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

Menin, the product of the <i>MEN1</i> gene, is a nuclear protein

17 Feb 1998

Abstract excerpt

The MEN1 gene, mutations in which are responsible for multiple endocrine neoplasia type 1 (MEN1), encodes a 610-amino acid protein, denoted menin. The amino acid sequence of this putative tumor suppressor offers no clue to the function or subcellular location of the protein. We report herein, based on immunofluorescence, Western blotting of subcellular fractions, and epitope tagging with enhanced green...

Read the complete abstract on PubMed

Topics

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

Share to Microtubule and mitosis dynamics
Share to Neuroblastoma Research and Treatments
Share to Neuroendocrine Tumor Research Advances

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 9465067
DOI: 10.1073/pnas.95.4.1630

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Menin, the product of the <i>MEN1</i> gene, is a nuclear proteinPMID 9465067Read ↗

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

Functional studies of the <i>MEN1</i> geneSemantic proximity Read ↗

Menin Molecular Interactions: Insights into Normal Functions and TumorigenesisSemantic proximity Read ↗

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

Twenty years of menin: emerging opportunities for restoration of transcriptional regulation in MEN1Semantic proximity Read ↗

MEN1 gene and its mutations: basic and clinical implications.Semantic proximity Read ↗

Clinically defined mutations in <i>MEN1</i> alter its tumor-suppressive function through increased menin turnoverSemantic proximity Read ↗

Molecular Pathology of the <i>MEN1</i> GeneSemantic proximity Read ↗

Review: multiple endocrine neoplasia type 1, sporadic neuroendocrine tumors, and MENIN.Semantic proximity Read ↗

MENIN loss as a tissue-specific driver of tumorigenesis.Semantic proximity Read ↗

The future: genetics advances in MEN1 therapeutic approaches and management strategiesSemantic proximity Read ↗

Menin in CancerSemantic proximity Read ↗

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