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1 opus laevis oocytes using two-microelectrode voltage clamp technique.
2 currents were recorded using a two-electrode voltage clamp technique.
3 l vein using the perforated patch whole-cell voltage clamp technique.
4 human blood eosinophils using the whole cell voltage clamp technique.
5 conductance (Gj) was measured with the dual voltage clamp technique.
6 with earlier studies using the two-electrode voltage clamp technique.
7 1) density was measured using the whole-cell voltage clamp technique.
8 neurons and dentate granule cells (DGCs) by voltage clamp technique.
9 sing immunoblot analysis and a two-electrode voltage clamp technique.
10 ion was assessed with the two-microelectrode voltage clamp technique.
11 s were recorded using the two-microelectrode voltage clamp technique.
12 in Xenopus oocytes using the two-electrode, voltage clamp technique.
13 e characterized using the two-microelectrode voltage clamp technique.
14 ton-activated current with the two-electrode voltage clamp technique.
15 r ovary (CHO-K1) cells, using the whole-cell voltage clamp technique.
16 f the dipeptide using the two-microelectrode voltage clamp technique.
17 ed by Ba(2+) (I(Ba)) using the two electrode voltage clamp technique.
18 were investigated using the dual whole-cell voltage clamp technique.
19 s (I(Na)) were measured by the two-electrode voltage clamp technique.
20 s, using the whole-cell configuration of the voltage-clamp technique.
21 ce (Gj) was measured by the dual 2-electrode voltage-clamp technique.
22 n Xenopus oocytes has been studied using the voltage-clamp technique.
23 f Rana temporaria with a double Vaseline-gap voltage-clamp technique.
24 function was studied using the two-electrode voltage-clamp technique.
25 s on GABAAR by means of a two-microelectrode voltage-clamp technique.
26 e-directed mutagenesis and the two-electrode voltage-clamp technique.
27 rrents were recorded using the two-electrode voltage-clamp technique.
28 ere measured by using the two-microelectrode voltage-clamp technique.
29 determined with standard two-microelectrode voltage-clamp technique.
30 opus laevis oocytes, using the two-electrode voltage-clamp technique.
31 investigated by using the two-microelectrode voltage-clamp technique.
32 -junctional currents using the two-electrode voltage-clamp technique.
33 oocytes and studied using the two-electrode voltage-clamp technique.
34 (mIPSCs) were recorded using the whole-cell voltage-clamp technique.
35 t isolated DRG neurones using the whole-cell voltage-clamp technique.
36 SCG) has been carried out using a whole-cell voltage-clamp technique.
37 nels expressed in Xenopus oocytes, using the voltage-clamp technique.
38 el inhibition evaluated using the whole-cell voltage-clamp technique.
39 s were measured using the two-microelectrode voltage-clamp technique.
40 rrents were measured using the two-electrode voltage-clamp technique.
41 ls were investigated by using the whole-cell voltage-clamp technique.
42 was measured using a dual two-microelectrode voltage-clamp technique.
43 hile membrane potential was controlled using voltage clamp techniques.
44 ns on cardiac K+ currents were studied using voltage clamp techniques.
45 ic epithelial cell line T84 using whole cell voltage clamp techniques.
46 tory currents were recorded using whole cell voltage clamp techniques.
47 -open oocyte voltage clamp and two-electrode voltage clamp techniques.
48 sing quantitative swelling and two-electrode voltage clamp techniques.
49 in Xenopus oocytes using two-microelectrode voltage clamp techniques.
50 ous expression system and two-microelectrode voltage clamp techniques.
51 ocytes were studied using two-microelectrode voltage-clamp techniques.
52 rom tiger salamander retina using whole-cell voltage-clamp techniques.
53 using two microelectrode and single channel voltage-clamp techniques.
54 lation and were recorded by using whole-cell voltage-clamp techniques.
55 stigated in retinal neurons using whole-cell voltage-clamp techniques.
56 t the single-channel level using tight-seal, voltage-clamp techniques.
57 nthetic A beta was measured using whole-cell voltage-clamp techniques.
58 the amphotericin or conventional whole-cell voltage-clamp techniques.
59 n Xenopus laevis oocytes using two-electrode voltage-clamp techniques.
