ライフサイエンスコーパス: H

1 H(2) formation is catalyzed by a biologically unique hex

2 H-MAGMA adds to existing analytic frameworks to help ide

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

4 at low concentrations (S. aureus, P < 0.001; H. influenzae, P < 0.0001) and in sputum-type specimens

5 (1) H NMR studies identified a 1400-fold rate enhancement un

6 However, so far only (1) H-(15) N dipolar couplings and (15) N chemical shifts ha

7 1D (1)H nuclear magnetic resonance spectra were acquired in pl

8 The present cross-sectional 3T (1)H MRS study is the first to use a multivoxel approach to

9 al ageing in these brain regions using 7T (1)H-MRS and findings indicate that glia-related metabolite

10 In this study, a (1)H qNMR method was developed for the analysis of propenyl

11 ned using (1)H, (13)C, (15)N, (29)Si, and (1)H DOSY NMR as well as X-ray diffraction studies.

12 MD) and showed the feasibility of MRI and (1)H MR spectroscopy to track disease progression over a wi

13 e and unique is the double probe given by (1)H and (11)B NMR tracing the reciprocally antipodal endoc

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

15 l nucleotides by 1-dimensional (1D) imino (1)H NMR as well as by 2D HyperW NMR spectra acquired upon

16 Most importantly, (1)H-(19)F coupling constants in this series are among the

17 unts, that were characterized by means of (1)H and (13)C NMR spectrometry as well as single-crystal X

18 grape varieties and 4 locations based on (1)H NMR spectra.

19 High-resolution magic-angle-spinning (1)H NMR spectroscopy (HR-MAS NMR) is a well-established te

20 ed labeling studies, variable-temperature (1)H NMR spectroscopy, and density functional theory calcul

21 ensed phases unambiguously assigned using (1)H, (13)C, (15)N, (29)Si, and (1)H DOSY NMR as well as X-

22 eparate, we compared (13)CO-detect versus (1)H(alpha)-detect experiments, showing that significant se

23 While (1)H NMR peak assignments have to be verified by (13)C NMR

24 dG(N(1)-H)(*) were formed as a result of the indirect and direct

25 ed loading, avoiding mutual nonspecific H(1)/H(2) hybridization.

26 posed strategy allowed the side arms of H(1)/H(2) to be sealed into the RNA sequence-programmed "zipp

27 rmulated as [Cu(81)(PhS)(46)((t)BuNH(2))(10)(H)(32)](3+) (Cu(81)), was successfully synthesized and f

28 th the longest alkoxy chains examined (OC(12)H(25)), which, although shown by in situ X-ray diffracti

29 In 2019, 128 H. zea neonates per isofamily for a total of 114 F(2) fa

30 ardness (mechanical stability) value of ~194 H(V) that is significantly higher compared to the pristi

31 itional S. aureus isolates and 25/92 (27.2%) H. influenzae isolates, which were more frequently disco

32 -733-dps is stable and shows no loss of C(2) H(2) adsorption capacity following multiple adsorption-d

33 -2) ) received primed continuous l-[ring-(2) H(5) ]phenylalanine before consuming a mixed meal.

34 itably isotopically-labelled cofactor ([4-(2)H]-NADH).

35 ough the formation of metastable [Ni(II)(C(2)H(2))(3)] complexes.

36 y C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.

37 ation of C(2)H(4) from a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.

38 (MOF) for highly efficient separation of C(2)H(4) from a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4

39 lexes, made by the reaction of Rh(eta(2)-C(2)H(4))(2)(acetylacetonate) with the support and anchored

40 m a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.

41 )/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.

42 ent separation of C(2)H(4) from a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mix

43 mologous perfluoroanion generation, (13)C/(2)H KIEs, LFERs, CF(2) transfer efficiency and selectivity

44 utilisation of NADH-dependent enzymes for (2)H-labelling is not straightforward, owing to difficultie

45 ectivity for borylation of aromatic C(sp(2))-H bonds over aliphatic C(sp(3))-H bonds(4).

