ライフサイエンスコーパス: positive potential

1 gative potentials, but to order with applied positive potential.

2 g the outer periphery with anodic current or positive potential.

3 and shorter ("scrunched") in regions of high positive potential.

4 nts in ERP waveforms--N1, N2, P3, and a late-positive potential.

5 ing cells were required to maintain the more positive potential.

6 atalyst films are activated by exposure to a positive potential.

7 x-active molecules in the medium at the more positive potential.

8 when the catalyst is exposed to an external positive potential.

9 e oxidation waves, one at significantly more positive potential.

10 ntial and the open channel is more stable at positive potential.

11 ural measure of emotional distress, the late positive potential.

12 results, indicating specificity of the late positive potential.

13 -defined irreversible oxidation peak at very positive potential.

14 ed by a negative potential and hindered by a positive potential.

15 ude and shifted the activation curves toward positive potentials.

16 tromotility saturation also to shift to more positive potentials.

17 ly blocking its activity at negative but not positive potentials.

18 egative potentials to its activated state at positive potentials.

19 e voltage dependence of inactivation to more positive potentials.

20 e dependence of channel inactivation to more positive potentials.

21 utward K+ current that rectifies inwardly at positive potentials.

22 three exponential components at negative and positive potentials.

23 hannel block that terminates current flow at positive potentials.

24 s, with the rate of increase larger for more positive potentials.

25 ubtraction of linear-charge displacements at positive potentials.

26 wever, V(1/2)m shifted progressively to more positive potentials.

27 potentials, but inhibited outward current at positive potentials.

28 higher current densities and a shift to more positive potentials.

29 ady state activation voltage shifted to more positive potentials.

30 phenol), which are oxidized at slightly more positive potentials.

31 ve potentials (<-80 mV) but was slow at more positive potentials.

32 e negative than 1.0 V vs SCE and one at more positive potentials.

33 tentials but increased significantly at high positive potentials.

34 vation and inactivation were shifted to more positive potentials.

35 little voltage sensitivity except at extreme positive potentials.

36 e dependence of channel availability to more positive potentials.

37 e potentials speeds and then slows with more positive potentials.

38 nd the magnitude of entering Ca2+ current at positive potentials.

39 teines shifted the g-V relationships to more positive potentials.

40 ivation and inactivation was shifted to more positive potentials.

41 age dependence of channel activation to more positive potentials.

42 with relief of block evident at large inside positive potentials.

43 desensitization by holding ganglion cells at positive potentials.

44 r, Ibetanull activated at significantly more positive potentials.

45 (L-type Ca2+ current) that activated at more positive potentials.

46 V, and showed strong inward rectification at positive potentials.

47 ge-dependent manner, with less block at more positive potentials.

48 annel, [Ca2+] was higher at negative than at positive potentials.

49 e dependence of current inactivation to more positive potentials.

50 to differ from the inactivation observed at positive potentials.

51 ation process that mediates rectification at positive potentials.

52 tiffness, shifts channel inactivation toward positive potentials.

53 tivate after fast-inactivating, even at very positive potentials.

54 larger glutamate-elicited outward current at positive potentials.

55 the latter of which becomes rate limiting at positive potentials.

56 m ICa,L), but increased at more negative and positive potentials.

57 ximal at -55 mV and declined steeply at more positive potentials.

58 ith less inhibition of Ba2+ currents at more-positive potentials.

59 onged inactivation kinetics, particularly at positive potentials.

60 eads to accelerated hydride decomposition at positive potentials.

61 rent through the activated voltage sensor at positive potentials.

62 by a voltammetric sweep through sufficiently positive potentials.

63 nced by a shift in the flat band toward more positive potentials.

64 to activation, reflecting VSD relaxation at positive potentials.

65 eving efficient nitrate reduction under more positive potentials.

66 eration range of the MXene electrodes toward positive potentials.

67 te and shift voltage activation towards more positive potentials.

68 half wave potential for HZ oxidation to less positive potentials.

69 s lower energy than the final 2 H2O state at positive potentials.

70 the voltage dependence of activation to more positive potentials.

71 in onset and greatly attenuates currents at positive potentials.

72 use of an outward omega current activated at positive potentials.

73 called the relaxed state, also populated at positive potentials.

74 and a shift of the activation curve to more positive potentials.

