=\/wp\/v2\/posts\/10","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=10"}],"version-history":[{"count":3,"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=\/wp\/v2\/posts\/10\/revisions"}],"predecessor-version":[{"id":18,"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=\/wp\/v2\/posts\/10\/revisions\/18"}],"wp:attachment":[{"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=10"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=10"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.szulc-euphenics.com\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=10"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}