mismatch repair MSH2
Selected indexed studies
- Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk. (Am J Hum Genet, 2021) [PMID:33357406]
- Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. (Oncol Rep, 2016) [PMID:27601186]
- Distinct mismatch-repair complex genes set neuronal CAG-repeat expansion rate to drive selective pathogenesis in HD mice. (Cell, 2025) [PMID:39938516]
_Worker-drafted node — pending editorial review._
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Sources
- Massively parallel functional testing of MSH2 missense variants conferring Lynch syndrome risk. (2021) pubmed
- Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population. (2016) pubmed
- Distinct mismatch-repair complex genes set neuronal CAG-repeat expansion rate to drive selective pathogenesis in HD mice. (2025) pubmed
- Identification of Lynch Syndrome. (2022) pubmed
- Mismatch Repair Protein Msh2 Is Necessary for Macronuclear Stability and Micronuclear Division in Tetrahymena thermophila. (2023) pubmed
- OTUB1 stabilizes mismatch repair protein MSH2 by blocking ubiquitination. (2021) pubmed
- Chromatin Rewiring by Mismatch Repair Protein MSH2 Alters Cell Adhesion Pathways and Sensitivity to BET Inhibition in Gastric Cancer. (2022) pubmed
- Induction of a mismatch repair deficient genotype by tailored chemical mutagenesis in experimental models of cancer. (2025) pubmed
- Mlh1 interacts with both Msh2 and Msh6 for recruitment during mismatch repair. (2022) pubmed
- Multigene Panel Testing Provides a New Perspective on Lynch Syndrome. (2017) pubmed