Analysis of MSH2 Loss of Heterozygosity, Expression, and IVS10+12G>A Polymorphism in Sporadic Colon Cancer | Anticancer Research
DNA Mismatch Repair Gene Variants | Encyclopedia MDPI
The UMD- MSH2 database: the protein
Genetics, diagnosis and treatment of Lynch syndrome: Old lessons and current challenges (Review)
Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer | Nature Communications
The MSH2 gene is located on chromosome 2 and the indicated allele has... | Download Scientific Diagram
IJMS | Free Full-Text | Novel Genetic Markers for Early Detection of Elevated Breast Cancer Risk in Women
MSH2 Gene Sequencing - Colorectal Cancer Test in Delhi | GDIC
Identification of novel pathogenic MSH2 mutation and new DNA repair genes variants: investigation of a Tunisian Lynch syndrome family with discordant twins | Journal of Translational Medicine | Full Text
Defective DNA mismatch repair and MLH1, MSH2 mutations in endometrial cancers
Analysis of expression of MSH2 and MSH3 genes in Mixed Lineage Leukemia (MLL)-Acute Lymphoblastic Leukemia (ALL) human cell lines — Journal of Young Investigators
MSH2 Gene - GeneCards | MSH2 Protein | MSH2 Antibody
Partial loss of heterozygosity events at the mutated gene in tumors from MLH1/MSH2 large genomic rearrangement carriers | BMC Cancer | Full Text
MSH2 - Wikipedia
Population-based Screening for Hereditary Colorectal Cancer Variants in Japan - ScienceDirect
Genetic and genomic basis of the mismatch repair system involved in Lynch syndrome | SpringerLink
MSH2 Protein Overview: Sequence, Structure, Function and Protein Interaction | Sino Biological
Protein MSH6 - an overview | ScienceDirect Topics
Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation - Raffaella Liccardo, Marina De Rosa, Francesca Duraturo, 2018
The properties of Msh2–Msh6 ATP binding mutants suggest a signal amplification mechanism in DNA mismatch repair - Journal of Biological Chemistry
Masking The Truth? | The DNA Exchange
Preferential loss of mismatch repair function in refractory and relapsed acute myeloid leukemia: potential contribution to AML progression | Cell Research
Characterization of a rare variant (c.2635-2A>G) of the MSH2 gene in a family with Lynch syndrome - Filomena Cariola, Vittoria Disciglio, Anna M. Valentini, Claudio Lotesoriere, Candida Fasano, Giovanna Forte, Luciana Russo,
