ライフサイエンスコーパス: V

1 subsequent dose of negative potential (-2.0 V) induces the release.

2 Applying positive potential (+2.0 V) to these PCPs promotes ethylene capture, and subseque

3 a high open circuit voltage of 1.08 +/- 0.01 V, attributed to the high lowest unoccupied molecular or

4 ng a low overpotential ( approximately 0.025 V) for a long cycle life.

5 than on the opposite side of the brain (0.03 V/m).

6 voltage of 1 V, a threshold voltage of 0.06 V, a subthreshold swing of 83 mV dec(-1) and an on/off r

7 ted current densities of 1 mA cm(-2) at 1.07 V vs NHE.

8 increase in OER activity ( approximately 0.1 V in overpotential shift at 10 mA cm(-2)) is observed fo

9 high open-circuit voltage of approximately 1 V and a striking fill factor of approximately 80%.

10 devices exhibited an operating voltage of 1 V, a threshold voltage of 0.06 V, a subthreshold swing o

11 y of 11.4% with an impressive V OC of over 1 V is recorded in photovoltaic devices, suggesting that I

12 quires a field strength of approximately 100 V/cm, yet it efficiently recovers proteins and nucleic a

13 s with applied potentials not exceeding 1000 V.

14 stronger in the stimulated hemisphere (0.12 V/m) than on the opposite side of the brain (0.03 V/m).

15 urring at 0.50 V (vs. Ag, compared with 1.15 V for Ag NPs capped in DNA alone).

16 applied reduction potentials (-0.53 to -0.17 V vs SHE), and Fe(2+) concentrations (up to 40 muM).

17 and a relatively low redox potential of 2.2 V vs. Li(+) /Li.

18 ow high redox potentials ( approximately 4.2 V vs Na/Na(+) ) with high charge capacity (190 mAh g(-1)

19 Upon application of a 2 V step in voltage, the resistor exhibited a steady-state

20 compared to the bandgap and high (>100 cm(2) V(-1) s(-1) ) intrinsic carrier mobilities.

21 nted 9 GHz charge-carrier mobility (71 cm(2) V(-1) s(-1) ), is demonstrated.

22 ranging from approximately 0.03 to 1.7 cm(2) V(-1) s(-1) .

23 from the original value of 1.8 to 3.2 cm(2) V(-1) s(-1) .

24 with electron mobility exceeding 2000 cm(2) V(-1) s(-1) and sheet carrier density above 1.07 x 10(13

25 effect mobilities (41 for holes and 80 cm(2) V(-1) s(-1) for electrons) and device stability are impr

26 trahigh Hall mobility value of >20,000 cm(2) V(-1) s(-1) is measured in as-grown Bi2O2Se nanoflakes a

27 t high Hall mobility values (up to 450 cm(2) V(-1) s(-1)), large current on/off ratios (>10(6)) and n

28 verage field-effect hole mobility (5.1 cm(2) V(-1) s(-1)).

29 iting hole mobility up to 0.15 and 6.4 cm(2) V(-1) s(-1), respectively.

30 lso increases the hole mobility to 560 cm(2) V(-1) s(-1), yielding a high mobility-lifetime product o

31 ility-lifetime product of 1.8 x 10(-2) cm(2) V(-1).

32 duced mobility values of 1.99 +/- 0.01 cm(2) V(-1)s(-1) at 175 degrees C.

33 ed the greatest shift in mobility (1.58 cm(2)V(-1)s(-1)) compared the DMMP monomer (1.63 cm(2)V(-1)s(

34 )s(-1)) compared the DMMP monomer (1.63 cm(2)V(-1)s(-1)).

35 r Hg3Se2I2 is estimated as 104 +/- 12 cm(2)/(V.s).

36 We tested the effect of acute DCS (10-20 V m(-1) for 3-5 s) on synaptic dynamics with constant ra

37 rol was achieved at applied potentials of 20 V.cm(-1), within 120 s of stimulation, using 0.1 M iron

38 3 mm as the applied field is varied from 200 V/mm to 800 V/mm, comparable to that of the human lens.

39 d to the desired value of platinum at (-0.25 V vs. SCE).

