About: Epistatic relationship between Waardenburg syndrome genes MITF and PAX3

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About: Epistatic relationship between Waardenburg syndrome genes MITF and PAX3 Goto Sponge NotDistinct Permalink

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description	article científic (ca) article scientific (oc) articol științific (ro) artigo científico (gl) artikull shkencor (sq) artikulong pang-agham (tl) artykuł naukowy (pl) bilimsel makale (tr) mokslinis straipsnis (lt) scienca artikolo (eo) teaduslik artikkel (et) tieteellinen artikkeli (fi) tudományos cikk (hu) vitenskapelig artikkel (nb) vitskapeleg artikkel (nn) επιστημονικό άρθρο (el) мақолаи илмӣ (tg) научна статия (bg) научная статья (ru) מאמר מדעי (he) სამეცნიერო სტატია (ka) บทความทางวิทยาศาสตร์ (th) bài báo khoa học (vi) naučni članak (sr-el) мақолаи илмӣ (tg-cyrl) научни чланак (sr-ec) scientific article (en) ശാസ്ത്ര പ്രബന്ധം (ml) سائنسی مضمون (ur) مقالهٔ علمی (fa) 1998 nî lūn-bûn (nan) 1998年の論文 (ja) 1998年論文 (zh-hk) 1998年論文 (zh-tw) 1998年論文 (zh-hant) 1998年論文 (yue) 1998年論文 (zh-mo) 1998年论文 (zh) 1998年论文 (zh-cn) 1998年论文 (zh-sg) 1998年论文 (zh-hans) 1998年论文 (wuu) 1998年论文 (zh-my) 1998년 논문 (ko) artigo científico (publicado na 1998) (pt-br) artículo científico publicado en 1998 (es) artículu científicu espublizáu en 1998 (ast) vědecký článek publikovaný v roce 1998 (cs) ১৯৯৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ (bn) 1998 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в березні 1998 (uk) 1998 թվականի մարտին հրատարակված գիտական հոդված (hy) wissenschaftlicher Artikel (veröffentlicht in 1998-03) (de) article scientifique (publié 1998-03) (fr) articolo scientifico (pubblicato il 1998-03) (it) artigo científico (publicado na 1998-03) (pt) научни чланак (објављен 1998-03) (sr) vedecký článok (publikovaný 1998-03) (sk) vetenskaplig artikel (publicerad på 1998-03) (sv) videnskabelig artikel (udgivet 1998-03) (da) wetenschappelijk artikel (gepubliceerd op 1998-03) (nl) مقالة علمية (نشرت في مارس 1998) (ar)
publication date	wds:Q24317196-A2F971EE-FDD6-478B-92D8-0575871EE6F8
publication date	1998-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q24317196-F735B581-9512-49AB-96D0-7D463FDC1B39
language of work or name	English
exact match	wds:Q24317196-7C948578-50E6-4B57-AFAA-6024ADD6F2DF
exact match	https://scigraph.springernature.com/pub.10.1038/ng0398-283
cites work	wds:Q24317196-03991272-2EC7-4B42-BB77-8764521A10B3 wds:Q24317196-04C3D4BF-6921-4C62-AB80-5FCA5DCEF75C wds:Q24317196-1E182894-ACCF-424C-BE6B-E3A81042D35E wds:Q24317196-1E5B3126-D020-46F9-989A-33D9CCC23B3A wds:Q24317196-308974CA-A8B2-4FC5-8FC9-EDD8F9845C63 wds:Q24317196-34292608-4A28-47DB-8043-03710BBBDDE4 wds:Q24317196-36D50035-4D21-433E-8884-9D815ECE8C64 wds:Q24317196-3B2B66A9-EFF8-4654-9FC0-76752BDF40E2 wds:Q24317196-589E4599-FA02-4BA9-833F-B1AD38F87D74 wds:Q24317196-5F2A50BE-ECC2-41D4-B4C3-0A119B7F33DA wds:Q24317196-6916DF14-BA74-480A-8ECA-AE8FF257F690 wds:Q24317196-77E45E25-A444-4A75-8CA4-554E019F5802 wds:Q24317196-7C26132A-5612-4236-86E6-039814BB671B wds:Q24317196-A06EFB00-AD22-4BFF-BC4D-3342140DD9DD wds:Q24317196-A83B2EB6-EB58-40EA-8976-C641BD55F0E2 wds:Q24317196-C4DD37E1-D9A3-4F44-AFD6-EA1A0FA56CA2 wds:Q24317196-C6D5FBB2-0E9D-4DBC-A5F2-94EAC4A38F6B wds:Q24317196-D1E54FA7-9D40-4F94-8660-2EC533639FA5 wds:Q24317196-DC7861EC-2470-450B-AF83-24C83EBCE8D9
cites work	The mutational spectrum in Waardenburg syndrome. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene Development of a highly efficient expression cDNA cloning system: application to oncogene isolation Rapid detection of octamer binding proteins with 'mini-extracts', prepared from a small number of cells Pax3 modulates expression of the c-Met receptor during limb muscle development Waardenburg syndrome The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3 Cochlear disorder associated with melanocyte anomaly in mice with a transgenic insertional mutation Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome Overlapping positive and negative regulatory elements determine lens-specific activity of the delta 1-crystallin enhancer Ectopic expression of MITF, a gene for Waardenburg syndrome type 2, converts fibroblasts to cells with melanocyte characteristics

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