75 l oxidation pathway on NiOOH enabled at more positive potentials.

76 e dependence of TRPM8 activation toward more positive potentials.

77 activation properties of the current to more positive potentials.

78 ge-insensitive step that is rate limiting at positive potentials.

79 on, so the third wave is shifted toward more positive potentials.

80 egative membrane potentials and inhibited at positive potentials.

81 probability mode becoming more prominent at positive potentials.

82 fidelity of ICa, which is known to be low at positive potentials.

83 Applying positive potential (+2.0 V) to these PCPs promotes ethyl

84 EEG analyses revealed positive potentials (400-700 ms) associated with relativ

85 the voltage dependence of activation to more positive potentials, a decrease in the maximum conductan

86 At positive potentials, a phase change is observed associat

87 Inactivation of ICl,vol at positive potentials, a typical hallmark of VRACs, strong

88 coupled H(2) oxidation to reduction of many positive potential acceptors, and it underwent anaerobic

89 At positive potentials, adsorbate-assisted anodic dissoluti

90 Memory updating was reflected in positive potentials after 700 ms that differentially pre

91 Patients also had smaller late-positive potential amplitude when compared with controls

92 Main Outcomes and Measures: The late positive potential amplitudes and ratings of liking and

93 In response to drug cues, the mean (SD) late positive potential amplitudes showed a parabolic traject

94 However, at positive potentials an outward current can be elicited b

95 and shifted voltage-dependent gating to less positive potentials, an effect partially conferred to WT

96 t below a certain critical level (<100 nA at positive potential and <25 nA at negative potential for

97 ield of 0.5-1 H2O2 molecules per electron at positive potential and 1.5-3 at negative potential.

98 s form heteromeric channels that activate at positive potential and decreased extracellular Ca(2+) co

99 ity, G230E exhibits outward rectification at positive potentials and a thiocyanate > NO(3) > I > Br >

100 abusers, the predictive ability of the late positive potentials and arousal ratings depended on insi

101 Results showed that pleasant-related late positive potentials and arousal ratings predicted pleasa

102 Voltage pulses to positive potentials and back to zero volts revealed that

103 on Ca2+ channel inactivation predominate at positive potentials and Ca2+ effects predominate at nega

104 d La3+ shifted the activation of INa to more positive potentials and decreased the maximal conductanc

105 used a shift of the activation curve to more positive potentials and F428S reduced the expression lev

106 oxygen into the cell shifted the OCP to more positive potentials and reduced the quantified H(ads); f

107 rret IKr, including the initial transient at positive potentials and the apparent discrepancy between

108 , like many other TRP channels, open at very positive potentials and thus rectify outwardly.

109 This blocker binds channels at positive potentials and unbinds at negative potentials,

110 hannels exhibited a large outward current at positive potentials and were constitutively active in th

111 tivated (in steady state) at about 5 mV more positive potential, and recovered faster from inactivati

112 he B ring of morin occurs first, at very low positive potentials, and is a one-electron, one-proton i

113 V(1/2)m was shifted to more positive potentials, and k(m) was doubled in the DeltaK1

114 , shift the threshold for excitation to more positive potentials, and prolong the relative refractory

115 (Po) of the channel is further augmented at positive potentials, and shows an e-fold voltage depende

116 redox potential of Eu(3+/2+) shifts to more positive potentials, and the diffusion coefficient for E

117 capable of operating under normal polarity (positive potentials applied to the electrode array) and

118 for the oxygen reduction reaction where high positive potentials are typically employed.

119 TTX-sensitive iNa inactivated at more positive potentials as compared to TTX-resistant iNa.

120 e of MsDps2, it is the interplay of negative-positive potentials at the pore that enables proper func

121 ide block was slow and greatly attenuated at positive potentials at which HERG rectifies.

