1 (Cav1.342A) expressed in tsA-201 cells using
whole cell patch-clamp.
2 icator dye and ionic current was recorded by
whole cell patch-clamp.
3 flow system, and the current was measured by
whole-cell patch clamp.
4 ust activation by PMA that was absent during
whole-cell patch clamp.
5 y isolated rabbit ventricular myocytes using
whole-cell patch clamp.
6 s, were evaluated using brainstem slices and
whole-cell patch-clamp.
7 to study their functional consequences using
whole-cell patch-clamp.
8 ded from rabbit and human atrial myocytes by
whole-cell-patch clamp.
9 d by oscillating pH electrodes combined with
whole-cell patch clamping.
10 pe and knock-out neurons was monitored using
whole-cell patch clamping.
11 ectroscopy and APOL1-dependent currents with
whole-cell patch clamping.
12 rization of SCN10A variants was performed by
whole-cell patch-clamping.
13 ciation, and electrical activity recorded by
whole-cell-patch clamp (
35-37 degrees C).
14 Whole cell patch clamp analysis demonstrated increased e
15 glucose sensing by Sf1 neurons, we performed
whole-cell patch clamp analysis of brain slices from con
16 f dendritic spines in the CeA and, moreover,
whole-cell patch clamp analysis of the basal amygdala to
17 gy was used to identify BNST CRF neurons for
whole-cell patch-clamp analysis in acutely prepared slic
18 Whole cell patch clamp and dynamic action potential clam
19 Using optogenetics, cell-specific ablation,
whole cell patch-clamp and immuno-electron microscopy, w
20 ip and antagonistic mechanism on TRPM2 using
whole-cell patch clamp and Calcium imaging in human embr
21 were heterologously expressed, recorded with
whole-cell patch clamp and conolidine/cannabidiol was ap
22 etraction in mouse embryonic hindbrain using
whole-cell patch clamp and imaging techniques.
23 Here, using
whole-cell patch clamp and Western blotting analysis, we
24 choline-induced currents were measured using
whole-cell patch clamping and a fast perfusion system to
25 Whole-cell patch clamping and confocal microscopy, coupl
26 By combining
whole-cell patch-clamp and 2-photon laser scanning micro
27 x months after SE or sham treatment, we used
whole-cell patch-clamp and fluorescence microscopy to re
28 By means of a combination of
whole-cell patch-clamp and Forster resonance energy tran
29 ation of DG granule cells while recording in
whole-cell patch-clamp and juxtacellular configuration f
30 Pharmacological, electrophysiological (
whole-cell patch clamp),
and behavioral approaches were
31 ce energy transfer, L-type Ca(2+) current by
whole-cell patch-clamp,
and cardiomyocyte shortening and
32 soproterenol exposure decreased IKs density (
whole cell patch clamp)
by 58% (P<0.0001), with correspo
33 BK channel currents were measured using
whole-cell patch clamp; [
cAMP](i), [cGMP](i) with ELISAs
34 a functional experimental rig for automated
whole-cell patch clamping can be set up in 1 week.
35 recorded in brain slices from SNL rats using
whole-cell patch-clamp conditions.
36 al terminals when recorded using the classic
whole-cell patch-clamp configuration.
37 We here used a combination of
whole-cell patch clamp,
confocal imaging, co-immunopreci
38 Whole-cell patch clamping demonstrates that plumbagin an
39 lated the fixed buffer fraction by prolonged
whole-cell patch-clamp dialysis and quantified its buffe
40 Whole cell patch clamp electrophysiological recordings o
41 Whole-cell patch-clamp electrophysiological recording is
42 Here, we used
whole-cell patch clamp electrophysiology and neuronal re
43 Using
whole-cell patch clamp electrophysiology in mouse midbra
44 C terminus alternatively spliced exons using
whole-cell patch clamp electrophysiology revealed a spli
45 ) were prepared from adult C57BL/6J mice and
whole-cell patch clamp electrophysiology was used to cha
46 Using
whole-cell patch clamp electrophysiology we demonstrate
47 t traffics to the plasma membrane, but using
whole-cell patch clamp electrophysiology we observed tha
48 trical properties of mouse MHb neurones with
whole-cell patch clamp electrophysiology, and investigat
49 Using
whole-cell patch clamp electrophysiology, we demonstrate
50 Using
whole-cell patch clamp electrophysiology, we examined ex
51 xpressed in tsA201 cells were measured using
whole-cell patch clamp electrophysiology.
