1 ion (20 Hz) activated PGNs up to 8 spikes/s (
current-clamp).
2 We next evoked action potentials under
current clamp.
3 bit only slow graded voltage responses under
current clamp.
4 affeine-induced DADs (cDADs) with whole-cell
current clamp.
5 bited regular spontaneous depolarisations in
current clamp.
6 not show spontaneous electrical activity in
current clamp.
7 pinal neurons using voltage or discontinuous
current clamp.
8 in eight neurons by using several levels of
current clamp.
9 algorithms and were assessed by voltage and
current clamp.
10 neous transient depolarizations (STDs) under
current clamp.
11 In
current clamp,
5-HT (20 microM) elicited a depolarizatio
12 In
current clamp,
a 10 pulse, 100 Hz stimulus train gave ri
13 Under
current clamp,
action potentials were elicited by depola
14 s: direct action potential phenotyping under
current-clamp,
activation of the aforementioned genetic
15 Under
current clamp,
ADP caused the membrane potential to fluc
16 onal electric coupling was established under
current clamping after impaling two adjacent glomus cell
17 Under
current clamp,
all cells continued firing spontaneously
18 Current clamp analysis demonstrated that hyperpolarizing
19 Current-clamp analysis in hippocampal neurons transfecte
20 Here, we report the voltage-clamp and
current-clamp analysis of a new Na(v)1.7 mutation, Q10R,
21 Current-clamp analysis of dorsal root ganglion neurons t
22 s in human embryonic kidney 293 cells and by
current-clamp analysis to determine the effects of A863P
23 vitro slice preparation were performed using
current clamp and conventional sharp-electrode intracell
24 Intracellular sharp electrode
current clamp and discontinuous single electrode voltage
25 tochemistry, were spontaneously active under
current clamp and generated transient inward (pacemaker)
26 correlated with lower firing probability in
current clamp and smaller synchronous EPSCs in voltage c
27 We examined this effect of EtOH under both
current clamp and voltage clamp conditions in the basola
28 ring and synaptic responses were recorded in
current clamp and voltage clamp from olig2(+) neurons in
29 We used a combination of
current clamp and voltage clamp recordings in an in vitr
30 In vitro intracellular
current clamp and voltage clamp recordings were performe
31 his heightened excitability was confirmed by
current-clamp and action potential phase-plot analyses,
32 On simultaneous
current-clamp and Ca(2+) imaging, early and delayed afte
33 Whole-cell
current-clamp and cell-attached recordings from labeled
34 are demonstrated in simulations and in vitro
current-clamp and dynamic-clamp experiments.
35 ared simulation results under voltage-clamp,
current-clamp and high [K(+)] membrane depolarized condi
36 We conducted whole-cell
current-clamp and single-unit recordings in NG neurons f
37 nic basis of this activity using interleaved
current-clamp and voltage-clamp experiments.
38 Current-clamp and voltage-clamp measurements were made b
39 Using combined
current-clamp and voltage-clamp recordings from neurons
40 By using in vivo whole-cell
current-clamp and voltage-clamp recordings, we found tha
41 sustained inward current (depolarization in
current clamp)
and increased the amplitude and frequency
42 ted with transient depolarizations of ICC in
current clamp,
and these events were blocked by niflumic
43 e, using structural modeling, voltage-clamp,
current-clamp,
and multielectrode array recordings, we h
44 Using a dynamic
current-clamp approach, we now show that the fear-induce
45 a-cells or hamster insulinoma tumor cells in
current clamp at 30-35 degrees C, using standard K+-rich
46 Under
current clamp,
beta-adrenergic stimulation (isoprenaline
47 Under
current clamp,
block of BKCa current increased depolariz
48 In
current clamp,
blocking L-type Ca channels with the spec
49 In
current-clamped CA1 pyramidal cells hypoxia induced a ra
50 , we demonstrate that induction of an ADP in
current clamp causes release of cannabinoids, and subseq
51 In
current-clamped cells the slow inverted current response
52 rev, equivalent to the membrane potential in
current-clamped cells) consistent with activation of Na+
53 In
current-clamped cells, membrane potentials were more neg
54 Under
current clamp,
cerebellar nuclear neurons fired spontane
55 Under
current clamp conditions rotenone and CN(-) caused a rap
56 Under zero
current clamp conditions this hormone induced amiloride-
57 Under
current clamp conditions we measured changes in membrane
58 , and membrane time constant) measured under
current clamp conditions were virtually identical.