122 e Cav3.1 T-type Ca2+ current is shifted to a positive potential, at which maximum current activation

123 he DNA-coated electrode, and shifted to more positive potentials attributed to the pre-concentration

124 ors for the detection of Sur based on buried positive-potential barrier layer structure and anti-surv

125 t the positive end of the amide dipole yield positive potentials because: 1) at allowed phi and psi a

126 Cocaine-related late positive potentials better predicted cocaine image choic

127 fting their oxidation potentials toward less positive potential but also enhanced their oxidation cur

128 p of the acid-induced currents was linear at positive potentials but an area of negative slope conduc

129 The bond is stable at positive potentials but cleaves at potentials more negat

130 ine methiodide not only inhibits currents at positive potentials but enhances N-type current at negat

131 currents were independent of Vm and Tl+o at positive potentials, but became more rapid at increasing

132 current activation was unaffected by pHo at positive potentials, but below 0 mV the activation rate

133 is reduced and activation is shifted to more positive potentials by acidification.

134 l of the zinc oxochlorins is shifted to more positive potentials by approximately 240 mV compared wit

135 x chemistry of the azo/hydrazo couple toward positive potentials by as much as 0.75 V.

136 S(2))W(CO)(4) derivatives is shifted to more positive potentials by ca. 0.5 V compared to the ca. -2

137 an serum increased outward currents (i.e. at positive potentials) by approximately 4-fold and inward

138 g but not sensor movement is shifted to more positive potentials, caused the loss of electromotility

139 3 catalyzes production at relatively positive potentials compared with other iron complexes.

140 The late positive potential component of electroencephalography,

141 lations identify a nearly continuous band of positive potential, consistent with an extended binding

142 feedback-related negativity, P300, and late positive potential could collectively encode saliency mo

143 Taken together, the late positive potential could serve as a biomarker to help pr

144 A centroparietal positive potential (CPP), which we previously establishe

145 measurements showed that maintaining a trans-positive potential definitely blocked fusion at steps fo

146 uction in maximal Ca2+ fluorescence at large positive potentials (DeltaF/Fmax) in double dysgenic/bet

147 negative potential drift is compensated by a positive potential drift related to the hydration of the

148 anism enables ethanol oxidation at much less positive potentials due to the fast kinetics for chlorid

149 Heightened late positive potential during reappraisal was associated wit

150 reas the MISUSE+ group showed increased late positive potential during reappraisal.

151 dimer radical is oxidized at a slightly more positive potential (E(1/2) = 0.47 V) to the correspondin

152 xidation state becomes accessible at a quite positive potential (E(1/2)) of -0.18 V vs Fc(+/0) upon c

153 eater effect on net membrane current at more positive potentials (EK channels) where total K(+) chann

154 Depolarizations to positive potentials elicited fluo-3 Ca2+ transients with

155 ial inside the target cell) but that a trans-positive potential eliminated all fusion.

156 ns show the effector domain produces a local positive potential, even when bound to a bilayer with 33

157 ni creates a region with a strong, localized positive potential for anion binding.

158 ontal negativity along with a decreased late positive potential for processing objects presented in m

159 e detection of chemosensory PS and BO showed positive potential for the determination of Cu(2+) in re

160 gative potential for 96% ethanol; < 40 nA at positive potential for water).

161 ctivity and structural changes, increasingly positive potentials from 0.1 up to 0.7 V vs Hg|HgO|1 M K

162 e package GRASP, revealing a large region of positive potential generated by a patch of positively ch

163 H-bond but usually requires the presence of positive potential generated by multiple cytosines, cons

164 al cAMP shifted the activation curve to more positive potentials, giving a V(1/2) of -74 mV; hence ar

165 At positive potentials (>0.5V(SCE)), a disordered layer of

166 Returning to more positive potentials, hydride decomposition begins above

167 Positive potentials (i.e., +0.2 V vs open circuit potent

168 rding to the results, SSG-ZMEO film may have positive potential impacts on increasing the shelf-life

169 It is often reported that more positive potentials improve acclimation and performance

170 -independent asymmetric reduction of a later positive potential in patients with schizophrenia resemb

171 mutant enzyme are consistent with increased positive potential in the active site, but the mutant en

172 onsistent with one function proposed for the positive potential in the active site-to stabilize the n

173 binding of PI(3)P significantly neutralizes positive potential in the region of the hydrophobic resi

174 l for Ru(bpy)3(2+) oxidation shifted to more positive potentials in a manner that was directly propor

175 KCNE1/KCNQ1 channel activation curve to more positive potentials in HEK cells.

176 tivation of I(Ca,L) was also shifted to more positive potentials in myocytes from diabetic versus non

177 ICa also reversed at slightly more positive potentials in rabbit (such that PCa/PCs might a

178 roxide shifts macropatch V0.5 values to more positive potentials, increases the rate of channel run-d

