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

Fine mapping of the MLK-3 gene within 11q13 and its exclusion as the MEN1 susceptibility gene.

Human genetics - 1 Jun 1997

Lassam N J, Lin Z, Shennan M G, Courseaux A, Teh B T, Gaudray P, Larsson C

Abstract excerpt

MLK-3 kinase is a widely expressed serine/ threonine kinase that bears multiple protein interaction domains and regulates signals mediated by the stress-responsive pathway. Thus, MLK-3 signaling affects numerous cellular processes, raising the possibility that MLK-3 might play a role in oncogenesis. In this report, we describe the fine mapping of the MLK-3 gene within the 11q13.1 chromosomal region. By...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human, Pair 11
Share to Cricetinae

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

Share to Cricetulus

Share to Genetic Predisposition to Disease

Share to Hybrid Cells

Share to In Situ Hybridization, Fluorescence

Share to Protein Serine-Threonine Kinases

Source

Identifiers

PMID: 9187672
DOI: 10.1007/s004390050447

Genes

MEN1
PYGM

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

Fine mapping of the MLK-3 gene within 11q13 and its exclusion as the MEN1 susceptibility gene.PMID 9187672Read ↗

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

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

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome.Semantic proximity Read ↗

Identification of a KEAP1 germline mutation in a family with multinodular goitre.Semantic proximity Read ↗

Molecular genetic analysis of the 3p- syndrome.Semantic proximity Read ↗

Cloning, expression, and chromosomal mapping of the human 14-3-3gamma gene (YWHAG) to 7q11.23.Semantic proximity Read ↗

Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.Semantic proximity Read ↗

Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.Semantic proximity Read ↗

Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice.Semantic proximity Read ↗

The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.Semantic proximity Read ↗

Mapping of human interferon regulatory factor 3 (IRF3) to chromosome 19q13.3-13.4 by an intragenic polymorphic marker.Semantic proximity Read ↗

Exclusion of the 13-kDa rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1.Semantic proximity Read ↗

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