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Duodecim; Laaketieteellinen Aikakauskirja|December 6, 2017
Disorders of DNA repair mechanisms and their clinical significanceMinttu Kansikas, Minna Nyström, Päivi PeltomäkiHuman Mutation|April 5, 2019
PMS2 expression decrease causes severe problems in mismatch repairMariann Kasela, Minna Nyström, Minttu KansikasHuman Mutation|December 2, 2010
Verification of the three-step model in assessing the pathogenicity of mismatch repair gene variantsMinttu Kansikas, Reetta Kariola, Minna NyströmGenes, Chromosomes & Cancer|June 4, 2008
The first functional study of MLH3 mutations found in cancer patientsMari K Korhonen, Elina Vuorenmaa, Minna NyströmHuman Mutation|June 14, 2014
Assessing how reduced expression levels of the mismatch repair genes MLH1, MSH2, and MSH6 affect repair efficiencyMinttu Kansikas, Mariann Kasela, Jukka Kantelinen, et al.Human Mutation|October 28, 2008
Mechanisms of pathogenicity in human MSH2 missense mutantsSaara Ollila, Denis Dermadi Bebek, Josef Jiricny, et al.International Journal of Cancer|May 13, 2008
Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classificationSaara Ollila, Denis Dermadi Bebek, Marc Greenblatt, et al.Oncology Reports|January 5, 2007
Conditional nuclear localization of hMLH3 suggests a minor activity in mismatch repair and supports its role as a low-risk gene in HNPCCMari K Korhonen, Tiina E Raevaara, Hannes Lohi, et al.Gastroenterology|January 27, 2023
Lynch Syndrome Genetics and Clinical ImplicationsPäivi Peltomäki, Minna Nyström, Jukka-Pekka Mecklin, et al.Human Molecular Genetics|May 23, 2002
Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndromeReetta Kariola, Tiina E Raevaara, Karin E Lönnqvist, et al.Pageof 4