ライフサイエンスコーパス: patch-clamp recording

1 g the presynaptic release function and using patch clamp recording.

2 d the protein in giant liposomes amenable to patch clamp recording.

3 e neocortical brain slices during whole-cell patch clamp recording.

4 ties of the encoded proteins with whole-cell patch-clamp recording.

5 ransduction, we examined its distribution by patch-clamp recording.

6 s using high-resolution confocal imaging and patch-clamp recording.

7 tate granule cells as measured by whole-cell patch-clamp recording.

8 performed using heterologous expression and patch-clamp recording.

9 in slices from trained rats using whole-cell patch-clamp recording.

10 g and performed whole-cell and cell-attached patch clamp recordings.

11 erived neurons are compared using whole-cell patch clamp recordings.

12 ow functional channel activity in whole-cell patch clamp recordings.

13 a preparation of peripheral nerve slices for patch-clamp recordings.

14 oaches in combination with lifted whole cell patch-clamp recordings.

15 ere a method for stable simultaneous octuple patch-clamp recordings.

16 red to wild-type mice could be detected with patch-clamp recordings.

17 es of L5 pyramidal neurons of mouse V1 using patch-clamp recordings.

18 neurons using optogenetic tools and in vitro patch-clamp recordings.

19 expressed in HEK293 cells and studied using patch-clamp recordings.

20 ) concentration ([Ca(2+)]i) measurements and patch-clamp recordings.

21 of MHbV (MHbVL and MHbVC) using brain slice patch-clamp recordings.

22 root ganglia (DRG) neurons using whole cell patch-clamp recordings.

23 ly induced nicotinic responses by performing patch-clamp recordings.

24 EK-293 cells using whole-cell and inside-out patch-clamp recordings.

25 Results from patch-clamp recordings agreed well with cellular assays

26 te mapping techniques with in vitro targeted patch-clamp recordings, allowed identifying a new type o

27 Patch-clamp recordings also showed increased CB1-sensiti

28 x vivo brain slice, combined with whole-cell patch clamp recording and capillary electrophoresis (CE)

29 We used patch clamp recording and substituted cysteine accessibi

30 f spine synapses were analyzed by whole cell patch clamp recording and two-photon image analysis of P

31 was impaired in eKO mice in single cells in patch clamp recordings and in the intact coronary circul

32 es was analyzed immunohistochemically and by patch clamp recordings and microfluorometry.

33 identified group of spinal INs, we combined patch-clamp recording and anatomical tracing with cluste

34 Using a combination of whole-cell patch-clamp recording and biochemical analyses in hippoc

35 sensitization/challenge to induce AIAD, (3) patch-clamp recording and Ca(2+) imaging to examine the

36 Using whole-cell patch-clamp recording and immunohistochemistry, we teste

37 ate cells in the cerebellum using whole-cell patch-clamp recording and photolytic uncaging of RuBi-GA

38 We have assessed, using whole-cell patch-clamp recording and RNA-sequencing (RNA-seq), the

39 itochondrial assays; in addition, using both patch-clamp recording and somatic Ca(2+) imaging, we hav

40 Here, using patch-clamp recording and two-photon Ca(2+) imaging in r

41 ase by a combination of membrane capacitance patch-clamp recordings and biochemical measurements of s

42 Patch-clamp recordings and Ca(2+) imaging demonstrate th

43 Here, we used patch-clamp recordings and confocal and electron microsc

44 Using a combination of whole-cell patch-clamp recordings and extracellular recordings in E

45 Here we have combined confocal microscopy, patch-clamp recordings and light-sensitive channel block

46 heterologous expression in mammalian cells, patch-clamp recordings and noise analysis to study and c

47 ne this, we used a combination of whole-cell patch-clamp recordings and optogenetics to demonstrate t

48 hway-specific retrograde tracing, whole-cell patch-clamp recordings and post hoc cell type identifica

49 used retrograde tracing in combination with patch-clamp recordings and recorded pre- and postsynapti

50 Patch-clamp recordings and synaptic CaV1.3 immunolabelin

51 ayers 2/3 of V1 of awake mice using targeted patch-clamp recordings and synchronous local field poten

52 , we used a combination of dual simultaneous patch-clamp recordings and targeted optogenetic stimulat