46 dding dimethyl sulfoxide (DMSO) into ZnCl(2)-H(2)O, in which DMSO replaces the H(2)O in Zn(2+) solvat

47 ing, targeting methanol formation from CO(2)/H(2) feeds at 170 degrees C and 1-8 bar pressure.

48 ZnT8 is a Zn(2+)/H(+) antiporter that belongs to SLC30 family and plays a

49 WT ClC-5 had a 2Cl(-)/H(+) exchange ratio at a V(h) of +40 mV with a [Cl(-)](o

50 PS) )}(6) (mu-OC(2) P(3) )(2) (mu-OC(2) P(3) H)(2) Rb(4) ] (5) featuring four five-membered [C(2) P(3

51 ts, which indicated that the gamma-C(sp(3) )-H bond cleavage is the rate-limiting step during the rea

52 cells using a Ca(2+) imaging assay and a [(3)H]ketanserin binding assay.

53 odide and tert-butyl iodide molecules (i-C(3)H(7)I and t-C(4)H(9)I) through a conical intersection be

54 the brain, and studies of modulation of [(3)H]muscimol binding by allosteric GABAergic modulators su

55 The binding of [(3)H]muscimol has been used to evaluate the distribution of

56 Using (3)H-leucine (the gold standard for LAT-1 transport studies

57 Enantioselective C(sp(3))-H aminations allow an efficient access to nonracemic chi

58 veraging the reactivity of benzylic C(sp(3))-H bonds to achieve reactivity at the homobenzylic positi

59 tic C(sp(2))-H bonds over aliphatic C(sp(3))-H bonds(4).

60 ective and chemoselective oxidative C(sp(3))-H methylation method that is compatible with late-stage

61 the subsequent adsorption of thiophene (C(4)H(4)S) depends strongly on the location on the edge of M

62 utyl iodide molecules (i-C(3)H(7)I and t-C(4)H(9)I) through a conical intersection between (3)Q(0)/(1

63 Ss) with a molecular weight (MW) of 212 (C(5)H(8)SO(7)), which are abundantly present in both ambient

64 he acetal unit considerably outpaces any 1,5-H shift and instead activates 1,5-methoxy migration, giv

65 el addition/intramolecular cyclization/[1,5]-H shift/cleavage of CS(2)/aromatization/nucleophilic acy

66 allogenic MHC-mismatched studies as C57BL/6 (H-2(b)) and BALB/cBy (H-2(d)) have disparate MHC haploty

67 a(Nacnac) (Nacnac=HC[C(Me)N(2,6-i-Pr(2) C(6) H(3) )](2) ).

68 [(tBu) LNi(S)] ((tBu) L={(2,6-(i) Pr(2) C(6) H(3) )NC((t) Bu)}(2) CH).

69 Me) LZn(S)] (2) ((Me) L={(2,6-(i) Pr(2) C(6) H(3) )NC(Me)}(2) CH), was isolated via reaction of [(Me)

70 )(2) C(2) B(9) H(9) }Dy{eta(2) :eta(5) -C(6) H(4) (CH(2) )(2) C(2) B(9) H(9) }(2) Li] 3Dy and show th

71 nd [(THF)(3) (mu-H)(3) Li](2) [{eta(5) -C(6) H(4) (CH(2) )(2) C(2) B(9) H(9) }Dy{eta(2) :eta(5) -C(6)

72 I) alkynyl [Cu(II)]-C=CAr (Ar = 2,6-Cl(2)C(6)H(3)) forms upon reaction of the alkyne H-C=CAr with the

73 efinated through the isolated (N, O)(Ph, C(6)H(4), C) oxaphosphetanes (Channel A), whereas MoBA compo

74 pounds decomposed faster via the isomer (C(6)H(4), O)(C, N, Ph) formed by P-stereomutation involving

75 A new strategy for the C(7)-H functionalization of indoline derivatives using first-

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

77 make dysprosiacarboranes, namely [(C(2) B(9) H(11) )(2) Ln(THF)(2) ][Na(THF)(5) ] (Ln=Dy, 1Dy) and [(

