1 ion (20 Hz) activated PGNs up to 8 spikes/s (
current-clamp).
2 bit only slow graded voltage responses under
current clamp.
3 affeine-induced DADs (cDADs) with whole-cell
current clamp.
4 bited regular spontaneous depolarisations in
current clamp.
5 not show spontaneous electrical activity in
current clamp.
6 pinal neurons using voltage or discontinuous
current clamp.
7 in eight neurons by using several levels of
current clamp.
8 algorithms and were assessed by voltage and
current clamp.
9 neous transient depolarizations (STDs) under
current clamp.
10 We next evoked action potentials 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 udied in hippocampal slices using whole-cell
current clamp and biocytin staining.
24 vitro slice preparation were performed using
current clamp and conventional sharp-electrode intracell
25 Intracellular sharp electrode
current clamp and discontinuous single electrode voltage
26 tochemistry, were spontaneously active under
current clamp and generated transient inward (pacemaker)
27 correlated with lower firing probability in
current clamp and smaller synchronous EPSCs in voltage c
28 We examined this effect of EtOH under both
current clamp and voltage clamp conditions in the basola
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 On simultaneous
current-clamp and Ca(2+) imaging, early and delayed afte
32 Whole-cell
current-clamp and cell-attached recordings from labeled
33 are demonstrated in simulations and in vitro
current-clamp and dynamic-clamp experiments.
34 ared simulation results under voltage-clamp,
current-clamp and high [K(+)] membrane depolarized condi
35 We conducted whole-cell
current-clamp and single-unit recordings in NG neurons f
36 nic basis of this activity using interleaved
current-clamp and voltage-clamp experiments.
37 Current-clamp and voltage-clamp measurements were made b
38 Using combined
current-clamp and voltage-clamp recordings from neurons
39 By using in vivo whole-cell
current-clamp and voltage-clamp recordings, we found tha
40 sustained inward current (depolarization in
current clamp)
and increased the amplitude and frequency
41 ted with transient depolarizations of ICC in
current clamp,
and these events were blocked by niflumic
42 e, using structural modeling, voltage-clamp,
current-clamp,
and multielectrode array recordings, we h
43 Using a dynamic
current-clamp approach, we now show that the fear-induce
44 a-cells or hamster insulinoma tumor cells in
current clamp at 30-35 degrees C, using standard K+-rich
45 Under
current clamp,
beta-adrenergic stimulation (isoprenaline
46 Under
current clamp,
block of BKCa current increased depolariz
47 In
current clamp,
blocking L-type Ca channels with the spec
48 Oxytocin neurones were characterized under
current clamp by the expression of a depolarization-acti
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 gically realistic currents into a cell under
current-clamp conditions, was used either to block I(Ade
70 ability and Ca(2+) influx under voltage- and
current-clamp conditions.
71 corded from L5 neurons by using a whole-cell
current clamp configuration.
72 ne potential were recorded in the whole cell
current-clamp configuration of the patch-clamp technique
73 and perforated-patch recording techniques in
current-clamp configuration.
74 events were identified both in voltage- and
current-clamp configurations.
75 width, and latency to first spike similar to
current clamp data from mouse dorsal striatum MSPN.
76 Voltage- and
current-clamp data showed that Rho-kinase inhibition red
77 In
current clamp,
depolarizing current injections from the
78 In
current clamp doses of 10 and 100 nM neuromedin C (NMC)
79 subgroups based on the visual inspection of
current clamp electrophysiological properties and morpho
80 Field potential recordings and whole-cell
current clamp electrophysiology were used to monitor the
81 ent mitral cell excitability as evaluated by
current-clamp electrophysiology.
82 sAHP conductance by spike-triggered dynamic-
current clamp enhanced the gain increase.
