ライフサイエンスコーパス: deoxygenation

1 , warming, changes in ocean circulation, and deoxygenation).

2 ecessary to reduce the ecosystems impacts of deoxygenation.

3 t the sensitivity of key bacterial groups to deoxygenation.

4 with young people despite similar levels of deoxygenation.

5 rfusion is not necessarily commensurate with deoxygenation.

6 ar scar were not associated with significant deoxygenation.

7 t into an aldehyde was observed to accompany deoxygenation.

8 -methyl-2'-deoxyguanosine (3) via 2'-radical deoxygenation.

9 of abnormal hemoglobin that polymerizes upon deoxygenation.

10 ad a low membrane conductance, unaffected by deoxygenation.

11 the 4-position show higher quantum yields of deoxygenation.

12 sitized photoreaction of 7Z in benzene being deoxygenation.

13 anges in threonine phosphorylation following deoxygenation.

14 ymerization could be implemented without pre-deoxygenation.

15 photolytic deoxygenation or radical-based 2'-deoxygenation.

16 y is released from this membrane precinct by deoxygenation.

17 self-associates to dimers and tetramers upon deoxygenation.

18 ctive oxygen scavengers, but is inhibited by deoxygenation.

19 lation occurred after initital, rapid muscle deoxygenation.

20 bal marine nitrogen cycle under severe ocean deoxygenation.

21 microbial oxygen consumption will cause reef deoxygenation.

22 t revealed loss of alpha-helical content and deoxygenation.

23 nic hydrogenation intermediates for glycerol deoxygenation.

24 LWHs and LANG hearts dropped steadily during deoxygenation.

25 ry coordination sphere that aids in oxyanion deoxygenation.

26 chieved by chemical doping, pressure, and/or deoxygenation.

27 t of a trisubstituted double bond by radical deoxygenation.

28 em-scale responses to abrupt, climate-forced deoxygenation.

29 tris(trimethylsilyl)silane-mediated radical deoxygenation.

30 Upon deoxygenation, a lower percentage of HBBAS3-transduced r

31 The combined transamination-deoxygenation activity places ColD in a class by itself.

32 plex formation as a prerequisite for the C-3 deoxygenation activity, we have carried out experiments

33 ine or mesyl chloride/triethylamine-mediated deoxygenation afforded 2H-indazoles.

34 A subsequent two-step deoxygenation affords the corresponding 1-bromo-8-methyl

35 bin to polymerise within erythrocytes during deoxygenation, altering red blood cell rheology and caus

36 oncentration of hemoglobin S and the rate of deoxygenation, among other factors.

37 s accompanied by the efficient nonreversible deoxygenation and 1-2 oxygen migration.

38 terminal hafnocene isocyanate and promoting deoxygenation and additional N-C bond formation resultin

39 formed into extended perylene derivatives by deoxygenation and aromatization with HCl/EtOH.

40 Deoxygenation and chain homologation steps complete the

41 ing, which may be limited by expanding ocean deoxygenation and declining prey availability.

42 xport increase near upwelling zones, causing deoxygenation and deeper carbon injection.

43 iethylborane-methanol system used in radical deoxygenation and dehalogenation processes has been inve

44 activity of hemoglobin is modulated by heme deoxygenation and heme redox potential, with maximal act

45 cation permeability, particularly following deoxygenation and hemoglobin (Hb) polymerisation.

46 This process depends at least partly on deoxygenation and may be influenced by the presence of o

47 re of the nitride complex to CO2 resulted in deoxygenation and N-C bond formation to form isocyanate

48 thropogenic CO2 -driven ocean acidification, deoxygenation and ocean circulation.

49 s have characterized the interaction between deoxygenation and other stimuli of NKCC activity.

50 cularly striking during cycles of hemoglobin deoxygenation and oxygenation in the presence of nitrite

51 e measured by means of sampling ports in the deoxygenation and oxygenation regions.

52 b S (approximately 11 v 18 g/dL) would favor deoxygenation and polymerization of human Hb S Antilles

53 rsion to NO, a process coupled to hemoglobin deoxygenation and protonation, and evince a new, simple

54 nstead, their variance increased during lake deoxygenation and recovery, and then stabilized.

55 Ocean warming, acidification, deoxygenation and reduced productivity are widely consid

56 ns an unprecedented route to interrogate the deoxygenation and reoxygenation of mitochondria, the mac

57 meability is increased, especially following deoxygenation and sickling, mediated by a pathway someti

58 tion conductance was reversibly induced upon deoxygenation and was permeable to both univalent (Na+,

59 properties by allowing release of NO during deoxygenation and/or by interaction with small-molecular

60 ed stresses of warming, ocean acidification, deoxygenation, and altered food inputs.