52 gy) in the gut of E11.5 and E12.5 mice using
whole-cell patch-clamp electrophysiology and compared th
53 To test this idea, we used
whole-cell patch-clamp electrophysiology and immunohisto
54 Whole-cell patch-clamp electrophysiology assessed sex di
55 Here, we combined
whole-cell patch-clamp electrophysiology in acute mouse
56 Whole-cell patch-clamp electrophysiology of neurons is a
57 Whole-cell patch-clamp electrophysiology subsequently re
58 Finally, we demonstrate using
whole-cell patch-clamp electrophysiology that netrin-1 i
59 nic kidney cells and used calcium imaging or
whole-cell patch-clamp electrophysiology to assess the e
60 LSPS) of caged glutamate in conjunction with
whole-cell patch-clamp electrophysiology to probe the in
61 anol (CIE) exposure to induce dependence and
whole-cell patch-clamp electrophysiology was used to exa
62 Using
whole-cell patch-clamp electrophysiology we demonstrate
63 Using
whole-cell patch-clamp electrophysiology, activation of
64 ng male D1tdTomato transgenic reporter mice,
whole-cell patch-clamp electrophysiology, and input-spec
65 Using
whole-cell patch-clamp electrophysiology, inhibitory GAB
66 ChIP2 with Kv4.2 in HEK293T cells, and, with
whole-cell patch-clamp electrophysiology, measured an ~1
67 polymerase chain reaction, Western blot, and
whole-cell patch-clamp electrophysiology, we examined th
68 Using
whole-cell patch-clamp electrophysiology, we observed di
69 The biological relevance was confirmed by
whole-cell patch-clamp electrophysiology.
70 her mutations in HEK293T cells and performed
whole-cell patch-clamp electrophysiology.
71 in the first postnatal weeks using in vitro
whole-cell patch-clamp electrophysiology.
72 C-1 when included in the pipette solution in
whole cell patch clamp experiments and when transiently
73 In
whole cell patch clamp experiments, this mutation reduce
74 Furthermore,
whole-cell patch clamp experiments and assessment of mem
75 hors purified KCNQ1 antibodies and performed
whole-cell patch clamp experiments as well as single-cha
76 We used mutagenesis and
whole-cell patch clamp experiments on TRPV3 channels end
77 -G2 exhibited similar channel properties in
whole-cell patch clamp experiments.
78 increases GABA-induced chloride currents in
whole-cell patch clamping experiments than either chemic
79 Whole-cell patch-clamp experiments in acute mouse brains
80 Whole-cell patch-clamp experiments performed on isolated
81 Whole-cell patch-clamp experiments showed that E299V pre
82 In
whole-cell patch-clamp experiments, we examined the effe
83 t reduces the IC(50) of TETS by ~700-fold in
whole-cell patch-clamp experiments.
84 Short-circuit current and
whole-cell patch-clamping experiments revealed that IL-8
85 tant hEAAT1 in mammalian cells and performed
whole-cell patch clamp,
fast substrate application, and
86 We
whole-cell patch clamped GFP-expressing (GFP(+)) cells w
87 al effects of the mutations were analyzed by
whole cell patch clamp in HEK293 cells; for 5 of the mut
88 on of four selected missense mutations using
whole cell patch-clamping in tsA201 cells-together with
89 Using dye-filling and
whole-cell patch clamping in brain slices, together with
90 Whole-cell patch clamping in vivo is an important neuros
91 Using
whole-cell patch-clamp in acute rat brain slices, we des
92 ctric mapping, isolation of atrial myocytes,
whole-cell patch clamping,
in vitro tachypacing of atria
93 Whole-cell patch-clamp measurements of the current, Ip,
94 Whole-cell patch-clamp measurements on root cell protopl
95 eotide effects were measured by means of the
whole-cell patch-clamp method.
96 t ganglion (DRG) neurons was examined by the
whole-cell patch-clamp method.