40 The input voltage (as low as 0.25 V) from the biofuel cell is converted to a stepped-up po

41 ured surface by applying a potential of -0.3 V during 180 s.

42 he results show that the cells stored at 2.3 V exhibited no change in cell capacity after 90 days; re

43 er-poly-Fe(vbpy)3(2+)|GCE electrode at -1.33 V vs. reversible hydrogen electrode (RHE) in 0.5 M KHCO3

44 with an input power responsivity of up to 38 V W(-1), referenced to incident illumination, and bandwi

45 20 600 W kg(-1) , and output voltage of 2.4 V can be delivered during >4000 cycles, which is far sup

46 chieve 10 mA cm(-2) at a low voltage of 1.44 V for 48 h in basic media for overall water splitting.

47 gh catalytic activity towards the HER (-0.46 V vs. SCE) upon the 1000th cycle, such potential is the

48 mory shows a large memory window of up to 47 V with an on/off current ratio larger than 10 000.

49 reduction to CO in tetrahydrofuran at -0.48 V vs NHE, the least negative potential reported for a mo

50 of surface functional groups and have a 1.5 V potential range for biogeochemical reactions that invo

51 e P2-O2 phase transition upon cycling to 4.5 V.

52 dation of the silver core, occurring at 0.50 V (vs. Ag, compared with 1.15 V for Ag NPs capped in DNA

53 y applying electric potentials as low as 500 V.

54 Here, using high-accuracy (75)As and (51)V nuclear magnetic resonance measurements, we investigat

55 C2-C3 products with onset potential at -0.53 V (vs. reversible hydrogen electrode, RHE) and C2-C3 far

56 r an applied potential (U) greater than -0.6 V (RHE) ethylene, the major product, is produced via the

57 e strong local electrical field (10(5)-10(6) V m(-2)) at the conductive nanoscale tip (4) .

58 g with 10 mA cm(-2) at a low voltage of 1.64 V is achieved using the ternary electrode as both the an

59 clearly shows a sub-bandgap emission at 1.7 V (bandgap 2.3 eV).

60 on, at fuel cell voltages greater than 0.75 V, were the same as those obtained with a Pt cathode at

61 c efficiency (FE) reaching 50% at only -0.75 V.

62 at 2 mA, cortical electric fields reach 0.8 V/m, the lower limit of effectiveness in animal studies.

63 arged to the capacitor to the voltage of 1.8 V.

64 applied field is varied from 200 V/mm to 800 V/mm, comparable to that of the human lens.

65 of 0.92 V, and a half-wave potential of 0.82 V.

66 of C2H4 along with CH4 at U less than -0.85 V arises from *CHO formation produced via an ER process

67 duction potential E degrees (Cl(*/-)) = 1.87 V vs NHE that is at least 300 meV more favorable than th

68 C-O containing polymeric species around 0.9 V (vs.

69 ion activity with an onset potential of 0.92 V, and a half-wave potential of 0.82 V.

70 8-17 DNAzyme adopts a V-shape fold, and the Pb(2+) cofactor is bound at the pr

71 The setup of a V-shaped optical cavity operating with a 3.29 mum cw ICL

72 To elucidate such requirements, we used a V(D)J passenger allele system to assay, in mouse GC B ce

73 otomous variable showed that patients with a V-wave decrease of >/=11 mm Hg were 3.8x more likely to

74 enhanced beta-glucosidase enzyme activities (V max ) but short-term drying and waterlogging caused a

75 , V, as a novel metric of nodal affiliation: V approximately 0 means that a node is consistently assi

76 nscriptome and 11,084 were annotated against V. v. vinifera reference genome.

77 The reduction of pH leads to much lower Al, V, and As mobility in the actively treated residue and t

78 Here we demonstrated an all-vanadium (all-V) continuous-flow photoelectrochemical storage cell (PE

79 ically bind the angiogenesis biomarker alpha V beta 3 integrin.

