ライフサイエンスコーパス: current-voltage relationship

1 egative slope resistance in the steady-state current-voltage relationship.

2 ion, and an inwardly rectifying steady-state current-voltage relationship.

3 ents) and voltage, but did not affect the Ca current-voltage relationship.

4 ) caused membrane currents or changes in the current-voltage relationship.

5 at -80 mV in whole cell mode, with a linear current-voltage relationship.

6 a fundamental change in rectification of the current-voltage relationship.

7 l cation current with an inwardly rectifying current-voltage relationship.

8 es, which causes inward rectification of the current-voltage relationship.

9 d sublinear-to-superlinear transition in the current-voltage relationship.

10 enhanced Cs+-sensitive rectification of the current-voltage relationship.

11 +/-1 pA/pF without altering the shape of the current-voltage relationship.

12 in reduced rectification of the steady-state current-voltage relationship.

13 3(M)beta3gamma2L receptors had a more linear current/voltage relationship.

14 lutions, the P2X7R current followed a linear current/voltage relationship.

15 h no change in action potential waveforms or current-voltage relationships.

16 Ca) over the range of potentials in standard current-voltage relationships.

17 rimarily contribute to preMN/MN subthreshold current-voltage relationships.

18 0.1 nA at -160 mV) or in inwardly rectifying current-voltage relationships.

19 polyamine block, and have relatively linear current-voltage relationships.

20 tern of discharge to depolarizing pulses and current-voltage relationships.

21 oM GABA were used to construct instantaneous current-voltage relationships.

22 A second type of channel had a linear current-voltage relationship, a slope conductance of 17.

23 reversal potential data, obtained from these current-voltage relationships, all corresponded to a 2 H

24 ation of some K+ channels, did not alter IKr current-voltage relationships, although it did decrease

25 maximal) displayed (i) a linear steady-state current-voltage relationship and (ii) time and voltage d

26 nel with little voltage dependence, a linear current-voltage relationship and a single-channel conduc

27 ator, caused a 3-14 mV leftward shift in the current-voltage relationship and also led to a hyperpola

28 e conductance was Cl- dependent and that the current-voltage relationship and anion permeation proper

29 isy' inward current at -50 mV with a similar current-voltage relationship and reversal potential to t

30 dent, Cl-selective channel with a rectifying current-voltage relationship and single channel conducta

31 CaV1.3 activity, causing a left shift in the current-voltage relationship and strongly potentiating p

32 tration of 1 mM produced effects on both the current-voltage relationship and the steady-state inacti

33 Both the current-voltage relationship and the time course of inac

34 The current-voltage relationship and the variance of current

35 hannel that exhibited an inwardly rectifying current-voltage relationship and was inhibited by extern

36 The current-voltage relationships and the reversal potential

37 ould quantitatively account for the observed current-voltage relationships and the transinhibition by

38 he two variants were similar with respect to current-voltage relationships and the voltage dependence

39 he NMDG+ current by P2X7Rs followed a linear current/voltage relationship and did not change with tim

40 e model to exhibit superlinear and sublinear current-voltage relationships, and show why alignment fi

41 of the dilution potentials, the linearity of current-voltage relationships, and the lack of influence

42 K1/2 (the dose causing 50% left shift in the current-voltage relationship) are additive in their abil

43 upancy, developed on the basis of single ion current-voltage relationships, are in agreement with the

44 Current-voltage relationships at different luminal pH va

45 e to calcium and display inwardly rectifying current-voltage relationships, because of blocking of ou

46 mean conductance of 56 +/- 1.8 pS, a linear current-voltage relationship between -80 and +60 mV with

47 6, as evidenced by their inwardly rectifying current-voltage relationship, blockade of AMPA receptor-

48 he inhibitory effect did not affect the peak current-voltage relationship but produced a negative shi

49 ions that would cause a maximal shift in the current-voltage relationship by each agent alone (Vmax),

50 The shift in the current-voltage relationship caused by 1alpha,25-D3 is r

51 leak cation currents, yielding the N-shaped current-voltage relationships, causing the resting membr

52 ted inward current was observed exhibiting a current-voltage relationship characteristic of high-volt

53 expressed TRPC5 exhibits a doubly rectifying current-voltage relationship characterized by relatively

54 -cell AMPA currents displayed roughly linear current-voltage relationships, consistent with the prese

55 A shift in the single-channel current-voltage relationship derived from antisense-trea

56 Current-voltage relationships, determined using depolari

57 out patches showed that in all Kir2 channels current-voltage relationships display a 'crossover' effe

58 The whole cell current-voltage relationship exhibited rectification abo

59 First, an expression for the current-voltage relationship for a biological oxygen ele

60 tivation produce inward rectification of the current-voltage relationship for human ether-a'-go-go-re

61 The current-voltage relationship for this K+ channel was alm

62 Subtraction currents yielded proctolin-like current-voltage relationships for all six substances, an

63 Current-voltage relationships for either ND7/23 cell or

64 removal of inactivation using this approach, current-voltage relationships for IKr ([K+]o, 1 to 20 mm

65 Current-voltage relationships for non-NMDA receptor-medi

66 Current-voltage relationships for the cotransporter, mea

67 hosphatidylcholine) bilayers, single-channel current-voltage relationships had an ohmic behavior at l

68 cation of single channel mustard oil (I(MO)) current-voltage relationships (I-V) and substantial modu

69 the transmembrane Na(+) gradient altered the current-voltage relationship in a fashion commensurate w

70 pH (pHin) of voltage-clamped oocytes, 2) the current-voltage relationship in solutions of various pH

71 anied by a negative shift in the peak of the current-voltage relationship in TG+ mice.

