Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease. - sprookjes - yvandenbroek - TriplyDB

Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

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Effects of NRG1 Polymorphisms on Hirschsprung's Disease Susceptibility: A Meta-analysis Genetic Background of Hirschsprung Disease: A Bridge Between Basic Science and Clinical Application.Large-scale replication study identified multiple independent SNPs in RET synergistically associated with Hirschsprung disease in Southern Chinese population.Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.Significance of neurexin and neuroligin polymorphisms in regulating risk of Hirschsprung's disease.Outcomes in patients with Hirschsprung disease following definitive surgery NRG1 variant effects in patients with Hirschsprung disease

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Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease.

http://www.wikidata.org/entity/Q37679036

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 03 March 2017

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

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Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

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type

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Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

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Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

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Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

@en

Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

@nl

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Scientific Reports

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Effects of RET, NRG1 and NRG3 ...... ion with Hirschsprung Disease.

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Dehua Yang

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Guoqing Cao

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Jun Yang

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Kang Li

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Li Yang

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Meng Jiang

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Shao-Tao Tang

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Shuai Li

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Xi Zhang

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Ying Zhou

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P2860

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

The neuregulin-I/ErbB signaling system in development and disease

A missense mutation of the endothelin-B receptor gene in multigenic Hirschsprung's disease

Mutations of the RET proto-oncogene in Hirschsprung's disease

Neuregulin 1 and susceptibility to schizophrenia.

Fine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophrenia

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

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

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43222

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scholarly article

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10.1038/SREP43222

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7

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2017-03-03T00:00:00Z

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28256518

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5335705

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