80 imarily cell autonomous, from loss of alpha3(V) chains normally produced by tumour cells, in which th

81 on by trace metals (Ag, Cd, Sb, Tl, but also V, Ni, and Mo which are enriched in bitumen) has been de

82 FCS: I, 48%; II, 11%; III, 15%; IV, 11%; and V, 15%).

83 fied serotypes were III (25%), Ia (23%), and V (19%).

84 trate an inverse relationship between Ca and V concentrations.

85 d preserved TC-NER (category 2: XP-C, E, and V).

86 revealed that many neurons in laminae I and V of the spinal cord dorsal horn and caudal spinal trige

87 ses caused by serotypes Ia, Ib, II, III, and V.

88 , as well as the Dut conserved motifs IV and V.

89 ial phospholipidome and complexes I, IV, and V activities.

90 HR, 5.96, P < .001, for classes III, IV, and V vs II, respectively), age (HR, 1.02, P = .001), and pr

91 is almost completely repressed under Mo- and V-limitation.

92 < .05), higher levels of apoptosis (Annexin V positivity, P < .005), and less lung allergic inflamma

93 Densities of C4d+ and C4d+/annexin V+ (C4d+/AVB+) microvesicles were also increased in AMR

94 lease assay, Hoechst 33342 staining, annexin V/PI staining, and JC-1 staining.

95 s were quantified by flow cytometry; annexin-V status identified apoptotic cells and phosphorylation

96 to the estrogen response element at the apoA-V promoter, implying the participation of SRC-1 in E2's

97 Aqueous V concentrations were controlled by Ca3(VO4)2 solubility

98 rease in advanced disease and AURKA is an AR-V target gene demonstrating a positive feedback mechanis

99 In arterioles, V, WSR, and WSS were lower in NDR (P </= 0.01).

100 yses show that V was released to solution as V(V) during dicalcium silicate dissolution and some V wa

101 As(V) was determined as the difference between total As and

102 to investigate the mechanism of arsenate (As(V)) tolerance and accumulation in rice.

103 c arsenic (arsenite, As(III) vs. arsenate As(V)) can be modulated by microbes.

104 peciation, and partitioning of associated As(V) and Sb(V) under anoxic conditions at pH 7.

105 S spectroscopy revealed some reduction of As(V) to As(III) at higher concentrations of Fe(2+), while

106 codes a rhodanase-like protein that shows As(V) reductase activity when expressed in Escherichia coli

107 OsHAC4 is the causal gene for the As(V)-hypersensitive phenotype.

108 The vacuolar H(+) ATPase (V-ATPase) is a complex multisubunit machine that regulat

109 ess the proton pumping vacuolar H(+)-ATPase (V-ATPase) and are extensively involved in acid-base home

110 Screening of all publically available V. cholerae genomes showed that numerous strains possess

111 he Artisan Myopia or Artisan Toric (Ophtec B.V., Groningen, The Netherlands) iris-fixated pIOL for th

112 e and porcine plasmapowder FG (PPFG; Sonac B.V.).

113 ministration of the phages up to 24 h before V. cholerae challenge reduces colonization of the intest

114 storing HapR expression in classical biotype V. cholerae repressed vieSAB transcription by binding to

115 domain AlmG substrate to that synthesized by V. cholerae.

116 we used classical (O395) and El Tor (C6706) V. cholerae biotypes in growth and biochemical assays.

117 CAL-V achieved by regenerative therapy in IBDs may have reta

118 TEMIS C terminus is dispensable for cellular V(D)J recombination and in vitro nuclease assays with C-

119 ally done by interrogation of paired H chain V region (VH) and L chain V region (VL) sequences of ind

120 of paired H chain V region (VH) and L chain V region (VL) sequences of individual and Ag-specific B

121 are thus needed to functionally characterize V-ATPase and to fully evaluate the therapeutic relevance

122 tion of halogens, we have synthesized [Cl3Sb(V)Pd(II)Cl2(o-dppp)2] (o-dppp = o-(Ph2P)C6H4), a palladi

123 or the infrainguinal bypass cohort) or class V (1131 [5.0%] vs 206 [0.3%]; P < .001) and to undergo e

124 nsistently assigned to a specific community; V >> 0 means it is inconsistently assigned to different

125 he codoped (Bi,Sb)2 Te3 films with varied Cr/V ratios reveals that magnetic codoping improves the hom

126 paritaprevir failure include R155K and D168E/V.

