Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations. - Wikidata - thesis-toulmin - TriplyDB

Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.

Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.

http://www.wikidata.org/entity/Q30474153

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White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathies Rapid cohort generation and analysis of disease spectrum of large animal model of cone dystrophy Male-biased aganglionic megacolon in the TashT mouse line due to perturbation of silencer elements in a large gene desert of chromosome 10 QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.Familiar hypopigmentation syndrome in sheep associated with homozygous deletion of the entire endothelin type-B receptor gene.Piebald mutation on a C57BL/6J background Identification of genetic loci affecting the severity of symptoms of Hirschsprung disease in rats carrying Ednrbsl mutations by quantitative trait locus analysis.A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosis QTL analysis of modifiers for pigmentary disorder in rats carrying Ednrb sl mutations.Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line.The developmental genetics of Hirschsprung's disease.Enterocolitis causes profound lymphoid depletion in endothelin receptor B- and endothelin 3-null mouse models of Hirschsprung-associated enterocolitis.Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease.

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P2860

Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.

http://www.wikidata.org/entity/Q30474153

description

2011 nî lūn-bûn

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2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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Genetic background strongly mo ...... carrying Ednrb(sl) mutations.

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Genetic background strongly mo ...... carrying Ednrb(sl) mutations.

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Genetic background strongly mo ...... carrying Ednrb(sl) mutations.

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Genetic background strongly mo ...... carrying Ednrb(sl) mutations.

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Genetic background strongly mo ...... carrying Ednrb(sl) mutations.

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Genetic background strongly mo ...... carrying Ednrb(sl) mutations.

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Daisuke Torigoe

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Kanako Moritoh

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Nobuya Sasaki

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Ruihua Dang

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Sari Suzuki

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Takashi Agui

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P2860

Novel mutations of the endothelin B receptor gene in patients with Hirschsprung's disease and their characterization

Mutation of the endothelin-3 gene in the Waardenburg-Hirschsprung disease (Shah-Waardenburg syndrome)

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

Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

A dinucleotide mutation in the endothelin-B receptor gene is associated with lethal white foal syndrome (LWFS); a horse variant of Hirschsprung disease

A missense mutation in the endothelin-B receptor gene is associated with Lethal White Foal Syndrome: an equine version of Hirschsprung disease

A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome)

Mutation of the endothelin-receptor B gene in Waardenburg-Hirschsprung disease

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Yoshiaki Kikkawa

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