Generation of assays and antibodies to facilitate the study of human 5′-tyrosyl DNA phosphodiesterase-Reference-Cited by-同舟云学术

Generation of assays and antibodies to facilitate the study of human 5′-tyrosyl DNA phosphodiesterase

Published:2013-05 Issue:2 Volume:436 Page:145-150
ISSN:0003-2697
Container-title:Analytical Biochemistry
language:en
Short-container-title:Analytical Biochemistry

Author:

Thomson Graeme,Watson Amanda,Caldecott Keith,Denneny Olive,Depledge Paul,Hamilton Nicola,Hopkins Gemma,Jordan Allan,Morrow Christopher,Raoof Ali,Waddell Ian,Ogilvie Donald

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference15 articles.

1. A human 5′-tyrosyl DNA phosphodiesterase that repairs topoisomerase-mediated DNA damage;Cortes Ledesma;Nature,2009

2. UnTTrapping the ends: A new player in overcoming protein linked DNA damage;Bahmed;Cell Res.,2010

3. 26S proteasome-mediated degradation of topoisomerase II cleavable complexes;Mao;J. Biol. Chem.,2001

4. Cellular processing pathways contribute to the activation of etoposide induced DNA damage responses;Fan;DNA Repair,2008

5. Mutant p53 cooperates with ETS2 to promote etoposide resistance;Do;Genes Dev.,2012

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