ライフサイエンスコーパス: O

1 O(2) unloading from RBCs was considerably slower than pr

2 O(2)- and O(4)-alkylated thymidine lesions are known to

3 O-(2-(18)F-fluoroethyl)-l-tyrosine ((18)F-FET) (7 studie

4 O-Vanillin also affected networks related to cell cycle

5 Focusing on Li(x)Ni(0.8)Co(0.15)Al(0.05)O(2) as a model compound, we use operando synchrotron X-

6 We show that hypoxia (1% O(2)) specifically increases matrix disassembly and incr

7 In flu ex1 safe1, all (1)O(2)-induced responses, including transcriptional rewiri

8 the anodic membrane side, is crucial for (1)O(2) generation.

9 oids (Thys) are specifically damaged upon (1)O(2) generation and associate with plastoglobules (PGs).

10 The 16-palladium(II)-oxo cluster [Pd(16) O(24) (OH)(8) ((CH(3) )(2) As)(8) ] (Pd(16) ) comprises

11 Variable-temperature (17) O NMR studies suggest that none of the complexes has a s

12 minor oxygen isotope compositions (Delta'(17)O) of atmospheric O(2) and [Formula: see text] are prima

13 -3.98 +/- 1.29 per mille (SD), and delta(17)O = -2.37 +/- 0.57 per mille (SD)), and human exhaled br

14 -5.41 +/- 1.47 per mille (SD), and delta(17)O = -2.92 +/- 0.79 per mille (SD)), GI fluid (GF; deltaD

15 -13.69 +/- 1.23 per mille (SD), and delta(17)O = -8.77 +/- 0.98 per mille (SD)) using a laser-based o

16 Furthermore, 2D proton-detected (1)H-(17)O heteronuclear correlation NMR experiments allow for a

17 ) values calculated from cellulose delta(18) O vs crown fluxes were remarkably consistent; both varie

18 However, estimated delta(18) O(cell) did not agree with measured delta(18) O(cell) wh

19 (cell) did not agree with measured delta(18) O(cell) when the proportion of exchangeable oxygen durin

20 = -119.63 +/- 7.27 per mille (SD), delta(18)O = -13.69 +/- 1.23 per mille (SD), and delta(17)O = -8.

21 D = -35.91 +/- 7.30 per mille (SD), delta(18)O = -3.98 +/- 1.29 per mille (SD), and delta(17)O = -2.3

22 = -36.59 +/- 10.64 per mille (SD), delta(18)O = -5.41 +/- 1.47 per mille (SD), and delta(17)O = -2.9

23 ndard deviations for delta(15)N and delta(18)O of +/-0.3 per mille and +/-0.3 per mille, respectively

24 ar transition in the marine benthic delta(18)O record for global ice volume and deep-sea temperature

25 Reconstructed delta(18)O(sw) displayed positive excursion during major El Nino

26 retation, whereas the foraminiferal delta(18)O-delta(34)S correlation indicates CH(4) advection at th

27 the human erythropoietin with a total of 188 O-glycopeptide spectra reported under 1% FDR.

28 Here, we confirm that the core 2 O-linked glycans mediate this lubricin-galectin-3 intera

29 '-hydroxyl group on the ribose at 3'-end (2'-O-methylation, 2'Ome) is critical for miRNA function in

30 hole-driven scission of the O-H bond in H(2) O is a critical, limiting step in plasmonic photosynthes

31 lutathione (GSH) and hydrogen peroxide (H(2) O(2) ) with high specificity on a basis of domino reacti

32 elopment of a unique hydrogen peroxide (H(2) O(2) )-sensing motif and its capacity for providing cell

33 (2) O(2) upregulated ENaC activity, and H(2) O(2) production was reduced in both the renal cortex and

34 (ORR) via a 2 e(-) pathway with a high H(2) O(2) selectivity of over 95 % in 0.10 m KOH.