179 mixing, ceased before complete transfer for positive potentials, indicating that reversion of hemifu

180 s use of an anionic surfactant which, when a positive potential is applied to the Au nanotube membran

181 When a positive potential is applied, the sensor is transported

182 This positive potential is discussed as an important electroc

183 ced by anodic oxidation of water at elevated positive potentials is an additional advantage as they a

184 ltage-dependent unblock of TRPP2 by mDia1 at positive potentials is mediated through RhoA-induced mol

185 n by shifting its voltage dependence to more positive potentials, it enhances the rate and extent of

186 A alloantibodies was studied in 128 antibody-positive, potential kidney transplant recipients over an

187 tentials and alkaline solutions, albeit also positive potentials lead to an increase in particle impa

188 ose an electro-inductive effect where a more positive potential leads to electron withdrawal on the N

189 Holding cells under voltage clamp at positive potentials leads to a rise in intracellular Ca2

190 (bpy)(CO)3](2-) via a second pathway at more positive potentials, likely avoiding the need for the ge

191 for kidney transplantation, with crossmatch positive potential living donors, were treated with vari

192 The magnitude of the positive potential located by the hydroxyl hydrogen atom

193 The two negative potential regions and the positive potential located by the hydroxyl hydrogen atom

194 sociated with autism - the N170 and the Late Positive Potential (LPP) - in response to faces as putat

195 rimary mechanistic outcome was parietal late positive potential (LPP) and P300 amplitude during posit

196 0) or waitlist (n = 58) at baseline and late positive potential (LPP) data from 99 children (44 assig

197 trol condition (n = 58) at baseline and late positive potential (LPP) data from 99 children (44 PCIT-

198 The late positive potential (LPP) is a commonly used event-relate

199 The late positive potential (LPP) is a reliable electrophysiologi

200 The late positive potential (LPP) is an event-related potential t

201 relevant stimuli (flowers), and higher Late Positive Potential (LPP) responses for emotional stimuli

202 neutral contexts, and a high amplitude Late Positive Potential (LPP) when preceded by emotional cont

203 event-related potentials (ERPs) in the late-positive potential (LPP) window have been observed.

204 npleasant and pleasant images while the late positive potential (LPP), an event-related potential com

205 age-related N400 and an emotion-related Late Positive Potential (LPP), both showing distinct latencie

206 ng earlier selective attention, and the Late Positive Potential (LPP), reflecting sustained attention

207 motional reactivity, as measured by the late positive potential (LPP).

208 posterior negativity (EPN), P3, and the late positive potential (LPP).

209 s, emotional pictures prompted a larger late positive potential (LPP, 400-700 ms) and a larger positi

210 erving highly aroused avatars increased Late Positive Potentials (LPP), in line with previous evidenc

211 d processing of these same stimuli (the late positive potential [LPP], an event-related potential) in

212 sitivity: RewP, Feedback-P3: FB-P3, and Late-Positive Potential: LPP).

213 Late positive potentials (LPPs) for 'to-be-remembered' (TBR)

214 t and unpleasant images prompted larger Late Positive Potentials (LPPs, a robust measure of motivatio

215 figuration of intracranial sources producing positive potentials maximal at 600-700 ms.

216 ed, the negative potential saturated but the positive potential (maximal approximately 110 ms) contin

217 potential calculations suggest that a highly positive potential near the secondary binding site may f

218 ading all decreased contractions at strongly positive potentials near ECa.

219 alytic activity toward oxygen reduction at a positive potential of 610 mV.

220 ch that the MISUSE- group decreased the late positive potential of the electroencephalography during

221 nomy be promoted instead, thus fostering the positive potential of the web?

222 ly to the active-site zinc ion to "mask" the positive potential of the zinc ion and lower the energy

223 A more positive potential of zero charge enhances CO(2)R activi

224 Positive potential on the side of protein addition resul

225 ethane (F4TCNQ) solutions imposed additional positive potentials on the P3HT RG, resulting in a lower

226 H 7, deltaDeltaPhi(SCR)(L) increases at more positive potentials or higher illumination power density

227 and overall composition, overall charge and positive potential patches on the protein surface.

