ライフサイエンスコーパス: O

1 O-Ethylation of phthalides with Meerwein's reagent follo

2 O-GlcNAc transferase (OGT) regulates a wide range of cel

3 O-GlcNAcylation is a common posttranslational modificati

4 O-Linked N-acetylglucosamine transferase (OGT) catalyzes

5 O. tauri is known to efficiently produce docosahexaenoic

6 identified that Ser255 is the site for Bmi-1 O-GlcNAcylation, and O-GlcNAcylation promoted Bmi-1 prot

7 , p-coumaric acid glucose ester (9.2%) and 1-O-beta-d-glucopyranosyl sinapate (5.6%), while caffeic a

8 o met for the major tacrolimus metabolite 13-O-desmethyl tacrolimus for AUC, but it failed the EMA cr

9 In addition, (15)O-H2O scans to measure cerebral blood flow were acquired

10 Here, we show that solid-state (17) O NMR spectroscopy can provide unique information about

11 Here, we analyze Delta(17)O data from four places (Taipei, Taiwan; South China Sea

12 relate with negative delta(13)C and delta(18)O anomalies, suggesting that explosive reactions between

13 e BTs, electrical conductivity, and delta(18)O in high-frequency streamwater samples taken during two

14 known but differing delta(13)C and delta(18)O isotopic composition allows standard uncertainties of

15 d to be achieved for delta(13)C and delta(18)O measurements, respectively.

16 rained by marine records, including delta(18)O of benthic foraminiferal calcite (delta(18)Oc).

17 Both delta(13)C and delta(18)O of the aragonite are enriched above the expected kinet

18 resolution deep-sea oxygen isotope (delta(18)O) record from the South Atlantic Ocean spanning an inte

19 delta(15)N and 0.5 per thousand for delta(18)O.

20 The oxygen-18 isotopic ((18)O) composition in CO2 provides an important insight into

21 Here, using in situ (18)O isotope labelling mass spectrometry, we provide direct

22 sed a stable isotope labeling technique ((18)O and (2)H) to determine the origin of the C2(1)-formyl

23 he faster substrate was excluded through (18)O-labeling studies.

24 ersion of "open" mitotic arrest deficient 2 (O-MAD2) into "closed" MAD2 (C-MAD2).

25 n distinct viral life cycles, the role of 2' O-methyl modifications in RNA stability and innate immun

26 The rate of miR487b editing, as well as 2'-O-ribose-methylation, is increased in murine muscle tiss

27 ve Epac activator 8-(4-chloro-phenylthio)-2'-O-methyladenosine-3', 5-cyclic monophosphate-AM (8-pCPT-

28 Here we challenged rRNA 2'-O-Me globally by inhibiting the rRNA methyl-transferase

29 However, whether rRNA 2'-O-Me is an adjustable feature of the human ribosome and

30 Our data establish rRNA 2'-O-Me plasticity as a mechanism providing functional spec

31 consisting of consecutive glucuronic acid 2-O-sulfate residues as selectively targeting HCII.

32 tents of rutin, zeaxanthin dipalmitate and 2-O-beta-d-glucopyranosyl-l-ascorbic acid.

33 Using the anionic redox reaction (O(2-) /O(-) ), this Mn-oxide is predicted to show high redox po

34 tructure is formulated [NaO4 (BuSn)12 (OH)3 (O)9 (OCH3 )12 (Sn(H2 O)2 )] (beta-NaSn13 ).

35 Hesperetin-3'-O-glucuronide and the colonic microbiota-derived catabol

36 are related to the population of the Fe(3+) -O-Co(3+) bonds, while the suppressed ferroelectric polar

37 ) in signaling events such as guanosine 5'-3-O-(thio)triphosphate binding and beta-arrestin2 recruitm

38 bubioside was higher than that of cyanidin 3-O-sambubioside with k values of 9.2.10(-7)s(-1) and 8.4.