61 , oxidatively induced reductive elimination, deoxygenation, and elimination reactions when treated wi

62 erization of hemoglobin in the red cell upon deoxygenation, and is characterized by vascular crises a

63 Double alkynylation, reductive deoxygenation, and subsequent oxidation using MnO2 furni

64 ncluding McMurry couplings, reductive ketone deoxygenations, and epoxide openings.

65 Deoxygenations are accomplished by Rh-catalyzed hydrogen

66 ntact intracellular signalling downstream of deoxygenation as indicated by preserved cAMP and ATP rel

67 ebullition are increasingly relevant to reef deoxygenation as reefs become dominated by fleshy algae.

68 re, and vasorelaxant activity is "linked" to deoxygenation, as illustrated herein.

69 ytes but redistributed to the cytoplasm upon deoxygenation, as seen in human erythrocytes.

70 ns above controls, indicating that reductive deoxygenation at C-9 of a xanthone precursor does not ta

71 erturbations on 2 were also studied, namely, deoxygenation at C5 (yielding 2,5-dideoxy-beta-D-erythro

72 dibenzothiophene S-oxide in water results in deoxygenation at significantly higher quantum yields tha

73 ,000-fold, whereas binding is retained after deoxygenation at the C-20 position.

74 t has been made on aliphatic primary alcohol deoxygenation by employing a ruthenium complex, with goo

75 Deoxygenation, by reduction or O atom abstraction reagen

76 This process involves C-2 deoxygenation, C-3 amination and methylation, C-5 epimer

77 composition (CH2O)n, modifications including deoxygenation, C-alkylation, amination, O- and N-methyla

78 The results suggest that deoxygenation causes activation of a kinase that either

79 DO diffusion from the sample stream into the deoxygenation chamber.

80 limited FENs' responses to ocean warming and deoxygenation confirms previous predictions made based s

81 be influenced by the presence of oxygenation/deoxygenation cycles and the frequency of cycling.

82 e subjected to approximately 180 oxygenation/deoxygenation cycles during 4 hours to evaluate RBC dehy

83 f the magnitude occurring during oxygenation-deoxygenation cycles had a minimal effect.

84 e involved, including, but not limited to 1) deoxygenation-dependent hemoglobin polymerization leadin

85 We find that deoxygenation-dependent rheologic processes are sufficie

86 Here, we chose to focus exclusively on deoxygenation-dependent rheologic processes in an effort

87 g a polydimethylsiloxane (PDMS) microfluidic deoxygenation device and ROXS, not only were the fluorop

88 tection strategies, including a microfluidic deoxygenation device.

89 N-Oxides are known to undergo deoxygenation during atmospheric pressure chemical ioniz

90 highly sensitive assay that exploits globin deoxygenation during respiration-catalyzed oxygen uptake

91 ment of perfusion is not sufficient to cause deoxygenation during stress.

92 Deoxygenation elevates glycolytic flux and lowers pentos

93 alcohol functions through a modified Barton deoxygenation employing hypophosphorous acid as the redu

94 ic foraminifera accompanying the most severe deoxygenation event indicates subsurface warming of up t

95 itrosothiol content, both during whole-blood deoxygenation ex vivo and during a 3-week protocol in wh

96 The smaller difference observed in the rapid deoxygenation experiment was associated with much faster

97 indicates, that faster kinetics in the rapid deoxygenation experiment were related to the initial pre

98 free magnesium concentration that occurs on deoxygenation (from 0.82 (S.D., 0.07) to 1.40 mm (S.D.,

99 scientific challenge in the field of alcohol deoxygenation has been direct catalytic sp(3) C-O defunc

100 n-specific cationic conductance activated by deoxygenation, HbS polymerisation and RBC sickling.

101 An aryl deoxygenation, however, also takes place in this overall

102 anthracenes employing a one-pot Pd-catalyzed deoxygenation/hydrogenation sequence.

103 ences between groups in duration of cerebral deoxygenation, hypotension or perioperative changes in l

104 and, along with AprD3, is responsible for 3'-deoxygenation in aminoglycoside biosynthesis.

105 exulose-3-dehydrase (E(1)) catalyzes the C-3 deoxygenation in the biosynthesis of 3,6-dideoxyhexoses

106 eanographic observations indicate increasing deoxygenation in the global oceans and an elevated frequ

107 bin (SNO-Hb), which releases the NO group on deoxygenation in the microcirculation.