35 We also found that H(2) O(2) upregulated ENaC activity, and H(2) O(2) production

36 ional oxygen vacancies in the 2D black In(2) O(3-) (x) nanosheets host, which enhances light harvesti

37 lfide as an electron donor will promote N(2) O and ammonium production, which is generally not desira

38 warming-induced rise in soil CH(4) and N(2) O emissions (1.84 Pg CO(2) -equivalent/year) could reduc

39 However, there is little information on N(2) O emissions from forest streams although they constitute

40 ilizer use efficiency and mitigation of N(2) O emissions.

41 ve and negative signs for net CH(4) and N(2) O flux.

42 sites that produce or consume CH(4) and N(2) O, such that a range of microsites occurs with both posi

43 emical performance of PANI-intercalated V(2) O(5) electrode is remarkable improved, exhibiting excell

44 uranospinite [Ca(UO(2))(2)(AsO(4))(2).10H(2)O] and becquerelite [Ca(UO(2))(6)O(4)(OH)(6).8(H(2)O)].

45 of deprotonated adenine, [N(4444)][Ad].2H(2)O, and thymine, [P(4444)][Thy].2H(2)O, as well as the do

46 Ad].2H(2)O, and thymine, [P(4444)][Thy].2H(2)O, as well as the double salt cocrystal, [P(4444)](2)[Ad

47 e salt cocrystal, [P(4444)](2)[Ad][Thy].3H(2)O.2HThy.

48 face of the semiconducting Bi(3.33)(VO(4))(2)O(2) and Bi(46)V(8)O(89) components, and the rectifying

49 between the Bi(4)O(7) and Bi(3.33)(VO(4))(2)O(2) phases acting afterward as a conventional p-n junct

50 MSO forms Zn(12)(SO(4))(3)Cl(3)(OH)(15).5H(2)O, ZnSO(3), and ZnS enriched-solid electrolyte interphas

51 response detection of Gsp using YbCl(3).6H(2)O and NdCl(3).6H(2)O solutions.

52 Specifically, O(2) and FeCl(3).6H(2)O catalyzed the cross-dehydrogenative coupling and aroma

53 of Gsp using YbCl(3).6H(2)O and NdCl(3).6H(2)O solutions.

54 The surface Al(2)O(3) layer, formed after an initial thermal oxidation, s

55 ations of SCN(-) near the neutral alpha-Al(2)O(3)(0001)/H(2)O interface show that the vSFG response i

56 upports such as carbon materials, gamma-Al(2)O(3), and zeolite, which is vital to their practical app

57 quired an increase in PEEP of 8[7, 10] cmH(2)O above traditional ARDSnet settings to improve lung fun

58 uctures of a uniaxial antiferromagnetic Cr(2)O(3) crystal and a heavy metal (Pt or Ta in its beta pha

59 minate the existence of twin domains in Cr(2)O(3) films, therefore significantly reducing leakage cur

60 The growth of Cr(2)O(3) on isostructural V(2)O(3) thin film electrodes help

61 he selectivity of a well-defined CeO(2)/Cu(2)O/Cu(111) catalyst from carbon monoxide and carbon dioxi

62 wever, the oxygen sensors based on beta-Ga(2)O(3) and other existing materials lack in response time

63 rted Pd catalysts, producing only CO and H(2)O as waste.

64 n angstroms to nanometers thick adsorbed H(2)O films.

65 nCl(2)-H(2)O, in which DMSO replaces the H(2)O in Zn(2+) solvation sheath due to a higher Gutmann don

66 ) near the neutral alpha-Al(2)O(3)(0001)/H(2)O interface show that the vSFG response in the C=N stret

67 tween 8.7 x 10(13) to 5.0 x 10(15) kg of H(2)O vapour instantaneously into the atmosphere.

68 dian [interquartile range], 11 [8-15] cm H(2)O vs. 31.5 [30-36] cm H(2)O; P < 0.0001), whereas other

69 placed by serine (C674S) were exposed to H(2)O(2) (100 umol/Lmu).

