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1 sociated, and ICa,L was recorded (whole-cell patch-clamp technique).
2 e the imaging technique with the traditional patch clamp technique.
3 ed and studied in the whole-cell mode of the patch clamp technique.
4 ductances expressed by these cells using the patch clamp technique.
5 ing techniques and the gramicidin-perforated patch clamp technique.
6 phyll cell protoplasts was studied using the patch clamp technique.
7 min, which we recorded using the whole cell patch clamp technique.
8 h membrane currents or APs recorded with the patch clamp technique.
9 ent (ICa,L) was studied using the whole-cell patch clamp technique.
10 (HUVEC), using the whole cell version of the patch clamp technique.
11 ode array (MEA) recording and the whole-cell patch clamp technique.
12 nduit and resistance PAMs using the standard patch clamp technique.
13 orded using the cell-attached single-channel patch clamp technique.
14 orded in the whole-cell configuration of the patch clamp technique.
15 -A lysine mutation in NBD1 (K464A) using the patch clamp technique.
16 1MF-2 were investigated using the whole cell patch clamp technique.
17 red with the whole-cell configuration of the patch clamp technique.
18 days old) were studied using the whole-cell patch clamp technique.
19 mal resting [Ca(2+)](i) using the perforated patch clamp technique.
20 orated patch configuration of the whole-cell patch clamp technique.
21 clamped at -60 1r1rqmV1qusing the perforated patch clamp technique.
22 clamp and in CV-1 cells using the whole cell patch clamp technique.
23 ical properties were examined via whole-cell patch clamp technique.
24 rized in mouse myotubes using the whole-cell patch clamp technique.
25 ts in lung endothelial cells was assessed by patch clamp technique.
26 BA and pentobarbital were recorded using the patch clamp technique.
27 e TRPV1 ion channels using the cell-attached patch clamp technique.
28 Ca(2)(+) entry as measured by the whole-cell patch clamp technique.
29 on Na/K ATPase currents using the whole-cell patch-clamp technique.
30 Chinese hamster ovary (CHO) cells using the patch-clamp technique.
31 cells were investigated using the whole-cell patch-clamp technique.
32 rat pituitary cell line, GH(4)C(1), with the patch-clamp technique.
33 ) currents were measured with the whole-cell patch-clamp technique.
34 in primary VMN cultures using the whole-cell patch-clamp technique.
35 yocytes at 37 degrees C using the perforated patch-clamp technique.
36 d the effects of ATP(o) using the whole-cell patch-clamp technique.
37 hytoplankton Coccolithus pelagicus using the patch-clamp technique.
38 icin B perforated-patch configuration of the patch-clamp technique.
39 sured in the whole-cell configuration of the patch-clamp technique.
40 cular myocytes recorded using the whole-cell patch-clamp technique.
41 e were measured in single myocytes using the patch-clamp technique.
42 ernal protons (H(+)(o)) using the whole-cell patch-clamp technique.
43 cle cells and in transfected HEK293 cells by patch-clamp technique.
44 by using the whole-cell configuration of the patch-clamp technique.
45 by the perforated-patch configuration of the patch-clamp technique.
46 using the cell-attached configuration of the patch-clamp technique.
47 (vagotomy) and examined with the whole-cell patch-clamp technique.
48 lls, using the cell-attached, single-channel patch-clamp technique.
49 g-term primary culture using the whole-cell, patch-clamp technique.
50 es using the whole-cell configuration of the patch-clamp technique.
51 currents were measured using the perforated patch-clamp technique.
52 < 10 cells) using the whole-cell perforated patch-clamp technique.
53 ig ventricular myocytes using the whole-cell patch-clamp technique.
54 tube system were recorded by the whole-cell, patch-clamp technique.
55 f rat cardiac myocytes, using the inside-out patch-clamp technique.
56 ptors was characterized using the whole-cell patch-clamp technique.
57 whole-cell currents were measured using the patch-clamp technique.
58 of primate retinal cell with the whole-cell patch-clamp technique.
59 tricular myocytes with use of the whole-cell patch-clamp technique.
60 nnel function is derived from the use of the patch-clamp technique.
61 cum aestivum L.) root cortex cells using the patch-clamp technique.
62 uated by in vitro organ bath studies and the patch-clamp technique.
63 , and Na(+) currents were recorded using the patch-clamp technique.
64 human embryonic kidney 293 cells, using the patch-clamp technique.
65 e performed in these cells by the whole-cell patch-clamp technique.
66 freshly isolated PASMCs using the perforated patch-clamp technique.
67 tability of the NBD dimeric states using the patch-clamp technique.
68 s too small to be resolved directly with the patch-clamp technique.
69 he inside-out and cell-attached modes of the patch-clamp technique.
70 ording LTCC currents using the cell-attached patch-clamp technique.
71 in both Kir6.1 and Kir6.2 using ion flux and patch clamp techniques.
72 pitation (Co-IP), immunoblot, and whole-cell patch clamp techniques.
73 lls using immunocytochemistry and whole cell patch clamp techniques.
74 measured using whole cell and single channel patch clamp techniques.
75 surface immunoprecipitation, and whole-cell patch clamp techniques.
