ライフサイエンスコーパス: nitrosation

1 st report of Sirt2 and Sirt6 inhibition by S-nitrosation.

2 of which have been reported as targets of S-nitrosation.

3 ion has been used as an index for endogenous nitrosation.

4 ly be applied for the detection of protein S-nitrosation.

5 ion of free NO as the primary mechanism of S-nitrosation.

6 onine requirements arising from homocysteine nitrosation.

7 sms, and obtained evidence of critical thiol nitrosation.

8 link dG-to-dG is an important product of DNA nitrosation.

9 and to which extent this effect depends on S-nitrosation.

10 to the N-nitrosoamidinium ion and reversible nitrosation.

11 ited slower reaction pathways required for S-nitrosation.

12 y, and this effect was also potentiated by S-nitrosation.

13 ttranslational modification of proteins by S-nitrosation.

14 reas electron-withdrawing ones decelerated N-nitrosation.

15 ing NO, an effect that is not prevented by S-nitrosation.

16 bly via reaction(s) of intracellular trans-S-nitrosation.

17 ometry were used to quantify the degree of S-nitrosation.

18 y regulate the direction of reversible S-(de)nitrosation.

19 on nitrosylation and S-nitrosation but not N-nitrosation.

20 DNA-binding by Cmr was severely impaired by nitrosation.

21 free thiols and site-specific analysis of S-nitrosation.

22 and dichloramine (NHCl(2)), which also form nitrosation agents.

23 combined effects of amine reactivity toward nitrosation and amine volatility.

24 like GSNO, NO does not elicit homocysteine S nitrosation and compensatory increases in methionine bio

25 organic azide synthesis through sequential N-nitrosation and dehydration of aryl hydrazines.

26 Nitrosation and denitrosation of caspase 3 was correlate

27 their activity, it has been suggested that S-nitrosation and denitrosation of cellular thiols are fun

28 sulted in a marked decrease in intracellular nitrosation and diminished NO-induced posttranslational

29 We here show that N-nitrosation and heme-nitrosylation are indeed as ubiquit

30 at neutral pH could be attributed to abiotic nitrosation and if N2O was consumed during N2 formation.

31 sociated with a drastic decrease in global S-nitrosation and in levels of SNO-Trx1 in the KI mice.

32 or and acute exercise reduced iNOS-induced S-nitrosation and increased insulin sensitivity in the mus

33 ported that compounds in garlic may suppress nitrosation and inhibit carcinogenesis.

34 es with mtH(2)O(2) production through KGDH S-nitrosation and may be useful in alleviating nonalcoholi

35 The highly disparate rates of aromatic nitrosation and nitration, despite the very similar (ele

36 ectron-transfer) mechanism for both aromatic nitrosation and nitration.

37 rculating pool of NO metabolites (oxidation, nitrosation and nitrosylation products) were measured in

38 Nitrosation and oxidation in the regulation of gene expr

39 lational modifications of p21ras including S-nitrosation and S-glutathiolation have been demonstrated

40 Cysteine S-nitrosation and S-sulfination are naturally occurring po

41 proteomic analysis demonstrates that both S-nitrosation and S-sulfination are widespread, yet exhibi

42 tissues reveals distinct profiles for both S-nitrosation and S-sulfination.

43 Since thiols can undergo nitrosation and the cell membrane is rich in thiol-conta

44 s posttranslational protein modifications, S-nitrosation, and genome-wide epigenetic modifications th

45 oute for NO bioactivity occurs via protein S-nitrosation, and involves the addition of a NO moiety to

46 to diverse modifications, such as oxidation, nitrosation, and lipidation.

47 books as electrophilic aromatic bromination, nitrosation, and nitration, respectively.

48 d liver modifications involved both S- and N-nitrosation, and RBC S-nitrosothiol formation emerged as

49 transfer mechanism in protein nitration and nitrosation are discussed.

50 Dietary N-nitroso compounds and endogenous nitrosation are important carcinogenic factors, but huma

51 eous when intracellular reactions of trans-S-nitrosation are to be studied.

52 t the need to study the risk of endogenous N-nitrosation associated with these products.

53 ciated from cSrc because of increased Cav1 S-nitrosation at Cys(156), leading to cSrc activation, con

54 hat this particular action of Trx requires S-nitrosation at Cys-69.

55 e plasmatic NO reaction products and limit S-nitrosation at low NO flux.

