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Article

Molecular mechanisms of the development of human disease caused by RET mutations.

Japanese journal of cancer research : Gann - 1 Jan 1997

Romeo G

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Share to Glial Cell Line-Derived Neurotrophic Factor
Share to Glial Cell Line-Derived Neurotrophic Factor Receptors
Share to Multiple Endocrine Neoplasia Type 2a

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9045887

Genes

RET

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

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Molecular mechanisms of the development of human disease caused by RET mutations.PMID 9045887Read ↗

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

Molecular Mechanisms of RET Activation in Human CancerSemantic proximity Read ↗

RET tyrosine kinase signaling in development and cancer.Semantic proximity Read ↗

Cellular mechanisms of RET receptor dysfunction in multiple endocrine neoplasia 2.Semantic proximity Read ↗

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

Rett Syndrome: Crossing the Threshold to Clinical Translation.Semantic proximity Read ↗

Rett syndrome: recent research progress.Semantic proximity Read ↗

RET proto-oncogene: role in kidney development and molecular pathology.Semantic proximity Read ↗

Minireview: RET: Normal and Abnormal FunctionsSemantic proximity Read ↗

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