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A subset of cancer cell lines is acutely sensitive to the Chk1 inhibitor MK-8776 as monotherapy due to CDK2 activation in S phase

DNA damage activates Checkpoint kinase 1 (Chk1) to halt cell cycle progression thereby preventing further DNA replication and mitosis until the damage has been repaired. Consequently, Chk1 inhibitors have emerged as promising anticancer therapeutics in combination with DNA damaging drugs, but their...

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Bibliografske podrobnosti
izdano v:Oncotarget
Main Authors: Sakurikar, Nandini, Thompson, Ruth, Montano, Ryan, Eastman, Alan
Format: Artigo
Jezik:Inglês
Izdano: Impact Journals LLC 2015
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4811467/
https://ncbi.nlm.nih.gov/pubmed/26595527
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