59 When applied together under
current clamp conditions, 5-HT reversed anaesthetic-indu
60 Under
current clamp conditions, application of the broad-spect
61 ing sag in negative voltage deviations under
current clamp conditions, or a large inward current with
62 Under
current clamp conditions, voltage-current (V-I) relation
63 ing and hyperpolarizing current pulses under
current clamp conditions.
64 induced significant hyperpolarization under
current clamp conditions.
65 Recordings under
current-clamp conditions revealed similar intrinsic elec
66 Under
current-clamp conditions, action potential durations wer
67 Under
current-clamp conditions, exposure to 4-AP or flecainide
68 Under intracellular
current-clamp conditions, the preferential block of the
69 ability and Ca(2+) influx under voltage- and
current-clamp conditions.
70 corded from L5 neurons by using a whole-cell
current clamp configuration.
71 and perforated-patch recording techniques in
current-clamp configuration.
72 events were identified both in voltage- and
current-clamp configurations.
73 width, and latency to first spike similar to
current clamp data from mouse dorsal striatum MSPN.
74 Voltage- and
current-clamp data showed that Rho-kinase inhibition red
75 In
current clamp,
depolarizing current injections from the
76 subgroups based on the visual inspection of
current clamp electrophysiological properties and morpho
77 was used to block Kv2 currents in whole-cell
current clamp electrophysiological recordings in rat lum
78 Field potential recordings and whole-cell
current clamp electrophysiology were used to monitor the
79 ent mitral cell excitability as evaluated by
current-clamp electrophysiology.
80 sAHP conductance by spike-triggered dynamic-
current clamp enhanced the gain increase.
81 In
current clamp,
estrogen enhanced the diazoxide-induced h
82 Current clamp experiments at body temperature show that
83 Current clamp experiments revealed that blood depressing
84 Current clamp experiments show that, physiologically, th
85 Current clamp experiments showed that in IHCs the SK cur
86 Voltage and
current clamp experiments showed that the delayed HCO(3)
87 erve stimulations, pharmacological block and
current clamp experiments suggest that this is due to a
88 In
current clamp experiments, NS309 enhanced the medium aft
89 d outward potassium currents in voltage- and
current clamp experiments.
90 In
current-clamp experiments alpha-DTX, used to eliminate t
91 Current-clamp experiments demonstrate that serotonergic
92 Current-clamp experiments indicated that these processes
93 Current-clamp experiments reveal that low concentrations
94 Current-clamp experiments show that Nav1.9 flows at subt
95 Current-clamp experiments showed that the specific Kv7/M
96 In
current-clamp experiments small neurons had more depolar
97 ly isolated neurons, mixed voltage-clamp and
current-clamp experiments were done at 37 degrees C to s
98 Current-clamp experiments were used to assess the functi
99 In
current-clamp experiments, APD and CaT alternans strongl
100 In
current-clamp experiments, non-inactivated VGSCs were su
101 In
current-clamp experiments,XE 991 per se caused membrane
102 -55 mV and did not induce depolarization in
current-clamp experiments.
103 cellular recordings under multiple levels of
current clamp from midbrain neurons in the mormyrid weak
104 Under
current clamp,
GIRK activation increased the cell membra
105 In
current clamp,
GTx (i) had almost no effect on the first
106 In
current clamp,
GTx had multiple effects: (i) increasing
107 In
current-clamp,
H(2)O(2) stimulated burst firing, but thi
108 In
current clamp,
halothane caused a membrane hyperpolariza
109 In
current clamped horizontal cells, BKCa channels subdue d
110 results for sodium channels using a dynamic
current clamp in neocortical fast spiking interneurons.
111 activating these receptors on the LTS, using
current-clamp intracellular recording in an in vitro sli
112 mpal slices of young and aging rabbits using
current-clamp,
intracellular recording techniques.
113 Current-clamped isolated neurons fired regularly ( appro
114 In
current clamp,
KO arterial smooth muscle cells have easi
115 This unprecedented combination of
current-clamp,
macroscopic-current, and single-channel r
116 Whole cell voltage- and
current clamp measurements were made from primary neuron
117 By combining
current-clamp measurements of electrophysiological prope
118 rom the DHC and the VHC using the whole-cell
current-clamp method.
119 By using
current clamp methods, it was found that the fAHP is red
120 dl-PAG neurons was recorded using whole cell
current-clamp methods.