78 (2) :eta(5) -C(6) H(4) (CH(2) )(2) C(2) B(9) H(9) }(2) Li] 3Dy and show that dicarbollide ligands imp

79 2) [{eta(5) -C(6) H(4) (CH(2) )(2) C(2) B(9) H(9) }Dy{eta(2) :eta(5) -C(6) H(4) (CH(2) )(2) C(2) B(9)

80 Interestingly, ABO(H) determinants are also expressed on several different

81 pecies is used as a strategy to avoid adding H(2)O(2) in the solution during the detection of phenoli

82 rs in angstroms to nanometers thick adsorbed H(2)O films.

83 )C(6)H(3)) forms upon reaction of the alkyne H-C=CAr with the copper(II) tert-butoxide complex [Cu(II

84 d neuronal degeneration, are mitigated by an H(3)R antagonist.

85 tudy is the longest prospective cohort of an H pylori eradication trial in a Hispanic population.

86 ng a stable compound insensitive to O(2) and H(2)O.

87 toredox catalysis enables C-H activation and H/D exchange in a number of additional substrates with f

88 hat H(2) O(2) upregulated ENaC activity, and H(2) O(2) production was reduced in both the renal corte

89 t stoichiometric operation) at the anode and H(2) at the cathode.

90 upported Pd catalysts, producing only CO and H(2)O as waste.

91 rophile, Pseudomonas, Enterobacteriaceae and H(2)S producing bacterial counts were obtained in PEF-1

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

93 W and H children were combined to produce FFMI models for each

94 record direct muscle responses (M-waves) and H-reflexes, both of which are comparable to those record

95 a bulky singly protonated cation that avoids H-bonding is ideal.

96 a-bond metathesis mediated (prevalent with B-H and B-R electrophiles).

97 verity and breath tests results at baseline (H(2) and/or CH(4) >= 15 ppm).

98 ty holding a single metal, to a binucleating H(2) ema(2-) with bridging sulfurs and carboxamide oxyge

99 damentally new transformation, in which both H atoms of dihydrogen are transferred to the same C atom

100 th donor (bm1 or F1) and third-party B10.BR (H-2) skin grafts.

101 eptide interactions, including salt bridges, H-bonds, and polar interactions.

102 that were infused with DMS (P < 0.01) and by H. gammarus larvae and A. tonsa on DMS-infused fibers an

103 ations showed that (*)OH oxidizes 6:2 FTS by H-abstraction from ethyl carbons.

104 membrane side and subsequently terminated by H(2)O(2) oxidation on the anodic membrane side, is cruci

105 d product chemoselectivity make asymmetric C-H oxidation a generally unsolved problem for nonenzymati

106 00 turnovers for the oxidation of benzylic C-H bonds were obtained.

107 nd stereoselective distal allylic/benzylic C-H functionalization of allyl and benzyl silyl ethers was

108 Despite efforts for beta-C-H functionalization in carbon-carbon and carbon-heteroat

109 ghts key advances in scalable biocatalytic C-H oxyfunctionalization reactions developed within the pa

110 nally, an aldehyde group was introduced by C-H amidation, enabling oxime ligation for the installatio

111 selenide reagent for both off- and on-DNA C-H selenylation under rhodium(III) catalysis.

112 Analogous photoredox catalysis enables C-H activation and H/D exchange in a number of additional

113 lly relied on precious-metal catalysts for C-H bond cleavage and, as a result, display high selectivi

114 e presented that reveal two mechanisms for C-H borylation, (i) electrophilic aromatic substitution (p

115 ive functionalizations of carbon-hydrogen (C-H) bonds represent a promising pathway toward this goal.

116 MMO-Q necessary to attack the highly inert C-H bonds of methane.

117 e ability of Zn to promote a rate-limiting C-H reductive elimination step, and calculations attribute

118 The regioselectivity of C-H activation is dominated by steric considerations and t

119 Phosphonate-directed ortho C-H borylation of aromatic phosphonates is reported.

120 ike H-bonding, solvent bonding, S-H...pai, C-H...pai, pai-pai stacking, charge-transfer complexation,

121 eloping on the C-O carbon atom progressing C-H abstraction.