83 In
current clamp,
estrogen enhanced the diazoxide-induced h
84 Current clamp experiments at body temperature show that
85 Current clamp experiments revealed that blood depressing
86 Current clamp experiments show that, physiologically, th
87 Current clamp experiments showed that in IHCs the SK cur
88 Voltage and
current clamp experiments showed that the delayed HCO(3)
89 erve stimulations, pharmacological block and
current clamp experiments suggest that this is due to a
90 In
current clamp experiments, AA was without effect on the
91 In
current clamp experiments, NS309 enhanced the medium aft
92 In
current-clamp experiments alpha-DTX, used to eliminate t
93 Current-clamp experiments demonstrate that serotonergic
94 Current-clamp experiments indicated that these processes
95 Current-clamp experiments reveal that low concentrations
96 Current-clamp experiments show that Nav1.9 flows at subt
97 Current-clamp experiments showed that the specific Kv7/M
98 In
current-clamp experiments small neurons had more depolar
99 ly isolated neurons, mixed voltage-clamp and
current-clamp experiments were done at 37 degrees C to s
100 Current-clamp experiments were used to assess the functi
101 In
current-clamp experiments, APD and CaT alternans strongl
102 In
current-clamp experiments, non-inactivated VGSCs were su
103 In
current-clamp experiments,XE 991 per se caused membrane
104 -55 mV and did not induce depolarization in
current-clamp experiments.
105 cellular recordings under multiple levels of
current clamp from midbrain neurons in the mormyrid weak
106 Under
current clamp,
GIRK activation increased the cell membra
107 In
current clamp,
GTx (i) had almost no effect on the first
108 In
current clamp,
GTx had multiple effects: (i) increasing
109 In
current clamp,
halothane caused a membrane hyperpolariza
110 In
current clamped horizontal cells, BKCa channels subdue d
111 results for sodium channels using a dynamic
current clamp in neocortical fast spiking interneurons.
112 activating these receptors on the LTS, using
current-clamp intracellular recording in an in vitro sli
113 mpal slices of young and aging rabbits using
current-clamp,
intracellular recording techniques.
114 Current-clamped isolated neurons fired regularly ( appro
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 In
current clamp mode, some cells developed spontaneous tra
131 potential was monitored under the whole cell
current clamp mode.
132 e perforated patch whole cell patch clamp in
current clamp mode.
133 Whole-cell patch clamp records under
current-clamp mode also showed a chloroquine-induced dep
134 ross an intact cell-attached patch using the
current-clamp mode of a conventional patch-clamp amplifi
135 Whole-cell recordings from SpL neurons in
current-clamp mode revealed EPSPs evoked by stimulation
136 In
current-clamp mode, Ang II (1 mumol/L) produced depolari
137 In
current-clamp mode, current-induced voltage oscillations
138 In the
current-clamp mode, extracellular acidosis evoked both a
139 In
current-clamp mode, fast local application of acetylchol
140 In the
current-clamp mode, GABA depolarized the cells to approx
141 In
current-clamp mode, in a model of mutant RyR2 that is ch
142 In
current-clamp mode, the mutant RyR2 model exhibited incr
143 of the membrane potential were also made in
current-clamp mode.
144 d injected transduction current waveforms in
current-clamp mode.
145 taset of 150 neurons recorded in whole-cell,
current-clamp mode.
146 bbit nodose ganglion cells with slow AHPs in
current-clamp mode.
147 ng frequency of L/M interneurons recorded in
current-clamp mode.
