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Msh3-/- cells are severely defective for CTG*CAG repeat (zeige CELF3 ELISA Kits) expansions but show full activity on contractions. Msh3 overexpression led to high expansion activity and elevated levels of MutSbeta complex, indicating that MutSbeta abundance drives expansions. Expression of 2 Msh3 polymorphic variants at normal levels showed no detectable change in expansions. These polymorphisms primarily affect Msh3 protein stability, not ac...
Findings indicate that carriers of the MSH5 (zeige MSH5 ELISA Kits) rs707939 T allele, the MSH2 (zeige MSH2 ELISA Kits) rs6544991 C allele, the MSH3 rs6151627 and rs6151670 G alleles, and the MSH3 rs7709909 T allele have poor toxicity tolerance to platinum-based chemotherapy in non-small cell lung cancer patients.
MSH3 is probably a modifier of disease progression in Huntington's disease.
data suggest that MSH3 mutations represent an additional recessive subtype of colorectal adenomatous polyposis
Three polymorphisms in MSH3 were associated with variation in somatic instability in myotonic dystrophy type 1.
Our meta-analysis results demonstrated that MSH3 rs26279 G > A polymorphism is associated with an increased risk of overall cancer, especially for the colorectal cancer and breast cancer.
The mismatch-binding protein MutS beta, a heterodimer of MSH2 and MSH3, activates ATR in response to DNA double-strand breaks.
Data show that single nucleotide polymorphisms in MutS homolog 3 (MSH3) had an impact on the chemotherapy response and prognosis of advanced non-small cell lung cancer (NCSLC) patients who were treated with platinum-based chemotherapy.
Our data present, for the first time, evidence that inherited MLH1 (zeige MLH1 ELISA Kits) c.-93G>A, MSH2 (zeige MSH2 ELISA Kits) c.211 + 9C>G, MSH3 c.3133G>A, and EXO1 (zeige EXO1 ELISA Kits) c.1765G>A abnormalities of DNA MMR (zeige MRC1 ELISA Kits) pathway are important determinants of head and neck squamous cell carcinoma
IL6 (zeige IL6 ELISA Kits) signaling disrupts the nuclear localization of hMSH3 and DNA repair, leading to elevated microsatellite alterations at selected tetranucleotide repeats in cancer cell lines.
MSH2 (zeige MSH2 ELISA Kits)-MSH3 suppresses chromosomal instability and modulates the tumor spectrum in p53 (zeige TP53 ELISA Kits)-deficient tumorigenesis.
naturally occurring MSH3 protein polymorphisms are modifiers of CAG repeat (zeige CELF3 ELISA Kits) instability, likely through variable MSH3 protein stability
Enhanced occupancy of Msh2 (zeige MSH2 ELISA Kits) and Msh3 proteins downstream of the FXN (zeige FXN ELISA Kits) expanded GAA (zeige GAA ELISA Kits) repeat, suggesting a model in which Msh2 (zeige MSH2 ELISA Kits)/3 dimers are recruited to this region to repair mismatches.
Stress treatment of mouse cells with ethanol or hydrogen peroxide caused the re-distribution of MSH3 into nuclear bodies containing the proliferating cell nuclear antigen (PCNA (zeige PCNA ELISA Kits)), a known binding partner of MutSbeta.
A (CTG)84 repeat was stable even in Msh3-deficient mice.
Data suggest that MutS homologues Msh2 (zeige MSH2 ELISA Kits), Msh3, and Msh6 (zeige MSH6 ELISA Kits) play overlapping and distinct roles during antibody diversification processes.
Data suggest that activation-induced cytidine deaminase (zeige AICDA ELISA Kits) has limited entry points into V and S regions in vivo, and subsequent mutation requires Msh2 (zeige MSH2 ELISA Kits)-Msh6 (zeige MSH6 ELISA Kits), but not Msh3, and DNA polymerase (zeige POLB ELISA Kits).
Frequencies and patterns in DNA mismatch repair in the context of mice deficient for Msh3.
The protein encoded by this gene forms a heterodimer with MSH2 to form MutS beta, part of the post-replicative DNA mismatch repair system. MutS beta initiates mismatch repair by binding to a mismatch and then forming a complex with MutL alpha heterodimer. This gene contains a polymorphic 9 bp tandem repeat sequence in the first exon. The repeat is present 6 times in the reference genome sequence and 3-7 repeats have been reported. Defects in this gene are a cause of susceptibility to endometrial cancer.
DNA mismatch repair protein Msh3
, DNA mismatch repair protein MSH3
, hypothetical protein
, divergent upstream protein
, mismatch repair protein 1
, protein repair-1
, protein repair-3