Varaico: Literature-Extracted Genetic Variants

Gene:MSH2
Variant:p.M1I
Back to variants list

MSH2

NM_000251.3:p.M1I

Associated Papers

Evolutionary origin of germline pathogenic variants in human DNA mismatch repair genes.

Lei H et al.

Human Genomics, 2024

38287404 (PubMed )
Supplement: 40246_2024_573_MOESM3_ESM.xls › MSH6

Understanding the Genetic Landscape of Pancreatic Ductal Adenocarcinoma to Support Personalized Medicine: A Systematic Review.

Pantaleo A et al.

Cancers, 2023

38201484 (PubMed )
Supplement: cancers-16-00056-s001.zip › Table_S3_Proof_final_version.xlsx › ATM_

A systematic CRISPR screen defines mutational mechanisms underpinning signatures caused by replication errors and endogenous DNA damage.

Zou X et al.

Nature Cancer, 2021

A Genetic Incompatibility Accelerates Adaptation in Yeast.

Bui DT et al.

Plos Genetics, 2015

Genealogical tree study as screening method in the Lynch syndrome prior to genetic test.

Delgado-Plasencia L et al.

American Journal of Clinical Oncology, 2010

Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.

Guillem JG et al.

Annals of Surgery, 2007

Detection of epidermal growth factor receptor variations by partially denaturing HPLC.

Chin TM et al.

Clinical Chemistry, 2007

Distinct mechanisms lead to HPRT gene mutations in leukemic cells.

Lin YW et al.

Genes, Chromosomes & Cancer, 2004

Palm mutants in DNA polymerases alpha and eta alter DNA replication fidelity and translesion activity.

Niimi A et al.

Molecular and Cellular Biology, 2004

The interaction of DNA mismatch repair proteins with human exonuclease I.

Schmutte C et al.

The Journal of Biological Chemistry, 2001

Human exonuclease I interacts with the mismatch repair protein hMSH2.

Schmutte C et al.

Cancer Research, 1998

BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer.

Couch FJ et al.

The New England Journal of Medicine, 1997

Loss of heterozygosity and base substitution at the APRT locus in mismatch-repair-proficient and -deficient colorectal carcinoma cell lines.

Phear G et al.

Molecular and Cellular Biology, 1996

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."