148 s range could alter cellular repolarization,
current-clamped myocytes were dialyzed with 0.5 or 1.0 m
149 When whole-cell responses were recorded from
current-clamped neurones using the gramicidin-perforated
150 calcium-activated potassium current, and in
current clamp,
nimodipine usually depolarized cells and
151 ted by L-type Ca2+ channels using whole-cell
current clamp of the SC in an isolated brainstem prepara
152 In
current-clamp or voltage-clamp recordings, histamine (10
153 Two-electrode
current-clamp or voltage-clamp techniques were used to r
154 M) SON magnocellular neurones (n = 27) under
current clamp,
or induced an outward current that revers
155 induced either a membrane depolarization in
current clamp,
or inward current under voltage clamp in
156 sent in VHCs, whole cell, voltage-clamp- and
current-clamp-
patch recordings were performed on isolate
157 Current-clamp pause protocols induced rate-dependent spo
158 In constant 100 mum lidocaine,
current-clamped Purkinje cells continued to fire spontan
159 During
current clamp recording IH caused time-dependent rectifi
160 Using dual whole-cell voltage and
current clamp recording techniques, we investigated the
161 In
current clamp recording, injection of the unclustering p
162 Using whole-cell
current clamp recording, we found that L2/3 pyramidal ne
163 whole-cell tight seal method of voltage and
current clamp recording.
164 Simultaneous Ca(2+) imaging and
current-clamp recording during apparent-motion stimulati
165 Current-clamp recording from the calyx showed that each
166 cretin neurons using whole-cell voltage- and
current-clamp recording in mouse whole hypothalamic slic
167 In
current-clamp recording, CsCl, which inhibits only I(H)
168 In striking contrast, using voltage and
current-clamp recording, we found that PYY(3-36) consist
169 Using whole-cell
current-clamp recording, we unexpectedly found that TRH
170 eurones by performing some experiments using
current-clamp recording.
171 Whole-cell
current clamp recordings demonstrated that, following di
172 rent injection were assessed with whole-cell
current clamp recordings from cells that were isolated s
173 Current clamp recordings from MSO neurones were made whi
174 Current clamp recordings from the LGN of ethanol naive m
175 ond to oscillatory inputs we made whole-cell
current clamp recordings from three different types of n
176 Using whole cell
current clamp recordings in acute hippocampal slices, we
177 of VMH glucose-sensing neurons in whole-cell
current clamp recordings in brain slices.
178 In
current clamp recordings obtained from inspiratory neuro
179 Current clamp recordings of isolated myocytes showed a 7
180 erentiation of RGC types, we made whole-cell
current clamp recordings of RGC responses to injected cu
181 Moreover,
current clamp recordings show that cannabidiol reduces o
182 Intracellular
current clamp recordings were made from CA1 pyramidal ne
183 In
current clamp recordings, 100 microM NE produced a hyper
184 In
current clamp recordings, ATP and UTP (but not CTP) depo
185 In
current clamp recordings, microinjection of cross-linked
186 In addition, in
current clamp recordings, SCH23390 can depolarize the me
187 tic CA3 pyramidal neurons were studied using
current clamp recordings; activation of M1 receptors and
188 In
current-clamp recordings and Ca(2+)-imaging experiments,
189 Current-clamp recordings and Ca2+-imaging experiments de
190 insight into this issue by using whole-cell
current-clamp recordings and immunocytochemistry to show
191 Dual
current-clamp recordings confirm that single motoneuron
192 firmed in acutely isolated STN neurons using
current-clamp recordings containing IPSPs as voltage-cla
193 Whole-cell
current-clamp recordings demonstrate that leptin (0.3-10
194 Whole-cell
current-clamp recordings demonstrated increased spontane
195 Current-clamp recordings during high frequency firing an
196 toring of synaptic activity using whole-cell
current-clamp recordings from a local astrocyte.
197 e properties, we compared somatic whole-cell
current-clamp recordings from basal and apical neurons o
198 uences synaptic strength, using voltage- and
current-clamp recordings from bushy cells in brain slice
199 d with synaptic stimulation using whole-cell
current-clamp recordings from CA1 pyramidal cells in hip
200 In
current-clamp recordings from GFP+ SO cells, linopirdine
201 Whole-cell
current-clamp recordings from neurones near the TS revea
202 Using whole-cell voltage-clamp and
current-clamp recordings in acute hippocampal slices and
203 Here, we performed both
current-clamp recordings in brain slices and voltage-cla
204 Using a combination of
current-clamp recordings in brain slices and whole-cell
205 Using loose-patch
current-clamp recordings in brainstem slices from rat pu
206 Using
current-clamp recordings in hippocampal slices, we find
207 t were studied using whole-cell voltage- and
current-clamp recordings in slices of rat cerebellum.
