Specificity of reversible ADP-ribosylation and regulation of cellular processes
Author:
Affiliation:
1. Sir William Dunn School of Pathology, University of Oxford, Oxford, UK;
2. Max Planck Institute for Biology of Ageing, Cologne, Germany;
3. Division of Molecular Biology, Ruđer Bošković Institute, Zagreb, Croatia
Funder
Wellcome Trust
Cancer Research UK
Deutsche Forschungsgemeinschaft
Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases
European Union’s Horizon
Croatian Science Foundation
Marie Skłodowska-Curie Actions, and Hrvatska Zaklada za Znanost
Publisher
Informa UK Limited
Subject
Molecular Biology,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10409238.2017.1394265
Reference226 articles.
1. In vivo vizualisation of mono-ADP-ribosylation by dPARP16 upon amino-acid starvation
2. Poly(ADP-ribose)–Dependent Regulation of DNA Repair by the Chromatin Remodeling Enzyme ALC1
3. Poly(ADP-ribose)-binding zinc finger motifs in DNA repair/checkpoint proteins
4. Loss of the Mono-ADP-ribosyltransferase, Tiparp, Increases Sensitivity to Dioxin-induced Steatohepatitis and Lethality
5. Molecular mechanism of poly(ADP-ribosyl)ation by PARP1 and identification of lysine residues as ADP-ribose acceptor sites
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