108 merization of the abnormal hemoglobin S upon deoxygenation in the tissues to form fibers in red cells

109 in the marine sulfate reservoir during ocean deoxygenation in the waning stages of the positive carbo

110 includes a minor portion of oxidant-forming deoxygenation, in contrast to previous conclusions.

111 reby SNO is released from Hb and RBCs during deoxygenation, in proportion to the degree of Hb deoxyge

112 y deoxygenated ferrous hemes, such that heme deoxygenation increases the rate of NO generation.

113 Deoxygenation-induced activation of the Gardos channel a

114 g RBC deformability in older adults restored deoxygenation-induced ATP release, whereas decreasing RB

115 rmability is a primary mechanism of impaired deoxygenation-induced ATP release, which may have implic

116 dehydration of RBCs from SCD patients - the deoxygenation-induced cation pathway (Psickle), the Ca(2

117 Many features of this deoxygenation-induced conductance (non-specificity for c

118 e o-vanillin also irreversibly inhibited the deoxygenation-induced conductance, partially at 1mM and

119 5HMF markedly reduced the deoxygenation-induced dehydration of RBCs whether in res

120 The deoxygenation-induced pathway was variable in magnitude.

121 er specificity not only during the transient deoxygenation ("initial dip") but also during the early

122 The initial deoxygenation involves a rate-determining step that cons

123 Deoxygenation is a global problem in coastal and open re

124 seudotuberculosis V, have shown that the C-3 deoxygenation is a process consisting of two enzymatic s

125 Deoxygenation is accompanied by an allosteric transition

126 This deoxygenation is accomplished via a photoinduced electro

127 This net two-step ester deoxygenation is an attractive alternative to the classi

128 Stimulation by deoxygenation is comparable with that caused by calyculi

129 that conversion of NAC to SNOAC during blood deoxygenation is necessary for the development of PAH in

130 on occurs above the LAT and that the rate of deoxygenation is sensitive to oxygen delivery.

131 -3,4-dihydroanthracen-1(2H)-one implies that deoxygenation is the first step in monodictyphenone bios

132 However, the biosynthetic mechanism of C3'-deoxygenation is unknown.

133 Although nitrene generation by exhaustive deoxygenation is widely accepted as the operating mechan

134 ction of xanthates using R3B and water (Wood deoxygenation) is presented.

135 Deoxygenations led ultimately to two new deoxy-vancomyci

136 By the same deoxygenation manifold with aliphatic aldehydes and keto

137 ixed-N inventory at an intermediate state of deoxygenation may represent a biogeochemical vulnerabili

138 ease of NO from SNO-Hb was not influenced by deoxygenation-mediated allosteric changes in Hb across a

139 Finally, we found that deoxygenation-mediated ATP release from isolated erythro

140 involve time-consuming, harsh and disruptive deoxygenation methods, while "grafting to" approaches re

141 a free radical mechanism, and the subsequent deoxygenation might also benefit from the weak complexat

142 Continuous deoxygenation (N2/5% CO2) at pH 6.8 generated both ID an

143 exercise below the LAT, neither progressive deoxygenation nor lactate accumulation occurred after in

144 /dL) SS discocytes to repetitive oxygenation-deoxygenation (O-D) cycles in vitro.

145 Analysis of the photoproducts indicated the deoxygenation occurred by at least two different pH-sens

146 cohol linked to a reactive functional group, deoxygenation occurred substantially more rapidly.

147 n to either PRF or SMF increased the rate of deoxygenation occurring several min to several hours aft

148 pport the hypothesis that progressive muscle deoxygenation occurs above the LAT and that the rate of

149 While the deoxygenation of 22 proved to be problematical, the uncy

150 A subsequent two-step deoxygenation of 3 represents the first synthesis of dib

151 Selective deoxygenation of a primary alcohol in the presence of a

152 Formation and deoxygenation of a SNO-Hb/Band 3 protein assembly does n

153 ately recreated based on measurements during deoxygenation of a tissue phantom of mouse erythrocytes.

154 ronsted acidity in the aldolization and self-deoxygenation of acetone to isobutene.

155 reaction provides a means for the effective deoxygenation of alcohols, as demonstrated by the highly

156 lly relevant steps and site requirements for deoxygenation of alkanols and alkanals.