39 Cyanidin-3-O-glucoside and delphinidin-3-O-glucoside inhibited EGFR

40 d that the degradation rate of delphinidin 3-O-sambubioside was higher than that of cyanidin 3-O-samb

41 =0.87 and 0.77, respectively), delphinidin-3-O-glucoside concentration with HT-29 inhibition (r=0.69)

42 Cyanidin-3-O-glucoside and delphinidin-3-O-glucoside inhibited EGFR (IC50=0.10 and 2.37microM, re

43 High contents in anthocyanins, flavonol-3-O-glycosides, phenolic acids and flavan-3-ols were found

44 In addition, luteolin 7-O-glucuronide 3-O-glucoside was identified for the first time in articho

45 However, 3-O-caffeoylquinic acid, 4-O-caffeoylquinic acid and salvi

46 -apiosylglucoside (apiin) and isorhamnetin-3-O-hexoside.

47 extracts from quince peel and pulp, namely 3-O-caffeoylquinic acid (3-CQA), 4-p-coumaroylquinic acid

48 dimethoxycinnamoyl hexoside and quercetin-3-O-rutinoside, (ii) dill: neochlorogenic acid and quercet

49 receptors, through recognition of a shared 3-O-sulfogalactosyl moiety.

50 id A, the deacetylation of uridyldiphospho-3-O-(R-hydroxydecanoyl)-N-acetylglucosamine by the enzyme

51 N-heterocycles at positions capable for 2-/4-O-pyridine-2-/4-pyridone tautomerism.

52 However, 3-O-caffeoylquinic acid, 4-O-caffeoylquinic acid and salvianolic acid I were only b

53 polysaccharides contain fucose, xylose and 4-O-methylglucuronic acid -residues.

54 d (3-CQA), 4-p-coumaroylquinic acid (HC1), 4-O-caffeoylquinic acid (4-CQA), 5-O-caffeoylquinic acid (

55 imulated to a greater extent by adenosine 5'-O-(thiotriphosphate) (ATPgammaS) than with WT particles.

56 entation caused a pronounced decrease in 3,5-O-dicaffeoylquinic acid and 5-O-caffeoylquinic acid in t

57 ecrease in 3,5-O-dicaffeoylquinic acid and 5-O-caffeoylquinic acid in the preparations.

58 id (HC1), 4-O-caffeoylquinic acid (4-CQA), 5-O-caffeoylquinic acid (5-CQA), derivative of p-coumaroyl

59 The effect of the chlorogenic acid isomer 5-O-caffeoylquinic acid (5-CQA) on digestion of potato sta

60 In addition, luteolin 7-O-glucuronide 3-O-glucoside was identified for the first

61 etected from July to November while tricin-7-O-diglucuronide was the major compound in all other mont

62 the RCC cell lines SN12PM-6-1 (SN12) and 786-O exhibited decreased survival and pronounced apoptosis

63 methyl (3.45%), hexa-decanoicacid (8.19%), 9,O-ctadecenoicacid (5.00%), butyl-6,9,12,15-octadecatetra

64 fically unlocks the nutritive potential of 9-O-acetylated mucus sialic acids for foraging by bacteria

65 e for melatonin synthesis, N-acetylserotonin-O-methyltransferase (ASMT), was cloned from apple rootst

66 tmosphere, indicating the presence of active O atoms, crucial for oxidation catalysts.Improving plati

67 reactions involving cleavage of the C(acyl)-O bond of aryl esters that proceed under mild conditions

68 Low efficacy for both drugs against O. viverrini was observed.

69 is cleaved rather than the weaker aliphatic O-R bond.

70 N-glycans from the original sample aliquot, O-glycans were chemically released from urinary exosomes

71 Porcupine is an O-acyltransferase that regulates Wnt secretion.

72 that predicted by theory and supporting an (O)S2 --> B2,5 --> (1)S5 conformational itinerary for GH1

73 istortion of the -1 subsite mannoside to an (O)S2 conformation, matching that predicted by theory and

74 number of symbionts, Orbicella annularis and O. faveolata, and species with reduced symbiont density

75 5 is the site for Bmi-1 O-GlcNAcylation, and O-GlcNAcylation promoted Bmi-1 protein stability and its

76 ables quantitative analysis of N-glycans and O-glycans from a single specimen and can be applied to a

77 species (O(MeAN)-LA) able to oxidize C-H and O-H bonds.

78 From the SFG spectra in the C-H and O-H regions, we found that the surface layers of Avicel

79 s, H(+) binding sites, Ce(3+) locations, and O vacancies on (100) facets.

80 ormal cellular trafficking depends on N- and O-glycosylation.

81 enrichment methods for enrichment of N- and O-linked glycopeptides.

