Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients.

Journal of human genetics - 1 Jan 2006

Sangkhathat Surasak, Kusafuka Takeshi, Chengkriwate Piyawan, Patrapinyokul Sakda, Sangthong Burapat, Fukuzawa Masahiro

Abstract excerpt

Mutation and polymorphism data for Hirschsprung disease (HSCR) varies among ethnic groups. Single nucleotide polymorphisms (SNP) of RET proto-oncogene (RET) were recently shown to be associated with the disease, and with disease severity, in different populations. In this study, comprehensive ana...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Glial Cell Line-Derived Neurotrophic Factor
Share to High Mobility Group Proteins
Share to Hirschsprung Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Proto-Oncogene Mas

Share to Proto-Oncogene Proteins c-ret

Share to Receptor, Endothelin B

Share to SOXE Transcription Factors

Share to Thailand

Source

Identifiers

PMID: 17009072
DOI: 10.1007/s10038-006-0064-7

Genes

RET
EDNRB
GDNF

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17009072-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations and polymorphisms of Hirschsprung disease candidate genes in Thai patients.PMID 17009072Read ↗

Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients.Semantic proximity Read ↗

Novel mutations of RET gene in Korean patients with sporadic Hirschsprung's disease.Semantic proximity Read ↗

Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.Semantic proximity Read ↗

Association analysis of the RET proto-oncogene with Hirschsprung disease in the Han Chinese population of southeastern China.Semantic proximity Read ↗

Comprehensive characterization of the genetic landscape of familial Hirschsprung's disease.Semantic proximity Read ↗

Single nucleotide polymorphisms in the RET gene and their correlations with Hirschsprung disease phenotype.Semantic proximity Read ↗

A study on genetic polymorphism of RET proto-oncogene in Hirschsprung's disease in children.Semantic proximity Read ↗

RET variants and haplotype analysis in a cohort of Czech patients with Hirschsprung disease.Semantic proximity Read ↗

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

Identification of a novel variant of the RET proto-oncogene in a novel family with Hirschsprung's disease.Semantic proximity Read ↗

Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.Semantic proximity Read ↗

RET polymorphisms and the risk of Hirschsprung's disease in a Chinese population.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.