121 t of ephedrine on dopamine-containing cells,
current-clamp microelectrode recordings were made from s
122 Under
current clamp,
ML-133 caused the depolarization of isola
123 tial in individual myocytes generated in the
current clamp mode but isometric tissue tension experime
124 assessed by whole-cell recording in the zero-
current clamp mode in the absence and presence of Ba(2+)
125 In
current clamp mode paired-pulse stimulation resulted in
126 In
current clamp mode with the resting membrane potential s
127 mode) nor a change in membrane potential (in
current clamp mode) occurred in response to vitronectin.
128 medium-diameter neurons recorded from in the
current clamp mode, 5-HT depolarized the resting membran
129 In
current clamp mode, in the presence of beta stimulation,
130 potential was monitored under the whole cell
current clamp mode.
131 e perforated patch whole cell patch clamp in
current clamp mode.
132 Whole-cell patch clamp records under
current-clamp mode also showed a chloroquine-induced dep
133 ross an intact cell-attached patch using the
current-clamp mode of a conventional patch-clamp amplifi
134 Whole-cell recordings from SpL neurons in
current-clamp mode revealed EPSPs evoked by stimulation
135 In
current-clamp mode, current-induced voltage oscillations
136 In the
current-clamp mode, extracellular acidosis evoked both a
137 In
current-clamp mode, fast local application of acetylchol
138 In the
current-clamp mode, GABA depolarized the cells to approx
139 In
current-clamp mode, in a model of mutant RyR2 that is ch
140 In
current-clamp mode, the mutant RyR2 model exhibited incr
141 of the membrane potential were also made in
current-clamp mode.
142 d injected transduction current waveforms in
current-clamp mode.
143 taset of 150 neurons recorded in whole-cell,
current-clamp mode.
144 bbit nodose ganglion cells with slow AHPs in
current-clamp mode.
145 s range could alter cellular repolarization,
current-clamped myocytes were dialyzed with 0.5 or 1.0 m
146 PD and CaT alternans in field-stimulated and
current-clamped myocytes.
147 When whole-cell responses were recorded from
current-clamped neurones using the gramicidin-perforated
148 calcium-activated potassium current, and in
current clamp,
nimodipine usually depolarized cells and
149 ted by L-type Ca2+ channels using whole-cell
current clamp of the SC in an isolated brainstem prepara
150 Two-electrode
current-clamp or voltage-clamp techniques were used to r
151 M) SON magnocellular neurones (n = 27) under
current clamp,
or induced an outward current that revers
152 induced either a membrane depolarization in
current clamp,
or inward current under voltage clamp in
153 sent in VHCs, whole cell, voltage-clamp- and
current-clamp-
patch recordings were performed on isolate
154 Current-clamp pause protocols induced rate-dependent spo
155 In constant 100 mum lidocaine,
current-clamped Purkinje cells continued to fire spontan
156 During
current clamp recording IH caused time-dependent rectifi
157 Using dual whole-cell voltage and
current clamp recording techniques, we investigated the
158 In
current clamp recording, injection of the unclustering p
159 Using whole-cell
current clamp recording, we found that L2/3 pyramidal ne
160 whole-cell tight seal method of voltage and
current clamp recording.
161 Simultaneous Ca(2+) imaging and
current-clamp recording during apparent-motion stimulati
162 Current-clamp recording from the calyx showed that each
163 cretin neurons using whole-cell voltage- and
current-clamp recording in mouse whole hypothalamic slic
164 In
current-clamp recording, CsCl, which inhibits only I(H)
165 In striking contrast, using voltage and
current-clamp recording, we found that PYY(3-36) consist
166 Using whole-cell
current-clamp recording, we unexpectedly found that TRH
167 eurones by performing some experiments using
current-clamp recording.
168 Whole-cell
current clamp recordings demonstrated that, following di
169 rent injection were assessed with whole-cell
current clamp recordings from cells that were isolated s
170 Current clamp recordings from MSO neurones were made whi
171 Current clamp recordings from the LGN of ethanol naive m
172 ond to oscillatory inputs we made whole-cell
current clamp recordings from three different types of n
173 Using whole cell
current clamp recordings in acute hippocampal slices, we
174 of VMH glucose-sensing neurons in whole-cell
current clamp recordings in brain slices.
