SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants. - Wikidata - awgldk - TriplyDB

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

http://www.wikidata.org/entity/Q35364550

about

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia.New insights into human enteric neuropathies.SOX10 is over-expressed in bladder cancer and contributes to the malignant bladder cancer cell behaviors.Genetic variants of IL-11 associated with risk of Hirschsprung disease.Expression of intermediate filament proteins and neuronal markers in the human fetal gut.Ablation of Ezh2 in neural crest cells leads to aberrant enteric nervous system development in mice

P2860

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P2860

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

http://www.wikidata.org/entity/Q35364550

description

2001 nî lūn-bûn

@nan

2001 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2001年の論文

@ja

2001年論文

@yue

2001年論文

@zh-hant

2001年論文

@zh-hk

2001年論文

@zh-mo

2001年論文

@zh-tw

2001年论文

@wuu

name

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

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SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

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type

label

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

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SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

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prefLabel

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

@ast

SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

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SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants.

@en

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Chen B

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Fu M

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Lui VC

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Sham MH

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Tam PK

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P2860

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

Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain.

Seven new members of the Sox gene family expressed during mouse development

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3

Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome

Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

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220-226

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scholarly article

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10.1136/GUT.49.2.220

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2

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49

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2001-08-01T00:00:00Z

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11454798

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1728391

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