56 the selectivity and redox dependence of Trx nitrosation at physiologically relevant concentrations a

57 ghly diffusible stable gas NO could initiate nitrosation at sites of neutrophil infiltration.

58 t, MitoSNO, to determine how mitochondrial S-nitrosation at the reperfusion phase of myocardial infar

59 ditions could be a favourable medium for Tau nitrosation, attention should be paid to potential situa

60 model promoted heme iron nitrosylation and S-nitrosation but not N-nitrosation.

61 r activity that increases with the degree of nitrosation, but S-nitroso derivatives show the greatest

62 , these effects are further potentiated by S-nitrosation, but this posttranslational modification is

63 Our results indicate that, in addition to nitrosation by the .NO derivative dinitrogen trioxide (N

64 tion (by measuring carbonyl groups), protein nitrosation (by measuring nitrosamines), and proteolysis

65 ather than NO autoxidation, explaining why S-nitrosation can compete effectively with nitrosylation.

66 The iNOS self-nitrosation characterized here appears appropriate to he

67 The acidic nitrosation chemistry of nine acyclic secondary and tert

68 are presented of a theoretical study of the nitrosation chemistry of pyrroline 1 (X = CH(2)), imidaz

69 line-based trigger that reacts with NO via N-nitrosation chemistry.

70 as a source of nitrosonium for nitrosothiol nitrosation, completing the catalytic cycle.

71 ential tests revealed that even under strong nitrosation conditions, polyDADEPC and related lower-ord

72 Sirt1 S-nitrosation correlated with Zn(2+) release from the cons

73 lational modification of Sirt1 by cysteine S-nitrosation correlates with increased acetylation of Sir

74 er enzymes are known to promote reversible S-nitrosation/denitrosation in biology.

75 uene) had various impacts on the extent of N-nitrosation, depending on the iron level.

76 The efficiency of PFC-mediated S-nitrosation depends on the amount of PFC in aqueous solu

77 ion of this residue, precluding hemoglobin S-nitrosation, did not change total red blood cell S-nitro

78 t not to NO2(-), combined with the lack of S-nitrosation during anoxia alone or by NO2(-) during norm

79 I(R)) to investigate protein oxidation and N-nitrosation during bovine meat digestion.

80 isothermal titration calorimetry as well as nitrosation experiments using S-nitrosocysteine demonstr

81 ates in nitration (Figure 8) but only one in nitrosation (Figure 7).

82 To further address the role of S-nitrosation for the overall antiapoptotic effect to Trx,

83 the reported oxygen-dependent promotion of S-nitrosation from SNO-Hb involves biochemical mechanisms

84 tion reactions; however, the kinetics of Trx nitrosation has not previously been investigated.

85 seudo-first-order rate constants for amidine nitrosation in aqueous acetic acid with excess nitrite a

86 e involvement of nitric oxide (NO) -mediated nitrosation in cell signaling and pathology.

87 Constitutive protein S-nitrosation in cells was detected by analysis with bioti

88 sulfur compounds found in garlic may inhibit nitrosation in humans.

89 N-Nitrosation in oxygenated nitric oxide (NO middle dot) s

90 bitors, decreased interferon-gamma-induced S-nitrosation in procaspase-9.

91 otentially be applied for the detection of S-nitrosation in protein systems.

92 t2, are modified and inhibited by cysteine S-nitrosation in response to exposure to both free nitric

93 However, the analysis of protein S-nitrosation in situ has been difficult because of the ab

94 S-nitrosation in the brain shows regional differences and

95 ne in the formation of N-nitrosamines during nitrosation in the presence of carbonyl compounds, espec

96 ults indicate that ONOO- may contribute to S-nitrosation in vivo and that direct nitrosation of thiol

97 -nitrosylation are indeed as ubiquitous as S-nitrosation in vivo and that the products of these react

98 y, aged iNOS-null mice were protected from S-nitrosation-induced insulin resistance.

99 binding assays were consistent with Sirt1 S-nitrosation inhibiting binding of both the NAD(+) and ac

100 S-Nitrosation is a post-translational modification of prot

101 S-nitrosation is a posttranslational, oxidative addition o

102 Nitrosation is an important reaction elicited by nitric

103 also raise the intriguing possibility that N-nitrosation is directly involved in the modulation of pr

104 A paradox of S-nitrosation is that only a small set of reactive cystein

105 Biomarkers of nitrosation, lipoperoxidation, and cytotoxicity were mea

106 itionally, pharmacologic agents disrupting S-nitrosation markedly increased cisplatin toxicity, where

107 dings suggest that the functional effects of nitrosation may be organized to occur within discrete do

108 ed and fully characterized, suggesting the S-nitrosation may proceed through the intermediary of anal

109 of GSNO, indicative of a direct nucleophilic nitrosation mechanism with elimination of HOO-.