122 carbamate esters bearing gamma-propargylic C-H bonds and furnishes versatile products in good yields

123 ategies to selectively halogenate pyridine C-H precursors are lacking.

124 he reaction allows valuable regioselective C-H modification of these N,O-chelated organoboron chromop

125 -metal-catalyzed, template-directed remote C-H activation reactions of alcohols, carboxylic acids, su

126 In this context, distinguishing remote C-H bonds on adjacent carbon atoms is an extraordinary cha

127 he fluorination and chlorination of remote C-H bonds under exceptionally mild conditions with exceedi

128 cals have long been known to enable remote C-H functionalization via 1,5-hydrogen atom abstraction.

129 atalyst system to promote a para-selective C-H functionalization reaction from benzylic electrophiles

130 chieving highly regio- and stereoselective C-H functionalization reactions using a newly developed Rh

131 active sites achieve activation of strong C-H bonds.

132 nalysis of the product films revealed that C-H functionalization by [B(12)X(11)](-) occurred in the p

133 This protocol enabled the C-H functionalization of substituted 2-methylquinolines wi

134 uld be engineered to further improve their C-H amination reactivity, which demonstrates their evolvab

135 ngle operation through a cascade of triple C-H bond activations is the beauty of this protocol.

136 volving the intramolecular coupling of two C-H bonds on gem-dialkyl groups has remained an elusive tr

137 vity are governed by various types of weak C-H hydrogen bonds.

138 ed studies as C57BL/6 (H-2(b)) and BALB/cBy (H-2(d)) have disparate MHC haplotypes.

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

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

141 ermally stable metalloradical, (P(3) (B) )Co(H(2) ), serves as a competent precursor for hydrogen ato

142 Upon loading with H(3) PO(4) , the COFs (H(3) PO(4) @COFs) realize an ultrahigh proton conductivi

143 ular dynamics is dominated by either complex H-bonded networks most probably leading to supramolecula

144 tion of wrinkle patterns as liquid crystals [H.

145 a indicate that multiple members of the CslF/H family fulfil important functions during grain develop

146 proton electrolyte is devised by dissolving H(3) PO(4) into acetonitrile.

147 r doping thus offers a pathway for efficient H doping in green solvent-processed metal oxide films an

148 tions of materials, and because the elements H, C, O, and N are among the most abundant in the univer

149 s in hydride bonds and reductively eliminate H(2) upon substrate binding.

150 e across 400 melanoma hematoxylin and eosin (H&E) specimens from The Cancer Genome Atlas.

151 uoroacetamide derivative engages in extended H-bond interactions in its crystal structure.

152 reciprocally antipodal endocyclic open face H(ec) and B(1).

153 tibody (mAb) that inhibited AQP3-facilitated H(2)O(2) and glycerol transport, and prevented liver inj

154 Genetic variants within complement factor H (CFH), a major alternative complement pathway regulato

155 tective genetic alleles of complement factor H (CFH), the Mediterranean diet had further beneficial e

156 of NiO is still limited by lacking favorable H adsorption sites.

157 d a dramatic increase of the coercive field (H(c) ) by more than 150% with an applied strain of 0.32%

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

159 ic decisions, where antibiotics are used for H. pylori eradication.

160 s, but shunt conductance facilitated further H(+)-ATPase-mediated endosomal acidification.

161 s this limitation by cathodically generating H(2)O(2) in situ.

162 he G, CP, and AgP groups compared with group H (P < 0.05).

163 or-dependent increase: CuO NP-induced OMVs > H(2)O(2)-induced OMVs > control OMVs.