76 es from neonatal rats were studied using the patch clamp techniques.
77 glia (DRG) neurons using calcium imaging and patch clamp techniques.
78 perties of Fb and MI-Fb were evaluated using patch clamp techniques.
79 ls expressed in mammalian TSA201 cells using patch clamp techniques.
80 c DRG neurons were measured using perforated patch-clamp techniques.
81 nd opening and closing rates of mPanx1 using patch-clamp techniques.
82 y myocytes at the single-channel level using patch-clamp techniques.
83 bition of these K+ channels using whole-cell patch-clamp techniques.
84 d human embryonic kidney HEK 293 cells using patch-clamp techniques.
85 nnels and neurotransmission using whole-cell patch-clamp techniques.
86 hippocampal CA1 interneurons in slices using patch-clamp techniques.
87 tagenesis and two-electrode voltage-clamp or patch-clamp techniques.
88 ents were recorded directly using whole-cell patch-clamp techniques.
89 gain of function as measured using standard patch-clamp techniques.
90 f acute slices were studied using whole-cell patch-clamp techniques.
91 mammalian cell lines and characterized using patch-clamp techniques.
92 lls by means of perforated and cell-attached patch-clamp techniques.
93 al neurons in rat brain slices by using dual patch-clamp techniques.
94 ane currents were analyzed using whole-cell, patch-clamp techniques.
95 s were examined in vitro by using whole-cell patch-clamp techniques.
96 ts from arteriolar smooth muscle cells using patch-clamp techniques.
97 insulin-secreting cell line BRIN-BD11 using patch-clamp techniques.
98 subunit Ca(2+) sensitivity was studied using patch-clamp techniques.
99 tudied in canine atrial cardiomyocytes using patch-clamp techniques.
100 perimental design, which is similar to other patch-clamp techniques.
101 and TRPC1-deficient (TRPC1(-/-)) mice using patch-clamp techniques.
102 ts in cultured rat hippocampal neurons using patch-clamp techniques.
103 ed tonic current (I(tonic)) using whole-cell patch-clamp techniques.
104 SVZ cells in adult mouse brain slices using patch-clamp techniques.
105 ges in extracellular pH using the whole-cell patch-clamping technique.
106 e release mechanisms can be dissected with a patch-clamping technique.
107 arge, ionic currents that can be detected by patch-clamping techniques.
108 neous ionic currents that can be detected by patch-clamping techniques.
109 dosome and lysosome (LEL) using the lysosome patch clamp technique, a proline substitution in TRPML1
111 corded from the interneurons by means of the patch-clamp technique: a nicotinic whole-cell current, d
112 amped in the whole-cell configuration of the patch-clamp technique according to described procedures.
113 amped in the whole-cell configuration of the patch-clamp technique according to described procedures.
115 's intracellular environment, the whole-cell patch clamp technique allows one to record the cell's ph
118 d by measuring transmembrane currents by the patch clamp technique and intracellular Ca(2+) transient
124 nuclear microdomains, we combined perforated patch-clamp technique and FRET microscopy for monitoring
126 ction on the NMDA receptor by the whole-cell patch-clamp technique and immunoblotting analysis using
128 conductance (g(j)) by the double whole-cell patch-clamp technique and intercellular transfer of Luci
131 ned their electrophysiological properties by patch-clamp techniques and determined the mechanism for
132 n vascular smooth muscle cells (VSMCs) using patch-clamp techniques and fura-2 fluorescence and on ar
133 Novel variants were characterized using patch-clamp techniques and in silico modeling was perfor
134 serotonin's effects on NTS-CA neurons using patch-clamp techniques and transgenic mice expressing an
135 We have now used confocal microscopy, the patch clamp technique, and biotin labeling to further ex
136 ) through VGCC, as measured by Fluo-4/AM and patch clamp techniques, and protected in Ca(2+) overload
137 (+) currents were recorded by the whole-cell patch-clamp technique, and APs were recorded by the micr
138 nnels and ion channels in general, using the patch-clamp technique, and begin to unravel the differen
140 rence contrast infrared video technology and patch-clamp techniques applied to slices in vitro has al
141 on thalamocortical neurons using whole-cell patch-clamp techniques applied to visualized neurons in
142 amic reticular nucleus (RT) using whole-cell patch-clamp techniques applied to visualized neurons in
143 sting methods such as immunofluorescence and patch clamp techniques are limited in their ability to l
144 ze plasma membrane ion channels, such as the patch-clamp technique, are not readily applicable to int
145 tion, we have developed a simple alternative patch clamp technique based on microfluidic junctions be
147 and characterized CLC-K/barttin channels by patch clamp techniques, biochemistry, and confocal micro
148 studied at the single-channel level with the patch clamp technique by removing divalent cations from
150 ing this approach, all configurations of the patch-clamp technique (cell-attached, inside-out, whole-
151 ted from tiger salamanders were studied by a patch-clamp technique combined with estimation of effect
152 rent in atrial myocytes using the whole-cell patch clamp technique, combined with pressurized fluid f
153 ional cell assays such as flow cytometry and patch clamp techniques for assessing cell electrophysiol
154 protocol detailing how to implement a manual patch-clamp technique for endolysosomal compartments.
