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Article

RET mutations in human disease.

Trends in genetics : TIG - 1 Apr 1996

Pasini B, Ceccherini I, Romeo G

Abstract excerpt

The RET proto-oncogene is at the origin of one of the most interesting models of human disease caused by mutations in a receptor tyrosine kinase gene. Somatic rearrangements of RET are involved in the aetiology of a variable proportion of papillary thyroid carcinomas (PTC), the most common type of thyroid tumour whose prevalence is increasing in areas heavily exposed to radioactive fallout after the Chernobyl...

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Source

Identifiers

PMID: 8901418
DOI: 10.1016/0168-9525(96)10012-3

Genes

RET

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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.

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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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RET receptor signaling: dysfunction in thyroid cancer and Hirschsprung's disease.Semantic proximity Read ↗

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