127 esulting in loss of adult NSCs and defective V-SVZ regeneration.

128 to SEM/EDS and muXANES analysis to determine V host phases and speciation in both primary and seconda

129 uts, and a mean residence time for dissolved V in seawater of about 130,000 y with respect to inputs

130 Overall, the budget of dissolved V in the oceans is remarkably well balanced-with about 4

131 se of outer hair cells exhibit a distinctive V-shape.

132 ing the Mo- as opposed to the less efficient V-nitrogenase.

133 sity (D), and joining (J) subgenic elements (V(D)J recombination).

134 s of volume of activation (Delta( not equal) V) and reaction volume (DeltaV) in understanding pressur

135 e decrease, resulting in a 42% increase in F&V consumption, corresponding values would be 451,900 CVD

136 MMCs) and economic incentives may increase F&V consumption.

137 n 2015 would increase the average national F&V consumption by 7% for 1 y and prevent approximately 18

138 mechanistic features of the oxidation by Fe(V)O of hydrocarbons including cyclohexane.

139 oth reaction classes described belongs to Fe(V)O.

140 authenticated reactive iron(V)oxo units (Fe(V)O), wherein the iron atom is two oxidation equivalents

141 e flux (V CS) and pyruvate carboxylase flux (V PC) in vivo.

142 hepatic mitochondrial citrate synthase flux (V CS) and pyruvate carboxylase flux (V PC) in vivo.

143 ween open and closed states is important for V. cholerae biofilm formation, as RbmA variants with swi

144 effector-immunity gene profiles observed for V. cholerae and closely related species.

145 widened the known antimicrobial spectrum for V. odorata cyclotides, including antibacterial activity

146 enthalpy of melting of the polymorphic form V, at higher storage temperatures, achieving greater sta

147 ion exons are assembled developmentally from V, D, J gene segments.

148 -with about 40 x 10(9) g V/y to 50 x 10(9) g V/y inputs and outputs, and a mean residence time for di

149 rkably well balanced-with about 40 x 10(9) g V/y to 50 x 10(9) g V/y inputs and outputs, and a mean r

150 Through mining of V ores (130 x 10(9) g V/y) and extraction and combustion of fossil fuels (600

151 nd combustion of fossil fuels (600 x 10(9) g V/y), humans are the predominant force in the geochemica

152 nts of mature bnAbs or unrearranged germline V, D, J segments (that can be assembled into variable re

153 pe of tri-antennary glycan, generated by GnT-V, is not a substrate for FUT8.

154 ducing more offspring and exhibiting greater V k* in the second sex.

155 However, protogynous species show greater V k*, especially pronounced in haremic species, resultin

156 lighter-for-age, and children in GMFCS group V had a lower FFM-for-height than those in GMFCS group I

157 sub-pocket at the interface between helices V and VI, which may facilitate the formation of an intra

158 GLP-1R and GCGR and located outside helices V-VII near the intracellular half of the receptor.

159 modulating the activity of this hypothalamic-V-SVZ connection.

160 Secondary diversification occurs when Ig V regions undergo somatic hypermutation (SHM) and affini

161 Growing III-V semiconductor materials on Si substrates for opto-elec

162 g(+) is an emerging electronic dopant in III-V and II-VI nanostructures, introducing intragap electro

163 igh-performance electro-optic devices in III-V semiconductor field.

164 ol over the low loss plasma frequency in III-V semiconductors.

165 research interest for the development of III-V/graphene functional hybrid heterostructures.

166 rsion efficiency of 11.4% with an impressive V OC of over 1 V is recorded in photovoltaic devices, su

167 decuple mutant of 12 diguanylate cyclases in V. cholerae.

168 ) and phenolics associated with increases in V max (enzyme production) and K m (indicative of competi

169 ransduction pathway that is nearly silent in V. cholerae of the El Tor biotype.

170 most-promising metal oxide catalysts include V(5+) surface species as a necessary constituent to conv

171 umidity, which can be explained by increased V-T relaxation.