53 Here we have used patch-clamp recordings and total internal reflection flu

54 Here, we used a combination of whole-cell patch-clamp recordings and two-photon Ca2+ imaging to re

55 By a combination of patch-clamp recordings and two-photon calcium imaging, w

56 nderlying startle habituation in rats, using patch-clamp recordings and voltage-sensitive dye imaging

57 lution immunoelectron microscopy, whole-cell patch-clamp recording, and computational modeling to inv

58 s were harvested and prepared for whole-cell patch-clamp recording, and in treated rats, this occurre

59 Here we use multiphoton imaging and patch-clamp recording, and observe sparse and stereotype

60 Using patch-clamp recordings, artificial dynamic conductance i

61 In this study, live imaging and paired patch clamp recording at the zebrafish neuromuscular syn

62 Using paired patch-clamp recordings between bipolar cell terminals an

63 This study used whole-cell patch clamp recordings combined with single-cell labelin

64 Dual soma-axon patch-clamp recordings combined with axonal Na(+) imagin

65 In patch-clamp recordings, compound 21 displayed a signific

66 Cell-attached patch clamp recordings confirmed that perisomatic Ih was

67 Patch-clamp recordings confirmed that KV1-C peptide atte

68 Whole-cell patch-clamp recordings confirmed that PVN AT1a deletion

69 Single-channel patch-clamp recordings confirmed that the human BK chann

70 o study these questions, we performed paired patch-clamp recordings, deconvolution analysis, and nume

71 Whole-cell patch-clamp recordings demonstrate that these transient

72 Whole-cell patch clamp recordings demonstrated that this decrease w

73 Single whole-cell patch-clamp recordings demonstrated that increased GABA

74 Ex vivo patch-clamp recordings demonstrated that the depolarizin

75 monstrated the pipettes' utility in targeted patch-clamp recording experiments and single-cell electr

76 ossal MNs from brain slices using whole-cell patch-clamp recording, followed by dye-filling these sam

77 Thus, we focused on optimizing whole-cell patch-clamp recordings for RVM neurons in animals older

78 We optimized whole-cell patch-clamp recordings for RVM neurons in animals older

79 Patch clamp recordings from auditory brainstem neurons a

80 e endbulb of Held was assessed by whole-cell patch clamp recordings from auditory neurons in mature (

81 e endbulb of Held was assessed by whole-cell patch clamp recordings from auditory neurons in mature (

82 ts of the variant vs. wild type NaV1.1 using patch clamp recordings from channels expressed in Chines

83 Using patch clamp recordings from infralimbic mPFC pyramidal n

84 Patch clamp recordings from layer V pyramidal neurons sh

85 Patch clamp recordings from mouse DRG neurones identifie

86 We have made patch clamp recordings from Purkinje cells in vivo to id

87 art-brainstem preparation to make whole cell patch clamp recordings from T3-4 SPNs (n = 98).

88 ical stimulation of the efferent fibres with patch clamp recordings from the IHCs to measure efferent

89 Patch-clamp recording from neurons in the sensory layers

90 Analysis of simultaneous multiple patch-clamp recordings from 6068 pairs of rat neurons wi

91 e, we used paired motor neuron target muscle patch-clamp recordings from a rapsyn-deficient mutant li

92 We demonstrate platform validation with patch-clamp recordings from a variety of cells in the mo

93 In whole-cell patch-clamp recordings from acute hippocampal slices, (+

94 action potential (AP) firing rates (FRs) in patch-clamp recordings from acutely isolated SAMs.

95 Whole-cell patch-clamp recordings from astrocytes further suggest t

96 shed light on these mechanisms, we performed patch-clamp recordings from basal amygdala (BA) neurons

