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Article

The search for the MEN1 gene. The European Consortium on MEN-1.

Journal of internal medicine - 1 Jun 1998

Abstract excerpt

The search for the gene whose mutations predispose individuals to multiple endocrine neoplasia type 1 (MEN-1) started in 1988 when the MEN1 locus was assigned to 11q13, close to PYGM. It came to an end with the recent identification of a gene expressed ubiquitously which harbours inactivating mutations associated with MEN-1. During these nine years, the genetic linkage interval had been slowly reduced, and losses...

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

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Source

Identifiers

PMID: 9681841
DOI: 10.1046/j.1365-2796.1998.00347.x

Genes

MEN1
PYGM
SCG2

Provenance

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

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

Research trail→

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The search for the MEN1 gene. The European Consortium on MEN-1.PMID 9681841Read ↗

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Positional cloning of the gene for multiple endocrine neoplasia-type 1.Semantic proximity Read ↗

Tracking the MEN1 gene.Semantic proximity Read ↗

Localization of the multiple endocrine neoplasia type I (MEN1) gene based on tumor loss of heterozygosity analysis.Semantic proximity Read ↗

Genetic mapping of the multiple endocrine neoplasia type 1 locus at 11q13.Semantic proximity Read ↗

Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1).Semantic proximity Read ↗

Menin: the protein behind the MEN1 syndrome.Semantic proximity Read ↗

Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors.Semantic proximity Read ↗

Genetic background of MEN1: from genetic homogeneity to functional diversity.Semantic proximity Read ↗

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