Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

MEN1 gene mutations in 12 MEN1 families and their associated tumors.

European journal of endocrinology - 1 Oct 1998

Bartsch D, Kopp I, Bergenfelz A, Rieder H, Münch K, Jäger K, Deiss Y, Schudy A, Barth P, Arnold R, Rothmund M, Simon B

Abstract excerpt

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant inherited tumor syndrome characterized by the development of multiple endocrine tumors. The gene responsible for the disease, termed MEN1 gene. has recently been isolated and germline mutations have been described in affected MEN1 individuals. Twelve unrelated (German MEN1 families and their associated tumors (5 parathyroid tumors, 1 vipoma, 1...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenoma
Share to Chromosomes, Human, Pair 11

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

Share to Germ-Line Mutation

Share to Loss of Heterozygosity

Share to Pancreatic Neoplasms

Share to Phenotype

Share to Polymorphism, Single-Stranded Conformational

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 9820618
DOI: 10.1530/eje.0.1390416

Genes

MEN1

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→

Click a neighbor to travelStep 1 · 12 closest

MEN1 gene mutations in 12 MEN1 families and their associated tumors.PMID 9820618Read ↗

Characterization of mutations in patients with multiple endocrine neoplasia type 1.Semantic proximity Read ↗

The MEN1 gene and associated diseases: an update.Semantic proximity Read ↗

Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the geneSemantic proximity Read ↗

Identification of Novel Variants in MEN1: A Study Conducted with Four Multiple Endocrine Neoplasia Type 1 Patients.Semantic proximity Read ↗

Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders.Semantic proximity Read ↗

MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1.Semantic proximity Read ↗

Mutation analysis of the MEN1 gene in multiple endocrine neoplasia type 1, familial acromegaly and familial isolated hyperparathyroidism.Semantic proximity Read ↗

Germline MEN1 mutations in sixteen Japanese families with multiple endocrine neoplasia type 1 (MEN1).Semantic proximity Read ↗

Mutation Analysis of the MEN1 Gene in Multiple Endocrine Neoplasia Type 1, Familial Acromegaly and Familial Isolated HyperparathyroidismSemantic proximity Read ↗

Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database.Semantic proximity Read ↗

Whole-genome sequencing of a multiple endocrine neoplasia type 1 proband identifies gross deletion in MEN1Semantic proximity Read ↗

Menin mutations in the diagnosis and prediction of multiple endocrine neoplasia type 1.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.