97 Here we use visually targeted patch-clamp recordings from basket cell terminals of mic

98 Moreover, we show in patch-clamp recordings from brain slices that VLPO neuro

99 Patch-clamp recordings from Cabp2(LacZ/LacZ) IHCs reveal

100 Whole-cell patch-clamp recordings from calyx endings were performed

101 We performed patch-clamp recordings from GPe neurons and found that b

102 We performed patch-clamp recordings from hippocampal CA3 pyramidal ne

103 Utilizing whole-cell patch-clamp recordings from morphologically identified C

104 Whole-cell patch-clamp recordings from neurons in slices removed at

105 We performed patch-clamp recordings from pyramidal cells in acute rat

106 Using whole-cell patch-clamp recordings from pyramidal neurons and fast-s

107 Using whole-cell patch-clamp recordings from rat cerebellar slices, we ha

108 ress this issue, we made two-photon targeted patch-clamp recordings from rat TC and TRN neuron dendri

109 Consistently, patch-clamp recordings from retrovirally labeled new gra

110 Targeted patch-clamp recordings from SbC-RGCs under two-photon gu

111 -of-function Fbxl3(Afh) mutation and perform patch-clamp recordings from SCN brain slices across the

112 Whole-cell patch-clamp recordings from SCN neurons revealed that ex

113 To test this, we performed patch-clamp recordings from soma and dendrites of rat hi

114 Using whole-cell patch-clamp recordings from spinal motoneurons and inter

115 Patch-clamp recordings from spiny projection neurones (S

116 We performed direct patch-clamp recordings from the dendrites of pyramidal n

117 ted cardiac myocytes, and performed targeted patch-clamp recordings from the latter.

118 asis of this effect, we performed whole-cell patch-clamp recordings from the set of identified visual

119 Here, we used dual patch-clamp recordings from turtle vestibular hair cells

120 Patch-clamp recordings further indicated that Fezf2-resp

121 e depletion to this activation pathway using patch clamp recording, GFP-PLCdelta1-PH imaging and co-l

122 Patch-clamp recording has enabled single-cell electrical

123 While in vivo patch-clamp recording has recently benefited from automa

124 Using a combination of patch clamp recording, immunoblotting, confocal imaging

125 ch-seq, a technique that combines whole-cell patch-clamp recording, immunohistochemistry, and single-

126 a single 24-hr episode of MD and whole-cell patch clamp recording in rat midbrain slices, we show th

127 s in hippocampal CA1 pyramidal neurons using patch clamp recordings in acute slices from mice at diff

128 Patch clamp recordings in GCs reveal that movement is ac

129 cine 1331 to valine) by obtaining whole-cell patch clamp recordings in human embryonic kidney 293T ce

130 Patch clamp recordings in isolated mitoplasts suggest in

131 ining high-yield and high-quality whole-cell patch clamp recordings in vivo.

132 ke the RVM a challenging area for whole-cell patch-clamp recording in adults.

133 nnelrhodopsin-2 in mouse MS neurons and used patch-clamp recording in brain slices to determine the r

134 Commensurately, patch-clamp recording in mPFC layer V pyramidal neurons

135 Using immunofluorescence and whole-cell patch-clamp recording in rat midbrain slices, we show th

136 The present study used voltage imaging and patch-clamp recording in slices of rat SC to test the hy

137 e inhibitory drive to PV+ INs using targeted patch-clamp recording in spinal cord slices from adult t

138 lfactory bulb slices and two-photon targeted patch-clamp recording in vivo to characterize the proper

139 Whole-cell patch-clamp recordings in acute brain slices revealed th

140 Here, by making patch-clamp recordings in acute slices of macaque retina

141 Patch-clamp recordings in acute slices showed that, 1 we

142 Moreover, patch-clamp recordings in acute VNO slices reveal that m

143 0 nm 3D resolution, which allows presynaptic patch-clamp recordings in all four configurations (cell-

144 Whole-cell patch-clamp recordings in brain slices revealed that int

145 stimulation in vivo and conducted whole-cell patch-clamp recordings in brain slices to reveal how nan

146 rphin-A on MCPO/SI cholinergic neurons using patch-clamp recordings in brain slices.