97 (VIP) or parvalbumin (PV) interneurons using
whole cell patch clamp methods.
98 nd rats with 24 h of femoral occlusion using
whole-cell patch clamp methods.
99 firing of dorsal root ganglia (DRG) neurons,
whole-cell patch clamp of transfected HEK cells revealed
100 Using
whole-cell patch clamping on human embryonic kidney 293
101 racterization of this splice variant through
whole-cell patch clamping on transfected mammalian cells
102 Here, we use
whole-cell patch-clamp on a rat model of withdrawal from
103 ly to adrenergic stimulation, as measured by
whole-cell patch clamp or a fluorescent intracellular Ca
104 acute passive infusion of alphaSyn PFFs from
whole-cell patch-clamp pipette decreased mEPSC frequency
105 bain-sensitive transient charge movements in
whole-cell patch-clamped rat cardiac ventricular myocyte
106 function of spine synapses were analyzed by
whole cell patch clamp recording and two-photon image an
107 Whole cell patch clamp recording demonstrated that mild
108 In this work, we used dual
whole cell patch clamp recording to examine the function
109 within an ex vivo brain slice, combined with
whole-cell patch clamp recording and capillary electroph
110 Using
whole-cell patch clamp recording combined with fluoresce
111 Using a single 24-hr episode of MD and
whole-cell patch clamp recording in rat midbrain slices,
112 A recent study using
whole-cell patch clamp recording of MNs in acute spinal
113 We used
whole-cell patch clamp recording to investigate the effe
114 Whole-cell patch clamp recording was used to examine the
115 ons in mouse neocortical brain slices during
whole-cell patch clamp recording.
116 Using a combination of
whole-cell patch-clamp recording and biochemical analyse
117 Using
whole-cell patch-clamp recording and immunohistochemistr
118 Here, using in vitro
whole-cell patch-clamp recording and intracellular filli
119 onto stellate cells in the cerebellum using
whole-cell patch-clamp recording and photolytic uncaging
120 We have assessed, using
whole-cell patch-clamp recording and RNA-sequencing (RNA
121 s region make the RVM a challenging area for
whole-cell patch-clamp recording in adults.
122 Using immunofluorescence and
whole-cell patch-clamp recording in rat midbrain slices,
123 Here, in vivo
whole-cell patch-clamp recording of excitatory neurons r
124 Applying
whole-cell patch-clamp recording of HEK cells, we found
125 specifically in the larval dHb and performed
whole-cell patch-clamp recording of IPN neurons.
126 Here we provide evidence from
whole-cell patch-clamp recording that dynorphin-A (Dyn-A
127 d high-resolution immunoelectron microscopy,
whole-cell patch-clamp recording, and computational mode
128 brain slices were harvested and prepared for
whole-cell patch-clamp recording, and in treated rats, t
129 18.5 hypoglossal MNs from brain slices using
whole-cell patch-clamp recording, followed by dye-fillin
130 veloped Patch-seq, a technique that combines
whole-cell patch-clamp recording, immunohistochemistry,
131 Using the
whole-cell patch-clamp recording, we found that THIK-1 c
132 By performing
whole-cell patch-clamp recording, we showed that TMEM16B
133 enic properties of the encoded proteins with
whole-cell patch-clamp recording.
134 nces in dentate granule cells as measured by
whole-cell patch-clamp recording.
135 al neurons in slices from trained rats using
whole-cell patch-clamp recording.
136 working heart-brainstem preparation to make
whole cell patch clamp recordings from T3-4 SPNs (n = 98
137 tobleaching (FRAP), quantitative RT-PCR, and
whole cell patch clamp recordings of GFP-encoding Mus mu
138 We performed
whole cell patch clamp recordings of hippocampal neurons
139 Whole cell patch clamp recordings of miniature excitator
140 while functional expression was confirmed by
whole cell patch clamp recordings of responses to GABA a
141 Whole cell patch clamp recordings showed that CRF increa
142 Whole cell patch clamp recordings were made from gastric
143 ibitions by purinergic receptor antagonists,
whole cell patch-clamp recordings of ATP-induced current
144 adult mouse spinal cord, allowing visualized
whole cell patch-clamp recordings of fluorescent lumbar
145 Whole cell patch-clamp recordings were performed on isol
146 emical approaches in combination with lifted
whole cell patch-clamp recordings.
