About: Association of megacolon with a new dominant spotting gene (Dom) in the mouse

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Attributes	Values
rdf:type	Item
description	artículu científicu espublizáu en 1984 (ast) vědecký článek publikovaný v roce 1984 (cs) 1984 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած (hyw) 1984 թվականի նոյեմբերին հրատարակված գիտական հոդված (hy) наукова стаття, опублікована в листопаді 1984 (uk) مقالة علمية (نشرت في نوفمبر 1984) (ar) scientific journal article (en) vedecký článok (publikovaný 1984/11/01) (sk) wetenschappelijk artikel (gepubliceerd op 1984/11/01) (nl) im November 1984 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28586637-62783CCB-B7AE-4D37-BC92-4D9B35D6702C
publication date	1984-11-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q28586637-A0EB68BE-8FF2-4017-8810-5E1718522E1C wds:Q28586637-F0CE4952-F1E6-42FC-A543-9E3C4A61DC15
author name string	P. W. Lane H. M. Liu
rdfs:label	Association of megacolon with a new dominant spotting gene (Dom) in the mouse (en) Association of megacolon with a new dominant spotting gene (Dom) in the mouse (nl) Association of megacolon with a new dominant spotting gene (Dom) in the mouse (ast)
skos:prefLabel	Association of megacolon with a new dominant spotting gene (Dom) in the mouse (en) Association of megacolon with a new dominant spotting gene (Dom) in the mouse (nl) Association of megacolon with a new dominant spotting gene (Dom) in the mouse (ast)
name	Association of megacolon with a new dominant spotting gene (Dom) in the mouse (en) Association of megacolon with a new dominant spotting gene (Dom) in the mouse (nl) Association of megacolon with a new dominant spotting gene (Dom) in the mouse (ast)
title	wds:Q28586637-53CF4871-4722-4BB6-BC1A-BD220B2F72AC
title	Association of megacolon with a new dominant spotting gene (Dom) in the mouse (en)
page(s)	wds:Q28586637-9E9CA59E-9987-406A-A319-89CD54AF5D72
page(s)	435–439
instance of	wds:Q28586637-1CB33B2B-8079-4363-8CFD-98AA7C602656
instance of	scholarly article
main subject	wds:Q28586637-55B335F1-378F-406C-B235-890151CE9F7C wds:Q28586637-D73A38EB-331A-49A1-9392-6E628DD1716F
main subject	megacolon SRY (sex determining region Y)-box 10
PubMed ID	wds:Q28586637-E7EF6322-E1FF-43AF-AE0B-0F3D4689D636
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6512238
PubMed ID	6512238
published in	wds:Q28586637-AB75DD85-5A8C-44B6-9CBB-BDC58D10D8DC
published in	Journal of Heredity
issue	wds:Q28586637-62B62D5B-FEC6-4E2E-9F76-A90889FA00CE
volume	wds:Q28586637-DDAB3971-B6BB-4AC3-A7BD-0541FE6B442D
issue	6
volume	75
DOI	wds:Q28586637-210BCE2E-EAF5-4DCD-8CBB-054F8DA4074E
DOI	http://dx.doi.org/10.1093/OXFORDJOURNALS.JHERED.A109980
DOI	10.1093/OXFORDJOURNALS.JHERED.A109980
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28586637
is cites work of	Enteric nervous system development: migration, differentiation, and disease Foal with Overo lethal white syndrome born to a registered quarter horse mare A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10. A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. Isolation and live imaging of enteric progenitors based on Sox10-Histone2BVenus transgene expression Hirschsprung disease, associated syndromes, and genetics: a review Wither polygenic inheritance: mapping Hirschsprung disease SOX10 mutations in patients with Waardenburg-Hirschsprung disease A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome) Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation A dual role for SOX10 in the maintenance of the postnatal melanocyte lineage and the differentiation of melanocyte stem cell progenitors The enteric nervous system Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development. Genetic screen for mutations affecting development and function of the enteric nervous system The transcription factor Sox10 is a key regulator of peripheral glial development. Review and update of mutations causing Waardenburg syndrome. Transgenic mice overexpressing the mouse homoeobox-containing gene Hox-1.4 exhibit abnormal gut development Null mutation of endothelin receptor type B gene in spotting lethal rats causes aganglionic megacolon and white coat color Analysis of early human neural crest development A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model Requirement of c-kit for development of intestinal pacemaker system Animal models in pediatric surgery Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease. Distant regulatory elements in a Sox10-beta GEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues. The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia Mouse models for four types of Waardenburg syndrome Sox proteins in melanocyte development and melanoma The mouse Col2a-1 gene is highly conserved and is linked to Int-1 on chromosome 15. Activation by GDNF of a transcriptional program repressing neurite growth in dorsal root ganglia The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10 Genetic basis of Hirschsprung's disease. Sympathoadrenal hyperplasia causes renal malformations in Ret(MEN2B)-transgenic mice Building a brain in the gut: development of the enteric nervous system Spatiotemporal regulation of endothelin receptor-B by SOX10 in neural crest-derived enteric neuron precursors. Hoxb3 vagal neural crest-specific enhancer element for controlling enteric nervous system development. Specification of neural crest into sensory neuron and melanocyte lineages The hairy ears (Eh) mutation is closely associated with a chromosomal rearrangement in mouse chromosome 15 The genetics of Hirschsprung disease The congenital goiter mutation is linked to the thyroglobulin gene in the mouse Genetic aspects of Hirschsprung's disease Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer. The RET proto-oncogene: a challenge to our understanding of disease pathogenesis Sox10 controls migration of B16F10 melanoma cells through multiple regulatory target genes. X-ray-induced deletion complexes in embryonic stem cells on mouse chromosome 15 A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus Hirschsprung disease and other enteric dysganglionoses Mouse chromosome 15. Mouse chromosome 15 The role of SOX10 during enteric nervous system development

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