72 The nonlinear current-voltage relationship in the presence of spermine

73 ly projecting PVN neurons exhibited a linear current-voltage relationship in Wistar-Kyoto (WKY) rats.

74 threonine, and l-methionine elicited complex current-voltage relationships in alkaline pH-dependent C

75 Construction of current-voltage relationships in the absence and presenc

76 or agonist-induced responses, linearized the current-voltage relationship, increased agonist and anta

77 Steady-state dose-response relationships, current-voltage relationships, ionic selectivities, and

78 an ohmic pore, but our results show that the current-voltage relationship is nonlinear with respect t

79 f vertebrate astrocytes, including a passive current-voltage relationship, low membrane resistance, h

80 From the current-voltage relationship measured at 1 ms from onset

81 4, 25-D3 inhibits the left shift in the peak current-voltage relationship mediated by either 1alpha,2

82 First, we study the current-voltage relationship obtained with fixed chemica

83 ated current amplitude, without changing the current- voltage relationship of the ATP-activated curre

84 The current-voltage relationship of basolaterally permeabili

85 The current-voltage relationship of Icat was not changed by

86 The low Ca(2+) permeability and nonrectified current-voltage relationship of most native AMPA recepto

87 Here we report the complete current-voltage relationship of NADPH oxidase, the first

88 After CFA treatment, the current-voltage relationship of NMDA receptor channels w

89 The effects on the current-voltage relationship of reduced pHin were oppose

90 probability, and inward rectification of the current-voltage relationship of single channels.

91 The current-voltage relationship of the acid-induced current

92 the prepulse holding potential followed the current-voltage relationship of the Ca2+ current found i

93 mM TEA + 5 mM 4-AP had little effect on the current-voltage relationship of the cells over the same

94 xtracellular divalent cations, as the linear current-voltage relationship of the channel could be res

95 ating that full-length LF and EF convert the current-voltage relationship of the heptameric PA63 ion

96 The current-voltage relationship of the RyR channel was N-sh

97 The current-voltage relationship of these injured neurons sh

98 In symmetrical 150 mm KCl, the current-voltage relationship of TRESK-2 was slightly inw

99 Furthermore, current-voltage relationships of AMPAR-mediated EPSCs sh

100 experiments of VDAC-1 show agreement for the current-voltage relationships of an "open" channel and t

101 l of hyperalgesia, there was a switch in the current-voltage relationships of capsaicin-induced mEPSC

102 We also show that the current-voltage relationships of glycine-evoked currents

103 Our data show that the current-voltage relationships of homomeric channels form

104 from the reversal potential by measuring the current-voltage relationships of the cotransporter at di

105 from its reversal potential by measuring the current-voltage relationships of the cotransporter at di

106 The current-voltage relationships of the kisspeptin-activate

107 Current-voltage relationships of the TRPC4G503S and TRPC

108 + current (ICa) density but no change in the current-voltage relationship or the kinetics of ICa inac

109 rsus PKCP, respectively) without a change in current-voltage relationships or peak I(Na).

110 The fully activated current-voltage relationship revealed that the drug incr

111 Current-voltage relationships revealed that D555E produc

112 Analysis of the current-voltage relationships revealed that nefiracetam

113 EGTA, Ishear showed an outwardly rectifying current-voltage relationship (reversal at -2 mV).

114 rties, including double rectification of the current-voltage relationship, sensitivity to a polyamine

115 The current-voltage relationship showed marked inward rectif

116 The current-voltage relationship showed no difference in the

117 The current-voltage relationship showed strong inward rectif

118 The current-voltage relationship showed that the spontaneous

119 a(1A) channels, alpha(1D) channels exhibited current-voltage relationships similar to those of native

120 ons with various IK1 gradient conditions and current-voltage relationships substantiated its major ro

121 display a permeability to calcium ions and a current-voltage relationship that differ from those of h

122 of TRPC1 and TRPV6 co-expression resemble in current-voltage relationship that of TRPV6.

123 mp, stretch elicited a current with a linear current-voltage relationship that was inward at membrane

124 These cardiomyocytes display N-shaped current-voltage relationships that cross the voltage axi

125 2 ion channel inhibitor, amantadine); b) had current-voltage relationships that shifted to more posit

126 typic pairs and showed a slightly asymmetric current-voltage relationship; the side expressing Cx35 e

127 reased ICa density and caused a shift in the current-voltage relationship to a similar extent to that

128 B2 slows Hslo1 channel gating and shifts the current-voltage relationship to more negative potentials

129 n resulted from a shift in 13 mV of the Ca2+ current-voltage relationship toward more negative potent

130 The current-voltage relationship under different ionic condi

131 105 mM internal K(+) (K(+)(1)), the unitary current-voltage relationship was fitted by the constant

132 s, the macroscopic fast rectification of the current-voltage relationship was fully explained at the

133 The current-voltage relationship was inwardly rectifying whi

134 The single channel current-voltage relationship was linear with a conductan

135 The current-voltage relationship was not altered by fluid fl

136 n conductance revealed that the open channel current-voltage relationship was outwardly rectifying wi

137 The current-voltage relationship was similar for the wild-ty

138 The current-voltage relationship was slightly inwardly recti

139 slow time course and a lack of change in the current-voltage relationship were consistent with an all

140 Single-channel current-voltage relationships were nonlinear in a way si

141 The current-voltage relationships were not altered after 3-m

142 d in reduced exchanger activity, and altered current-voltage relationships were observed with mutatio

143 ich identified a 20-mV leftward shift in the current-voltage relationship when palmitoylation at C243

144 eceptors showed outward rectification of the current-voltage relationship, whereas current-voltage re

145 pS), low permeability to calcium ions, and a current-voltage relationship which resembles that of cha

146 Na(+) currents exhibited essentially linear current-voltage relationships which were mildly inhibite