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Both microsatellite length and sequence context determine frameshift mutation rates in defective DNA mismatch repair

It is generally accepted that longer microsatellites mutate more frequently in defective DNA mismatch repair (MMR) than shorter microsatellites. Indeed, we have previously observed that the A(10) microsatellite of transforming growth factor beta type II receptor (TGFBR2) frameshifts −1 bp at a faste...

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Dettagli Bibliografici
Autori principali: Chung, Heekyung, Lopez, Claudia G., Holmstrom, Joy, Young, Dennis J., Lai, Jenny F., Ream-Robinson, Deena, Carethers, John M.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2010
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2912546/
https://ncbi.nlm.nih.gov/pubmed/20418486
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddq151
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