HUGO ID Detailed Result 7873


HUGO ID 7873
Symbol NOS2A
Name nitric oxide synthase 2A (inducible, hepatocytes)
#Occurrence 68
#Paper 20

 


PMID Match String Actual String Score Flanking text Edited by Edit
11978481iNOSiNOS2.7oxide synthase (eNOS), eNOS and inducible nitric oxide synthase (iNOS) iNOS 
12663085iNOSiNOS2.7Wong et al reported that AGE-positive astrocytes and microglia expressing iNOS were found in AD brains and concluded that the activation 
12663085NOSNOS2.7by antioxidants aminoguanidine and inhibitors of nitric oxide synthase (NOS) NOS 
12663085NOSNOS2.7glycation AG has antioxidant properties 81 and also inhibits inducible NOS (iNOS) iNOS 100 
12663085iNOSiNOS2.7has antioxidant properties 81 and also inhibits inducible NOS (iNOS) iNOS 100 
12663085iNOSiNOS2.7properties 81 and also inhibits inducible nitric oxide synthase (iNOS) iNOS 100 
12663085NOSNOSs2.7pentosidine were negative for stress-response proteins (SRPs), SRPs HNE acrolein NOSs and nitrotyrosine as representative markers of oxidative stress 35 
14739060iNOSiNOS1.9NO synthase (nNOS; nNOS type I inducible NO synthase (iNOS; iNOS typeII which is produced in very large amounts by activated 
14739060iNOSiNOS1.9in pathologic conditions especially NO coming from activated microglia (iNOS) iNOS or and from endothelial cells (eNOS) eNOS 
15896810iNOSiNOS2.7(eNOS; eNOS type III and (c) c inducible NOS (iNOS, iNOS type II 
15896810iNOSiNOS2.7In contrast to nNOS and eNOS iNOS can bind to calmodulin even at very low concentration of 
15896810iNOSiNOS2.7calmodulin even at very low concentration of intracellular calcium thus iNOS can exert its activity in a calcium-independent manner 
15896810iNOSiNOS2.7The levels of iNOS in the CNS are generally fairly low 
15896810iNOSiNOS2.7However an increased expression of iNOS in astrocytes and microglia occurs following viral infection and trauma 
15896810iNOSiNOS2.7Activation of iNOS requires gene transcription and the induction can be influenced by 
15964487iNOSiNOS2.2expression of cycloxygenase-2 caspase-1 and inducible nitric oxide synthase (iNOS) iNOS mRNA have been described ( Chen et al. 2000 
15964487iNOSiNOS2.2death by other mechanisms such as inhibition of methaloproteases or iNOS expression ( Chen et al 2000 and Sadowski and Steinmeyer 
16194581iNOSiNOS2.2activation genes such as the inducible nitric oxide synthase (iNOS), iNOS interleukin-1_amp_#x3b2 (IL-1_amp_#x3b2;), IL-1_amp_#x3b2 tumor necrosis factor-_amp_#x3b1 (TNF-_amp_#x3b1;), TNF-_amp_#x3b1 and nuclear 
16242643iNOSiNOS2.5Furthermore malonate did not induce the expression of the iNOS caspase-3 -8 and -9 genes which have been shown to 
16242643iNOSiNOS2.5expression of interleukin 1 beta inducible nitric oxide synthase (iNOS), iNOS caspase-3 and -1 ( Chen et al. 2000 
16242643iNOSiNOS2.5no modifications in the expression of the mRNA's encoding for iNOS caspase-3 -8 and -9 after malonate additions were found we 
16242643iNOSiNOS2.5iNOS caspase-3 -8 and -9 mRNA expression levels are not modulated 
16242643iNOSiNOS2.5Among them the down-regulation of caspases and iNOS and the up-regulation of Bcl-2 have been documented recently ( 
16242643iNOSiNOS2.5cell death we first analyzed the pattern of expression of iNOS caspase-3 -8 and -9 and the antiapoptotic gene Bcl-2 in 
16242643iNOSiNOS2.5in cell viability does not modify the expression of the iNOS caspase-3 -8 and -9 genes 
16242643iNOSiNOS2.5mRNA expression of caspase-3 -8 and -9 as well as iNOS it decreases the mRNA of the antiapoptotic protein Bcl-2 an 
16242643iNOSiNOS2.5be modulated by minocycline after different neurotoxic stimuli such as iNOS and several members of the caspase family ( Chen et 
16242643iNOSiNOS2.5no changes in the expression of the genes coding for iNOS caspase-3 -8 and -9 
16242643iNOSiNOS2.5Fig 6._amp_#xa0 Malonate does not affect iNOS caspase-3 -8 and -9 but significantly reduces Bcl-2 mRNA expression 
16242643iNOSiNOS2.5(A) A Lack of effects of malonate on the iNOS caspase-3 -8 and -9 mRNA expression levels 