70 naling cascade, which leads to increased H(2)O(2) and Ca(2+) levels and F-actin reorganization, but t

71 results demonstrated that the synergy of H(2)O(2) and gluconic acid is essential for the antibacteria

72 dy (mAb) that inhibited AQP3-facilitated H(2)O(2) and glycerol transport, and prevented liver injury

73 Using H(2)O(2) as oxidant, up to ~300 turnovers for the oxidation

74 aiming at the design of a biosensor for H(2)O(2) detection.

75 reports from other models, mitochondrial H(2)O(2) emission and oxidative damage were greater in Taz(K

76 is limitation by cathodically generating H(2)O(2) in situ.

77 es is used as a strategy to avoid adding H(2)O(2) in the solution during the detection of phenolic co

78 Here we report that H(2)O(2) is spontaneously produced in water microdroplets fo

79 rane side and subsequently terminated by H(2)O(2) oxidation on the anodic membrane side, is crucial f

80 tion pathway in peroxisomes and leads to H(2)O(2) production.

81 ence for mAb inhibition of AQP3-mediated H(2)O(2) transport as therapy for macrophage-dependent liver

82 , by a mechanism involving AQP3-mediated H(2)O(2) transport.

83 Hydrogen peroxide (H(2)O(2)) is a reactive oxygen species (ROS) that mediates e

84 ependent increase: CuO NP-induced OMVs > H(2)O(2)-induced OMVs > control OMVs.

85 asma by the physiologically relevant MPO-H(2)O(2)-NO(2) (-) system.

86 signals from pH changes, histamine, and H(2)O(2).

87 becquerelite [Ca(UO(2))(6)O(4)(OH)(6).8(H(2)O)].

88 The dehydrated molecule [M-H(2)O+H](+) was the base peak of the spectrum and no further

89 g dimethyl sulfoxide (DMSO) into ZnCl(2)-H(2)O, in which DMSO replaces the H(2)O in Zn(2+) solvation

90 stable compound insensitive to O(2) and H(2)O.

91 number (29.8) of DMSO than that (18) of H(2)O.

92 , 11 [8-15] cm H(2)O vs. 31.5 [30-36] cm H(2)O; P < 0.0001), whereas other variables differed later.

93 ative to demand, continuously adjusting JH(2)O(2) production and, in turn, the rate at which energy i

94 The reduction of NO to N(2)O by flavodiiron nitric oxide reductases (FNORs) is rela

95 ly be used as an effective way to reduce N(2)O emission from hypoxic soil in agricultural production

96 The cumulative N(2)O emissions were between 60 and 600 g N(2)O-N ha(-1), sm

97 opriate SOFs applied were able to reduce N(2)O production and maintain greater nitrate-N levels in fl

98 s provide a mechanistic understanding of N(2)O production in eukaryotic phototrophs and represent an

99 nitrogen fertilizer exhibited increased N(2)O production, by 74 times in mineral soil and 2 times in

100 ction of greenhouse gases nitrous oxide (N(2)O) and nitrogen (N(2)) in arable soils include high nitr

101 an ozone-depleting agent, nitrous oxide (N(2)O) plays a critical role in the global climate.

102 bly mild conditions (25 degrees C, 1 bar N(2)O), together with high turnover numbers (TON, up to 6700

103 (2)O emissions were between 60 and 600 g N(2)O-N ha(-1), smaller than predicted based on a fertilizer

104 ating oxygen vacancy (V(O)) in spinel NiCo(2)O(4).

105 trium ruthenium pyrochlores Y(1.8)M(0.2)Ru(2)O(7-delta) (M = Cu, Co, Ni, Fe, Y) controls the concentr

106 ctively) were induced by the stiff (Bi,Sm)(2)O(3) nanopillars embedded.

