Cargando…
A quasi-quantitative dual multiplexed immunoblot method to simultaneously analyze ATM and H2AX Phosphorylation in human peripheral blood mononuclear cells
Pharmacologic inhibition of DNA repair may increase the efficacy of many cytotoxic cancer agents. Inhibitors of DNA repair enzymes including APE1, ATM, ATR, DNA-PK and PARP have been developed and the PARP inhibitor olaparib is the first-in-class approved in Europe and the USA for the treatment of a...
Autores principales: | Bakkenist, Christopher J., Czambel, R. Kenneth, Hershberger, Pamela A., Tawbi, Hussein, Beumer, Jan H., Schmitz, John C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4468340/ https://www.ncbi.nlm.nih.gov/pubmed/26097887 |
Ejemplares similares
-
Radiation therapy induces the DNA damage response in peripheral blood
por: Bakkenist, Christopher J., et al.
Publicado: (2013) -
Functional analyses of ATM, ATR and Fanconi anemia proteins in lung carcinoma: ATM, ATR and FA in lung carcinoma
por: Beumer, Jan H., et al.
Publicado: (2015) -
Clustered DNA damage induces pan-nuclear H2AX phosphorylation mediated by ATM and DNA–PK
por: Meyer, Barbara, et al.
Publicado: (2013) -
ATM activation accompanies histone H2AX phosphorylation in A549 cells upon exposure to tobacco smoke
por: Tanaka, Toshiki, et al.
Publicado: (2007) -
AIF-mediated caspase-independent necroptosis requires ATM and DNA-PK-induced histone H2AX Ser139 phosphorylation
por: Baritaud, M, et al.
Publicado: (2012)