147 rat dorsal root ganglia (DRG) neurons using
whole cell patch-clamp recordings.
148 e lack of A-type K(+) channel conductance in
whole cell patch-clamp recordings.
149 We combined
whole-cell patch clamp recordings (n = 440) of NMDAR-med
150 e anxiety levels and general locomotion; (2)
whole-cell patch clamp recordings and biocytin labeling
151 This study used
whole-cell patch clamp recordings combined with single-c
152 Whole-cell patch clamp recordings conducted 2-4 days aft
153 Whole-cell patch clamp recordings demonstrated that this
154 ssion at the endbulb of Held was assessed by
whole-cell patch clamp recordings from auditory neurons
155 ssion at the endbulb of Held was assessed by
whole-cell patch clamp recordings from auditory neurons
156 In
whole-cell patch clamp recordings from cultured rat spin
157 cid and leucine 1331 to valine) by obtaining
whole-cell patch clamp recordings in human embryonic kid
158 ically obtaining high-yield and high-quality
whole-cell patch clamp recordings in vivo.
159 n slices were prepared following stress, and
whole-cell patch clamp recordings of inhibitory postsyna
160 Whole-cell patch clamp recordings of spontaneous miniatu
161 In
whole-cell patch clamp recordings of transfected HEK293T
162 nderwent one of the following procedures: 1)
whole-cell patch clamp recordings to characterize AMPAR
163 We performed
whole-cell patch clamp recordings using cultured DRG neu
164 Whole-cell patch clamp recordings were used to compare t
165 Using in vivo
whole-cell patch clamp recordings, we found that many gl
166 In
whole-cell patch clamp recordings, we observed larger ma
167 de high resolution flow cytometry assays and
whole-cell patch clamp recordings, we revealed that the
168 trol iPSC-derived neurons are compared using
whole-cell patch clamp recordings.
169 ytes and show functional channel activity in
whole-cell patch clamp recordings.
170 We used
whole-cell patch-clamp recordings and an optogenetic app
171 Using a combination of
whole-cell patch-clamp recordings and extracellular reco
172 Whole-cell patch-clamp recordings and high-resolution 3D
173 using a combination of immunohistochemistry,
whole-cell patch-clamp recordings and optogenetic stimul
174 To examine this, we used a combination of
whole-cell patch-clamp recordings and optogenetics to de
175 , using pathway-specific retrograde tracing,
whole-cell patch-clamp recordings and post hoc cell type
176 Here, we used a combination of
whole-cell patch-clamp recordings and two-photon Ca2+ im
177 Using
whole-cell patch-clamp recordings combined with optogene
178 Whole-cell patch-clamp recordings confirmed that PVN AT1
179 Whole-cell patch-clamp recordings demonstrate that loss
180 Whole-cell patch-clamp recordings demonstrate that these
181 Whole-cell patch-clamp recordings demonstrated that alph
182 Single
whole-cell patch-clamp recordings demonstrated that incr
183 Thus, we focused on optimizing
whole-cell patch-clamp recordings for RVM neurons in ani
184 We optimized
whole-cell patch-clamp recordings for RVM neurons in ani
185 In
whole-cell patch-clamp recordings from acute hippocampal
186 We used
whole-cell patch-clamp recordings from acutely prepared
187 Whole-cell patch-clamp recordings from astrocytes furthe
188 Whole-cell patch-clamp recordings from calyx endings wer
189 Acute
whole-cell patch-clamp recordings from GrCs in brain sli
190 Utilizing
whole-cell patch-clamp recordings from morphologically i
191 s this question studies were performed using
whole-cell patch-clamp recordings from mouse hypoglossal
192 Using multiple
whole-cell patch-clamp recordings from neurons in acute
193 Whole-cell patch-clamp recordings from neurons in PFC sl
194 Whole-cell patch-clamp recordings from neurons in slices
195 Using
whole-cell patch-clamp recordings from pyramidal neurons
196 Using
whole-cell patch-clamp recordings from rat cerebellar sl
197 Whole-cell patch-clamp recordings from SCN neurons revea
198 Using
whole-cell patch-clamp recordings from spinal motoneuron
199 cellular basis of this effect, we performed
whole-cell patch-clamp recordings from the set of identi
200 Whole-cell patch-clamp recordings in acute brain slices
201 Whole-cell patch-clamp recordings in brain slices reveal
202 ippocampal stimulation in vivo and conducted
whole-cell patch-clamp recordings in brain slices to rev
203 In vivo
whole-cell patch-clamp recordings in cat visual cortex r
204 Moreover, we use
whole-cell patch-clamp recordings in combination with lo
205 th muscle (aSM)-like activity patterns using
whole-cell patch-clamp recordings in HEK293 cells (Cav1.