60 of calcium currents (I(Ca)) using whole-cell voltage-clamp techniques.
61 nd currents recorded with two-microelectrode voltage-clamp techniques.
62 ells of skate were examined using whole-cell voltage-clamp techniques.
63 ingle-channel properties were recorded using voltage-clamp techniques.
64 3 null alleles, as determined by whole-cell, voltage-clamp techniques.
65 cortical pyramidal neurons using whole-cell voltage-clamp techniques.
66 the current study, we used the two-electrode voltage-clamp technique alone or in combination with pH/
68 h muscle cells using conventional whole-cell voltage clamp technique and high temporal resolution mic
69 d human embryonic kidney 293 cells using the voltage clamp technique and photodiode-based displacemen
70 nopus laevis oocytes using the two-electrode voltage clamp technique and simulated interactions using
73 d KCNJ2 mutations using a two-microelectrode voltage-clamp technique and correlated the findings with
74 We characterized I(h) using the whole-cell, voltage-clamp technique and found the current expressed
75 d on a functional level using the whole-cell voltage-clamp technique and on a molecular level using t
77 on whole oocytes, we used the two-electrode voltage-clamp technique, as well as pH- and voltage-sens
79 rabbit ileum studied with the Ussing chamber-voltage clamp technique, EGF stimulation of active NaCl
85 ns (SPNs) were recorded using the whole-cell voltage clamp technique in slices of neonatal rat spinal
86 s discovered by Hodgkin and Huxley using the voltage clamp technique in their landmark series of pape
88 urements were combined with action potential voltage clamp techniques in a physiologically relevant h
89 3)(beta(2))(2) receptors using two-electrode voltage clamp techniques in Xenopus laevis oocytes indic
91 This study investigates, using current and voltage-clamp techniques in brain slices from young mice
92 ession of inhibition' (DSI) using whole-cell voltage-clamp techniques in Ca1 pyramidal cells of rat h
93 nule neurones were analysed using whole-cell voltage-clamp techniques in order to explore the functio
94 ion channel function using the two-electrode voltage clamp technique on 16 cloned ion channels (12 K(
95 Ce1-mediated currents with the two-electrode voltage-clamp technique or pHi changes using Vm/pH-sensi
96 nopus laevis oocytes using the two-electrode voltage clamp technique showed GHB to be a partial agoni
98 TX dose-response curve, using the whole cell voltage-clamp technique, showed three populations of fib
99 dy, using patch-pipet whole-cell current and voltage clamp techniques, synaptic interactions of these
100 study, we demonstrate, using dual whole-cell voltage-clamp techniques, that coexpression of connexin
102 e injected Xenopus oocyte with two-electrode voltage clamp techniques to characterize the action of A
103 dy, we used the oocyte expression system and voltage clamp techniques to determine the functional con
104 n oocyte Vaseline gap and two microelectrode voltage clamp techniques to determine the voltage depend
105 cells using the perforated patch whole-cell voltage-clamp technique to ascertain whether this Ca2+ u
107 ences, we have applied the double-whole-cell voltage-clamp technique to freshly isolated pairs of cel
108 this study we have used the cut-open oocyte voltage-clamp technique to investigate the relationship
109 ed Ca2+ channels, by applying the whole-cell voltage-clamp technique to isolated dendritic segments (
112 t study, we used standard two-microelectrode voltage-clamp techniques to further characterize the eff
114 To elucidate the mechanisms of IH, we used voltage-clamp techniques to investigate the [H]o, [Na]o,
115 the range of 1-780 nm) by the two-electrode voltage clamp technique using a standard Xenopus oocyte
116 s were studied using the permeabilized-patch voltage-clamp technique, using an applied NH4+ gradient
117 lying the potentiation, the whole-cell patch voltage clamp technique was used to study VMN neurons in
128 nine-scanning mutagenesis and the whole cell voltage clamp technique were used to investigate the fun
133 sis of the decreased conductance, whole-cell voltage-clamp techniques were used to record evoked, GAB
137 llular compartments, and (b) patch clamp and voltage clamp techniques, which investigate transporters
139 s were studied using the permeabilized-patch voltage-clamp technique, with an applied NH4+ gradient t