82 ChIP-sequencing experiments using an anti-O-GlcNAc antibody revealed significant chromatin enrichm

83 cient utilization of LigM as a tool for aryl O-demethylation and as a component of synthetic biology

84 ed amide-containing medicinal drugs, such as O-Me-alibendol and -buclosamide.

85 Alternatively, the single-atom, O-to-S modification of peptide backbone thioamidation ha

86 gle genes encode enzymes for its attachment (O-GlcNAc transferase (OGT)) and removal (O-GlcNAcase (OG

87 of 3-QCA with DOM molecules of above-average O/C and H/C ratios.

88 all cysteine-rich protein motifs that can be O-glycosylated by several ER-localized enzymes, includin

89 otocols have been developed to remove benzyl O-protective groups from oxyarene N-heterocycles at posi

90 only beta-O-4 linkages, or both 5-5 and beta-O-4 linkages, showed major 1,2-eliminations of neutral c

91 Deprotonated compounds with only beta-O-4 linkages, or both 5-5 and beta-O-4 linkages, showed

92 ich show that the energy differences between O-protonation and N-protonation are very small.

93 ravel a previously unidentified link between O-GlcNAcylation, lipid metabolism and the regulation of

94 The BiB2 O(-) and Bi2 B(-) clusters are produced by laser vaporiz

95 odium phenolates to form the substrate-bound O(MeAN)-RPhO(-) species that leads to ortho-hydroxylatio

96 otein kinase (PKG2) to activate forkhead box O (FoxO) in colon cancer cells and in the colon epitheli

97 ble addition of LiCF2P(O)(OEt)2 and BrMgCF2P(O)(OEt)2 reagents to N-t-butanesulfinyl glycosylamines i

98 hat the caspases may be directly affected by O-GlcNAcylation as a potential antiapoptotic mechanism.

99 epigenetic regulation of MYBL1 expression by O-GlcNAc, thereby significantly affecting tumor progress

100 of Hippo pathway (YAP) is O-GlcNAcylated by O-GlcNAc transferase (OGT) at serine 109.

101 t protein modification that is hydrolyzed by O-GlcNAcase (OGA).

102 of colorectal adenocarcinoma progression by O-GlcNAc, we have focused on the O-GlcNAc-mediated epige

103 lkylation; 1,2- 1,3-, or 1,4-addition; and C-O bond formation.

104 catalyzed tandem isomerization followed by C-O and C-C bond formation reaction strategy developed by

105 d to the heme a3 iron atom, with a bent Fe-C-O angle of approximately 142 degrees .

106 he two C-B functions were transformed into C-O systems to allow unambiguous stereochemical assignment

107 Rate-limiting C-O bond cleavage occurs to generate a three-coordinate pr

108 at open circuit voltage then is reduced to C-O containing polymeric species around 0.9 V (vs.

109 ng some important insights for this C-C vs C-O bond shift.

110 nvolving various gamma-hydroxy lactams and C/O/S nucleophiles at room temperature.

111 approach was further developed to catalytic O-transfer from N2O to Si-H bonds.

112 cetylglucosamine transferase (OGT) catalyzes O-GlcNAcylation of target proteins and regulates numerou

113 Additionally, catechol-O-methyltransferase (COMT) polymorphism has been reporte

114 urinary hydroxytyrosol and HVAL and catechol-O-methyltransferase (COMT) rs4680 genotypes were measure

115 ression of tyrosine hydroxylase and catechol-O-methyltransferase (COMT).

116 pCZ1 with the cloned Salmonella Choleraesuis O-antigen gene cluster was introduced into three constru

117 The E coli O-antigen is a promising vaccine target.

118 The conventional O-H insertion product is essentially suppressed by judic

119 he solid state, depending on the counterion, O-protonated or N-protonated cations can be formed, in a

120 gy by oxidase enzymes, includes the critical O-O bond reductive cleavage step.

121 ate how rainfall in the region responds to D-O events.

122 ibbean hydroclimate change associated with D-O variability and particularly with stadial intervals, r

123 (R)-2,3-Di-O-benzylglyceraldehyde and N-tosyl homoallylamine underg

124 al line(C horizontal line)mO] and diketones [O horizontal line(C horizontal line)mO], in order to elu

125 Nutrient-driven O-GlcNAcylation is strikingly abundant in the brain and

126 racteristics in these patients using dynamic O-(2-(18)F-fluoroethyl)-l-tyrosine ((18)F-FET) PET.