206 in mediating these adaptations, we conducted
whole-cell patch-clamp recordings in NAc core MSNs of "i
207 Using
whole-cell patch-clamp recordings in posthearing mice, w
208 Whole-cell patch-clamp recordings in rat DRG neurons rev
209 Whole-cell patch-clamp recordings in RPE derived from hu
210 tic suppression of HP inputs onto MSNs using
whole-cell patch-clamp recordings in slices from adult r
211 Whole-cell patch-clamp recordings in spinal cord slices
212 We tested this by obtaining
whole-cell patch-clamp recordings in the "fictively" cal
213 Here we used paired
whole-cell patch-clamp recordings in the cockroach Perip
214 xpressed in tsA201 cells were measured using
whole-cell patch-clamp recordings in the presence and ab
215 Whole-cell patch-clamp recordings in the spinal cord sli
216 Here we combined
whole-cell patch-clamp recordings in vivo and dynamic cl
217 erves the intact cell-medium interface using
whole-cell patch-clamp recordings in vivo and in vitro.
218 Whole-cell patch-clamp recordings indicate sustained, th
219 Whole-cell patch-clamp recordings indicated that food re
220 Here, using
whole-cell patch-clamp recordings of CA1 pyramidal neuro
221 Using
whole-cell patch-clamp recordings of EPSCs in nucleus ac
222 By performing
whole-cell patch-clamp recordings of human embryonic kid
223 This study used
whole-cell patch-clamp recordings of ligand activated G-
224 We performed
whole-cell patch-clamp recordings of medium spiny neuron
225 Whole-cell patch-clamp recordings of neurons from male m
226 We used
whole-cell patch-clamp recordings of over 460 neurons to
227 Whole-cell patch-clamp recordings of presynaptic termina
228 We performed
whole-cell patch-clamp recordings of principal neurons i
229 Whole-cell patch-clamp recordings of striatal spiny proj
230 Whole-cell patch-clamp recordings of synaptic conductanc
231 Whole-cell patch-clamp recordings of VTA dopamine neuron
232 Whole-cell patch-clamp recordings of XII motoneurons sho
233 Whole-cell patch-clamp recordings reveal that detection
234 Whole-cell patch-clamp recordings revealed increased exc
235 Whole-cell patch-clamp recordings revealed that DEX (1-1
236 lating the LHb from the SCN, we show through
whole-cell patch-clamp recordings that LHb neurones exhi
237 vo pharmacological manipulations and ex vivo
whole-cell patch-clamp recordings to dissect the local c
238 bination of retrograde labeling and in vitro
whole-cell patch-clamp recordings to examine the effect
239 First, we used
whole-cell patch-clamp recordings to measure the physiol
240 SIC composition in muscle afferents, we used
whole-cell patch-clamp recordings to study the propertie
241 In mouse brain slices, we used
whole-cell patch-clamp recordings to study the role of C
242 viral tracer in male lean and db/db mice and
whole-cell patch-clamp recordings were conducted.
