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1 tion causes a dramatic positive shift of the inactivation curve.
2 ated state and a hyperpolarized steady-state inactivation curve.
3 ctivation curve of I(A) without altering the inactivation curve.
4  manner without affecting their steady-state inactivation curve.
5 nificant, negative shift of the steady-state inactivation curve.
6 ionship but produced a negative shift in the inactivation curve.
7 r an additional hyperpolarizing shift of the inactivation curve.
8 erimposed after voltage shifting, as did the inactivation curves.
9  position of the activation and steady state inactivation curves.
10 we find that vixotrigine shifts steady-state inactivation curves.
11 ss of the sodium current, while shifting the inactivation curve ~10 mV toward more hyperpolarized pot
12  shift of the voltage-dependent steady-state inactivation curve, a slower inactivation, and a faster
13 hyperpolarizing shifts of the activation and inactivation curves and enhanced fast inactivation.
14 l overlap of its activation and steady-state inactivation curves and its persistent nature suggest th
15 curves negative, decreasing the slope of the inactivation curve, and increasing the percentage of non
16 uM, negatively shifted the voltage-dependent inactivation curve, and slowed its recovery from inactiv
17  protocols (such as I-V curves, steady-state inactivation curves, and measurements of inactivation ra
18 g, shifting both steady state activation and inactivation curves, as well as accelerating channel kin
19  the midpotential of the hKv2.1 steady-state inactivation curve by approx. 15 mV in the hyperpolarizi
20  a hyperpolarizing shift in the steady-state inactivation curve completely abolished EADs in myocytes
21                             The trace of the inactivation curve could not be altered by preincubating
22  current" between the voltage activation and inactivation curves, decreasing the tonically active I(A
23                                              Inactivation curves dependency on heating technology sug
24 s dominating and, consequently, the prepulse inactivation curves exhibit depolarizing shifts (DeltaV
25 tion in inside-out patches, the steady-state inactivation curve exhibits a hyperpolarizing shift of a
26 the qPCR-based method to establish a UV(254) inactivation curve for HuNoV (inactivation rate constant
27  a hyperpolarizing shift in the steady-state inactivation curve for the sodium current.
28 nt-voltage relationship and the steady-state inactivation curve for the TTX-R INa which were indistin
29                            When steady-state inactivation curves for the L current were fitted with a
30 oltage-dependent activation and steady-state inactivation curves for these currents were shifted nega
31 polarizing shift in the apparent Na+ channel inactivation curves generated from Vmax and theta2, resp
32 urrents at rest and shifted the steady-state inactivation curve (h infinity) toward the hyperpolarizi
33               Current-voltage activation and inactivation curves indicated that adding 0.5 and 2 mM c
34 s altered the shape of the voltage-dependent inactivation curve indicating that the suppression of IK
35 d in the depolarized direction, and the fast-inactivation curve is less steep compared with mu1.
36 ate constants by as much as 600%, shortening inactivation curve lag phase by up to 73% and lowering C
37 -93 shifted the midpoint of the steady-state inactivation curve leftward and markedly slowed the reco
38   In addition, we find that the steady-state inactivation curve of modified Na channels is made much
39                             The steady-state inactivation curve of Na(v)1.2a was shifted +12 mV in Na
40 hat from control rats (109.4 pA/pF), and the inactivation curve of the IA current was displaced to mo
41  effects on the position of the steady state inactivation curve of the Kv4.3 channel.
42 dings revealed a hyperpolarized shift in the inactivation curve of transient, A-type K(+) currents th
43         As a consequence, the activation and inactivation curves of ASIC3 but not other ASICs overlap
44 cantly increased at 38 h after ischemia; the inactivation curves of I(A) shifted toward the depolariz
45 ation, shifts of steady-state activation and inactivation curves of I(Na) to more depolarized potenti
46                               Activation and inactivation curves of ICa currents in cells expressing
47 t density, and right-shifted the V1/2 of the inactivation curve, of hindpaw innervating DRG neurons,
48 tive radicals, and electric field on E. coli inactivation curves, rate of DNA leakage and visual appe
49 g peptides caused depolarizing shifts in the inactivation curves seen with CaM(WT) coexpression with
50 y-state channel availability relationships ("inactivation curves") shifted toward more negative membr
51                               Activation and inactivation curves showed no shift in the voltage depen
52 to changes in the steady-state activation or inactivation curves, the time course of current decay, t
53 o higher pH values and a slight shift of the inactivation curve to lower pH values.
54  in the rate of inactivation and shifted the inactivation curve to more hyperpolarized potentials, bu
55 eduction of I(Ca,L) density and shift of the inactivation curves to more depolarized potentials).
56 near 0 mV and shifted the Na+ activation and inactivation curves to the left.
57 ss acidic pH but a shift in the steady state inactivation curve toward more acidic pH.
58             The midpoint of the steady-state inactivation curve was approximately 25 mV more negative
59 The midpoints of steady-state activation and inactivation curves were 1.1 mV and -61.4 mV, respective
60                                          All inactivation curves were nonlinear and followed Weibull
61 ches, respectively, n = 16, P < 0.01), while inactivation curves were not significantly different.
62 ng measurements, bell-shaped Ca2+ activation/inactivation curves were obtained in media containing di
63                                 Steady-state inactivation curves were shifted by approximately 10 mV
64                                 Steady-state inactivation curves were shifted to more depolarized pot
65                                 Steady-state inactivation curves were similar in the two populations.
66  depolarizing shift of the steady-state fast inactivation curve, whereas EE1314,15RR produced a hyper