Results 161 to 170 of about 26,541 (200)

The role of DNA mismatch repair mutS/mutL homolog genes in spermatogenesis and male infertility: a systematic review and cohort study. [PDF]

open access: yesReprod Biol Endocrinol
Podgrajsek R   +12 more
europepmc   +1 more source

DNA mismatch repair system expression in salivary gland tumors: A Systematic Review. [PDF]

open access: yesMed Oral Patol Oral Cir Bucal
Alves GM   +4 more
europepmc   +1 more source

Mesonephric-like Adenocarcinoma of the Uterine Corpus: Comparison Between Mismatch Repair Protein Immunostaining and Microsatellite Instability Testing

Anticancer Research, 2023
Background/Aim: The utility of mismatch repair (MMR) immunohistochemistry (IHC) and microsatellite instability (MSI) testing in uterine mesonephric-like adenocarcinoma (MLA) has seldom been reported. This study aimed to compare MMR IHC and MSI testing in
Hyunjin Kim, Hyun-Soo Kim
semanticscholar   +1 more source

Identification of SNPs in hMSH3/MSH6 interaction domain affecting the structure and function of MSH2 protein

Biotechnology and applied biochemistry, 2021
MutS homolog 2 (MSH2) is a mismatch repair gene that plays a critical role in DNA repair pathways, and its mutations are associated with different cancers.
Sidhartha Singh   +2 more
semanticscholar   +1 more source

Cadmium(Cd)-induced oxidative stress down-regulates the gene expression of DNA mismatch recognition proteins MutS homolog 2 (MSH2) and MSH6 in zebrafish (Danio rerio) embryos

Aquatic Toxicology, 2013
DNA mismatch repair (MMR) of simple base mismatches and small insertion-deletion loops in eukaryotes is initiated by the binding of the MutS homolog 2 (MSH2)-MSH6 heterodimer to mismatched DNA. Cadmium (Cd) is a genotoxic heavy metal that has been recognized as a human carcinogen.
Todd, Hsu   +4 more
openaire   +2 more sources

Expression status of MLH1 and MSH2 mismatch repair proteins in colorectal carcinoma

Egyptian Journal of Pathology, 2023
Colorectal carcinoma (CRC) is a main cause of morbidity and mortality worldwide. Lynch syndrome or hereditary nonpolyposis colorectal carcinoma is a cancer syndrome that accounts for 5–10% of cases of CRCs, and it is caused by a germline mutation ...
Said A-A Mohamed   +3 more
semanticscholar   +1 more source

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