172 rmine acts as an exogenous cue that inhibits V. cholerae biofilm formation through the NspS-MbaA sign

173 ractions between the paramagnetic interlayer V ions and a Kondo screening of these V moments.

174 the structurally authenticated reactive iron(V)oxo units (Fe(V)O), wherein the iron atom is two oxida

175 t commonly types Ia (40% [69/172 isolates]), V (23% [40/172 isolates]), II (14% [24/172 isolates]), a

176 n the formation of fully characterized Ir(IV,V) and Ir(III,III) complexes.

177 La and 17 other elements (Na, K, V, Ni, Co, Cu, Zn, Ga, As, Se, Mo, Cd, Sn, Sb, Ba, W, an

178 plex 1 (RAPTOR), the serine/threonine kinase V-Akt murine thymoma viral oncogene homolog 1 (AKT1), an

179 pG to modulate established disease in the L (V) panamensis mouse model.

180 No differences were observed in strains of L.V. panamensis by LRV-1 status.

181 fected with the prevalent related species L.(V.) braziliensis.

182 ve no clear effect on kinase activity, L290P/V mutations enhance ERK3's cytoplasmic localization by i

183 R254C/Zfnbrain revealed a reduction in layer V (CTIP2+) neurons, while the overall cell density of th

184 lum in mice 4 months of age and 18% in layer V of the cortex in mice 8 months of age.

185 le, daily cocaine injections, t-LTP in layer V pyramidal neurons is induced at +30 ms, a normally ine

186 ermined using whole-cell recordings in layer V pyramidal neurons.

187 the increasing of firing rates, and in layer V, where the major effect is the reduction in noise corr

188 ileptiform discharges were recorded in layer V-VI pyramidal neurons and fast-spiking interneurons in

189 napses in the apical dendritic tuft of layer V pyramidal neurons in the mPFC.

190 uts arising from superficial layers to layer V.

191 Since it is bioluminescent, imaging LOTUS-V does not require external light illumination.

192 dium-based bimetallic nanocrystals (PdM, M = V, Mn, Fe, Co, Ni, Zn, Sn, and potentially extendable to

193 cies at pol codons K103N, Y181C, G190A, M184 V, or K65R by oligonucleotide ligation assay and Illumin

194 ntial role in adaptive immunity by mediating V(D)J recombination in developing lymphocytes.

195 sue of the Journal of Clinical Microbiology, V.

196 lated mannan oligomers, MOS-III, MOS-IV, MOS-V and MOS-VI consist of tetra-, penta-, hexa-, and hepta

197 hannel correlates with the capacity of motif V to twist and order in the SaPI-inducing disposition, w

198 mical energy to directional motion in myosin V is examined by careful simulations that include two co

199 motes highly selective and processive myosin V.

200 In Saccharomyces cerevisiae, the myosin V motor Myo2 binds the vacuole-specific adapter Vac17 to

201 More specifically, n(V) increases at forward bias because of an attractive el

202 e, Th and U), common heather (Co, K, Mg, Na, V), sage (Ag, Cd, Cu), and bearberry (Ba, Fe, Pb, Sb, Zn

203 The design principle of NDP-V is to reduce the conformational disorder in the backbo

204 orphology of the donor-acceptor (PTB7-Th:NDP-V) blend, which is evidenced by the enhanced hole and el

205 r, naphthodiperylenetetraimide-vinylene (NDP-V), featuring a backbone of altenating naphthodiperylene

206 rain activity during the unimodal A (but not V) presentation.

207 renal ablation (Nx), being divided into: Nx+V, receiving vehicle, Nx+Eple, given eplerenone, 150 mg/

208 The El Tor and classical biotypes of O1 V. cholerae show striking differences in their resistanc

209 phosphoethanolamine (pEtN) to the lipid A of V. cholerae El Tor that is not functional in the classic

210 redominant force in the geochemical cycle of V at Earth's surface.

211 Given the potential dispersion of V. velutina, we conclude that vigilance is required over

212 ts is likely to lead to greater emissions of V to the atmosphere in the near future.