243 Whole-cell patch-clamp recordings were made from layer V
244 Whole-cell patch-clamp recordings were made from rat dor
245 Whole-cell patch-clamp recordings were obtained from Pur
246 Whole-cell patch-clamp recordings were obtained from ret
247 After >40 days of withdrawal,
whole-cell patch-clamp recordings were performed in NAc
248 First,
whole-cell patch-clamp recordings were performed on prep
249 Whole-cell patch-clamp recordings were performed to exam
250 We used in vitro
whole-cell patch-clamp recordings with laser-scanning ph
251 Whole-cell patch-clamp recordings, immunohistochemistry,
252 In
whole-cell patch-clamp recordings, reduced LIS1 function
253 sciplinary approach included Ca(2+) imaging,
whole-cell patch-clamp recordings, skin-nerve and gut-ne
254 Using paired
whole-cell patch-clamp recordings, trains of action pote
255 Here, using
whole-cell patch-clamp recordings, we assessed whether c
256 Using
whole-cell patch-clamp recordings, we found that Tg2576
257 By combining single-cell RNA-seq with
whole-cell patch-clamp recordings, we identified Ptgds a
258 Using
whole-cell patch-clamp recordings, we observed a K(+) co
259 Here, using in vitro
whole-cell patch-clamp recordings, we show that 5-HT hyp
260 onto D2R-containing MSNs as measured by dual
whole-cell patch-clamp recordings.
261 say, intracellular calcium measurements, and
whole-cell patch-clamp recordings.
262 obustly blocks anesthetic TREK-1 currents in
whole-cell patch-clamp recordings.
263 Whole-cell, patch clamp recordings demonstrate that both
264 injection of pseudorabies virus PRV-152) and
whole-cell, patch clamp recordings were obtained in brai
265 of specific thalamic afferents combined with
whole-cell, patch-clamp recordings of MSNs and electrica
266 Whole-cell patch clamp showed that CASK-silencing increa
267 Examination of neuronal activity by
whole-cell patch-clamp shows elevated levels of glutamat
268 Using
whole-cell patch-clamping,
single-cell RT-PCR to assay e
269 stimulation of afferent fibres coupled with
whole-cell patch-clamp somatic recordings to study the f
270 Whole-cell patch clamp studies revealed that the mutant
271 This is in part because
whole-cell patch-clamp studies in RVM to date have been
272 Immunofluorescence and dual
whole-cell patch-clamp studies were performed to determi
273 Whole cell patch clamp technique was used to assess the
274 s to a cell's intracellular environment, the
whole-cell patch clamp technique allows one to record th
275 embrane current in atrial myocytes using the
whole-cell patch clamp technique, combined with pressuri
276 rophysiological properties were examined via
whole-cell patch clamp technique.
277 physical properties were further assessed by
whole-cell patch clamp technique.
278 al characteristics of these neurons by using
whole-cell patch-clamp technique in vitro Our results sh
279 I(Ca,L) density was measured by the
whole-cell patch-clamp technique on days 0-3 in cardiomy
280 The
whole-cell patch-clamp technique was employed to investi
281 ordings were performed in these cells by the
whole-cell patch-clamp technique.
282 We used the
whole-cell, patch clamp technique to characterize the ef
283 In this study we used
whole cell patch-clamping techniques in rat horizontal b
284 We show by
whole-cell patch clamping that treatment of hepatocytes
285 rophysiological studies were conducted using
whole cell patch-clamp to explore biophysical properties
286 ythmias (VA) were probed by optical mapping,
whole-cell patch clamp to measure action potential durat
287 We used
whole-cell patch clamp to study the electrophysiological
288 or genetic approaches that we confirmed with
whole-cell patch clamp to substantially reduce Ih curren
289 se a combination of protein biochemistry and
whole-cell patch clamping to determine effects of diet m
290 We then used
whole-cell patch-clamping to evaluate NMDAR-mediated cur
291 ) in the dorsal root ganglion (DRG), and the
whole cell patch clamp was used to examine the amplitude
292 Whole-cell patch clamp was used to assess K(+) channel c
293 Whole-cell patch clamp was used to assess silent synapse
294 Whole-cell patch-clamp was used to measure sodium curren
295 NCX current (INCX), measured with
whole cell patch clamp,
was inhibited in response to cyt
296 Finally, using
whole-cell patch clamping we demonstrate that activation
297 Using
whole-cell patch clamp,
we found that the activation of
298 Using
whole-cell patch clamp,
we have demonstrated that NTnC d
299 n of mefenamic acid's effect on I (Ks) Using
whole-cell patch clamp,
we show that mefenamic acid enha
300 The combination of
whole-cell patch clamp with single cell cytoplasm metabo