The zinc finger domains of PARP-1 are selectively and potently inhibited by the Au(I)-based drugs sodium aurothiomalate and aurothioglucose. [PDF]
Bashtanova U, Duer MJ.
europepmc +1 more source
Histone γH2AX and Poly(ADP-Ribose) as Clinical Pharmacodynamic Biomarkers
C. Redon +8 more
semanticscholar +1 more source
Structural basis for the inhibition of poly(ADP-ribose) polymerases 1 and 2 by BMN 673, a potent inhibitor derived from dihydropyridophthalazinone. [PDF]
Aoyagi-Scharber M +5 more
europepmc +1 more source
Chromatin relaxation dynamics and histone PTMs in the early DNA damage response. [PDF]
Qian J, Xie Z, Zhou L, Zhu WG.
europepmc +1 more source
The nicotinamide hypothesis revisited-plant defense signaling integrating PARP, nicotinamide, nicotinic acid, epigenetics, and glutathione. [PDF]
Berglund T, Ohlsson AB.
europepmc +1 more source
Identifying Direct Protein Targets of Poly-ADP-Ribose Polymerases (PARPs) Using Engineered PARP Variants-Orthogonal Nicotinamide Adenine Dinucleotide (NAD+) Analog Pairs. [PDF]
Carter-O'Connell I, Cohen MS.
europepmc +1 more source
Global research trends in PARP inhibitors for ovarian cancer: a bibliometric analysis. [PDF]
Wang X, Ding G, He J, Huang Y, Wang Q.
europepmc +1 more source

