1 urons that synthesize POMC, as determined by
whole cell recording.
2 stably transfected in HEK293 cells, by using
whole-cell recording.
3 stably transfected in HEK293 cells, by using
whole-cell recording.
4 these cells with conventional and perforated
whole-cell recording.
5 ve K(+) current measured under conditions of
whole-cell recording.
6 hClCa1 in HEK293 and NCIH522 cell lines and
whole cell recordings.
7 iability, yield and quality of freely moving
whole-cell recordings.
8 ry, retrograde tracing, calcium imaging, and
whole-cell recordings.
9 RAC) activity was assessed from conventional
whole-cell recordings.
10 activity were determined by perforated patch
whole-cell recordings.
11 in the frontal azimuthal plane with in vivo
whole-cell recordings.
12 reases NMDA receptor currents in patch-clamp
whole-cell recordings.
13 gonists, we performed simultaneous field and
whole-cell recordings.
14 s observed by PS in dialyzed (nonperforated)
whole-cell recordings.
15 with recent experimental data obtained using
whole-cell recordings.
16 ulnerable and resilient rats, using in vitro
whole-cell recordings.
17 To this end, we performed
whole-cell recording and biocytin labeling of PrS neuron
18 Using
whole-cell recording and calcium imaging in rat slices,
19 Using
whole-cell recording and cerebellar slices, we found tha
20 To answer these questions, we use in vitro
whole-cell recording and dynamic-clamp somatic current i
21 Using
whole-cell recording and immunostaining, heteromeric cha
22 Here we use in vivo
whole-cell recording and two-photon Ca(2+) imaging in aw
23 uced into neocortical pyramidal cells during
whole-cell recording and, using a combination of experim
24 Furthermore,
whole-cell recordings and biochemical experiments reveal
25 In vitro
whole-cell recordings and biocytin staining demonstrated
26 We investigated this idea using multisite,
whole-cell recordings and Ca2+ imaging and found that pr
27 o have resonant properties and, based on our
whole-cell recordings and computational modeling, that a
28 Using
whole-cell recordings and direct measures of postsynapti
29 Whole-cell recordings and dye filling revealed a nucleus
30 In
whole-cell recordings and inside-out patches, H(2)O(2) o
31 Here, we used paired
whole-cell recordings and optogenetic approaches in mous
32 vitro ischaemia, using pre- and postsynaptic
whole-cell recordings and presynaptic Ca(2+) imaging at
33 pal CA1 region of murine brain slices, using
whole-cell recordings and single-cell Ca(2+) imaging.
34 Using
whole-cell recordings and two-photon microscopy, we show
35 Channel function was determined by
whole cell recordings,
and subunits trafficking and cell
36 We then used two-photon glutamate uncaging,
whole-cell recording,
and Ca(2+) imaging to analyze the
37 ous activity patterns using calcium imaging,
whole-cell recording,
and multielectrode array recording
38 Amphetamine self-administration,
whole-cell recordings,
and electron microscopy were perf
39 Using homologous binding and
whole-cell recording assays, we found that an RNA aptame
40 range nearly identical to the I(h) found in
whole-cell recordings before hearing onset.
41 or no effect when applied intracellularly in
whole-cell recording,
but blocks effectively and rapidly
42 ory bulb of adult zebrafish by pharmacology,
whole-cell recordings,
calcium imaging, and optogenetics
43 ddress this issue, we used single and paired
whole-cell recordings combined with stimulation of corti
44 Using simultaneous multi-site
whole-cell recordings complemented by computational mode
45 Third, in vitro
whole-cell recordings demonstrate that 50% (18/36) of OV
46 In vitro
whole-cell recordings demonstrate the majority of OVLT n
47 Immunolocalization and
whole-cell recordings demonstrated that Cftr and the epi
48 Using nTS as a model,
whole-cell recordings demonstrated that increased Fos ex
49 Whole-cell recordings demonstrated that neurons with dem
50 Paired
whole-cell recordings detected unitary GABA(A)ergic syna
51 t silencing of STN neurons as measured using
whole-cell recording ex vivo.
52 Simultaneous paired
whole cell recordings from amphibian cones and horizonta
53 t responses of cones and by obtaining paired
whole cell recordings from cones and HCs in salamander r
54 he photoresponses of all five cell types, by
whole-cell recording from fluorescently labelled ipRGCs
55 By combining
whole-cell recording from identified L6 principal cells
56 We combined
whole-cell recording from individual thalamocortical neu
57 that were exposed to cocaine in utero, using
whole-cell recording from mPFC layer V pyramidal neurons
58 ighly synchronized activity as assessed with
whole-cell recording from pairs of mitral cells.