164 We find that a single gene, Hairy (H), which is needed to repress trichome fate, underlies

165 ens in Africa and whether H. heidelbergensis/H. rhodesiensis was a direct ancestor of our species(13,

166 ated, although a predicted helix-loop-helix (H-L-H) was suggested to form pores by virtue of its simi

167 ing of the TiO(2) support during heterolytic H(2) adsorption; evidence for this phenomenon was observ

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

169 Consistent with higher H(2) abundance, sediment microbial communities from the

170 us, we identified a potential role for hnRNP H in basal and dynamic mitochondrial function that infor

171 Hydrogen (H(2)) is a potent reductant that can be generated when w

172 Free hydrogen (H(2)) is a basal energy source underlying chemosynthetic

173 Importantly, H. pylori-induced replication stress and DNA damage depe

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

175 read resistance to Cry1 and Cry2 proteins in H. zea will challenge the long-term efficacy of Vip3Aa t

176 signaling cascade, which leads to increased H(2)O(2) and Ca(2+) levels and F-actin reorganization, b

177 nterlayer SC phase coherence with increasing H( ).

178 , UV-irradiation of ubiquitin did not induce H/D scrambling in the nonfragmented precursor ion popula

179 Light-induced H(2) production from water represents one of the most cr

180 tate and transient kinetic studies involving H/D and (13)C/(12)C exchange, coupled with operando infr

181 st 40 years ago when one of the authors (K.J.H.) published an organized system to quantify the accura

182 s of a significant kinetic isotope effect (k(H) /k(D) =5.7) for the reactions of diphenyl ether under

183 , although a predicted helix-loop-helix (H-L-H) was suggested to form pores by virtue of its similari

184 ocycles, along with the dimeric model of LDH-H, constitute promising pharmacological tools for the de

185 produced up to two orders of magnitude less H(2) than their modern counterparts, consistent with Fe-

186 lizes multiple noncovalent interactions like H-bonding, solvent bonding, S-H...pai, C-H...pai, pai-pa

187 A well-saturated magnetization M-H loop with remanent magnetization of 3.5 emu/cm(3) was

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

189 hyrin rings) have different pathways to make H(2) .

190 We hypothesized that maternal H. pylori status affects the maternal intestinal microbi

191 n to phenocopy the PYCR1 knockdown in MCF10A H-RAS(V12) breast cancer cells by inhibiting de novo pro

192 evidence for mAb inhibition of AQP3-mediated H(2)O(2) transport as therapy for macrophage-dependent l

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

194 ous reports from other models, mitochondrial H(2)O(2) emission and oxidative damage were greater in T

195 High-purity 69.69 mmol-H(2)/(dry-ash-free)g-brown seaweed is produced with a co

196 n plasma by the physiologically relevant MPO-H(2)O(2)-NO(2) (-) system.

197 d equal 97.5% (468/484) specificity; 64% MSI-H and 73% MMR deficient tumours unexplained by LS or MLH

198 programmed death-ligand 1 expression and MSI-H/MMR-D status were not associated with objective respon

199 bitals, investigations of [(P(6)ArC)Fe(2)(mu-H)](+1) and [(P(6)ArC)Fe(2)(mu-H)](-1) by pulse EPR reve

200 )ArC)Fe(2)(mu-H)](+1) and [(P(6)ArC)Fe(2)(mu-H)](-1) by pulse EPR revealed that redox chemistry induc

201 [Na(THF)(5) ] (Ln=Dy, 1Dy) and [(THF)(3) (mu-H)(3) Li](2) [{eta(5) -C(6) H(4) (CH(2) )(2) C(2) B(9) H

202 nucleophilic substitution of hydrogen (S(N)(H)) was first applied for the direct modification of non

203 functional groups, providing a variety of N-H pyrroles in good yields and with high regioselectivity

204 ngstrom of the X-ray structure) using only N-H RDCs from one alignment medium.

205 confirmed the presence of peaks related to N-H bending vibration, C-N stretching and symmetric, and a

206 d stimulate non- HCO3- transporters (e.g. Na-H exchangers) by accelerating CO(2) / HCO3- -mediated bu

207 ly shorter lag times and faster rates of net H(2) oxidation and dark carbon dioxide (CO(2)) fixation

208 -terphenyl substituents that can host two Ni-H units in close proximity.

