ADP-ribosylation: from molecular mechanisms to human disease
Author:
Affiliation:
1. Universidade de São Paulo, Brazil
2. University of Sussex, UK; Institute of Histology and Embryology of Mendoza, Argentina
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v43n1s1/1415-4757-GMB-43-1-s1-2019-0075.pdf
Reference161 articles.
1. Proteomic analyses identify ARH3 as a serine mono-ADP-ribosylhydrolase;Abplanalp J;Nat Commun,2017
2. Poly(ADP-ribose)-dependent regulation of DNA repair by the chromatin remodeling enzyme ALC1;Ahel D;Science,2009
3. NAD+ depletion is necessary and sufficient for poly(ADP-ribose) polymerase-1-mediated neuronal death;Alano CC;J Neurosci,2010
4. The zinc-finger domains of PARP1 cooperate to recognize DNA strand breaks;Ali AAE;Nat Struct Mol Biol,2012
5. Molecular mechanism of poly(ADP-ribosyl)ation by PARP1 and identification of lysine residues as ADP-ribose acceptor sites;Altmeyer M;Nucleic Acids Res,2009
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