107 of 2H-azirines with triflic anhydride (Tf(2)O) forms an electrophilic 1-trifloyl-aziridin-2-yl trifl

108 The growth of Cr(2)O(3) on isostructural V(2)O(3) thin film electrodes helps eliminate the existence

109 NA and decreased or absent heparan sulfate 2-O-sulfotransferase 1 in two of three fibroblast cell lin

110 The 24-palladium(II)-oxo cluster [Pd(24) O(44) (OH)(8) ((CH(3) )(2) As)(16) ] (Pd(24) ) can be co

111 ible, possess weak magnetic remanence (Fe(3) O(4) ), or cannot be implemented in nanofabrication sche

112 urfaces regulated by inorganic Cr(3) (mu(3) -O) trimers.

113 agnetic charge transfer insulator YBa(2)Cu(3)O(6.1) revealed rapid demagnetization within 90 fs of ph

114 tic nanocrystals composed of magnetite (Fe(3)O(4)) or greigite (Fe(3)S(4)), enveloped by a lipid bila

115 Separable diastereoisomeric 3-O-camphanate esters of (+/-)-6-O-p-methoxy-benzyl-1,2:4,

116 In Hs3st1(-/-) (HS 3-O-sulfotransferase-1 knockout) cells, reduced 3-O-S leve

117 Kaempferol-3-O-galactoside was the predominant compound in almond ski

118 fined HS oligosaccharides show that a rare 3-O-sulfation (3-O-S) of HS significantly enhances tau bin

119 ulfotransferase-1 knockout) cells, reduced 3-O-S levels of HS diminished both cell surface binding an

120 accharides show that a rare 3-O-sulfation (3-O-S) of HS significantly enhances tau binding.

121 Meanwhile, the ultrasmall size of Cu(5.4)O USNPs enables rapid renal clearance of the nanomateria

122 and the rectifying contact between the Bi(4)O(7) and Bi(3.33)(VO(4))(2)O(2) phases acting afterward

123 composition of a complex metal M oxide (M (4)O(5)) with a stoichiometry of (Fe(3+) (2.15)Fe(2+) (1.59

124 The anion [P(4)O(11)](2-), employed as its bis(triphenylphosphine)imini

125 PAC-Ti(4)O(7) REM was tested with tap water spiked with 0.11 mg L

126 decomposed faster via the isomer (C(6)H(4), O)(C, N, Ph) formed by P-stereomutation involving a M(B2

127 c electrolyte (Li(6.5) La(3) Zr(0.5) Ta(1.5) O(12) ) to fabricate symmetric cells, which exhibit stab

128 ity of highly lithiated phase of Li(7) Ti(5) O(12) for Deep Neural Network applications is reported,

129 y for the low lithiated phase of Li(4) Ti(5) O(12) toward Spiking Neural Network applications, due to

130 Considering Hf(0.5)Zr(0.5)O(2) as the ferroelectric material, we study 180 degrees

131 A 1,5-O -> N carbamoyl shift, a new variation of the anionic F

132 tic data demonstrate the significance of 1,5-O...Ch interactions in enantioselective catalysis.

133 tion of chlorogenic acid (CGA) measured as 5-O-caffeoylquinic acid (5-CQA).

134 ))(2).10H(2)O] and becquerelite [Ca(UO(2))(6)O(4)(OH)(6).8(H(2)O)].

135 nterface of Pt NPs and linker-deficient Zr(6)O(8) nodes resting on the Pt NP surface.

136 Resveratrol and 6-O-methylalaternin were isolated from the Rhubarb for the

137 reoisomeric 3-O-camphanate esters of (+/-)-6-O-p-methoxy-benzyl-1,2:4,5-di-O-isopropylidene-myo-inosi

138 superstructure of Na(0.75)[Li(0.25)Mn(0.75)]O(2), present in almost all oxygen-redox compounds, is l

139 ducting Bi(3.33)(VO(4))(2)O(2) and Bi(46)V(8)O(89) components, and the rectifying contact between the

140 polarization in the ion-conducting Bi(46)V(8)O(89) constituent.

