Gene interactions and pathways from curated databases and text-mining

◀ Back to NOS2

NOS2 — PARP16

Text-mined interactions from Literome

Wang et al., Ann N Y Acad Sci 2003 (Disease Models, Animal...) : The mechanisms of MPTP induced neurotoxicity are not yet fully understood but involve activation of N-methyl-D-aspartate ( NMDA ) receptors by glutamate, production of NO by nNOS and iNOS , oxidative injury to DNA, and activation of the DNA damage sensing enzyme poly ( ADP-ribose ) polymerase ( PARP )
Kujundzić et al., Immunol Lett 2008 : Inhibition of poly ( ADP-ribose ) polymerase ( PARP ), a nuclear enzyme involved in DNA repair, replication and transcription, which cleaves NAD into nicotinamide and ADP-ribose, down regulated iNOS gene transcription and NO production in ChIFN-gamma stimulated HD11 cells
von Lukowicz et al., Cardiovasc Res 2008 (Atherosclerosis...) : PARP inhibition or PARP1 deletion reduced PARP activity and diminished expression of inducible nitric oxide synthase , vascular cell adhesion molecule-1, and P- and E-selectin
Mittal et al., Mol Cell Biochem 2011 (Respiratory Distress Syndrome, Adult) : Therefore, surfactant may regulate lung homeostasis by neutralizing acidic microenvironment in inflammatory lesions that leads to the upregulation of iNOS activity through the activation of NF-?B pathway and by PARP activation
Qin et al., Biochim Biophys Acta 2013 (Inflammation) : Moreover, PARP-1 inhibition attenuated LSS induced iNOS and ICAM-1 upregulation by inhibiting nuclear factor kappa B ( NF-?B ) nuclear translocation and activity, with a reduced NF-?B phosphorylation
Czapski et al., Neurochem Int 2013 (Inflammation) : PARP activity plays a role in regulation of expression of iNOS , the main enzyme responsible for oxidative/nitrosative stress in SIR