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

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.

Disease markers - 1 Jan 2004

Peltomäki Päivi, Vasen Hans

Abstract excerpt

In 1994, the International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer (ICG-HNPCC) established an international database of mutations identified in families with Lynch (HNPCC) syndrome. The data are publicly available at http://www.nfdht.nl. The information stored in the data...

Read the complete abstract on PubMed

Topics

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

Share to Adenosine Triphosphatases
Share to Base Pair Mismatch
Share to Colorectal Neoplasms, Hereditary Nonpolyposis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Repair Enzymes

Share to Mismatch Repair Endonuclease PMS2

Share to MutL Protein Homolog 1

Share to MutL Proteins

Share to MutS Homolog 2 Protein

Source

Open in PubMed Open full text

Identifiers

PMID: 15528792
DOI: 10.1155/2004/305058
PMCID: PMC3839397

Genes

MLH1
MSH2
MSH6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15528792-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutations associated with HNPCC predisposition -- Update of ICG-HNPCC/INSiGHT mutation database.PMID 15528792Read ↗

The genetics of HNPCC: application to diagnosis and screening.Semantic proximity Read ↗

Update on Lynch syndrome genomics.Semantic proximity Read ↗

Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study. The International Collaborative Group on Hereditary Nonpolyposis Colorectal Cancer.Semantic proximity Read ↗

Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. Online.Semantic proximity Read ↗

Distinct mutations in MLH1 and MSH2 genes in hereditary non-polyposis colorectal cancer (HNPCC) families from China.Semantic proximity Read ↗

Racial differences in MLH1 and MSH2 mutation: an analysis of yellow race and white race based on the InSiGHT database.Semantic proximity Read ↗

Hereditary cancer syndromes.Semantic proximity Read ↗

Germline susceptibility variants impact clinical outcome and therapeutic strategies for stage III colorectal cancerSemantic proximity Read ↗

UMD-MLH1/MSH2/MSH6 databases: description and analysis of genetic variations in French Lynch syndrome families.Semantic proximity Read ↗

Germline mutations in MLH1, MSH2 and MSH6 in Korean hereditary non-polyposis colorectal cancer families.Semantic proximity Read ↗

Analysis of mismatch repair gene mutations in Turkish HNPCC patients.Semantic proximity Read ↗

Two germline alterations in mismatch repair genes found in a HNPCC patient with poor family history.Semantic proximity Read ↗

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