141 )Ni(2+) (0.17)Cu(+) (0.04))(Sigma) (=) (3.95)O(5) We further suggest a possible link between this pha

142 protein by transfer of N-acetylglucosamine (O-GlcNAc) to serine and threonine hydroxyls.

143 vide a mechanistic explanation for the acute O(2) regulation of breathing, reveal an unanticipated ro

144 ) affords an easy way to discover additional O-glycosylations on a multiply glycosylated peptide by v

145 o a planar bicyclic frame with a terminal Al-O(*-) radical site, accompanied by a change from the Fe(

146 at runs in polynomial time and guarantees an O(ln n) approximation.

147 t with ~20% each of the WT conformer and an "O" state in which d(z)(2) Ni(p)(I) (g( ) > g(||) ~ 2) su

148 een groups (O:E = 0.65 vs 1.00, P = 0.11 and O:E = 0.79 vs 1.00, P = 0.15, respectively).

149 O(2)- and O(4)-alkylated thymidine lesions are known to be poorly

150 ved miRNAs, cel-miR-71-5p and bma-lin-4, and O-150 repeat DNA were assessed.

151 LFNG to inhibit JAG1-NOTCH2 activation, and O-fucosylation on EGF9 was important for trafficking of

152 -based and NH-linked analogs, CoPc-based and O-linked MOFs have lower activation energies in the form

153 that apparently high concentrations of C and O at depths up to 1 um in SIMS profiles do not represent

154 articles of the electrode, such as the C and O K-edges to track the stability of carbonate-based elec

155 Monophyly of the M, C, and O lineages is strongly supported, but the A lineage appe

156 we present the first analysis of the N- and O- and glycosphingolipid-glycans from total human lungs,

157 constrains stroke volume, cardiac output and O(2) delivery, thereby impairing VO2 peak and thus exerc

158 cteria peritonitis (SBP), and pneumonia; and O: the CLIF consortium organ failure score (CLIF-C OFs).

159 the reference genome, our de novo assembled O. nubilalis mitochondrial genomes contained 82 intraspe

160 pe compositions (Delta'(17)O) of atmospheric O(2) and [Formula: see text] are primarily regulated by

161 led dimeric lignin model compounds with beta-O-4 linkages were evaporated and ionized using negative

162 me, satisfaction and risk of failure between O and S.

163 Blocking O-glycan elaboration also partially blocked viral entry.

164 on, and methylated Pontin binds Forkhead Box O 3a (FOXO3a).

165 nosomal karyotypes.See related commentary by O'Hagan et al., p.

166 The distance penetrated by O(2) into the roots was shorter at lower O(2) .

167 of materials, and because the elements H, C, O, and N are among the most abundant in the universe, ma

168 carboxamide oxygens within Mn-mu-S-CH(2) -C-O, 5-membered rings.

169 Cross-dehydrogenative C-O coupling of N-hydroxyimides with ketones, esters, and

170 The applicability of this direct C-O bond formation method is shown by synthesizing several

171 applied to the asymmetric construction of C-O bonds at fully substituted carbon centers in the synth

172 rmediates, which promotes the formation of C-O bonds.

173 In this conformation, ring sigma(C-O)* orbitals oriented antiperiplanar to the allyloxocarb

174 partial positive charge developing on the C-O carbon atom progressing C-H abstraction.

175 ight be modified by variants of the catechol-O-methyltransferase (COMT) gene.

176 electric power via fuel cells or combustors, O(2) may be used as a component of oxyfuel in the cement

177 ated Cu particles or atomically dispersed Cu-O-Zr sites only catalyze the reverse water-gas shift rea

178 active site for the formation of a stable Cu-O(2) intermediate.

179 duct, confirmed to be the Vi monomer both de-O- and de-N-acetylated by mono- and bidimensional Nuclea

180 ers of (+/-)-6-O-p-methoxy-benzyl-1,2:4,5-di-O-isopropylidene-myo-inositol allowed the preparation of

181 n part, to impaired convective and diffusive O(2) delivery, and thus V O(2) , especially within fast-

182 7 l min(-1) , P < 0.05) and muscle diffusive O(2) conductance (6.6 +/- 0.8 vs.