175 In
current clamp recordings obtained from inspiratory neuro
176 Current clamp recordings of isolated myocytes showed a 7
177 erentiation of RGC types, we made whole-cell
current clamp recordings of RGC responses to injected cu
178 Moreover,
current clamp recordings show that cannabidiol reduces o
179 In
current clamp recordings, 100 microM NE produced a hyper
180 In
current clamp recordings, ATP and UTP (but not CTP) depo
181 In
current clamp recordings, microinjection of cross-linked
182 In addition, in
current clamp recordings, SCH23390 can depolarize the me
183 tic CA3 pyramidal neurons were studied using
current clamp recordings; activation of M1 receptors and
184 In
current-clamp recordings and Ca(2+)-imaging experiments,
185 Current-clamp recordings and Ca2+-imaging experiments de
186 insight into this issue by using whole-cell
current-clamp recordings and immunocytochemistry to show
187 Dual
current-clamp recordings confirm that single motoneuron
188 firmed in acutely isolated STN neurons using
current-clamp recordings containing IPSPs as voltage-cla
189 Whole-cell
current-clamp recordings demonstrate that leptin (0.3-10
190 Whole-cell
current-clamp recordings demonstrated increased spontane
191 Current-clamp recordings during high frequency firing an
192 toring of synaptic activity using whole-cell
current-clamp recordings from a local astrocyte.
193 e properties, we compared somatic whole-cell
current-clamp recordings from basal and apical neurons o
194 uences synaptic strength, using voltage- and
current-clamp recordings from bushy cells in brain slice
195 d with synaptic stimulation using whole-cell
current-clamp recordings from CA1 pyramidal cells in hip
196 In
current-clamp recordings from GFP+ SO cells, linopirdine
197 Whole-cell
current-clamp recordings from neurones near the TS revea
198 Using whole-cell voltage-clamp and
current-clamp recordings in acute hippocampal slices and
199 Here, we performed both
current-clamp recordings in brain slices and voltage-cla
200 Using a combination of
current-clamp recordings in brain slices and whole-cell
201 Using loose-patch
current-clamp recordings in brainstem slices from rat pu
202 Whole-cell
current-clamp recordings in cultured Schwann cells revea
203 Using
current-clamp recordings in hippocampal slices, we find
204 t were studied using whole-cell voltage- and
current-clamp recordings in slices of rat cerebellum.
205 red from male and female ChAT-EGFP mice, and
current-clamp recordings obtained from BFCNs chronically
206 Whole-cell
current-clamp recordings obtained from MGE-derived cells
207 Current-clamp recordings of dopamine neurons showed that
208 Current-clamp recordings of electrocyte APs reveal that
209 Whole-cell
current-clamp recordings of GnRH neurons in brain slices
210 On-cell
current-clamp recordings of olfactory receptor neurons f
211 To investigate, we obtained whole-cell
current-clamp recordings of pyramidal neurons in visual
212 Current-clamp recordings reveal that the desynchronized
213 Voltage-clamp and
current-clamp recordings revealed that knockdown of Navb
214 Current-clamp recordings revealed that the firing rates
215 s apical dendritic tuft and trunk whole-cell
current-clamp recordings revealed that the pharmacologic
216 Whole-cell
current-clamp recordings showed that 4-AP changed the en
217 Simultaneous [Ca2+]i and
current-clamp recordings showed that Ca2+ and Vm oscilla
218 Whole-cell
current-clamp recordings showed that each burst ended wi
219 Current-clamp recordings showed that neurons expressing
220 Current-clamp recordings showed that the fast activation
221 Voltage- and
current-clamp recordings suggested a high level of inact
222 Conventional
current-clamp recordings using excitatory ramp or square
223 s whole-cell voltage-clamp and cell-attached
current-clamp recordings we have defined both mathematic
224 Whole-cell
current-clamp recordings were made as extracellular gluc
225 Current-clamp recordings were made during and following
226 Whole-cell
current-clamp recordings were made from mouse basal spir
227 Whole-cell
current-clamp recordings were made from neurons in the r
228 Whole-cell voltage- and
current-clamp recordings were made of GFP-identified GnR
229 ifferential experience, sharp microelectrode
current-clamp recordings were obtained in CA1 pyramidal
230 Whole-cell voltage- and
current-clamp recordings were performed in acutely isola
231 Whole-cell
current-clamp recordings were performed on neurons from
232 -clamp and gramicidin-based perforated-patch
current-clamp recordings were then used to study the rel
233 Intracellular
current-clamp recordings with high-resistance micropipet
234 In
current-clamp recordings, decreasing [Ca2+]o induced sus
235 In
current-clamp recordings, depolarizing step current inje
236 In
current-clamp recordings, halothane depressed EPSP ampli
237 In
current-clamp recordings, inhibition of T-type calcium c
238 In
current-clamp recordings, LEV reduced the amplitude of t
239 In
current-clamp recordings, low-frequency stimulation of t
240 In
current-clamp recordings, noise-reared BCs had greater s
241 solutions that are used in voltage-clamp and
current-clamp recordings, only limited information can b
242 We confirmed, with whole-cell
current-clamp recordings, our previous finding from shar
243 In
current-clamp recordings, PDC dramatically increased the
244 k channels increased channel opening and, in
current-clamp recordings, produced narrowing of action p
245 In
current-clamp recordings, regular and irregular trains o
246 In
current-clamp recordings, SST preferentially inhibited b
247 In
current-clamp recordings, the increased K(Na) current in
248 ing multielectrode array, voltage-clamp, and
current-clamp recordings, we assessed a newly identified
249 MDA in deep-layer PL-PFC neurons analyzed by
current-clamp recordings.
