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1 e characterized using the two-microelectrode voltage clamp technique.
2  conductance (Gj) was measured with the dual voltage clamp technique.
3 with earlier studies using the two-electrode voltage clamp technique.
4 1) density was measured using the whole-cell voltage clamp technique.
5  neurons and dentate granule cells (DGCs) by voltage clamp technique.
6 ion was assessed with the two-microelectrode voltage clamp technique.
7 s were recorded using the two-microelectrode voltage clamp technique.
8  in Xenopus oocytes using the two-electrode, voltage clamp technique.
9 ton-activated current with the two-electrode voltage clamp technique.
10 r ovary (CHO-K1) cells, using the whole-cell voltage clamp technique.
11 f the dipeptide using the two-microelectrode voltage clamp technique.
12 ed by Ba(2+) (I(Ba)) using the two electrode voltage clamp technique.
13  were investigated using the dual whole-cell voltage clamp technique.
14 s (I(Na)) were measured by the two-electrode voltage clamp technique.
15 currents were recorded using a two-electrode voltage clamp technique.
16 l vein using the perforated patch whole-cell voltage clamp technique.
17 human blood eosinophils using the whole cell voltage clamp technique.
18 s, using the whole-cell configuration of the voltage-clamp technique.
19 ce (Gj) was measured by the dual 2-electrode voltage-clamp technique.
20 n Xenopus oocytes has been studied using the voltage-clamp technique.
21 s on GABAAR by means of a two-microelectrode voltage-clamp technique.
22 f Rana temporaria with a double Vaseline-gap voltage-clamp technique.
23 function was studied using the two-electrode voltage-clamp technique.
24 e-directed mutagenesis and the two-electrode voltage-clamp technique.
25 rrents were recorded using the two-electrode voltage-clamp technique.
26 ere measured by using the two-microelectrode voltage-clamp technique.
27 nels expressed in Xenopus oocytes, using the voltage-clamp technique.
28  determined with standard two-microelectrode voltage-clamp technique.
29 opus laevis oocytes, using the two-electrode voltage-clamp technique.
30 investigated by using the two-microelectrode voltage-clamp technique.
31 s were measured 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 el inhibition evaluated using the whole-cell voltage-clamp technique.
38 rrents were measured using the two-electrode voltage-clamp technique.
39 ls were investigated by using the whole-cell voltage-clamp technique.
40 was measured using a dual two-microelectrode voltage-clamp technique.
41 tory currents were recorded using whole cell voltage clamp techniques.
42 hile membrane potential was controlled using voltage clamp techniques.
43 ns on cardiac K+ currents were studied using voltage clamp techniques.
44 ic epithelial cell line T84 using whole cell voltage clamp techniques.
45 sing quantitative swelling and two-electrode voltage clamp techniques.
46 -open oocyte voltage clamp and two-electrode voltage clamp techniques.
47  in Xenopus oocytes using two-microelectrode voltage clamp techniques.
48 ous expression system and two-microelectrode voltage clamp techniques.
49 ocytes were studied using two-microelectrode voltage-clamp techniques.
50 rom tiger salamander retina using whole-cell voltage-clamp techniques.
51  using two microelectrode and single channel voltage-clamp techniques.
52 lation and were recorded by using whole-cell voltage-clamp techniques.
53 stigated in retinal neurons using whole-cell voltage-clamp techniques.
54 t the single-channel level using tight-seal, voltage-clamp techniques.
55 nthetic A beta was measured using whole-cell voltage-clamp techniques.
56  the amphotericin or conventional whole-cell voltage-clamp techniques.
57 n Xenopus laevis oocytes using two-electrode voltage-clamp techniques.
58 of calcium currents (I(Ca)) using whole-cell voltage-clamp techniques.
59 nd currents recorded with two-microelectrode voltage-clamp techniques.
60 ells of skate were examined using whole-cell voltage-clamp techniques.
61 ingle-channel properties were recorded using voltage-clamp techniques.
62 3 null alleles, as determined by whole-cell, voltage-clamp techniques.
63  cortical pyramidal neurons using whole-cell voltage-clamp techniques.
64 the current study, we used the two-electrode voltage-clamp technique alone or in combination with pH/
65                      Using the two-electrode voltage clamp technique and alpha4beta2 nAChRs in the Xe
66 h muscle cells using conventional whole-cell voltage clamp technique and high temporal resolution mic
67 d human embryonic kidney 293 cells using the voltage clamp technique and photodiode-based displacemen
68               We have used the two-electrode voltage clamp technique and the patch clamp technique to
69      We used giant-patch and cut-open oocyte voltage clamp techniques and applied solutes which are t
70 d KCNJ2 mutations using a two-microelectrode voltage-clamp technique and correlated the findings with
71  We characterized I(h) using the whole-cell, voltage-clamp technique and found the current expressed
72 d on a functional level using the whole-cell voltage-clamp technique and on a molecular level using t
73                   A variety of patch pipette voltage clamp techniques are available to characterize i
74  on whole oocytes, we used the two-electrode voltage-clamp technique, as well as pH- and voltage-sens
75  cells was investigated using the whole-cell voltage-clamp technique at 35 degrees C.