157 This study reports evidence for catalytic deoxygenation of alkanols, alkanals, and alkanediols on

158 C3'-deoxygenation of aminoglycosides results in their decrea

159 ctive transformations are the regioselective deoxygenation of an advanced enone intermediate and the

160 al intermediate in the thiourethane-mediated deoxygenation of an alcohol (Barton-McCombie reaction) c

161 Deoxygenation of capillary electrophoresis separation bu

162 g with its reductase (E3), catalyzes the C-3 deoxygenation of CDP-4-keto-6-deoxy-D-glucose to form th

163 xulose-3-dehydrase (E1), which catalyzes C-3 deoxygenation of CDP-4-keto-6-deoxyglucose in the biosyn

164 triethylphosphite (including a rapid, direct deoxygenation of certain classes of benzoisothiazolones

165 d singlet ((1)B(1)) methylene formation from deoxygenation of CH(2)O by C ((1)D) atom as suggested by

166 ng service causes warming, acidification and deoxygenation of deep waters, leading to decreased food

167 mical strategies developed for the selective deoxygenation of E-O compounds remain as a feasible alte

168 A novel, mild, ecofriendly protocol for the deoxygenation of epoxides to alkenes using indium metal

169 Deoxygenation of ferret erythrocytes stimulates Na+-K+-2

170 xy-D-mannose-3-dehydrase responsible for C-3 deoxygenation of GDP-4-keto-6-deoxy-D-mannose.

171 Deoxygenation of Hb was initiated using the reducing age

172 his observation provides a mechanism for how deoxygenation of hemoglobin/myoglobin could facilitate n

173 applied independently, increased the rate of deoxygenation of human hemoglobin (Hb) in a cell-free as

174 In sickle cell disease, deoxygenation of intra-erythrocytic hemoglobin S leads t

175 Efficient depolymerization and deoxygenation of lignin while retaining the aromatic fun

176 s been developed via the palladium-catalyzed deoxygenation of mandelate esters.

177 n plane movement of cobalt which accompanies deoxygenation of myoglobin also occurs in cobalt hemoglo

178 -exchanged ZSM-5 zeolite crystals during the deoxygenation of nitrogen oxides with propene.

179 azones and nitro-benzyl bromide, followed by deoxygenation of ortho-nitrostyrenes, and subsequent cyc

180 In this respect, the energy-intense deoxygenation of oxo compounds of silicon, phosphorus, a

181 These probes were monitored in gels after deoxygenation of oxyHb and after CO binding to deoxyHb,

182 In the presence of PtCo/NOMC, full deoxygenation of phenolic compounds and a biomass-derive

183 cid lactone, cyclization, and regioselective deoxygenation of phloroglucinol methyl ether affords res

184 been found in Nature but is obtained through deoxygenation of pukalide, the first naturally occurring

185 Third, deoxygenation of RBCs dislodges all GEs from the membran

186 Thus, cyclic deoxygenation of sickle cells under these conditions app

187 in net fluxes of Na(+) and K(+) produced by deoxygenation of SS RBCs.

188 avodoxin/flavodoxin reductase, catalyzes C-3 deoxygenation of TDP-4-keto-2,6-dideoxy-D-glucose.

189 two enzymes act sequentially to catalyze C-2 deoxygenation of TDP-4-keto-6-deoxy-D-glucose to form th

190 first example of enantioselective reductive deoxygenation of tertiary alcohols.

191 l)aniline and DBU in DMF; (3) hydrogenolytic deoxygenation of the "top" unit over Pearlman's catalyst

192 Stannyl radical-mediated deoxygenation of the 3'-O-TBS-2'-thionocarbamate derivat

193 the electronic changes induced by metabolic deoxygenation of the 3-amino-1,2,4-benzotriazine 1,4-dio

194 However, deoxygenation of the C(13)-hydroxyl of 16 provided the 1

195 ound has been efficiently prepared by Barton deoxygenation of the C-2- and C-14-hydroxyl groups on a

196 Deoxygenation of the C4 ketone proved difficult but was

197 ted forms (haterumalides NA, NB, and NE; via deoxygenation of the C9-hydroxyl).

198 ith p-methoxybenzaldehyde, which proceeds by deoxygenation of the carbonyl group and formation of the

199 on of the Cu coordination resulting from the deoxygenation of the CuO chains, as confirmed by first-p

200 The key step is the regioselective deoxygenation of the desired hydroxyl group as either th

201 The subsequent reductive deoxygenation of the Diels-Alder adducts with Fe2(CO)9 f

202 the presence of n-butyllithium, followed by deoxygenation of the double adducts with low-valent tita

203 of epothilone B followed by tungsten-induced deoxygenation of the epoxide moiety.

