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Article

The MENX syndrome and p27: relationships with multiple endocrine neoplasia.

Progress in brain research - 1 Jan 2010

Molatore Sara, Pellegata Natalia S

Abstract excerpt

In the past 3 years new insight into the etiopathogenesis of hereditary endocrine tumors has emerged from studies conducted on MENX, a rat multiple endocrine neoplasia (MEN) syndrome. MENX spontaneously developed in a rat colony and was discovered by serendipity when these animals underwent complete necropsy, as they were found to consistently develop multiple endocrine tumors with a spectrum similar to both MEN...

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Topics

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Share to Cyclin-Dependent Kinase Inhibitor p27
Share to MEN1 gene
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple Endocrine Neoplasia

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Source

Identifiers

PMID: 20541671
DOI: 10.1016/S0079-6123(10)82013-8

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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