110 s mutagenic, in the present article tyramine nitrosation mechanisms have been characterized in order

111 igma-complex, whereas this Wheland adduct in nitrosation merely represents a high energy (transition-

112 toward elucidating the mechanism by which S-nitrosation modulates a protein's function is identifica

113 dation peaks and only glyphosate is prone to nitrosation, n-nitroso glyphosate and glufosinate were u

114 e nitrosylation (e.g., DAF radical + NO) and nitrosation (NO+ addition).

115 xidase (MPO), a mediator of inflammation, on nitrosation observed during NO autoxidation.

116 To better understand how nitrosation occurs in biological systems, we assessed th

117 Little is known about whether such nitrosation occurs in physiological conditions and, if s

118 during normoxia places constraints on how S-nitrosation occurs in vivo and on its mechanisms of card

119 Although trans-nitrosation occurs with methanol, 1 degree, 2 degree, an

120 el of NO in the media was also observed, and nitrosation of 2,3-diaminonapthalene was increased great

121 QTOs were prepared by nitrosation of 2,4-quinolinediols.

122 Nitrosation of 2-amino-3-methylimidazo[4,5-f]quinoline (

123 o-4-nitroisoxazoles has been developed using nitrosation of 4-nitroisoxazole-based enamines with tert

124 benzoxazinone-3-sulfonamide was prepared by nitrosation of a beta-ketosulfonamide followed by intram

125 Nitrosation of a conserved cysteine residue at position

126 Here we show that S-nitrosation of adult human hemoglobin (Hb A(0)) or sickl

127 Nitrosation of amine, thiol, and hydroxyl residues can m

128 rite with no significant risk of artifactual nitrosation of amines.

129 our-membered ring lactones, resulting in the nitrosation of amino carboxylic acids, the fraction of E

130 This study examines nitrosation of aminothiones in acidic solutions and re-e

131 c-oxide synthase (NOS) inhibitors regulate S-nitrosation of an initiator caspase, procaspase-9, in a

132 In contrast, S-nitrosation of ATP synthase alpha subunit in DHF hearts

133 steric mechanisms for hemoglobin, based on S-nitrosation of beta-chain cysteine 93, raise the possibi

134 a-chain (betaCys93) and, specifically, for S-nitrosation of betaCys93 to form S-nitrosohemoglobin (SN

135 hypothesis is that red meat facilitates the nitrosation of bile acid conjugates and amino acids, whi

136 Nitrosation of biological thiols is believed to be media

137 nitrosyl group, and in one subunit, partial nitrosation of bound NOHA.

138 Nitrosation of bovine serum albumin with acidified NaNO2

139 , our data support an important role for the nitrosation of brain proteins.

140 131, R135, K150, and H154) that facilitate S-nitrosation of C151.

141 act as an anti-apoptotic factor via trans-S-nitrosation of caspase 3.

142 isplatin treatment, resulting in augmented S-nitrosation of caspase-3 and prolyl-hydroxylase-2, the e

143 Neither S-nitrosation of caspase-3 nor induction of Hsp70 appeared

144 demonstrate that modulation of NO-mediated S-nitrosation of cellular proteins is strongly associated

145 The nitrosation of cellular thiols has attracted much intere

146 Reversible S-nitrosation of complex I slows the reactivation of mitoc

147 of complex I is afforded by the selective S-nitrosation of Cys39 on the ND3 subunit, which becomes s

148 S-Nitrosation of cysteine beta93 in hemoglobin (S-nitrosoh

149 competes for DAF-2, whereas AA decreases the nitrosation of DAF-2 to a larger extent, possibly becaus

150 Quenching of DHR oxidation by azide and nitrosation of diaminonaphthalene were exclusively obser

151 modifluoromethyl)trimethylsilane followed by nitrosation of difluorinated organozinc species with an

152 olites mediate the oxidation, nitration, and nitrosation of DNA bases, amino acids, and lipids.

