Mismatch Repair-Deficient Crypt Foci in Lynch Syndrome – Molecular Alterations and Association with Clinical Parameters

Lynch syndrome is caused by germline mutations of DNA mismatch repair (MMR) genes, most frequently MLH1 and MSH2. Recently, MMR-deficient crypt foci (MMR-DCF) have been identified as a novel lesion which occurs at high frequency in the intestinal mucosa from Lynch syndrome mutation carriers, but ver...

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Vydáno v:PLoS One
Hlavní autoři: Staffa, Laura, Echterdiek, Fabian, Nelius, Nina, Benner, Axel, Werft, Wiebke, Lahrmann, Bernd, Grabe, Niels, Schneider, Martin, Tariverdian, Mirjam, von Knebel Doeberitz, Magnus, Bläker, Hendrik, Kloor, Matthias
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2015
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4376900/
https://ncbi.nlm.nih.gov/pubmed/25816162
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0121980
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