183 asurements reveal time profiles of dissolved O(2) in each sample vial, from which Threshold Time of s

184 differences in the inductor structure (i.e., O vs CH(2)).

185 Energy requirement (EE/O) for the treatment of PFOA and PFOS from SBs ranged fr

186 d exclusively at the N-terminus would enable O-glycoproteomic methods to rely solely on collision-bas

187 the large majority of molecules (especially, O-atom bearing molecules) are solvent accessible.

188 etine resulted in elevated 7-ethoxyresorufin-O-deethylase (EROD) activity of cytochrome P450 enzymes

189 with phenotype L, 58 (43%) had a Pa(O(2))/Fi(O(2)) < 150.

190 method to tryptic peptides originating from O-GlcNAcylated proteins TAB1 and Polyhomeotic confirmed

191 ative-flux lower boundary condition, -0.25 g O(2) m(-2) d(-1), was found to more accurately describe

192 one of these types of polyphenol extract (G, O or T), using a homogenizer.

193 with significantly lower risk in blood group O individuals.

194 month and 1 year was similar between groups (O:E = 0.65 vs 1.00, P = 0.11 and O:E = 0.79 vs 1.00, P =

195 nic phosphinite moiety was performed by N -> O phosphinyl migration of aminophosphines borane by heat

196 e C=N stretch region originates from a SCN-H-O-Al complex, suggesting the surface site specificity of

197 e oxygen (O(2)) status of the tumor and HBOC O(2) affinity may play a role in increased O(2) delivery

198 ssociation spectra, O-Pair Search identifies O-glycopeptides via an ion-indexed open modification sea

199 ange from the Fe(+III)/O(-II) to the Fe(+II)/O(-I) valence state.

200 he copper(II) tert-butoxide complex [Cu(II)]-O(t)Bu.

201 e, accompanied by a change from the Fe(+III)/O(-II) to the Fe(+II)/O(-I) valence state.

202 ring twitch contractions reflecting impaired O(2) delivery-to-utilization matching.

203 Importantly, O -> S substitution in squaramide synthons resulted in s

204 C may respond to climate-mediated changes in O(2) dynamics.

205 Overnutrition stimulates an increase in O-GlcNAc signaling in macrophages.

206 C O(2) affinity may play a role in increased O(2) delivery to the tumor.

207 Indeed, O-glycopeptides modified exclusively at the N-terminus w

208 Here, we infer *O. megalodon body dimensions based on anatomical measure

209 d superior performance in identifying intact O-glycopeptides of the human erythropoietin with a total

210 was generated during our attempt to isolate O-benzyl-N-((trimethylsilyl)methyl)hydroxylamine.

211 istine structures of the Fe(III) and Fe(IV) =O redox states of a B-type DyP.

212 25 degrees C) normoxia, warm hypoxia (12 kPa O(2) ), cold (5 degrees C) normoxia, or cold hypoxia.

213 metry analyses reveal that HIPK2 is at least O-GlcNAc modified at S852, T1009, and S1147 residues.

214 tates the formation of superoxo/peroxo-like (O(2) )(n) (-) species, i.e., NiOO*, for enhancing OER ac

215 dexed open modification search and localizes O-glycosites using graph theory and probability-based lo

216 by O(2) into the roots was shorter at lower O(2) .

217 as VO(2)peak responders (ie, Delta >=1.32 mL O(2).kg(-1).min(-1)).

218 ng, driven in part by formation of molecular O(2) inside the solid.

219 portantly, direct elimination of one or more O-glycans under negative-mode MS(2) affords an easy way

220 and (2) prebake at 700 degrees C in 20 mTorr O(2) is shown by atomic force microscopy to yield nearly

221 rval (CI) 5; 172) lower FFM compared to MUAC-O.