59 To test this idea, we performed in vivo
whole-cell recordings from antennal lobe neurons misexpr
60 ned the cellular basis for this rescue using
whole-cell recordings from CA1 hippocampal pyramidal cel
61 Using
whole-cell recordings from CA1 pyramidal cells and field
62 Here, we made
whole-cell recordings from calyceal terminals in newborn
63 Simultaneous
whole-cell recordings from characterized neurones establ
64 We investigated adaptation during in vitro
whole-cell recordings from chick nucleus magnocellularis
65 Simultaneous multiple
whole-cell recordings from connected fast-spiking intern
66 We examined this possibility using
whole-cell recordings from cultured embryonic mouse hipp
67 Using targeted
whole-cell recordings from direct- and indirect-pathway
68 tivated rhodopsin (metarhodopsin = M( *)) in
whole-cell recordings from Drosophila photoreceptors by
69 Here, we report the first
whole-cell recordings from duration-selective neurons in
70 Using in vivo targeted
whole-cell recordings from excitatory and inhibitory neu
71 We obtained
whole-cell recordings from excitatory neurons and somato
72 We used
whole-cell recordings from granule cells in acute slices
73 Whole-cell recordings from HEK293 cells showed the mutat
74 We conducted
whole-cell recordings from HEK293 cells transiently tran
75 During
whole-cell recordings from hippocampal and neocortical s
76 ith combined 2-photon time-lapse imaging and
whole-cell recordings from hippocampal neurons, we find
77 tergic transmission in the hippocampus using
whole-cell recordings from hippocampal slices.
78 Whole-cell recordings from identified cell types, facili
79 We conducted our experiments using
whole-cell recordings from identified gastric-projecting
80 Whole-cell recordings from identified layer 1 interneuro
81 t methods were involved in our approach: (i)
whole-cell recordings from identified retinal ganglion c
82 Here we present the results of dual
whole-cell recordings from identified, synaptically conn
83 We used
whole-cell recordings from Im neurons in acute slices of
84 tance changes: DeltaC(m)) were measured with
whole-cell recordings from immature gerbil hair cells us
85 populations of retinal neurons and by making
whole-cell recordings from individual AIIs and alpha-RGC
86 In
whole-cell recordings from L2/3 neurons in vivo, brief d
87 cerebellar activity during learning, we made
whole-cell recordings from larval zebrafish Purkinje cel
88 We performed
whole-cell recordings from layer 2/3 and layer 4 visual
89 By performing two-photon guided
whole-cell recordings from layer 2/3 excitatory and inhi
90 In this study, we performed in vivo
whole-cell recordings from layer 5 (L5) pyramidal neuron
91 Whole-cell recordings from layer V medial PFC pyramidal
92 In this study we used simultaneous
whole-cell recordings from mitral cell pairs to show tha
93 Whole-cell recordings from mPFC layer V pyramidal neuron
94 the dendrites, we made dendritic and somatic
whole-cell recordings from MSO principal neurons in brai
95 By performing
whole-cell recordings from multiple cell types identifie
96 We hypothesize that D1 inhibition in
whole-cell recordings from neonatal rats may be mediated
97 We performed multiple
whole-cell recordings from neurons in layer 5 (L5) of th
98 Here, in vivo
whole-cell recordings from neurons in the rat primary au
99 Here, we performed
whole-cell recordings from neurons in upper-layer primar
100 Simultaneous
whole-cell recordings from pairs of cells show that the
101 Whole-cell recordings from principal cells of rat cortic
102 Here, we performed in vivo
whole-cell recordings from pyramidal neurons in the rat
103 We made
whole-cell recordings from RA and HVC neurons in acute b
104 Here, in vivo
whole-cell recordings from rat auditory cortical neurons
105 We made
whole-cell recordings from rat locus coeruleus and prima
106 Using a combination of
whole-cell recordings from rat neocortical neurons and c
107 dy used the combination of intracellular and
whole-cell recordings from rats and mice, as well as liv
108 We made paired
whole-cell recordings from rod bipolar (RB) and AII amac
109 Whole-cell recordings from rod bipolar cells showed, bot
110 Whole-cell recordings from SRKO retinal ganglion cells s
111 ribute to this imbalance, we obtained paired
whole-cell recordings from striatal direct- and indirect
112 Using triple and dual
whole-cell recordings from synaptically connected human
113 o address this question, we performed paired
whole-cell recordings from synaptically coupled nRT and
114 In
whole-cell recordings from targets of auditory nerve fib
115 Whole-cell recordings from the CA1 neurons showed that D
116 otentials) and outputs (spikes) with in vivo
whole-cell recordings from the IC of awake Mexican free-
117 ated FM directional selectivity with in vivo
whole-cell recordings from the inferior colliculus of aw
118 Using dual
whole-cell recordings from the IO of young adult rhesus
119 Dual
whole-cell recordings from the soma and distal apical de
120 present work addresses these questions using
whole-cell recordings from the spiral process of type II
121 (Tadarida brasilensis mexicana) with in vivo
whole-cell recordings from which we derived excitatory a
122 Whole-cell recordings further revealed that the silencin
123 Whole-cell recordings further showed that synaptically r
124 In
whole-cell recordings,
G2019S SPNs exhibited a fourfold
125 Recent in vivo
whole-cell recordings have revealed how sensory stimuli
126 Using in vivo
whole-cell recordings,
I show (1) that a subset of GCs i
127 In
whole-cell recordings,
IgG-IC induced a nonselective cat
128 We combined
whole cell recording in an in vitro slice preparation wi
129 ecorded postsynaptic currents using in vitro
whole cell recordings in acute slices and measured cysti
130 Using
whole cell recordings in coronal hypothalamic slices fro
131 fy the conductance activated by leptin using
whole-cell recording in EGFP-POMC neurons from transgeni
132 Using
whole-cell recording in ex vivo brain slices from cocain
133 VMH) glutamatergic neurons was studied using
whole-cell recording in hypothalamic slices from a novel
134 ulvinar nucleus relay neurons using in vitro
whole-cell recording in juvenile and adult tree shrew (T
135 ory cortex using variance analysis of paired
whole-cell recording in olfactory cortex slices.