147 otent role of gap junctions was confirmed in patch-clamp recordings in bulb slices from wild-type and

148 In vivo whole-cell patch-clamp recordings in cat visual cortex revealed sma

149 loping the first robot to perform sequential patch-clamp recordings in cell culture and in vivo witho

150 Moreover, we use whole-cell patch-clamp recordings in combination with local electri

151 In situ patch-clamp recordings in genetic mosaics reveal that Dm

152 aSM)-like activity patterns using whole-cell patch-clamp recordings in HEK293 cells (Cav1.2 alpha1-su

153 l of neuropathic pain in Long-Evans rats and patch-clamp recordings in layer II/III pyramidal neurons

154 dial entorhinal stellate cells, we performed patch-clamp recordings in mice navigating in a virtual-r

155 elrhodopsin-2 (ChR2) in TMN neurons and used patch-clamp recordings in mouse brain slices to examine

156 g these adaptations, we conducted whole-cell patch-clamp recordings in NAc core MSNs of "incubated ra

157 Using whole-cell patch-clamp recordings in posthearing mice, we show that

158 We used patch-clamp recordings in prefrontal cortical slices fro

159 Whole-cell patch-clamp recordings in rat DRG neurons revealed that

160 a(+)/K(+)-ATPase role was investigated using patch-clamp recordings in rat MnPO dissociated neurons.

161 Whole-cell patch-clamp recordings in RPE derived from human-induced

162 sion of HP inputs onto MSNs using whole-cell patch-clamp recordings in slices from adult rats.

163 Whole-cell patch-clamp recordings in spinal cord slices revealed th

164 Here we used paired whole-cell patch-clamp recordings in the cockroach Periplaneta amer

165 The present study combines patch-clamp recordings in the intact neonatal rat spinal

166 Whole-cell patch-clamp recordings in the spinal cord slice preparat

167 Here, we used patch-clamp recordings in visual cortex of anesthetized

168 With multiple patch-clamp recordings in vitro, we show that the cell s

169 Here we combined whole-cell patch-clamp recordings in vivo and dynamic clamp recordi

170 ntact cell-medium interface using whole-cell patch-clamp recordings in vivo and in vitro.

171 Here we perform dendritic and somatic patch-clamp recordings in vivo combined with optogenetic

172 Using dual patch-clamp recordings in vivo, we reveal that in the pr

173 calbindin-D28k, and calretinin in mice with patch-clamp recording, in vivo physiology, and mathemati

174 Whole-cell patch-clamp recordings indicate sustained, thermally sta

175 docking, molecular dynamics simulations, and patch-clamp recordings indicate that residues K526 and K

176 Whole-cell patch-clamp recordings indicated that food restriction a

177 Targeted patch-clamp recording is a powerful method for character

178 = 44) and with sclerosis (n = 75) combining patch clamp recording, K(+) concentration analysis, elec

179 ine-regulated potassium current (IKACh) with patch clamp recording, messenger ribonucleic acid expres

180 We combined whole-cell patch clamp recordings (n = 440) of NMDAR-mediated curre

181 A recent study using whole-cell patch clamp recording of MNs in acute spinal cord slices

182 Using patch clamp recording of olfactory bulb slices in the wh

183 (FRAP), quantitative RT-PCR, and whole cell patch clamp recordings of GFP-encoding Mus musculus nACh

184 We performed whole cell patch clamp recordings of hippocampal neurons to determi

185 re prepared following stress, and whole-cell patch clamp recordings of inhibitory postsynaptic curren

186 Patch clamp recordings of isolated rat vagal neurons sho

187 quantitative PCR (q-PCR), immunostaining and patch clamp recordings of membrane current and voltage,

188 Whole-cell patch clamp recordings of spontaneous miniature postsyna

189 In whole-cell patch clamp recordings of transfected HEK293T cells, cha

190 used high-throughput calcium-flux assays and patch clamp recordings of transiently transfected HEK-29

191 Here, in vivo whole-cell patch-clamp recording of excitatory neurons revealed var

192 Applying whole-cell patch-clamp recording of HEK cells, we found that wild-t

193 Here, we used in situ patch-clamp recording of myenteric neurons from mice to

194 spite an age-dependent dendritic spine loss, patch-clamp recording of synaptic activity revealed an i

195 We used in vivo patch-clamp recordings of binaural neurons in the Mongol

196 Here, through patch-clamp recordings of channel population ensembles a

197 METHODS AND Patch-clamp recordings of cultured neonatal rat ventricu

198 microcircuit was investigated with targeted patch-clamp recordings of DA amacrine cells in TH-RFP mi