127 o oxygen but also activates it for efficient O-O bond cleavage.

128 Cancers display elevated O-GlcNAcylation and suppression of O-GlcNAcylation inhib

129 ino)propyl]amine) that featured an elongated O-O bond but did not lead to O-O cleavage or reactivity

130 es to determine effects on 7-ethoxyresorufin-O-deethylase (EROD) activity, porphyrin accumulation, an

131 Endothelial cells (ECs) express O-glycoproteins that are believed to play important role

132 Comparison of reactivities of [(PyTACN)Fe(O)(X)](+) generated in different spin states and bearing

133 o stabilize the quintet state of [(PyTACN)Fe(O)(X)](+), whereas trifluoroacetate and nitrate stabiliz

134 +) are energetically accessible pathways for O-O bond formation.

135 -1 in cancer and suggests a crucial role for O-GlcNAc signaling in transducing nutritional state to r

136 ical composition of the aqueous extract from O. odorifera leaves and evaluate the correlation of thei

137 nd/or C-terminal prior glycosylation (GalNAc-O-Ser/Thr) preferences modulated by the lectin domain.

138 ma active compounds also distinguished by GC-O.

139 es were characterized by GC-Olfactometry (GC-O) and Aroma Extract Dilution Analysis (AEDA): volatile

140 Thanks to GC-O and GC-MS analysis, cooked fruit notes were identified

141 that (S)P(MeAN) can be activated to generate O(MeAN) and perform the oxidation of external substrates

142 gulation.O-linked beta-N-acetyl glucosamine (O-GlcNAc) is an important protein modification that is h

143 benzoate where the halogen bonding and C-H...O hydrogen bonding are well-matched.

144 ring of the EPK and the catalyst) and C-H...O interactions (between the catalyst and LiClO4) are not

145 2H groups and the important roles of CF2-H...O hydrogen bonds in influencing intermolecular interacti

146 m in a concerted, four-center (H3C...*...H...O*)() transition state.

147 pect thus exists that H2 [(CF3 )7 TpFPP]2 H2 O and cognate structures may act as supramolecular synth

148 d [NaO4 (BuSn)12 (OH)3 (O)9 (OCH3 )12 (Sn(H2 O)2 )] (beta-NaSn13 ).

149 y complex class II (MHC-II)-like molecule H2-O, a negative regulator of antigen presentation.

150 studies are necessary in moderate and heavy O. viverrini infections.

151 biomarkers of the consumption of hesperetin-O-glycoside-containing OJ and other citrus products.

152 Average indoor-to-outdoor (I/O) abundance ratios for the majority of elements were cl

153 ographic characterization of [(N4Py)Fe(III) -O-Ce(IV) (OH2 )(NO3 )4 ](+) (3), a complex obtained from

154 Bk(III)-O and Bk(IV)-O bond lengths are shorter than anticipated

155 nding adaptability and specificity to OGA in O-GlcNAc regulation.O-linked beta-N-acetyl glucosamine (

156 l in the Lao People's Democratic Republic in O. viverrini-infected adults.

157 model for superconductivity is satisfied in O-doped Y2 O2 Bi.

158 uding oxidative stress, results in increased O-GlcNAcylation of numerous proteins, and this increase

159 Furthermore, we find that increasing O-GlcNAcylation decreases spontaneous CA3 pyramidal cell

160 this probe is selectively incorporated into O-GlcNAcylated proteins over cell-surface glycoproteins.

161 igand before the barrier; the other involves O-O homolysis, where the phenol remains H-bonding to the

162 the core component of Hippo pathway (YAP) is O-GlcNAcylated by O-GlcNAc transferase (OGT) at serine 1

163 This observation suggests that Fe(IV) =O complexes may avail of reaction pathways involving mul

164 CMe)](2+) with 2 equiv CAN or [(N4Py)Fe(IV) =O](2+) (2) with Ce(III) (NO3 )3 in MeCN.

165 st is the effect of spin state of the Fe(IV)(O) unit.

166 Bk(III)-O and Bk(IV)-O bond lengths are shorter than anticipated and provide

167 trong credence to the intermediacy of Co(IV)-O species in cobalt-catalysed oxidation of organic subst

168 n adult female rats.-Chen, J.-R., Lazarenko, O.