153 Our results show that S-nitrosation of endogenous procaspase-9 occurs in the HT-

154 nes with a biotin tag enabled us to reveal S-nitrosation of endogenous procaspase-9 that was immunopr

155 ploying a synthetic strategy that involves C-nitrosation of enoldiazoacetates, while the diazo functi

156 osation reactions, a systematic study of the nitrosation of ethylbenzene, phenethylamine, and tyramin

157 tional model of ceruloplasmin in mediating S-nitrosation of external thiols, with implications for bi

158 of nitrite (20 nM/min) but failed to elicit nitrosation of extracellular 2,3-diaminonapthalene.

159 pounds in the formation of N-nitrosamines by nitrosation of five secondary amines via different pathw

160 processes and are inversely linked to the S-nitrosation of GAPDH and (ii) that the NO sensitivity of

161 rmed that the NO effects are all linked to S-nitrosation of GAPDH at Cys-152.

162 Nitrosation of GSH could theoretically proceed via inter

163 nstrate that GSNO binding does not precede S-nitrosation of GSTP1-1.

164 It involves nitrosation of H2O2 at pH> or = 12.5 by isoamyl or butyl

165 S-nitrosation of Hb (SNO-Hb) may confer vasodilatory prope

166 ity and R-state character that result from S-nitrosation of Hb S would be expected to decrease its po

167 NO breathing increases S-nitrosation of hemoglobin beta-chain cysteine 93, howeve

168 tch method were used to confirm endogenous S-nitrosation of iNOS.

169 (S)-nitrosation of Keap1 may contribute to nuclear accumulat

170 phosphate pathway and NRF2 pathway through S-nitrosation of Keap1, thereby preserving myocardial oxid

171 Aging increased iNOS expression and S-nitrosation of major proteins involved in insulin signal

172 Nitrosation of MDEA, a tertiary amine, is not catalyzed

173 )(u-NO)](2+) complex is also competent for O-nitrosation of MeOH.

174 We found that protection is due to the S-nitrosation of mitochondrial complex I, which is the ent

175 oxide by cardiac myoglobin and subsequent S-nitrosation of mitochondrial membrane proteins reduced m

176 f mitochondrial respiration as a result of S-nitrosation of NADH: ubiquinone oxidoreductase (complex

177 When comparing the rate of DEANO-mediated nitrosation of Ng with other sulfhydryl-containing compo

178 -1-(3-pyridyl)-1-butanone (NNK) is formed by nitrosation of nicotine and has been identified as the m

179 -1-(3-pyridyl)-1-butanone (NNK) is formed by nitrosation of nicotine and has been identified as the m

180 omponent in cigarette smoke and is formed by nitrosation of nicotine.

181 ntact, gas-to-skin deposition, and epidermal nitrosation of nicotine.

182 e emitted during smoking and form indoors by nitrosation of nicotine.

183 propose a cationic chain mechanism in which nitrosation of nitrosothiol produces a nitrosated cation

184 elective, and convenient method for the ipso-nitrosation of organotrifluoroborates using nitrosonium

185 Late bloomer: Nitrosation of peracetylated sialic acid glycosides foll

186 conjunction with ischemia led to extensive S-nitrosation of protein thiols across all cellular compar

187 osure to ischemia alone results in minimal S-nitrosation of protein thiols.

188 rly neurodegeneration identified increased S-nitrosation of proteins important for synapse function,

189 ucible nitric oxide synthase (iNOS) in the S-nitrosation of proteins involved in the early steps of t

190 ccumulating evidence has demonstrated that S-nitrosation of proteins plays a critical role in several

191 to quantify the extent of NO2(-)-dependent S-nitrosation of proteins thiols in vivo Using this approa

192 rosylation reaction that is coupled to the S-nitrosation of sGC cysteines.

193 of nano-antioxidant (SNO-Man-HSA) via the S-nitrosation of SH-Man-HSA.

194 NOS1-dependent S-nitrosation of SOCS1 impairs its binding to p65 and targ

195 is bimolecular attack by N(2)O(3); (iii) the nitrosation of taurine affords ethanesultone (ES), which

196 An S-nitrosation of the aconitase [4Fe-4S] center catalyzed b

197 sation pathway is general and results in the nitrosation of the amine Ph2NH and alcohol (t)BuOH to gi

198 benzothiazolines (2) were synthesized by the nitrosation of the corresponding 2-iminobenzothiazolines

199 ations of FL(5) versus FL(5)-NO reveal how N-nitrosation of the fluorophore ligand brings about the f

200 The nitrosothiol 2 was prepared via direct S-nitrosation of the hydrochloride of L-cysteine ethyl est

201 d medium to nitrous acid, which leads to the nitrosation of the indole that is generated by tryptopha

202 ctivation, we show that NO activates TACE by nitrosation of the inhibitory motif of the TACE prodomai

203 n aged mice is mainly mediated through the S-nitrosation of the insulin-signaling pathway.

