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

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

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

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

7 results, indicating specificity of the late positive potential.

8 -defined irreversible oxidation peak at very positive potential.

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

10 e dependence of channel inactivation to more positive potentials.

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

12 three exponential components at negative and positive potentials.

13 hannel block that terminates current flow at positive potentials.

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

15 ubtraction of linear-charge displacements at positive potentials.

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

17 potentials, but inhibited outward current at positive potentials.

18 ady state activation voltage shifted to more positive potentials.

19 te and shift voltage activation towards more positive potentials.

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

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

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

23 tentials but increased significantly at high positive potentials.

24 vation and inactivation were shifted to more positive potentials.

25 little voltage sensitivity except at extreme positive potentials.

26 e dependence of channel availability to more positive potentials.

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

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

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

30 ivation and inactivation was shifted to more positive potentials.

31 age dependence of channel activation to more positive potentials.

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

33 desensitization by holding ganglion cells at positive potentials.

34 r, Ibetanull activated at significantly more positive potentials.

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

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

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

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

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

40 e dependence of current inactivation to more positive potentials.

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

42 to differ from the inactivation observed at positive potentials.

43 ation process that mediates rectification at positive potentials.

44 tiffness, shifts channel inactivation toward positive potentials.

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

46 larger glutamate-elicited outward current at positive potentials.

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

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

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

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

51 the voltage dependence of activation to more positive potentials.

52 in onset and greatly attenuates currents at positive potentials.

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

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

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

56 e dependence of TRPM8 activation toward more positive potentials.

57 activation properties of the current to more positive potentials.

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

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

60 onged inactivation kinetics, particularly at positive potentials.

61 egative membrane potentials and inhibited at positive potentials.

62 probability mode becoming more prominent at positive potentials.

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

64 tromotility saturation also to shift to more positive potentials.

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

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

67 egative potentials to its activated state at positive potentials.

68 e voltage dependence of inactivation to more positive potentials.

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

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

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

72 At positive potentials, a phase change is observed associat

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

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

75 At positive potentials, adsorbate-assisted anodic dissoluti

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

122 3 catalyzes production at relatively positive potentials compared with other iron complexes.

123 The late positive potential component of electroencephalography,

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

155 This positive potential is discussed as an important electroc

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

178 Positive potential on the side of protein addition resul

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

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

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

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

183 Steps to positive potentials produced greater augmentation of the

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

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

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

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

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

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

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

191 A positive potential reversibly opened OmpF and TolC chann

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

207 At positive potentials the longer burst duration was increa

208 At positive potentials, the channel exhibited a single cond

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

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

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

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

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

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

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

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

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

218 1000 ms) and late (1000-2000 ms) window late positive potentials were collected; (ii) self-reported a

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

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

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

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

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

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