250 nglion cell, were measured during whole cell
current-clamp recordings.
251 estigated using whole-cell voltage-clamp and
current-clamp recordings.
252 ones in the hippocampus and dentate gyrus in
current-clamp recordings.
253 itability of GABAergic neurons determined by
current-clamp recordings.
254 ) were also observed in dendritic whole-cell
current-clamp recordings.
255 s (eEPCs) under voltage-clamp, which, unlike
current-clamp records, were independent of the changes i
256 In
current clamp,
repetitive activation of the GABAergic ax
257 Using a prerecorded
current-clamp response to capsaicin as a voltage-clamp c
258 Comparisons of voltage- and
current-clamp responses obtained from the same Purkinje
259 Current-clamp responses were recorded from CA1 pyramidal
260 al (AP) in these cells based on voltage- and
current-clamp results together with measurements of Ca(2
261 Whole-cell
current clamping revealed distinct excitability patterns
262 Current-clamp revealed GnRH neurons fired more action po
263 Current-clamp,
sharp electrode and whole-cell voltage-cl
264 ation of action-potential backpropagation in
current-clamp simulations of a CA1 pyramidal neuron.
265 Under
current clamp,
single Purkinje cells from RyR2/RyR2(R449
266 We combined
current-clamp somatic and dendritic recordings, outside-
267 Under
current clamp stimulation SR Ca2+ content increased in l
268 When
current-clamp stimuli approximated the mean physiologica
269 Current clamp studies reveal complex spontaneous firing
270 In
current clamp studies, these drugs also led to a depolar
271 In
current-clamp studies neither R(+)-WIN nor R(+)-methanan
272 Current-clamp studies reveal that mutant channels decrea
273 Current-clamp studies reveal that R1279P depolarizes res
274 Consequently, under whole-cell
current clamp,
synaptically released GABA produced short
275 We have used whole-cell voltage and
current clamp techniques to characterize Ih in neurons f
276 ffort, electrophysiologists commonly utilize
current clamp techniques to gain a detailed characteriza
277 Whole-cell voltage- and
current-clamp techniques were used to record L-type Ca2+
278 transient BK current was also examined using
current-clamp techniques.
279 otoreceptors were studied using voltage- and
current-clamp techniques.
280 by intracellular recording using whole-cell
current-clamp techniques.
281 (tau), were measured with either voltage- or
current-clamp techniques.
282 potentials were recorded using voltage- and
current-clamp techniques.
283 hin dorsal root ganglion neurons and show by
current-clamp that R185H renders dorsal root ganglion ne
284 ined when depolarizations were eliminated by
current-clamping the membrane potential.
285 In
current clamp,
the activation of I(KA) reduced neuronal
286 In
current clamp,
the prolonged rebound firing rate after h
287 TP and Ca2+ channel conductances to cells in
current clamp to assess the role of Ca2+ and KATP channe
288 se predictions physiologically using dynamic
current clamping to apply model-derived synaptic conduct
289 Here, we use whole-cell
current-clamp to demonstrate that aged rat (29-32 months
290 In
current clamp,
upregulation of persistent current was as
291 Under
current clamp,
UTP increased action potential (AP) firin
292 addition, the amplitude of APs evoked under
current clamp was inhibited by the action of vesicular p
293 a nonlinear leak conductance with a dynamic
current clamp,
was able to restore wild-type firing prop
294 Using
current clamp,
we show that A1632E renders dorsal root g
295 In addition, using whole-cell
current-clamp,
we find that deletion of Kcnab2 leads to
296 Using
current-clamp,
we show that the expression of Q10R induc
297 The effects of the enzyme in voltage and
current clamp were noted in 0 Mg2+ media but were abolis
298 calcium dependent, we conducted voltage- and
current-clamp whole-cell recordings while pharmacologica
299 Under
current-clamp,
whole-cell recordings in single dissociat
300 inspiratory PBC neurons (n = 44) recorded in
current clamp within the active network revealed a signi