The diverse biological roles of mammalian PARPS, a small but powerful family of poly-ADP-ribose polymerases.
By P. Hassa, M. Hottiger. Frontiers in Bioscience, 2008
604 citations recorded by the source corpus.
Subfields: Oncology
View Paper: https://www.semanticscholar.org/paper/2b04169f84c7a4a6de1d7e9e63d07161a29b7052
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Citations in the corpus
- The PARP Side of the Nucleus: Molecular Actions, Physiological Outcomes, and Clinical Targets (2010, neutral): “The modification most likely occurs on glutamate, aspartate, or lysine residues, although historically the evidence for covalent modification of specific residues has been weak (D’Amours et al., 1999; Hassa and Hottiger, 2008).”
- Stereospecific PARP trapping by BMN 673 and comparison with olaparib and rucaparib (2013, background): “Mol Cancer Ther; 13(2) February 2014 Molecular Cancer Therapeutics 434”
- Age Related Changes in NAD+ Metabolism Oxidative Stress and Sirt1 Activity in Wistar Rats (2011, background): “Moreover, NADH is also able to promote the formation of H2O2 in the presence of iron [78].”
- PARP inhibition: PARP1 and beyond (2010, background): “The amino-terminal DNA-binding domain contains two zinc fingers that are important for the binding of PARP1 to single-strand breaks and double-strand breaks (DSBs”