199 Using whole-cell patch-clamp recordings of EPSCs in nucleus accumbens, we

200 Patch-clamp recordings of excitatory and inhibitory curr

201 spinal cord, allowing visualized whole cell patch-clamp recordings of fluorescent lumbar MN cell bod

202 Patch-clamp recordings of Ih currents in cells expressin

203 roscopy of the prokaryotic homolog GltPh and patch-clamp recordings of mammalian EAATs to determine h

204 Perforated patch-clamp recordings of MOPr-mediated activation of G-

205 thalamic afferents combined with whole-cell, patch-clamp recordings of MSNs and electrical stimulatio

206 Here, we obtained dual patch-clamp recordings of neighboring IO neurons from yo

207 We used whole-cell patch-clamp recordings of over 460 neurons to characteri

208 Whole-cell patch-clamp recordings of presynaptic terminals from S21

209 We performed whole-cell patch-clamp recordings of principal neurons in the media

210 Altogether, patch-clamp recordings of single-photon responses in mou

211 Whole-cell patch-clamp recordings of synaptic conductances showed a

212 to underlie these differences using in vitro patch-clamp recordings of synaptic events and multiscale

213 x slices were prepared enabling simultaneous patch-clamp recordings of up to four labeled corticospin

214 Whole-cell patch-clamp recordings of XII motoneurons showed that DN

215 ned with emergent technologies for automatic patch-clamp recordings, permits automated, in vitro high

216 s (bright-field microscopy with simultaneous patch-clamp recording, phase contrast microscopy, and tr

217 Using patch-clamp recording, real-time PCR, Western blotting,

218 Patch-clamp recordings reveal that exposed MOR23 neurons

219 Patch clamp recordings revealed facilitated opening of C

220 Clomeleon imaging and patch clamp recordings revealed that inhibition of NKCC1

221 Outside-out patch clamp recordings revealed that the maximum Na(+) c

222 Ca(2)(+) imaging and patch-clamp recording revealed cell-wide propagating SCW

223 Whole-cell patch-clamp recordings revealed increased excitatory and

224 Patch-clamp recordings revealed increased inhibitory syn

225 Patch-clamp recordings revealed that 72% of the thoracic

226 Patch-clamp recordings revealed that anatomical rewiring

227 xpress NPY Y1 receptor immunoreactivity, and patch-clamp recordings revealed that both NPY and alpha-

228 Whole-cell patch-clamp recordings revealed that DEX (1-10 microM) r

229 ect measurement of I(KA) using cell-attached patch-clamp recordings revealed that there was significa

230 Here, we use a combination of paired patch-clamp recordings, serial EM, and large-scale multi

231 opathic pain, in vivo two-photon imaging and patch clamp recording showed initial loss and subsequent

232 Whole cell patch clamp recordings showed that CRF increased inhibit

233 Perforated patch clamp recordings showed that noradrenalin changes

234 Consistent with this observation, in vitro patch clamp recordings showed that reducing postsynaptic

235 Ca(2+) imaging and patch-clamp recordings showed that although the platelet

236 hat combines whole-cell electrophysiological patch-clamp recordings, single-cell RNA-sequencing and m

237 sted, stable, simultaneous quadruple-viguple patch-clamp recording system.

238 s these questions, we developed a perforated patch-clamp recording technique and recorded from single

239 HEK293 cells, and studied p7 channels using patch-clamp recording techniques.

240 Here we provide evidence from whole-cell patch-clamp recording that dynorphin-A (Dyn-A) directly

241 LHb from the SCN, we show through whole-cell patch-clamp recordings that LHb neurones exhibit heterog

242 Here we demonstrate, using in vivo patch-clamp recordings, that four medulla neurons implem

243 Using patch-clamp recordings, this study measures dendritic pr

244 In this work, we used dual whole cell patch clamp recording to examine the functional effects

245 We have used patch clamp recording to identify high affinity Cd(2+) b

246 We used whole-cell patch clamp recording to investigate the effect of chron

247 We then used patch clamp recording to monitor PNU potentiation of sin

248 Here, we use paired patch clamp recording to study neuromuscular transmissio

249 e of the following procedures: 1) whole-cell patch clamp recordings to characterize AMPAR transmissio