213 philic quinazolines modulate the function of V-ATPase in cells.

214 oals of this work were the identification of V. v. sylvestris exclusive transcripts and the character

215 To investigate the mechanism of V-ATPase regulation by reversible disassembly, we recent

216 Through mining of V ores (130 x 10(9) g V/y) and extraction and combustion

217 with a recently developed metabolic model of V. fischeri provides us with a clearer picture of the me

218 Existing small-molecule modulators of V-ATPase either are restricted to targeting one membrano

219 d the role of adenosine in the regulation of V-ATPase in ICs.

220 fully evaluate the therapeutic relevance of V-ATPase in human diseases.

221 icted to targeting one membranous subunit of V-ATPase or have poorly understood mechanisms of action.

222 Translocation of V-type ATPase after 1 h of exposure to 30,000 muatm was

223 However, geochemical controls on V mobility within coke deposits remain poorly constraine

224 eristic peptides [M132LGSXMSRPL141 (X = A or V), Y153XENMY158 (X,= H or R), and Y166RPVDXY172 (X = H,

225 that when group IV (i.e., Ti, Zr, and Hf) or V (i.e., Nb and Ta) transition metals are substituted in

226 lectrophilic [ClP(mu-NR)]2 to give P(III) /P(V) hexameric rings or reacted with I2 to give trimeric P

227 rings or reacted with I2 to give trimeric P(V) variants.

228 sociated with SMIC included Kudo pit pattern V, a depressed component (0-IIc), rectosigmoid location,

229 studies in humans demonstrate that the V PC/V CS ratio measured by PINTA is similar to that determin

230 sly developed high-performance acceptor, PDI-V, a perylenediimide-vinylene polymer.

231 enuates the sensitivity to DCS from 1.1% per V m(-1) to 0.55%.

232 ation of benzene from an unstable phosphorus(V) intermediate, yielding (C5 Me5 )2 Th[kappa(2) -(C,C')

233 tion that is sufficient to achieve d33>10 pm V(-1), when incorporated in a non-centrosymmetric DA mul

234 e non-coding RNAs produced by Pol IV and Pol V.

235 dDM pathway, including RNA POLYMERASE V (POL V), DOMAINS REARRANGED METHYLTRANSFERASE 2 (DRM2) and SA

236 f the RdDM pathway, including RNA POLYMERASE V (POL V), DOMAINS REARRANGED METHYLTRANSFERASE 2 (DRM2)

237 bnAb KI models expressing deduced precursor V(D)J rearrangements of mature bnAbs or unrearranged ger

238 ctor that directly regulates the two primary V. cholerae virulence factors.

239 consequences of Ab fucosylation, we produced V-gene-matched recombinant anti-RhD IgG Abs of the four

240 and synaptic vesicular proton pump protein (V-ATPase H) levels.

241 umented a reduction of the highly soluble Pu(V,VI) to the less mobile Pu(IV) within the argillaceous

242 process, generating viologen cation radical (V(*+)).

243 After the senior radiologist (V.M.C.) reviewed the radiographs, the patient was called

244 excludes the intermediacy of mer-(ONO(Q))Re(V)O2(IMes) in this oxygen atom transfer reaction.

245 Mutation of either oxyR2 or ahpC rendered V. cholerae more resistant to H2O2 RNA sequencing analys

246 rther demonstrate that a previously reported V-ATPase inhibitor, 3-bromopyruvate, also targets the sa

247 s deoxygenated by PMe2Ph to give the rhenium(V) compound (ONO(Cat))ReO(IMes), which can be independen

248 Sb(V) forms a precipitate, whereas Sb(III) needs to be oxid

249 and partitioning of associated As(V) and Sb(V) under anoxic conditions at pH 7.

250 ES spectroscopy indicated no reduction of Sb(V).

251 , whereas Sb(III) needs to be oxidized to Sb(V) before being incorporated in the new phase.

252 ring dicalcium silicate dissolution and some V was incorporated into neo-formed Ca-Si-H.

253 y and caused by defects in lymphoid-specific V(D)J recombination.