204 at the sex difference was mediated by lesser deoxygenation of the knee extensors during exercise.

205 2-nitrobiphenyls was achieved via reductive deoxygenation of the nitro groups using a slight excess

206 Palladium-mediated deoxygenation of the resulting allylic alcohol was follo

207 Deoxygenation of the sample could be accomplished by hea

208 lectron reductive coupling and proceeds with deoxygenation of the starting enone or enal.

209 tic investigations indicate that the twofold deoxygenation of the sulfonyl substrate proceeds by the

210 sisted in situ N-Boc-deprotection, selective deoxygenation of the xanthate ester, and lactam hydrolys

211 eir RBCs are misshapen in vivo, and in vitro deoxygenation of their blood induces 30% to 50% of the R

212 ctronic changes resulting from the metabolic deoxygenation of tirapazamine analogues might be exploit

213 Earlier experiments indicated that reductive deoxygenation of versicolorin A is not the first step.

214 ion to determine the redox potential for the deoxygenation of ZnO.

215 Deprotection (deoxygenation) of 12 was accomplished using Lawesson's r

216 f electro-organic synthesis (dehalogenation, deoxygenation) of pharmaceutically relevant building blo

217 y induced seizure causes a stronger cerebral deoxygenation on the side ipsilateral to the electrical

218 Hypoxia and CO accelerated muscle deoxygenation only for exercise above the LAT; for exerc

219 in compared with controls but no evidence of deoxygenation or hypoperfusion during vasodilatory stres

220 by a thioacetyl unit, followed by photolytic deoxygenation or radical-based 2'-deoxygenation.

221 emicals has often focused on either complete deoxygenation or the production of high-volume platform

222 on of RBCs whether in response to maintained deoxygenation or to cyclical deoxygenation/re-oxygenatio

223 osynthesis of GDP-L-colitose represent a new deoxygenation paradigm in deoxysugar biosynthesis.

224 fluence of ocean warming, acidification, and deoxygenation, poses a serious threat to marine organism

225 13 followed by the two-step Barton-McCombie deoxygenation procedure.

226 in the absence of any additives or external deoxygenation procedures using low-organic content media

227 actions, we developed a two-step epoxidation/deoxygenation process that results in overall inversion

228 hat of the plain electrode, while an in situ deoxygenation process, based on GOx-glucose enzyme react

229 orate the mechanism proposed for the overall deoxygenation process.

230 ported conditions used in dehalogenation and deoxygenation processes.

231 s are purportedly consumed during hemoglobin deoxygenation, producing nitric oxide and coupling intra

232 d without rigorous substrate purification or deoxygenation protocols.

233 yranones and subsequent regioselective alpha-deoxygenation provides 1,3-trans-beta-hydroxy-delta-lact

234 Deoxygenation quantum yields are also less solvent depen

235 tantial FEN expansion with ocean warming and deoxygenation, rather than FEN maintenance or contractio

236 e to maintained deoxygenation or to cyclical deoxygenation/re-oxygenation.

237 r with its reductase (E3), catalyzes a novel deoxygenation reaction essential for the biosynthesis of

238 le beta-oxygen effect in the Barton-McCombie deoxygenation reaction is operating where, according to

239 ic camera flash instantaneously triggers the deoxygenation reaction of GO by photothermal heating.

240 Moreover, a revision of the mechanism of the deoxygenation reaction of xanthates using R3B and water

241 groups adjacent to the oxirane ring for the deoxygenation reaction to occur.

242 mophenyl)-3-phenylprop-2-yn-1-one and in the deoxygenation reaction with phenylboronic acid.

243 he phenyl thionoformate unit as a prelude to deoxygenation reactions of polyols.