76 rabbit ileum studied with the Ussing chamber-voltage clamp technique, EGF stimulation of active NaCl
77                           In addition, using voltage clamp technique, four individual RNAs increase t
78                                  The somatic voltage clamp technique has revolutionized understanding
79                                              Voltage-clamp techniques have revolutionized clinical el
80                                Using in vivo voltage-clamp techniques, here we show that dendritic PI
81                             Using whole-cell voltage clamp techniques, I(Na) density was lower in ank
82 ns (SPNs) were recorded using the whole-cell voltage clamp technique in slices of neonatal rat spinal
83 s discovered by Hodgkin and Huxley using the voltage clamp technique in their landmark series of pape
84 udies were performed using the two-electrode voltage clamp technique in Xenopus oocytes.
85 3)(beta(2))(2) receptors using two-electrode voltage clamp techniques in Xenopus laevis oocytes indic
86                             Using whole-cell voltage-clamp technique in conjunction with pharmacologi
87   This study investigates, using current and voltage-clamp techniques in brain slices from young mice
88 ession of inhibition' (DSI) using whole-cell voltage-clamp techniques in Ca1 pyramidal cells of rat h
89 nule neurones were analysed using whole-cell voltage-clamp techniques in order to explore the functio
90 ion channel function using the two-electrode voltage clamp technique on 16 cloned ion channels (12 K(
91 Ce1-mediated currents with the two-electrode voltage-clamp technique or pHi changes using Vm/pH-sensi
92 nopus laevis oocytes using the two-electrode voltage clamp technique showed GHB to be a partial agoni
93                            The two-electrode voltage clamp technique showed there was a marked reduct
94 TX dose-response curve, using the whole cell voltage-clamp technique, showed three populations of fib
95 dy, using patch-pipet whole-cell current and voltage clamp techniques, synaptic interactions of these
96 study, we demonstrate, using dual whole-cell voltage-clamp techniques, that coexpression of connexin
97               We adapted the dual whole cell voltage clamp technique to in situ analysis of electrica
98 dy, we used the oocyte expression system and voltage clamp techniques to determine the functional con
99 n oocyte Vaseline gap and two microelectrode voltage clamp techniques to determine the voltage depend
100  cells using the perforated patch whole-cell voltage-clamp technique to ascertain whether this Ca2+ u
101         In this study we used the whole-cell voltage-clamp technique to assess the effects of dietary
102 ences, we have applied the double-whole-cell voltage-clamp technique to freshly isolated pairs of cel
103  this study we have used the cut-open oocyte voltage-clamp technique to investigate the relationship
104 ed Ca2+ channels, by applying the whole-cell voltage-clamp technique to isolated dendritic segments (
105                                  We used the voltage-clamp technique to study synaptic transmission i
106             In this study, we use whole-cell voltage-clamp techniques to analyze light responses of i
107 t study, we used standard two-microelectrode voltage-clamp techniques to further characterize the eff
108                         We used conventional voltage-clamp techniques to identify and characterize A-
109   To elucidate the mechanisms of IH, we used voltage-clamp techniques to investigate the [H]o, [Na]o,
110  the range of 1-780 nm) by the two-electrode voltage clamp technique using a standard Xenopus oocyte
111 s were studied using the permeabilized-patch voltage-clamp technique, using an applied NH4+ gradient
112 lying the potentiation, the whole-cell patch voltage clamp technique was used to study VMN neurons in
113                     When the cut-open oocyte voltage clamp technique was used, membrane depolarizatio
114                               The whole-cell voltage-clamp technique was used in rat cardiac myocytes
115                               The whole-cell voltage-clamp technique was used to examine opioid regul
116                              The 2-electrode voltage-clamp technique was used to record currents via
117                               The whole-cell voltage-clamp technique was used with normal transmembra
118                           Using the cut-open voltage clamp technique, we have simultaneously recorded
119                   Using a two-microelectrode voltage clamp technique, we investigated possible mechan
120                    Using a double whole-cell voltage-clamp technique, we determined macroscopic and s
121                      Using the two-electrode voltage-clamp technique, we examined metaflumizone inhib
122                Using the permeabilized patch voltage-clamp technique, we studied the temperature depe
123 nine-scanning mutagenesis and the whole cell voltage clamp technique were used to investigate the fun
124                              Dual whole-cell voltage clamp techniques were used to analyze macroscopi
125                                              Voltage-clamp techniques were used to examine the persis
126                                   Whole-cell voltage-clamp techniques were used to investigate the ca
127                           Two-microelectrode voltage-clamp techniques were used to record currents, a
128 sis of the decreased conductance, whole-cell voltage-clamp techniques were used to record evoked, GAB
129               Two-electrode current-clamp or voltage-clamp techniques were used to record from muscle
130                                   Whole-cell voltage-clamp techniques were used to study the alterati
131                  Microchamber and whole-cell voltage-clamp techniques were used.
132 llular compartments, and (b) patch clamp and voltage clamp techniques, which investigate transporters
133                          Using two-electrode voltage-clamp techniques with hDAT-expressing Xenopus la
134 s were studied using the permeabilized-patch voltage-clamp technique, with an applied NH4+ gradient t

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