254 receptor potential cation channel subfamily V, receptor 1 (TRPV1)-substance P nociceptive signaling

255 e compared variance in reproductive success (V k*) and effective population sizes (N e) in several sp

256 he DNA of one T cell receptor beta (TCRbeta) V-to-DJ-joined allele in a functional configuration, whi

257 muXANES analyses show that V was released to solution as V(V) during dicalcium sili

258 Finally, we show that V. fischeri, purified EroS, and other bacterial chondroi

259 The results suggest that V. fischeri may help modulate the host stress responses

260 The V LSSE peak at 75 K is attributed to the H KS and M S (

261 tween MULE, hAT and Transib elements and the V(D)J recombinase.

262 mal degradation of HIF1alpha, disrupting the V-ATPase results in intracellular iron depletion, thereb

263 trafficking caused by genetic defects in the V-ATPase complex.

264 ication mechanism that only functions in the V. cholerae El Tor biotype.

265 ts illustrate that for the top 20 meters the V S models that is well constrained by the data, we obta

266 review, we describe unique components of the V-SVZ that may permit or promote tumor growth within the

267 ; the other 40% of cells have recombined the V to the DJ segments on both alleles, with only one of t

268 ation studies in humans demonstrate that the V PC/V CS ratio measured by PINTA is similar to that det

269 rovides long-range regionalized input to the V-SVZ niche and can regulate specific NSC subpopulations

270 shows selection for rearrangement within the V region of a number of genes and for CD8 and CD4 cells.

271 start at CDR3 position four, well within the V region.

272 rlayer V ions and a Kondo screening of these V moments.

273 Fe, Co, Ni, Cu, early transition metals (Ti, V, Cr, Zr, Nb and W) and their nanocomposites with empha

274 dataset 81,064 transcripts were annotated to V. v. vinifera reference transcriptome and 11,084 were a

275 54 eyes, 42 were Reese-Ellsworth group IV to V, and 37 were International Classification of Retinobla

276 ctural with SIFSIX-14-Cu-i, exhibited a type V isotherm and no phase change.

277 type II myosins Myo2p and Myp2p and the type V myosin Myo51p [2].

278 conditions, compared with that of wild-type V strains.

279 ere equally severe in Fitzpatrick skin types V to VI and I to IV, with minimal erythemal doses to mon

280 is capable to clearly characterize U(IV), U(V), and U(VI) existing simultaneously in the same sample

281 step in the process, reduction of U(VI) to U(V) .

282 estimated equilibrium constants (Keq) for U-V bearing minerals were more than 6 orders of magnitude

283 These effects are relevant for understanding V. cholerae pathogenicity and are mediated through the p

284 However, marine tests show that vanadium (V) is preferentially extracted over U and many other cat

285 ld enhance the reductive removal of vanadium(V) and inhibit the reoxidation of its reduction product

286 With molar ratios of phosphate to vanadium(V) varying from 0 to 1, phosphate accelerated the reduct

287 ntigen receptor gene assembly from variable (V), diversity (D), and joining (J) subgenic elements (V(

288 rovascular involvement of all hepatic veins (V) or portal bifurcation (P), contiguous extrahepatic tu

289 ing this approach, we introduce versatility, V, as a novel metric of nodal affiliation: V approximate

290 the most recently discovered NCRs is VISTA (V-domain Ig-containing Suppressor of T cell Activation).

291 tual machine that was developed to visualize V(D)J gene usage.

292 the temperature dependences of LSSE voltage (V LSSE), magnetocrystalline anisotropy field (H K) and s

293 tomachs, but the predominant response of W/W(V) stomachs was contraction.

294 Intestinal colonization with V. cholerae results in expenditure of host lipid stores

295 f the variation in junction conductance with V b .

296 ed by large numbers of smaller icebergs with V-shaped keels.

297 Similar model with V-wave change as a dichotomous variable showed that pati

298 romagnetic topological insulator (Bi, Sb)2-x V x Te3.

299 e mammalian ventricular-subventricular zone (V-SVZ) presents the highest neurogenic potential in the

300 SCs) in the ventricular-subventricular zone (V-SVZ) produce diverse olfactory bulb (OB) neurons.