250 Here the authors use patch clamp recordings to show that selective tuning of

251 Here, we used patch-clamp recording to measure NMDAR-mediated currents

252 In this study, we use 2-photon-guided patch-clamp recordings to characterize responses of vesi

253 logical manipulations and ex vivo whole-cell patch-clamp recordings to dissect the local circuit mech

254 retrograde labeling and in vitro whole-cell patch-clamp recordings to examine the effect of trace fe

255 re, we exploited the high time resolution of patch-clamp recordings to examine the effects of Zn(2+)

256 performed paired motor neuron target muscle patch-clamp recordings to investigate the mechanisms cau

257 We used dendritic patch-clamp recordings to measure dendritic excitability

258 We used site-directed mutagenesis and patch-clamp recordings to probe the ion channel extracel

259 Here, we use in vivo patch-clamp recordings to show that locomotion can be di

260 tion in muscle afferents, we used whole-cell patch-clamp recordings to study the properties of acid-e

261 ws simultaneous presynaptic and postsynaptic patch-clamp recording, to show that the postsynaptic res

262 Here, we performed patch-clamp recordings, together with pharmacological an

263 Using paired whole-cell patch-clamp recordings, trains of action potentials at 1

264 terize SbC-RGCs in mice, and target them for patch-clamp recordings under two-photon guidance.

265 Patch-clamp recording was used to analyze glutamatergic

266 , computational fluid dynamics modeling, and patch clamp recording, we discovered that OSNs situated

267 Using 2-photon Ca(2+) imaging and patch clamp recordings, we demonstrate that dantrolene t

268 Using in vivo whole-cell patch clamp recordings, we found that many glutamatergic

269 Lastly, using gramicidin-perforated patch clamp recordings, we found that the GluK2-mediated

270 Using confocal microscopy and patch clamp recordings, we investigated the relevance of

271 olution flow cytometry assays and whole-cell patch clamp recordings, we revealed that the surface den

272 Here, using whole-cell patch-clamp recordings, we assessed whether cocaine self

273 Using dual patch-clamp recordings, we find that ON and OFF RGCs rec

274 With multiple patch-clamp recordings, we found that CeL neurons made c

275 fic transgenic mouse lines, optogenetics and patch-clamp recordings, we found that dentate gyrus cell

276 Using whole-cell patch-clamp recordings, we found that Tg2576 DG granule

277 Using whole-cell patch-clamp recordings, we observed a K(+) conductance m

278 Here, using in vitro whole-cell patch-clamp recordings, we show that 5-HT hyperpolarizes

279 Using in situ hybridization and patch-clamp recordings, we show that D1 receptors are al

280 Using perforated patch-clamp recordings, we show that developing IHCs fir

281 Using paired patch-clamp recordings, we show that excitatory projecti

282 Using a combination of somatic and dendritic patch-clamp recordings, we show that the threshold for L

283 Patch clamp recordings were made from bulbospinal RVLM n

284 Whole cell patch clamp recordings were made from gastric-projecting

285 Whole-cell patch clamp recordings were used to compare the electrop

286 -gated Ca(2+) channel currents determined by patch-clamp recording were greater in neurons on stiff s

287 r in male lean and db/db mice and whole-cell patch-clamp recordings were conducted.

288 Whole-cell patch-clamp recordings were made from layer V pyramidal

289 Whole-cell patch-clamp recordings were made from rat dorsal motor n

290 Whole-cell patch-clamp recordings were obtained from retrobead-labe

291 After >40 days of withdrawal, whole-cell patch-clamp recordings were performed in NAc core medium

292 Whole cell patch-clamp recordings were performed on isolated naive

293 First, whole-cell patch-clamp recordings were performed on prepubertal mal

294 Whole-cell patch-clamp recordings were performed to examine the eff

295 a platform for automated two-photon targeted patch-clamp recording, which solves this problem by maki

296 o calculate ion concentration changes during patch-clamp recordings, which validated our experimental

297 Combining patch clamp recording with measurement of PLS, we show t

298 he core nucleus accumbens (NAc) by combining patch-clamp recordings with calcium imaging and optogene

299 We used in vitro whole-cell patch-clamp recordings with laser-scanning photostimulat

300 medial nucleus of the thalamus by combining patch-clamp recordings with two-photon fluorescence micr