17099894iNOSiNOS3.2MNs accumulate NADPH diaphorase and inducible nitric oxide synthase (iNOS)-like iNOS -like immunoreactivity and iNOS gene deletion extends significantly the life 
17099894iNOSiNOS3.2and inducible nitric oxide synthase (iNOS)-like iNOS -like immunoreactivity and iNOS gene deletion extends significantly the life span of G93A-mSOD1 mice 
17099894NOSNOS2.7of MN mitochondria with enhanced toxic potential from distal terminals NOS localization in MN mitochondria and peroxynitrite damage and early degeneration 
17174478iNOSiNOS2.7(nNOS), nNOS endothelial NOS (eNOS) eNOS and inducible NOS (iNOS) iNOS nNOS and eNOS are constitutively expressed isozymes controlling basal NO 
17174478iNOSiNOS2.7synthesizing NO in response to increases in intracellular calcium levels iNOS is expressed in response to specific cytokines growth factors or 
17191135iNOSiNOS3.2and interferon-G (IFN-G) IFN-G promotes a rapid increase in both iNOS expression and nitrite levels followed by enhancement of Hsp70 3 
17191135iNOSiNOS-derived2.73 20 whereas the modulation of HO-1 mRNA expression by iNOS-derived NO following stimulation with LPS has also been reported in 
17191135iNOSiNOS3.2Moreover the early increase in iNOS protein levels observed in endothelial cells exposed to low oxygen 
17191135NOSNOS2.7(ii) ii decreasing the neuronal 3-nitrotyrosine levels and therefore inducible NOS activity and (iii) iii by the well known direct free 
9675268nitric oxide synthasenitric oxide synthase1.0oxidative insult to normal neurons also results from catalytically active redox metal ions i.e iron and copper and particular ros generating enzymes and peptides e.g nitric oxide synthase xanthine oxidase _amp_#x3b2; amyloid etc. present in the brain.  
10930589nitric oxide synthasenitric oxide synthase1.0neither nitroarginine a nitric oxide synthase inhibitor or vitamin e altered the ros levels.  
10930589nitric oxide synthasenitric oxide synthase1.0quercetin a bio flavonoid molecule with antioxidant properties [ 26 ] showed effects similar to ascorbic acid. nitroarginine an inhibitor of nitric oxide synthase nos [ 27 ] did not affect the c dcf fluorescence in resting cells of any group.  
11223912nitric oxide synthasenitric oxide synthase1.0phenylhydrazone|kainic acid|2 4 dinitrophenol|glutamic acid|calmidazolium|cyclosporine|n methylaspartate|calcium|dizocilpine maleate|alpha amino 3 hydroxy 5 methyl 4 isoxazolepropionic acid|dibucaine|nitric oxide synthase|nitric oxide synthase type i|nos1 protein rat|superoxide dismutase|calcium calmodulin dependent protein kinase type 2|calcium calmodulin dependent protein kinases|  
11223912nitric oxide synthasenitric oxide synthase1.0|nitric oxide synthase type i|nos1 protein rat|superoxide dismutase|calcium calmodulin dependent protein kinase type 2|calcium calmodulin dependent protein kinases|  
11978481nitric oxide synthasenitric oxide synthase1.0the generation of nitric oxide no _amp_#x2022; from arginine by nitric oxide synthase is a process which is involved in neurotransmission regulation of vascular relaxation and in inflammatory processes.  
11978481nitric oxide synthasenitric oxide synthase1.0the source of the nitric oxide is possibly from upregulation of an inducible nitric oxide synthase in neurofibrillary tangle bearing neurons or from nitric oxide synthase in astrocytes and microglia adjacent to senile plaques [ 38 and 39 ].  
12663085nitric oxide synthasenitric oxide synthase1.0the cytotoxic effects were attenuated by antioxidants aminoguanidine and inhibitors of nitric oxide synthase nos .  
12663085nitric oxide synthasenitric oxide synthase1.0in addition to its suppressive effect on glycation ag has antioxidant properties [ 81 ] and also inhibits inducible nitric oxide synthase inos [ 100 ].  
12909279nitric oxide synthasenitric oxide synthase1.0nf _amp_#x3ba;b modulates the expression of several proteins such as nitric oxide synthase nos [ 93 ] and cox2 [ 70 ] that might be involved in mechanisms of inflammation mediated neurodegeneration and be crucial in the pathogenesis of als.  