228 At positive potentials Po and the longer mean open time wer

229 imately 200 ms after the flash, with a small positive potential preceding it.

230 nt-related potentials, specifically the late positive potential, predict choice to view cocaine image

231 Steps to positive potentials produced greater augmentation of the

232 ell as reactivate during repolarization from positive potentials, producing a "resurgent" current.

233 ting the relationship with voltage to a more positive potential range.

234 in rectifying outward currents and, at more positive potentials, rapidly inactivating ( approximatel

235 of activation and fast inactivation to more positive potentials, relative to WT.

236 ge-voltage relationship to more negative and positive potentials, respectively.

237 s decreased and shifted to more negative and positive potentials, respectively.

238 Conclusions and Relevance: The late positive potential responses to drug cues, indicative of

239 A positive potential reversibly opened OmpF and TolC chann

240 is a shift in voltage dependence toward more positive potentials, reversing the trend toward negative

241 e electrode history: it is different for the positive potential scan direction than for the reverse d

242 Cyclic voltammetry revealed a positive potential shift for the first reduction of enca

243 ctivation of the voltage gate (V(j) gate) at positive potentials shifted the accessibility limit for

244 show greatly increased conductance at inside positive potentials, significantly larger than in oocyte

245 d the conductance-voltage curves toward more positive potentials, slowed activation, and speeded deac

246 Since the positive potential stability range in diluted aqueous el

247 ve in triggering Ca2+ release than pulses to positive potentials suggesting that the Ca(2+)-induced C

248 potential maps reveal that the channel has a positive potential, suggesting that it binds negatively

249 ains polyphenols that are oxidised at a less positive potential than extract EII, i.e., it shows bett

250 in which the Mn(V) species formed at a less positive potential than that in MnO(x) , displayed only

251 ation of the phenol dyad occurring at larger positive potential than that of a typical phenol.

252 n(mesbpy)(CO)3](-), is formed at 300 mV more positive potential than the corresponding state is forme

253 e with a valence band edge located at a more positive potential than the oxidation potential of Co(2+

254 ed by an irreversible oxidation at much more positive potentials than for 1,2-dithiin and 3,6-dimethy

255 Na(+) currents of PG cells activate at more positive potentials than those of typical CNS neurons.

256 elatively neutral compared to the asymmetric positive potential that surrounds eukaryotic TBPs.

257 Prepulses to positive potentials that relieve the Ca(2+) channel bloc

258 At positive potentials the longer burst duration was increa

259 At positive potentials, the channel exhibited a single cond

260 As the electrode potential is swept to positive potentials through both redox transitions, an i

261 Adsorption is promoted by scanning to positive potentials (through the ferrocene wave) and by

262 This oxidation is enhanced upon applying a positive potential to the Pt electrode or raising the el

263 use of an external power source to supply a positive potential to the working electrode of a given d

264 bsequently scanning the ring linearly toward positive potentials to yield H(2)SeO(3).

265 We find that the cluster signal is stable at positive potentials up to 0.5 V but that cluster destruc

266 erfluorooctanoic acid (PFOA) was observed at positive potentials via the molecule's hydrophobic long-

267 boundary layer that contributed to low level positive potential vorticity.

268 When a positive potential was applied, leakage was severe, obsc

269 ormation was much lower compared to when the positive potential was applied.

270 Its relief at positive potentials was consistent with omega-Aga-IVA ac

271 The early posterior negativity and late positive potential were greatest in amplitude for erotic

272 1000 ms) and late (1000-2000 ms) window late positive potentials were collected; (ii) self-reported a

273 n 600 nM time-dependent currents elicited by positive potentials were typical of Slow Vacuolar (SV) c

274 a surface and polarization to high negative/positive potentials, where partial denaturation/unfoldin

275 rent that has a large transient component at positive potentials, whereas the other two channels are

276 to be converted into chloride conductance at positive potentials, whereas whole-cell currents at nega

277 tion activity in the sample generates a more positive potential, which enhances the PB absorbance tha

278 cation selective and exhibits gating at low positive potentials, while alpha-hemolysin is weakly ani

279 of pacing; (2) counterclockwise rotation of positive potentials with time for epicardial pacing, clo

280 hese gating modes occur at both negative and positive potentials, with the high open probability mode

281 referential emotional reactivity (i.e., late positive potential) within the first second of viewing a