157 PC5 currents were recorded by the whole-cell patch clamp technique from human embryonic kidney 293 ce
158 GABA-evoked currents were recorded using the patch-clamp technique from cells transfected with cDNA e
163 ssion in the sarcolemma using the whole-cell patch clamp technique in normal, dyspedic, and RyR-1-exp
165 characterize the action of AMPH, we used the patch clamp technique in the whole-cell configuration co
166 ation currents were studied using whole cell patch clamp techniques in HEK-293 cells, a null backgrou
169 ies with electrical field stimulation or the patch-clamp technique in beating cardiac myocytes, we id
170 ibres was studied by means of the whole-cell patch-clamp technique in canine cardiac single Purkinje
171 capsaicin were recorded using the giga-seal patch-clamp technique in cell-attached and excised (insi
174 tion of the Kv11.1 mutant was carried out by patch-clamp technique in human embryonic kidney 293 cell
175 cells as the deprotonated anion, we used the patch-clamp technique in protoplasts isolated from the t
177 To investigate this hypothesis, we used the patch-clamp technique in vitro and in situ to measure cu
178 ristics of these neurons by using whole-cell patch-clamp technique in vitro Our results showed that P
179 how ghrelin modulates TH-EGFP neurons using patch-clamp techniques in a horizontal brain slice prepa
180 to N-type Ca(2+) channels was examined using patch-clamp techniques in F11 rat dorsal root ganglion x
183 mediated IPSCs were recorded with whole-cell patch-clamp techniques in visually identified CA1 pyrami
186 of unitary currents from the ASICs with the patch-clamp technique indicate that ASIC1 localizes to t
191 ABA-gated current, assessed using whole cell patch clamp techniques on acutely isolated hippocampal p
193 Ca,L) density was measured by the whole-cell patch-clamp technique on days 0-3 in cardiomyocytes isol
194 d its response to membrane tension using the patch-clamp technique on either a heterologous expressio
199 single-molecule observations afforded by the patch-clamp technique revealed an unanticipated kinetic
200 es and functional characterization using the patch-clamp technique revealed that the channels are gat
201 +) radiotracer, Fura-2 microfluorimetry, and patch-clamp techniques revealed that neurounina-1 stimul
204 this method is a visually controlled, direct patch-clamp technique similar to conventional patch-clam
205 yramidal neurons was studied using dual-cell patch-clamp techniques simultaneous with an extracellula
207 e developed a novel high-resolution scanning patch-clamp technique that enables the study of ion chan
209 59A) and examined by radioligand analysis or patch clamp technique their interaction with the AChBP,
211 the alternatively used planar endolysosomal patch-clamp technique, this method is a visually control
212 ce of GV-58 effects on Ca(2+) channels using patch clamp techniques; this showed the effects of GV-58
214 wo-electrode voltage clamp technique and the patch clamp technique to investigate the regulation of R
222 e whole-cell patch and gramicidin-perforated patch clamp techniques to measure their basic electrophy
225 murine small intestine were studied with the patch-clamp technique to characterize regulation of pace
226 on of the beta subunits we have utilized the patch-clamp technique to compare the properties of 'toni
230 sure intracellular Ca(2+) and the perforated patch-clamp technique to measure SR Ca(2+) content.
232 ng the perforated-patch configuration of the patch-clamp technique to monitor the whole-cell currents
233 annel currents, applying the dual whole-cell patch-clamp technique to pairs of N2A neuroblastoma cell
234 h preserved cellular architecture and used a patch-clamp technique to study AMPA-receptor (AMPAR)-med
235 s of nicotine, we used a nystatin-perforated patch-clamp technique to study Ca(2+) channels and Ca(2+
240 these channels, we have used the whole-cell patch-clamp technique to study the human cold-sensitive
244 ell invasion (transwell migration assay) and patch-clamp techniques to investigate the role of volume
246 s using whole-cell and gramicidin-perforated patch-clamp techniques to measure Cl- reversal potential
248 channels, as well as more broadly for using patch-clamp techniques to study ion channels and neurona
249 d-patch and whole-cell configurations of the patch clamp technique using cell capacitance measurement
252 The amphotericin B-perforated whole-cell patch clamp technique was used to determine the modulati
260 s, the perforated-patch configuration of the patch-clamp technique was used to determine the effect o
265 The perforated-patch configuration of the patch-clamp technique was used to monitor whole-cell cur
268 -like small-conductance K (SK) channels, the patch-clamp technique was used to study the effect of in
271 outward potassium current, recorded with the patch-clamp technique, was inhibited by exogenous applic
276 Using the whole cell configuration of the patch clamp technique, we show that ectopic expression o
277 s, using confocal microscopy combined with a patch clamp technique, we show that ryanodine receptor C
292 nnel (ENaC) is a target of oxidative stress, patch clamp techniques were used to determine whether EN
297 nels employing the whole-cell variant of the patch-clamp technique.Western blotting analysis showed t
299 degrees C, using the perforated or ruptured patch clamp techniques with Fura-2-AM to record Ca2+i.
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