208 Whole-cell
current-clamp recordings obtained from MGE-derived cells
209 Current-clamp recordings of dopamine neurons showed that
210 Current-clamp recordings of electrocyte APs reveal that
211 Whole-cell
current-clamp recordings of GnRH neurons in brain slices
212 On-cell
current-clamp recordings of olfactory receptor neurons f
213 Current-clamp recordings reveal that the desynchronized
214 Voltage-clamp and
current-clamp recordings revealed that knockdown of Navb
215 Current-clamp recordings revealed that the firing rates
216 s apical dendritic tuft and trunk whole-cell
current-clamp recordings revealed that the pharmacologic
217 Whole-cell
current-clamp recordings showed that 4-AP changed the en
218 Simultaneous [Ca2+]i and
current-clamp recordings showed that Ca2+ and Vm oscilla
219 Whole-cell
current-clamp recordings showed that each burst ended wi
220 Current-clamp recordings showed that neurons expressing
221 Current-clamp recordings showed that the fast activation
222 Voltage- and
current-clamp recordings suggested a high level of inact
223 Conventional
current-clamp recordings using excitatory ramp or square
224 s whole-cell voltage-clamp and cell-attached
current-clamp recordings we have defined both mathematic
225 Whole-cell
current-clamp recordings were made as extracellular gluc
226 Current-clamp recordings were made during and following
227 Whole-cell
current-clamp recordings were made from mouse basal spir
228 Whole-cell
current-clamp recordings were made from neurons in the r
229 Whole-cell voltage- and
current-clamp recordings were made of GFP-identified GnR
230 ifferential experience, sharp microelectrode
current-clamp recordings were obtained in CA1 pyramidal
231 Whole-cell voltage- and
current-clamp recordings were performed in acutely isola
232 Whole-cell
current-clamp recordings were performed on neurons from
233 -clamp and gramicidin-based perforated-patch
current-clamp recordings were then used to study the rel
234 Intracellular
current-clamp recordings with high-resistance micropipet
235 In
current-clamp recordings, decreasing [Ca2+]o induced sus
236 In
current-clamp recordings, depolarizing step current inje
237 In
current-clamp recordings, halothane depressed EPSP ampli
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, SP (100 nM) applied by superfu
247 In
current-clamp recordings, SST preferentially inhibited b
248 Using whole-cell voltage-clamp and
current-clamp recordings, this study shows for the first
249 ing multielectrode array, voltage-clamp, and
current-clamp recordings, we assessed a newly identified
250 nglion cell, were measured during whole cell
current-clamp recordings.
251 estigated using whole-cell voltage-clamp and
current-clamp recordings.
252 itability of GABAergic neurons determined by
current-clamp recordings.
253 ones in the hippocampus and dentate gyrus in
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 Under
current clamp stimulation SR Ca2+ content increased in l
267 When
current-clamp stimuli approximated the mean physiologica
268 Current clamp studies reveal complex spontaneous firing
269 In
current clamp studies, these drugs also led to a depolar
270 Previous
current-clamp studies in rat hippocampal slice CA1 neuro
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 Whole-cell voltage- and
current-clamp techniques were used to record L-type Ca2+
277 potentials were recorded using voltage- and
current-clamp techniques.
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 hin dorsal root ganglion neurons and show by
current-clamp that R185H renders dorsal root ganglion ne
283 ined when depolarizations were eliminated by
current-clamping the membrane potential.
284 In
current clamp,
the activation of I(KA) reduced neuronal
285 In
current clamp,
the prolonged rebound firing rate after h
286 TP and Ca2+ channel conductances to cells in
current clamp to assess the role of Ca2+ and KATP channe
287 were recorded from dissociated neurons under
current clamp to investigate the role of the resurgent c
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