169 phase and the development of the MnO and Li2 O phases with preferred orientations is demonstrated, wh

170 ereoselective and tunable addition of LiCF2P(O)(OEt)2 and BrMgCF2P(O)(OEt)2 reagents to N-t-butanesul

171 sform optically we can overcome the limiting O(nlogn) complexity of fast Fourier transform algorithms

172 ations predict an additional role for linker O-glycans, namely that they are responsible for maintain

173 r composition of NOM to higher H/C and lower O/C ratios.

174 undergo rapid internal rotation about the M-O bond.

175 Loss of WciG-mediated O-acetylation in serotypes 33X1 and 33X2, however, resul

176 oil per palm (O/P) and oil-to-dry mesocarp (O/DM).

177 t CCSC compartment observed after modulating O-GlcNAc levels is therefore likely to result, at least

178 atures based on the molar mass and molecular O:C ratio of SOA components, and we used the global chem

179 and redox isomerization of {[LCu(III)]2-(mu-O)2}(2+) are energetically accessible pathways for O-O b

180 n at -30 degrees C to yield {[Cu(tmpa)]2-(mu-O)}(2+) (2).

181 and the decay of the asymmetric [Ni(III) (mu-O)2 Co(III) ](2+) core through aromatic hydroxylation re

182 lic reactivity of the symmetric [Ni(III) (mu-O)2 Ni(III) ](2+) complex and the decay of the asymmetri

183 re-earth (RE) nonanuclear [RE9(mu3-OH)12(mu3-O)2(O2C-)12] carboxylate-based cluster, points of extens

184 Elemental compositions (C, H, N, O, S), Py-GC/FID, Py-GC/MS and SEM imaging reveal extens

185 emperature stable, acyclic, two-coordinate N,O-silylene 7 exhibiting a fascinating siloxy ligand was

186 thermore, representative pyrrolidines were N,O-debenzylated in a selective way and used for further s

187 II) with electron transfer and concomitant N-O heterolysis liberating an intermediate having a nitrog

188 t nitrogen inversion or rotation about the N-O bond.

189 f 2.74-2.75 A and an intense light-atom (C/N/O) scattering interaction 1.8 A from the Fe.

190 N2 O was not detectably released from surface-sterilized fe

191 wth and turnover of nitric oxide (NO) and N2 O at low cell densities of Nitrosomonas europaea (AOB) a

192 mbles to predict jointly productivity and N2 O emissions at field scale is discussed.

193 erstanding of soil N cycling pathways and N2 O production.

194 The remaining six accumulated NO and N2 O to varying degrees and genome sequencing of four indic

195 c denitrification was the main source for N2 O production, and was not impacted by the application of

196 ch was taken complemented by detection of N2 O released and nitrogen isotope determinations of fern b

197 Soil N2 O and CH4 fluxes were measured for five crop-years (2011

198 Relative contributions of AOA and AOB to N2 O production, therefore, reflect their respective contri

199 round Na and effectively soften the short Na-O bond along the polar axis - an effect that is proposed

200 ol (NNAL), NNAL-N-beta-glucuronide, and NNAL-O-beta-glucuronide.

201 plete, as the reported structure contains no O-acetylation.

202 contained the greatest relative abundance of O-acetylated derivatives, Binocrit expressed the least N

203 n greatly accelerate the C-H alkenylation of O-, S-, and N-heteroarenes.

204 The alteration of O-GlcNAcylation was also seen in the ischemic areas of p

205 bles real-time simultaneous deconvolution of O(105) traces of whole-brain larval zebrafish imaging da

206 enabling the first large-scale discovery of O-glycosylation on signaling peptides.

207 nexpectedly, many transcriptional effects of O-GlcNAc transferase (OGT) inhibition were due to the ac

208 Interference of the transient elevation of O-GlcNAcylation pharmacologically or genetically aggrava

209 revealed significant chromatin enrichment of O-GlcNAc-modified proteins at the promoter of the transc

210 removal of N-glycans prior to enrichment of O-linked glycopeptides by HILIC improved identification

211 omains (DBD) of R insert in major grooves of O pre-TS, forming most Coulombic interactions of RO and

212 peptides by HILIC improved identification of O-linked glycopeptides by mass spectrometry.

213 e vacancies that induce the incorporation of O as necessary stabilization of the crystal structure.