222 d SALSA), a large glycoprotein with multiple O-glycosylation repeats.

223 ivatives olefinated through the isolated (N, O)(Ph, C(6)H(4), C) oxaphosphetanes (Channel A), whereas

224 es a sustainable alternative for preparing N,O-biaryl compounds that are widely used as ligands and c

225 e regioselective C-H modification of these N,O-chelated organoboron chromophores incorporating differ

226 ring conformations in the vicinity of the N-O bond.

227 posttranslational control over the nighttime O(2) consumption rate (R(N)) in mature leaves of Arabido

228 We detect an age-dependent decrease in NSC O-GlcNAc levels coincident with decreased neurogenesis a

229 e verify that TgSPY is the nucleocytoplasmic O-fucosyltransferase (OFT) by 1) complementation with Tg

230 lving the strong and/or selective binding of O(2).

231 a broad range of microsite concentrations of O(2) , which then determines the PDF of microsites that

232 Linking microsite consumption of O(2) with a diffusion model generates a broad range of m

233 nts with this mutation are caused by loss of O-fucosylation on TSR3 and impaired ADAMTSL2 secretion.

234 ignals were produced, which allow mapping of O(2) in the tissue within 20 s.

235 In the presence of O(2) , Aer2 signaling increases the autophosphorylation

236 we suggest that electrostatic stabilizers of O(2)-bound intermediates are more crucial for cobalt por

237 s from grape seed (G), grape seed and olive (O) or grape total (T), called ESG, ESO and EST, respecti

238 the more remarkable impact of saturation on O(i), polyunsaturation indicated a higher contribution t

239 ided into two groups of isomers, named open (O-) and closed (C-), based on the ring conformations in

240 adily separated and sequestered, H(2) and/or O(2) may be used to generate electric power via fuel cel

241 chemical properties relative to the original O-based analogue.

242 tational analysis indicated that the oxygen (O(2)) status of the tumor and HBOC O(2) affinity may pla

243 of bipyridine, or using the excess of the >P(O)H reagent as the P-ligand.

244 d by us that the P-C coupling reaction of >P(O)H reagents with PhX (X = I and Br) in the presence of

245 patients with phenotype L, 58 (43%) had a Pa(O(2))/Fi(O(2)) < 150.

246 of Re[Cl(8)TpCF(3)PC](O), Re[Cl(8)TpCH(3)PC](O), and Re[Br(8)TpFPC](O) revealed mild saddling for one

247 ystal X-ray structures of Re[Cl(8)TpCF(3)PC](O), Re[Cl(8)TpCH(3)PC](O), and Re[Br(8)TpFPC](O) reveale

248 ical kinetics with the reaction of gas phase O(3) and aqueous maleic acid droplets.

249 period, demonstrated by high photosynthetic O(2) and CO(2) fluxes and effective yields of PSI and PS

250 he oxo complex [U(O)(NP(pip)(3))(4)], 2-U(PN)O.

251 n important structural aspect of [Fe(IV)poat(O)](-) is the inclusion of an auxiliary site capable of

252 igh pH, concurrently producing a high-purity O(2)/CO(2) gas mixture (1:2 molar ratio at stoichiometri

253 g diacids with oxygen-to-carbon molar ratio (O:C > 1) significantly reduced the rate of polycatechol

254 Released O-glycans were purified by an optimized protocol to elim

255 d Polyhomeotic confirmed previously reported O-GlcNAc sites in TAB1 (S395 and S396) and uncovered new

256 We obtained spatially resolved O-PTIR and AFM-IR spectra confirming the presence of pea

257 ate) with the support and anchored by two Rh-O bonds at framework tetrahedral sites, as shown by infr

258 would need to reliably contain only a single O-glycosite.

