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PARI overexpression promotes genomic instability and pancreatic tumorigenesis

Treatment options for patients with pancreatic ductal adenocarcinoma remain limited. Therapeutic targets of interest include mutated molecules that predispose to pancreatic cancer such as KRAS and TP53. Here we show that an element of the homologous recombination pathway of DNA repair, the PARP-bind...

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Detalhes bibliográficos
Main Authors: O’Connor, Kevin W., Dejsuphong, Donniphat, Park, Eunmi, Nicolae, Claudia M., Kimmelman, Alec C., D’Andrea, Alan D., Moldovan, George-Lucian
Formato: Artigo
Idioma:Inglês
Publicado em: 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3630264/
https://ncbi.nlm.nih.gov/pubmed/23436799
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/0008-5472.CAN-12-3313
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