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Article

Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissues

24 Nov 2012

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

Identifiers

PMID: 23228367
DOI: 10.1016/j.dnarep.2012.10.006

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Tissue-specific mismatch repair protein expression: MSH3 is higher than MSH6 in multiple mouse tissuesPMID 23228367Read ↗

Structural, molecular and cellular functions of MSH2 and MSH6 during DNA mismatch repair, damage signaling and other noncanonical activitiesSemantic proximity Read ↗

Single-cell whole-genome sequencing reveals mutational landscapes of DNA mismatch repair deficiency in mouse primary fibroblastsSemantic proximity Read ↗

An integrative pan-cancer analysis reveals the oncogenic role of mutS homolog 6 (MSH6) in human tumors.Semantic proximity Read ↗

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer.Semantic proximity Read ↗

Mbd4 and MutSα protect cells from spontaneous deamination of 5-methylcytosine.Semantic proximity Read ↗

Loss of Msh2 and a single-radiation hit induce common, genome-wide, and persistent epigenetic changes in the intestineSemantic proximity Read ↗

Complex Mutation Profiles in Mismatch Repair and Ribonucleotide Reductase Mutants Reveal Novel Repair Substrate Specificity of MutS Homolog (MSH) ComplexesSemantic proximity Read ↗

Mbd4 and MutSα protect cells from spontaneous deamination of 5-methylcytosineSemantic proximity Read ↗

Mismatch repair dissection by in vivo RNAi reveals dose-dependent modulators of somatic instability and proteome remodeling in Huntington’s diseaseSemantic proximity Read ↗

Complex mutation profiles in mismatch repair and ribonucleotide reductase mutants reveal novel repair substrate specificity of MutS homolog (MSH) complexes.Semantic proximity Read ↗

Oxidative Stress Accelerates Repeat Instability and Base Substitutions, Promoting Gastrointestinal Driver Mutations under MSH2 DeficiencySemantic proximity Read ↗

MutS Homologues hMSH4 and hMSH5: Genetic Variations, Functions, and Implications in Human DiseasesSemantic proximity Read ↗

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