244 O) in desulfurization, denitrogenation, and deoxygenation reactions.

245 ogenation reactions; (4) oxo-metal catalyzed deoxygenation reactions; and (5) catalyst discovery via

246 In response to haemoglobin deoxygenation, red blood cells (RBCs) release ATP, which

247 Deoxygenation/reoxygenation cycling of oxyHb in the pres

248 A cycle of deoxygenation/reoxygenation does not cause loss of NO or

249 C-O hydrogenolysis becomes the preferred deoxygenation route on Cu-based catalysts, thus avoiding

250 with the percentage of sickled cells at the deoxygenation sampling port and was observed only in the

251 rocyclic di-N-oxide that undergoes enzymatic deoxygenation selectively in the oxygen-poor (hypoxic) c

252 DFT calculations define a two-stage deoxygenation sequence for the reductive C-N coupling.

253 thylsilyl chloride followed by a Barton type deoxygenation sequence of the 3'-hydroxyl groups afforde

254 13-20a) macrocycle, an effective epoxidation/deoxygenation sequence to isomerize the C(13,14) olefin,

255 significantly increased conductance and, on deoxygenation, showed a further rise in membrane conduct

256 Although kinetically invisible, the second deoxygenation stage is implicated as the critical C-N pr

257 The exothermicity of the deoxygenation step for carbon atom reaction with methoxy

258 This eliminated the need for the deoxygenation step that is essential for existing TTA-ba

259 lowed for chain extension without additional deoxygenation steps or exogenous monomer addition.

260 had been only addressed by classic multistep deoxygenation strategies with stoichiometric reagents.

261 ves a tandem aryne Diels-Alder cycloaddition-deoxygenation strategy.

262 ible biological relevance of oxygenation and deoxygenation studies is discussed.

263 In contrast, during intervals of intense deoxygenation such as Cretaceous ocean anoxic event (OAE

264 An inexpensive and quick deoxygenation system for measuring protein phosphorescen

265 responses during 2 conditions of erythrocyte deoxygenation (systemic hypoxia and graded handgrip exer

266 Unlike most deoxygenation systems, carbon monoxide was used as the t

267 In addition to deoxygenation, tert-N-oxides containing an alkyl or benz

268 tituted DBTOs show higher quantum yields for deoxygenation than does the parent molecule, in the orde

269 that future warming can lead to more intense deoxygenation than previously anticipated.

270 enables a novel Barton-McCombie-type radical deoxygenation that proceeds efficiently with visible lig

271 With continuous deoxygenation, the density shift was decreased by inhibi

272 d have provided a positive feedback on ocean deoxygenation through increased nutrient utilization and

273 (DTT) in an assay that allowed the time for deoxygenation to be controlled (from several min to seve

274 histidine swings out of the heme pocket upon deoxygenation to form a bond with a carboxyl group of a

275 osose to hydroxyhydroquinone, and subsequent deoxygenation to form hydroquinone.

276 ydration to 1,2,3,4-tetrahydroxybenzene, and deoxygenation to form pyrogallol.

277 olecules via electrochemical decarboxylation/deoxygenation to improve the stability of fuels and chem

278 reactants were found to increase the rate of deoxygenation to some extent, but in the presence of rea

279 laxed (R, oxygenated) conformation, and that deoxygenation to tense (T) state destabilizes the SNOHb

280 ygenation, in proportion to the degree of Hb deoxygenation, to regulate vessels directly.

281 The effects of acidification and deoxygenation together were not additive.

282 hermal elimination via cyclic ortho ester or deoxygenation via cyclic thionocarbonate.

283 Photobleaching is dramatically reduced by deoxygenation via gas diffusion through porous channel w

284 the products by tert-butyl deprotection or N-deoxygenation was demonstrated.

285 blood flow during conditions of erythrocyte deoxygenation was markedly reduced in aging humans, and

286 The time course of Hb deoxygenation was observed using visible light spectrosc

287 Deoxygenation was the major physiological stimulus for N

288 r at all workloads and APD reductions during deoxygenation were blunted in both LWHs and LANG hearts.

289 Stimulation by calyculin A and deoxygenation were not additive.

290 nd surprising conformational consequences of deoxygenation were revealed for one of the new compounds

291 lood cells (RBCs) release ATP in response to deoxygenation, which can increase blood flow to help mat

292 argest signal arose from a focal increase in deoxygenation, which lasted for approximately 2 sec, con

293 as a consequence of climate change, yet how deoxygenation will affect the microbial communities that

294 with diisobutylaluminum hydride followed by deoxygenation with boron trifluoride etherate in the pre

295 for the physiologic coupling of erythrocyte deoxygenation with increased NO bioactivity in vivo.

296 Deoxygenation with reclamation of the mu-pdt parent comp

297 he silane reductant influences the degree of deoxygenation, with diethylsilane effecting the complete

298 nd effect of cell membrane stiffening during deoxygenation, with granular RBC shapes leading to the g

299 ndoles under identical conditions results in deoxygenation without cyclization.

300 addition to their utility in Barton-McCombie deoxygenations, xanthates can engage in 5-exo-trig radic