204 nthase and nitric oxide production through S-nitrosation of the NRF2-negative regulator Keap1.

205 The data show that S-nitrosation of the zinc tetrathiolate cysteine results i

206 in the presence of Zn(2+), consistent with S-nitrosation of the Zn(2+)-tetrathiolate as the primary s

207 ge DNA by deamination of DNA bases following nitrosation of their primary amine functionalities.

208 A redox-neutral S-nitrosation of thiol has been achieved at a dicopper(I,I

209 Although the nitric oxide (.NO)-mediated nitrosation of thiol-containing molecules is increasingl

210 ; 2b), which is extensively used for trans-S-nitrosation of thiol-containing proteins, has a limited

211 The results suggest that oxidation and nitrosation of thiols by superoxide and NO are determine

212 ute to S-nitrosation in vivo and that direct nitrosation of thiols or other nucleophilic substrates b

213 ced apoptosis to a degree similar to hTrx, S-nitrosation of this protein, which lacks Cys-69, failed

214 nsecticide) to photoinduce the nitration and nitrosation of three aromatic probes (phenol, resorcinol

215 roduced in a residue specific manner via the nitrosation of tryptophan, which enables an easily trigg

216 ogy studies have shown that the product of C-nitrosation of tyramine is mutagenic, in the present art

217 The nitrosations of MEA, DEA, and MMEA are first order in ni

218 The chemical changes (oxidation/nitrosation) of meat proteins during digestion lead to a

219 ctivities, and inhibition capacity against N-nitrosation) of seven neglected and underutilized specie

220 Protein S-nitrosation on cysteine residues has emerged as an impor

221 t the hypothesis that the reaction occurs by nitrosation on the imino nitrogen, followed by the addit

222 lobin), and Tyr-130 (beta-globin) as well as nitrosation on Tyr-24 (alpha-globin) were identified.

223 a significant factor in the advent of either nitrosation or oxidation chemistry in biological systems

224 and their functions can be modified by thiol nitrosation or oxidation.

225 veral of these phytochemicals either inhibit nitrosation or the formation of DNA adducts or stimulate

226 tivities of these enzymes are inhibited by S-nitrosation, our data thus indicate that modulation of i

227 This nitrosation pathway is general and results in the nitros

228 This is consistent with nitrosation potentiation by MPO, not peroxynitrite.

229 The S-nitrosation proceeds by a mixed-valence [Cu(II) Cu(III)

230 This redox- and proton-neutral S-nitrosation process is the first functional model of cer

231 on of NO(3)(-)/NO(2)(-) to the nitration and nitrosation processes was found to be minor under our ex

232 The uric acid nitration/nitrosation product may play a pivotal role in human pat

233 Nicotine and its nitrosation product, nicotine-derived nitrosamine ketone

234 2), this result suggesting that the yield of nitrosation products in the human stomach would increase

235 The principal nitrosation products were amides derived from the amino

236 types of DNA were lower than the morpholine nitrosation rate constant by a factor of approximately 1

237 ) yields close to unity, validating the slow nitrosation rates hypothesized for tertiary amines.

238 The antioxidant or inhibiting nitrosation reaction properties of vegetables and fruits

239 The role of nitrite in the nitrosation reaction was probed at elevated temperatures

240 ts into identifying the protein targets of S-nitrosation reactions and their potential role in cell f

241 Nitrosation reactions are quenched by O-2, while the oxi

242 analysis and spectroscopic studies show that nitrosation reactions are sustained at sulfur, oxygen, n

243 Recent work has illuminated enzymatic N-nitrosation reactions in microbial natural product biosy

244 ic study with UV-visible spectroscopy of the nitrosation reactions of both molecules, as well as of L

245 Nitrosation reactions span a diverse range of applicatio

246 Nitrosation reactions sustained at additional nucleophil

247 To determine the kinetic course of nitrosation reactions, a systematic study of the nitrosa

248 cell-surface PDI reacts with NO, catalyzes S-nitrosation reactions, and facilitates NO transfer from

249 r thioredoxin (Trx) in controlling protein S-nitrosation reactions.