15031734nitric oxide synthasenitric oxide synthase1.0n redox active metals and oxygen species via reactions such as the fenton and haber weiss reactions or via indirect pathways involving the calcium activation of metallo enzymes such as phospholipases nitric oxide synthase and xanthine dehydrogenase also known as xanthine oxidase 22 .  
15031734nitric oxide synthasenitric oxide synthase1.0alzheimer's disease amyotrophic lateral sclerosis friedreich's ataxia huntington's disease nitric oxide synthase parkinson's disease stroke wilson's disease  
15208263nitric oxide synthasenitric oxide synthase1.0cytokines|enzyme inhibitors|lipopolysaccharides|noc 18|nitric oxide donors|nitroso compounds|reactive oxygen species|ng nitroarginine methyl ester|interferon type ii|catalase|nitric oxide synthase|sod1 g93a protein|superoxide dismutase 1|superoxide dismutase|caspase 1|  
15896810nitric oxide synthasenitric oxide synthase1.0the enzyme responsible for no synthesis is the nitric oxide synthase nos family of enzymes which catalyse the conversion of arginine to citrulline and no.  
15964487nitric oxide synthasenitric oxide synthase1.0the exact mechanisms by which minocycline plays these neuroprotective effects remain unknown although a reduced expression of cycloxygenase 2 caspase 1 and inducible nitric oxide synthase inos mrna have been described chen et al. 2000 .  
16043017nitric oxide synthasenitric oxide synthase1.0also elevation of inflammation related genes e.g. induced nitric oxide synthase proinflammatory cytokines occurs at 11 weeks of age in the presymptomatic stage before motor neuron death in g93a sod1 transgenic mice suggesting that neuroinflammation mediated oxidative stress is a 
16194581nitric oxide synthasenitric oxide synthase1.0neuroinflammation has been connected to enhanced signal transduction leading to the activation genes such as the inducible nitric oxide synthase inos interleukin 1_amp_#x3b2; il 1_amp_#x3b2; tumor necrosis factor _amp_#x3b1; tnf _amp_#x3b1; and nuclear factor kappa b nf _amp_#x3ba;b [1] [49] [60] [65] [69] [72] [81] and [86] .  
16242643nitric oxide synthasenitric oxide synthase1.0in this sense tetracyclines can inhibit the matrix metalloproteases activity and superoxide production and can also down regulate the levels of expression of interleukin 1 beta inducible nitric oxide synthase inos caspase 3 and 1 chen et al. 2000 .  
17099894nitric oxide synthasenitric oxide synthase1.0mitochondria in msod1 mouse mns accumulate nadph diaphorase and inducible nitric oxide synthase inos like immunoreactivity and inos gene deletion extends significantly the life span of g93a msod1 mice.  
17174478nitric oxide synthasenitric oxide synthase1.0keywords: amyotrophic lateral sclerosis ataxia telangiectasia like disorder werner syndrome xeroderma pigmentosum nitric oxide synthase superoxide dismutase  
17174478nitric oxide synthasenitric oxide synthase1.0cu zn sod with essential cellular components bruijn et al. 1998 johnston et al. 2000 cleveland and rothstein 2001 and this has been demonstrated with the copper chaperone for sod ccs kato et al. 2001 nitric oxide synthase nos and phosphorylated neurofilaments chou et al. 1996 .  
17174478nitric oxide synthasenitric oxide synthase1.0ros and nitric oxide synthase  
17174478nitric oxide synthasenitric oxide synthase1.0no is a small easily diffusible and transient free radical whose availability is controlled at the synthesis level by the nitric oxide synthase nos enzymes.  
17174478nitric oxide synthasenitric oxide synthase1.0ros and nitric oxide synthase  
17174478nitric oxide synthasenitric oxide synthase1.0ros and nitric oxide synthase  
17191135nitric oxide synthasenitric oxide synthase1.0in addition ad lymphocytes showed an increased expression of inducible nitric oxide synthase ho 1 hsp72 hsp60 and trxr [ 96 ].  
17368952nitric oxide synthasenitric oxide synthase1.0expression of inducible _amp_#xb7; nitric oxide synthase nos increases during the development of als in the g93a transgenic mice compared with normal sod1 mice and nc mice almer et al. 1999 .  
17496232nitric oxide synthasenitric oxide synthase1.0peroxynitrite; hydrogen peroxide; mitochondrial nitric oxide synthase; mitogen activated protein kinase  
17634371nitric oxide synthasenitric oxide synthase1.0although an exogenous source of nitric oxide is not required for ngf to induce sod1 motor neuron death n nitro l arginine methyl ester name 1 m m a general nitric oxide synthase nos inhibitor and 1 2 trifluoromethylphenyl imidazole trim 10 micro m a specific inhibitor of the neuronal isoform of nos prevented ngf induced apoptosis in sod1 motor neurons fig 3 e .