209 trolled loading, avoiding mutual nonspecific H(1)/H(2) hybridization.

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

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

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

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

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

215 tential in decalin indicate that addition of H to the aromatic ring is involved in the rate-limiting

216 e proposed strategy allowed the side arms of H(1)/H(2) to be sealed into the RNA sequence-programmed

217 These proteins contain a continuous chain of H-bonds that impart stability, causing difficulty in dig

218 nt research, the main bioactive compounds of H. dulcis pseudofruits were characterised using phytoche

219 and are inhibited by high concentrations of H(2)O(2) upon adsorption on an electrode.

220 intercept was used to estimate the effect of H pylori status on the score over time.

221 teria must overcome the silencing effects of H-NS.

222 her questions about the mode of evolution of H. sapiens in Africa and whether H. heidelbergensis/H. r

223 ite high infection rates, only a fraction of H. pylori-infected individuals develop gastric cancer.

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

225 Hadi et al. was resulted from high levels of H-RasV12 overriding anti-cancer mechanisms of the naked

226 nodominant TMEV peptide VP2(121-130) Loss of H-2D(b) on CD11c(+) APCs mitigates the CD8 T cell respon

227 al function is maintained in the presence of H(2)S in sulfide spring P. mexicana but not ancestral li

228 ity and specificity toward the production of H(2) O(2) .

229 that likely influenced the growth regime of H. tuna.

230 If biomass is used as a source of H(2), the process can be considered carbon-neutral.

231 Our results demonstrated that the synergy of H(2)O(2) and gluconic acid is essential for the antibact

232 ls based on the arrival of multiple waves of H. sapiens into Europe coming into contact with declinin

233 ere and a positive dependence of the rate on H(2) chemical potential in decalin indicate that additio

234 5-mediated exchange of two Cl(-) out for one H(+) in is not permissible.

235 of glutathione (GSH) and hydrogen peroxide (H(2) O(2) ) with high specificity on a basis of domino r

236 e development of a unique hydrogen peroxide (H(2) O(2) )-sensing motif and its capacity for providing

237 Hydrogen peroxide (H(2)O(2)) is a reactive oxygen species (ROS) that mediat

238 rhodium complex (eta(5)-C(5)Me(5))Rh((Me)PhI)H ((Me)PhI = N-methyl-1-phenylethan-1-imine) exhibited h

239 previously reported (eta(5)-C(5)Me(5))Rh(ppy)H (ppy = 2-phenylpyridine).

240 This primary H/D KIE leads to the inference that hole-driven scission

241 These findings indicate that SMOX promotes H. pylori-induced carcinogenesis by causing inflammation

242 ub-1-nm protein pores with ultrahigh proton (H(+)) selectivity over other ions.

243 anic semiconductor photocatalyst with proven H(2) evolution ability.

244 An additional Rh-H...C stabilization in some intermediates or transition

245 eractions like H-bonding, solvent bonding, S-H...pai, C-H...pai, pai-pai stacking, charge-transfer co

246 The first example of enantioselective S-H insertion reactions of sulfoxonium ylides is reported.

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

248 2) may be readily separated and sequestered, H(2) and/or O(2) may be used to generate electric power

249 Several H-H bond forming pathways have been proposed for the hyd

250 d WT and CSE(-/-) macrophages using the slow H(2)S releaser GYY3147 and the CSE inhibitor DL-propargy

251 drogen-deuterium exchange mass spectrometry (H/D exchange MS), to characterize the global and peptide

252 with all the subunits including the subunit H, which is essential for ATPase activity.

