1. Khailany, Rozhgar A, Ozaslan, Mehmet. 2021. Exonic sequencing and MLH3 gene expression analysis of breast cancer patients. In Cellular and molecular biology (Noisy-le-Grand, France), 67, 35-43. doi:10.14715/cmb/2021.67.3.5. https://pubmed.ncbi.nlm.nih.gov/34933735/
2. Valle, Laura, de Voer, Richarda M, Goldberg, Yael, Castellvi-Bel, Sergi, Hemminki, Kari. 2019. Update on genetic predisposition to colorectal cancer and polyposis. In Molecular aspects of medicine, 69, 10-26. doi:10.1016/j.mam.2019.03.001. https://pubmed.ncbi.nlm.nih.gov/30862463/
3. Lipkin, S M, Wang, V, Jacoby, R, Elliott, R M, Collins, F S. . MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability. In Nature genetics, 24, 27-35. doi:. https://pubmed.ncbi.nlm.nih.gov/10615123/
4. Flores-Rozas, H, Kolodner, R D. . The Saccharomyces cerevisiae MLH3 gene functions in MSH3-dependent suppression of frameshift mutations. In Proceedings of the National Academy of Sciences of the United States of America, 95, 12404-9. doi:. https://pubmed.ncbi.nlm.nih.gov/9770499/
5. Nawaz, Shoaib, Ullah, Muhammad Imran, Hamid, Beenish Samreen, Hussain, Shabir, Ahmad, Wasim. 2021. A loss-of-function variant in DNA mismatch repair gene MLH3 underlies severe oligozoospermia. In Journal of human genetics, 66, 725-730. doi:10.1038/s10038-021-00907-z. https://pubmed.ncbi.nlm.nih.gov/33517345/
6. Liu, Hong-Xu, Li, Yu, Jiang, Xue-Dong, Wang, Yu, Yang, Jun. . Mutation screening of mismatch repair gene Mlh3 in familial esophageal cancer. In World journal of gastroenterology, 12, 5281-6. doi:. https://pubmed.ncbi.nlm.nih.gov/16981255/
7. Roesner, Lennart M, Mielke, Christian, Faehnrich, Silke, Drexler, Hans G, Dirks, Wilhelm G. 2014. Localization of MLH3 at the centrosomes. In International journal of molecular sciences, 15, 13932-7. doi:10.3390/ijms150813932. https://pubmed.ncbi.nlm.nih.gov/25116689/
8. Al-Sweel, Najla, Raghavan, Vandana, Dutta, Abhishek, Nishant, K T, Alani, Eric. 2017. mlh3 mutations in baker's yeast alter meiotic recombination outcomes by increasing noncrossover events genome-wide. In PLoS genetics, 13, e1006974. doi:10.1371/journal.pgen.1006974. https://pubmed.ncbi.nlm.nih.gov/28827832/
9. Ferguson, Ross, Goold, Robert, Coupland, Lucy, Flower, Michael, Tabrizi, Sarah J. 2024. Therapeutic validation of MMR-associated genetic modifiers in a human ex vivo model of Huntington disease. In American journal of human genetics, 111, 1165-1183. doi:10.1016/j.ajhg.2024.04.015. https://pubmed.ncbi.nlm.nih.gov/38749429/
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