250 tilized for the NO(+) transfer processes and nitrosation reactions.

251 ile acetone and benzaldehyde did not promote nitrosation reactions.

252 he most mutagenic, underwent two consecutive nitrosation reactions.

253 rts have studied thermodynamic end points of nitrosation reactions; however, the kinetics of Trx nitr

254 one via reductive alkylation with acetone, N-nitrosation, reduction, and cyclization.

255 We, therefore, suggest that S-nitrosation regulates activation of endogenous procaspas

256 Protein S-nitrosation represents a recently described form of post

257 Reversal of S-nitrosation resulted in full restoration of Sirt1 activi

258 ns suggested that Zn(2+) loss due to Sirt1 S-nitrosation results in repositioning of the tetrathiolat

259 Although GSNO inactivated hBCATm, neither S-nitrosation, S-glutathionylation, nor dimerization could

260 ide (NO) modification, which can result in S-nitrosation, S-thiolation, or disulfide bond formation.

261 using quantitative proteomics to determine S-nitrosation site occupancy.

262 s occurs, and the functional importance of S-nitrosation sites across the mammalian proteome, remain

263 Here we define two specific non-heme iNOS nitrosation sites discovered by combining UV-visible spe

264 that PAF stimulates hyperpermeability via S-nitrosation (SNO) of adherens junction proteins.

265 function in a cGMP-independent manner, via S-nitrosation (SNO), a redox-based modification of cystein

266 Protein S-nitrosation (SNO-protein), the nitric oxide-mediated pos

267 Here we present an N-nitrosation strategy for deamination under mild conditio

268 l-probe and blot-based assays for cysteine S-nitrosation, sulfenylation, and glutathionylation.

269 actions (amination, amidation, nitration and nitrosation) that involve the use of boronic acids and s

270 nd inhibits complex I by posttranslational S-nitrosation; this dampens electron transfer and effectiv

271 with (Ph,Me) TpZn(SNO) turns on competing S-nitrosation to form (Ph,Me) TpZn-SH and RSNO, the latter

272 te in [Cu(II)](kappa(2)-O2N) that leads to S-nitrosation to give the S-nitrosothiol RSNO and copper(I

273 sformation ("metabolic shunting") from thiol nitrosation to heme nitrosylation.

274 The sensitivities of N-nitrosation to these intra- and intermolecular electroni

275 he only dipeptide that underwent significant nitrosation under these conditions.

276 Renin-angiotensin system-induced Cav1 S-nitrosation was associated with increased Cav1-endotheli

277 The impact of a second cooking stage on nitrosation was evaluated.

278 The rate of nitrosation was found to vary in a systematic way with t

279 Sirt1 S-nitrosation was reversed upon exposure to the thiol-base

280 Maximum inhibition on n-nitrosation was showed by O. gratissimum and E. foetidum

281 ever, the mechanism of Sirt1 inhibition by S-nitrosation was unknown.

282 M: disulfide bond, S-glutathionylation and S-nitrosation were assessed.

283 These sites of nitrosation were confirmed at the peptide level using a

284 mechanisms and kinetic laws of tryptophan N-nitrosation were determined.

285 trations of IgG modified by chlorination and nitrosation were measured in synovial fluids from inflam

286 In a similar fashion, the nitrosations were accelerated in polar solvents but were

287 ased, such that there was a 95% reduction in nitrosation when the fluxes of NO and O-2 were nearly eq

288 cysteine residues that can be subjected to S-nitrosation, whereby this process often acts as an activ

289 the most favoured reaction in tyramine is C-nitrosation, which generates mutagenic products.

290 d in hyperoxia-exposed GGT(enu1) mice except nitrosation, which showed a diminished decrease compared

291 rimental results suggest a mechanism for the nitrosation, whose rate-limiting step is bimolecular att

292 ituted methylamines, followed by their alpha-nitrosation with sodium nitrite and subsequent base medi

293 their R-state conformations in response to S-nitrosation, with increased oxygen affinity and decrease

294 An increase in nitrosation within eggs is evident seconds after insemin

295 er processes; however, consumption of NO and nitrosation within intact cells were exponential.

296 Maximum nitrosation yields were obtained at an oxygen concentrat