253 Dysregulation of hydrogen sulfide (H(2)S) by inhibition of cystathionine gamma-lyase (CSE)

254 Recently, we achieved sustainable H(2) photoproduction by shifting algae from continuous i

255 T(H)17 cells are believed to orchestrate MS pathology, in

256 into a number of subsets, including T(H)1, T(H)2, T(H)9, T follicular helper, T follicular regulatory

257 number of subsets, including T(H)1, T(H)2, T(H)9, T follicular helper, T follicular regulatory, and r

258 CVID-associated immune dysregulation is a T(H)1-mediated inflammatory process driven by the IFN-gamm

259 expressing IMs in the development of acute T(H)2-cell-dependent allergic airway inflammation.

260 epithelial activation, ILC2 expansion, and T(H) 2 differentiation.

261 mTOR activation in IL-17(+) gammadelta and T(H)17 cells.

262 nificantly increased GM-CSF production and T(H)2 cell differentiation.

263 Anti-T(H) 2 therapies have the potential to effectively reduce

264 he lung, but those cells release decreased T(H) 2 cytokine levels.

265 iation into a number of subsets, including T(H)1, T(H)2, T(H)9, T follicular helper, T follicular reg

266 bal transcriptome reversion and normalized T(H)17 cell/IL23 signaling, whereas dupilumab led to a str

267 deficiency could induce higher numbers of T(H) 2 cells in the lung, but those cells release decrease

268 pressed the development of IL-17-producing T(H)17 cells but increased the generation of those produci

269 We showed that TSLP can directly promote T(H)2-cell differentiation in the lung, independent of the

270 Targeting H(2)S to the mitochondria may be of therapeutic benefit

271 ibitor DL-propargylglycine demonstrated that H(2)S is the effector molecule regulating Mtb survival i

272 We also found that H(2) O(2) upregulated ENaC activity, and H(2) O(2) produ

273 Here we report that H(2)O(2) is spontaneously produced in water microdroplet

274 we summarize recent work that suggests that H(2)S/RSS impacts bacterial survival in infected cells a

275 The H. pylori infection-induced downregulation of NEIL2 was

276 unique hexanuclear iron cofactor denoted the H-cluster.

277 r-protic solvent combinations to disrupt the H-bonds and hydrophobic interactions holding together th

278 reaction from rhodium to carbon to form the H-C bond.

279 We were also able to generate the H(inact) state anaerobically via both chemical and elect

280 This is found in the H-transfer from the tetrazole ring in 5-(2-pyridyl)tetra

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

282 repair was the ability of the A analogues to H-bond with the Hoogsteen face of OG.

283 Nickel binding to H. pylori NikR (HpNikR) induces an allosteric response f

284 s replaced by serine (C674S) were exposed to H(2)O(2) (100 umol/Lmu).

285 xidation pathway in peroxisomes and leads to H(2)O(2) production.

286 he lowest fraction of KED on the transferred H-atom and the highest chance to follow rebound hydroxyl

287 The vacuolar-type H(+)-ATPases (V-ATPase) hydrolyze ATP to pump protons ac

288 yzing benzene/pyridine solutions of 4a under H(2) and D(2) atmospheres (150 psi), which leads to the

289 7) for the reactions of diphenyl ether under H(2) and D(2) atmosphere and a positive dependence of th

290 ilarly, a/x and c/z ions have also undergone H/D scrambling due to UV-induced heating of the precurso

291 nate catchment, indicating adaptation to use H(2) as a reductant in basaltic catchments.

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

293 r-F bond and is ultimately regenerated using H(2) and base.

294 ne at 359.0 K was calculated to be Delta(vap)H = 91.27 +/- 0.28 kJ/mol compared to Delta(vap)H(corr)

295 91.27 +/- 0.28 kJ/mol compared to Delta(vap)H(corr) = 91.44 kJ/mol for the reference correlation.

296 r pocket" stitches the gelators through weak H-bonding interactions to facilitate the formation of an

297 volution of H. sapiens in Africa and whether H. heidelbergensis/H. rhodesiensis was a direct ancestor

298 arry insertions that are not correlated with H-NS binding.

299 Upon loading with H(3) PO(4) , the COFs (H(3) PO(4) @COFs) realize an ultr

300 of the clinical and radiological signs with H-ABC patients.