259 Specifically, O(2) and FeCl(3).6H(2)O catalyzed the cross-dehydrogenat

260 on- and electron-based dissociation spectra, O-Pair Search identifies O-glycopeptides via an ion-inde

261 agenesis approach, we identify loss of STAT3 O-GlcNAc at Threonine 717 as a driver of astrocyte diffe

262 Steady O(2) depletion shows good quantitative correlation with

263 omoter is present in a progenitor subspecies O. nivara and thus was acquired early during the evoluti

264 ained genes for tetracycline resistance [tet(O)], the Type IV secretion system, conjugative transfer

265 Our results demonstrate that O-GlcNAc controls detained intron splicing to tune syste

266 The results show that O(3) oxidation in the dark diminishes light absorption o

267 Besides, the O. subterraneum mtDNA was also subjected to additional H

268 showed glucose as the major component in the O-glycans of the three SLPs; however, some differences i

269 Interestingly, elimination of the O-fucose site on EGF12 allowed LFNG to inhibit JAG1-NOTC

270 e inference that hole-driven scission of the O-H bond in H(2) O is a critical, limiting step in plasm

271 ating the dehydration scars imprinted on the O-glycosylated sites.

272 ult, we show that it is possible to tune the O(2) affinity at the open metal sites of MOFs for applic

273 The versatility of this O-sulfation strategy was demonstrated in the scalable sy

274 tic interfacial interaction mechanisms of Ti-O-C covalent bonding, sliding of MXene nanosheets, and p

275 ical for OGT activity, and 3) its ability to O-fucosylate itself and a model substrate and to specifi

276 k, yielding a stable compound insensitive to O(2) and H(2)O.

277 Acute cardiorespiratory responses to O(2) deficiency are essential for physiological homeosta

278 nation/Michael addition, are not specific to O-glycan release and can also eliminate phosphoryl subst

279 ), Re[Cl(8)TpCH(3)PC](O), and Re[Br(8)TpFPC](O) revealed mild saddling for one Cl(8) structure and th

280 xpression of both tumor-associated truncated O-linked glycans and their receptor, macrophage galactos

281 l bipyramidal geometry of the oxo complex [U(O)(NP(pip)(3))(4)], 2-U(PN)O.

282 Moreover, using O-GlcNAc-specific mass spectrometry analysis of the agin

283 PET using O-(2-(18)F-fluoroethyl)-l-tyrosine ((18)F-FET) has been

284 systemic K(ATP) channel inhibition reduces V O(2) max and critical speed during treadmill running in

285 tive and diffusive O(2) delivery, and thus V O(2) , especially within fast-twitch oxidative skeletal

286 ials whereby an increased concentration of V(O) sites correlates with a superior OER activity.

287 y of HCOO* protonation is decreased on the V(O) -rich N-SnO(2) NS, thus enhancing HCOO(-) selectivity

288 roles of the three ion pairs formed by the V(O) defect, including Cu(1+) -Ti(4+) , Ti(3+) -Ti(4+) and

289 concentration of surface oxygen vacancies (V(O)) in these materials whereby an increased concentratio

290 ive dopant to modulate the oxygen vacancy (V(O) ) concentration and Ti(3+) formation, which markedly

291 terojunctions and creating oxygen vacancy (V(O)) in spinel NiCo(2)O(4).

292 point to a novel "thiol-blocked" [(PDT)Mo(V)O(S(Cys))(thiolate)](-) structure, which is supported by

293 The clustered and variable O-glycans make the IgA1 glycomic analysis challenging an

294 IR spectroscopy revealed the presence of a W=O moiety arising from the in situ reaction of the W=C(t)

295 cale, PM(2.5) was positively correlated with O(3), daily maximum and minimum temperature, and negativ

296 us environment control reactivity of Cu with O(2).

297 coordinate sites that selectively react with O(2) relative to the remaining six-coordinate sites.

298 After adjustments, WLZ-O had 89 g (95% confidence interval (CI) 5; 172) lower F

299 the electronic properties of the Sn(1-x)Pb(x)O ternary oxide system.

300 Yet, O(2) limitation may differentially impact kinetic or the