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Article

Genetic analysis of RET, EDNRB, and EDN3 genes and three SNPs in MCS + 9.7 in Chinese Patients with isolated Hirschsprung disease.

Biochemical genetics - 1 Aug 2007

Zhang Xian-Ning, Zhou Miao-Ni, Qiu Yun-Qing, Ding Shi-Ping, Qi Ming, Li Ji-Cheng

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17554617
DOI: 10.1007/s10528-007-9093-y

Genes

EDN3
EDNRB
RET

Provenance

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Related research

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Genetic analysis of RET, EDNRB, and EDN3 genes and three SNPs in MCS + 9.7 in Chinese Patients with isolated Hirschsprung disease.PMID 17554617Read ↗

Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.Semantic proximity Read ↗

Significant Association of rs2147555 Genetic Polymorphism in the EDNRB Gene with Hirschsprung Disease in Southern Chinese Children.Semantic proximity Read ↗

High incidence of EDNRB gene mutation in seven southern Chinese familial cases with Hirschsprung's disease.Semantic proximity Read ↗

Exome sequencing identified a novel pathogenic RET variant with high variable expressivity and incomplete penetrance in an extended pedigree with Hirschsprung diseaseSemantic proximity Read ↗

Low RET mutation frequency and polymorphism analysis of the RET and EDNRB genes in patients with Hirschsprung disease in Taiwan.Semantic proximity Read ↗

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

Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant.Semantic proximity Read ↗

[The role of ret gene in the pathogenesis of Hirschsprung disease].Semantic proximity Read ↗

Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease.Semantic proximity Read ↗

Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese.Semantic proximity Read ↗

A Scoring System to Predict the Severity of Hirschsprung Disease at Diagnosis and Its Correlation With Molecular Genetics.Semantic proximity Read ↗

Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms.Semantic proximity Read ↗

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