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Article

Functional Analysis of RET With Hirschsprung Mutations Affecting Its Kinase Domain

1 Jul 2001

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 11438491
DOI: 10.1053/gast.2001.25515

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Functional Analysis of RET With Hirschsprung Mutations Affecting Its Kinase DomainPMID 11438491Read ↗

Molecular heterogeneity of RET loss of function in Hirschsprung's disease.Semantic proximity Read ↗

Multiple functional effects of RET kinase domain sequence variants in Hirschsprung disease.Semantic proximity Read ↗

Novel RET mutation produces a truncated RET receptor lacking the intracellular signaling domain in a 3-generation family with Hirschsprung disease.Semantic proximity Read ↗

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's diseaseSemantic proximity Read ↗

New mutations associated with Hirschsprung disease.Semantic proximity Read ↗

Functional analyses of RET mutations in Chinese Hirschsprung disease patients.Semantic proximity Read ↗

[New mutations associated with Hirschsprung disease].Semantic proximity Read ↗

Variability in proliferative and migratory defects in Hirschsprung disease-associated RET pathogenic variants.Semantic proximity Read ↗

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

Current concepts in RET-related genetics, signaling and therapeutics.Semantic proximity Read ↗

RET oncogene.Semantic proximity Read ↗

RET receptor tyrosine kinase gene mutations: molecular biological, physiological and clinical aspects.Semantic proximity Read ↗

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