214 e was recently reported, but the presence of O-acetyltransferase genes in the serotype 35C cps locus

215 ds (LA's) to form an unprecedented series of O-type species (O(MeAN)-LA) able to oxidize C-H and O-H

216 were detected in all developmental stages of O. viverrini.

217 the relative energies of the spin states of O atom, Fe(2+) ion, and FeF2 and characterizes their exc

218 European isolates represent novel strains of O. ophiodiicola.

219 elevated O-GlcNAcylation and suppression of O-GlcNAcylation inhibits cancer invasion and metastasis.

220 e of CaO, which facilitates the transport of O(2-) anions, drastically improves the reaction kinetics

221 oreover, we present the [Co(II)xNi4-x(dpy{OH}O)4(OAc)2(H2O)2](ClO4)2 (CoxNi4-xO4-dpk) series as the f

222 PLA1 in mice impaired the formation of omega-O-acylceramides and led to an accumulation of nonesterif

223 ce analysis from C. glutamicum OMP and other O-acylated proteins in bacteria and eukaryotes revealed

224 e reaction employing an internally oxidizing O-N bond as a directing group.

225 K/F), mesocarp-to-fruit (M/F), oil per palm (O/P) and oil-to-dry mesocarp (O/DM).

226 the-annulus threading of calix[5]arene penta-O-ethers by dialkylammonium cations coupled to the loose

227 Peptidoglycan O-acetyltransferase B (PatB) catalyzes the O-acetylation

228 ture of the reaction is that the stronger Ph-O bond is cleaved rather than the weaker aliphatic O-R b

229 with benzoyl peroxide afforded [Cp*2Fe][PhC(O)OE(C6F5)3] (E = B 5, Al 6).

230 hich encodes a plant-specific polysaccharide O-acetyltransferase involved in xylan acetylation.

231 Alternatively, protein O-linked mannose beta-1,2-N-acetylglucosaminyltransferas

232 eral ER-localized enzymes, including protein O-glucosyltransferase 1 (POGLUT1) and POFUT1.

233 Together, our data suggested that protein O-mannosylation is required for normal sensory feedback

234 nd that previous cocaine exposure enhanced R-O associations in DLS.

235 sition of its anti-tetherin activity, RBF206 O-Vpu potently suppresses NF-kappaB activation and reduc

236 Using the anionic redox reaction (O(2-) /O(-) ), this Mn-oxide is predicted to show high r

237 FeO/Pt(111) interface and undergoes readily O-H and C-H dissociations with the aid of interfacial ox

238 nd specificity to OGA in O-GlcNAc regulation.O-linked beta-N-acetyl glucosamine (O-GlcNAc) is an impo

239 nt (O-GlcNAc transferase (OGT)) and removal (O-GlcNAcase (OGA)).

240 ith carbon dioxide (CO2) gave the respective O-[Zr] bonded cyclic boratacarbonate product.

241 ssumed that populations of living wild rice, O. rufipogon, are descendants of the ancestral populatio

242 mercial rice protein (RP) products, RP-G, RP-O, RP-RM, RP-RS1, and RP-RS2, were analyzed.

243 -H functionalization most likely involves Ru-O coordinate bond.

244 n of aryl-alkynes possessing ortho-EMe (E=S, O) groups represents a simple, metal-free method for the

245 minant interaction in the gas phase (SO2)S...O(H2O) to the dominant interaction on the water nanodrop

246 interaction between SO2 and H2O is (SO2)S...O(H2O), consistent with previous density-functional theo

247 The present findings suggest S/O/W emulsions are potential delivery systems to incorpor

248 , rainbow trout (O. mykiss), Chinook salmon (O. tshawytscha), Atlantic salmon (Salmo salar), and Arct

249 -bisselenylvinylene (DESVS), with novel Se...O noncovalent conformational locks is designed and synth

250 % specific for detection of E. coli serotype O:157.

251 how that SiO2 first undergoes a change in Si-O coordination number from fourfold to sixfold between 1

252 nt class of compounds, their catalysis of Si-O bond hydrolysis and condensation was investigated with

253 e decay is intrinsic to the nature of the Si-O bond.

254 ly defined major antigenic sites II and site O.

255 that specifically recognizes antigenic site O at the apex of the pre-F protein trimer.

256 2.5 x 10(-6)) was observed with CCDC62 (SKAT-O [p = 6.89 x 10(-7)], combined multivariate collapsing

257 nt interaction on the water nanodroplet (SO2)O...H(H2O) may incur effects on the SO2 chemistry in atm

258 hat the hydrogen-bonding interaction of (SO2)O...H(H2O) becomes increasingly important with the incre

259 rization being consistent within the species O. cf. ovata, a certain degree of toxin variability was

260 m an unprecedented series of O-type species (O(MeAN)-LA) able to oxidize C-H and O-H bonds.

261 ion proceeds by H2O(+) abstracting a surface O-atom, then forming an excited precursor state, which d

262 Surprisingly, O-mannosylation of cadherins and protocadherins does not

263 Our data indicate that O-glycosylation is not necessary for the natural replica

264 We show that O-acetylation driven by Adr protects the peptidoglycan o

265 We show that O-acetylation of peptidoglycan, a mechanism utilized by

266 ules approaching the surface, activating the O-H bonds and inducing deprotonation.

267 uranal, their 7-methoxy derivatives, and the O-prenylated natural products boropinols A and C.

268 with various long-chain substitutions at the O-8 position extensively inhibit SERCA1a-mediated Ca(2+)

269 n O-acetyltransferase B (PatB) catalyzes the O-acetylation of PG in Gram (-) bacteria, which aids in

270 ree times as much (15) N was retained in the O and A soil layers when N was derived from litter decom

271 imarily because of increased recovery in the O layer.

272 ardiac ion channels were integrated into the O'Hara-Rudy myocyte model modified to include dynamic dr

273 These findings link the O-GlcNAc modification to mammalian neurogenesis and high

274 ast to alpha-dystroglycan, and moreover, the O-Man glycans on cadherins are not elongated.

275 se virus (FMDV), particularly strains of the O and SAT serotypes, is notoriously unstable.

276 Full chemical analysis of the O-antigens of these strains identified gtr-dependent glu

277 llular processes through the addition of the O-GlcNAc sugar moiety to thousands of protein substrates

278 of copper and the enhanced weakening of the O-O bond from the higher electron density in the d orbit

279 gression by O-GlcNAc, we have focused on the O-GlcNAc-mediated epigenetic regulation of human colon c

280 tron Radiation Facility to check whether the O- to C-state transition in fully activated fibers of fa

281 tini, Dobromir Dobrev, Jordi Heijman, Thomas O'Hara, Crystal Ripplinger, Zhilin Qu, Jamie Vandenberg,

282 populate the surface with titanium oxyl (Ti-O(*)) radicals.

283 ed an elongated O-O bond but did not lead to O-O cleavage or reactivity toward external substrates.

284 g group is critical since the observed N- to O-Bz transfer during the process prevents later undesire

285 almon (Oncorhynchus kisutch), rainbow trout (O. mykiss), Chinook salmon (O. tshawytscha), Atlantic sa

286 of hepatocyte growth factor or unmethylated O(6)-methylguanine-DNA methyltransferase may benefit fro

287 echanistic features of the oxidation by Fe(V)O of hydrocarbons including cyclohexane.

288 uthenticated reactive iron(V)oxo units (Fe(V)O), wherein the iron atom is two oxidation equivalents a

289 h reaction classes described belongs to Fe(V)O.

290 e prepared from monosaccharide stannanes via O-glycosylation with Schmidt-type donors, glycal epoxide

291 c acid and is predominantly expressed on VWF O-glycans.

292 rge amount of external waste water to form W/O/W microreactor system.

293 altodextrin through water in oil in water (W/O/W) multiple emulsions.

294 This species reacts with weak O-H bonds in TEMPO-H and 4-dimethylaminophenol ((NMe2)Ph

295 s excellent peroxidase mimetic activity with O-phenylenediamine in the presence of hydrogen peroxide.

296 Xenograft tumors from colon tumor cells with O-linked N-acetylglucosamine transferase (OGT) knockdown

297 Pharmacological inhibition of Rpn11 with O-phenanthroline (OPA) blocks cellular proteasome functi

298 , creating an optical Fourier transform with O(n) apparent complexity.

299 excretion in hyperoxaluric mice treated with O. formigenes CM reflects the in vivo retention of biolo

300 YAP O-GlcNAcylation disrupts its interaction with upstream k