136 RNA sequencing, ultrastructural imaging, and
whole-cell recording in wild-type mice suggest that cont
137 g its postsynaptic neuron, we performed dual
whole-cell recordings in acute brain slices from rats an
138 Using
whole-cell recordings in acute cortical slices, we inves
139 and identify postsynaptic target neurons by
whole-cell recordings in acute slices.
140 Using voltage-clamp
whole-cell recordings in acute thalamocortical brain sli
141 We used simultaneous targeted
whole-cell recordings in an active slice preparation and
142 Whole-cell recordings in BDNF mutant VMH neurons reveale
143 o-photon calcium imaging in combination with
whole-cell recordings in both unanesthetized and anesthe
144 Using optogenetics and
whole-cell recordings in brain slices, we find that a la
145 Using
whole-cell recordings in brain slices, we found that dyn
146 Using
whole-cell recordings in brain slices, we identified a t
147 Whole-cell recordings in cortical slices from NrCAM-null
148 Whole-cell recordings in freely moving animals can be ob
149 nces between place and silent cells by using
whole-cell recordings in freely moving rats.
150 Whole-cell recordings in intact and hemisected spinal co
151 ac effects of Rgs6 ablation were analyzed by
whole-cell recordings in isolated cardiomyocytes and ECG
152 Whole-cell recordings in L2/3 of awake mice revealed tha
153 smission in the rat PL were determined using
whole-cell recordings in layer V pyramidal neurons.
154 Using a combination of optogenetics and
whole-cell recordings in mice, we now provide physiologi
155 We used dual
whole-cell recordings in mouse brain slices to study the
156 sured using fast-scan cyclic voltammetry and
whole-cell recordings in mouse brain slices.
157 ivity and spike synchrony, we performed dual
whole-cell recordings in mouse entorhinal cortical slice
158 Here,
whole-cell recordings in mouse retina showed that cholin
159 Using
whole-cell recordings in parasagittal rat brain slices t
160 ection of rat hippocampal slice cultures and
whole-cell recordings in pyramidal neurons.
161 Here, we show, using
whole-cell recordings in rat hippocampal slices, that gr
162 Using dendritic and somatic
whole-cell recordings in rat hippocampal slices, we meas
163 We therefore used
whole-cell recordings in rat midbrain slices to investig
164 synaptic inputs to dorsal horn neurons using
whole-cell recordings in rat spinal cord slices.
165 Using in vivo
whole-cell recordings in rat visual cortex, we show that
166 Whole-cell recordings in rhythmically active newborn mou
167 Here, using paired
whole-cell recordings in rodent hippocampal slices, we r
168 ing mice and concomitant field potential and
whole-cell recordings in slice preparations we found tha
169 Here, we used
whole-cell recordings in slices from bacterial artificia
170 Whole-cell recordings in slices from delta-subunit knock
171 ifferences were observed with PV or GAD(67),
whole-cell recordings in slices revealed abnormal respon
172 Whole-cell recordings in striatal slices demonstrated th
173 In vivo
whole-cell recordings in the hypothalamus confirmed near
174 Here, in vivo
whole-cell recordings in the mouse V1 revealed that simp
175 imulation of two sites along each branch and
whole-cell recordings in the parent neurons.
176 TRPV2 desensitization was not altered in
whole-cell recordings in the presence of calmodulin inhi
177 Whole-cell recordings in vitro showed that AIA enhanced
178 Whole-cell recordings in vitro showed that both MRGPRA3+
179 Here, we used cell-attached and
whole-cell recordings in vitro to study activity of pyra
180 ween V1 L2/3 neurons assayed by simultaneous
whole-cell recordings in vitro to their response propert
181 to glycinergic afferents in the ICC and made
whole-cell recordings in vitro while exciting glycinergi
182 -photon calcium imaging in vivo and multiple
whole-cell recordings in vitro.
183 ergic neurons using immunohistochemistry and
whole-cell recordings in vitro.
184 c basis for orientation selectivity, we made
whole-cell recordings in vivo from mouse V1 neurons, com
185 synaptic integration across species, we made
whole-cell recordings in vivo from the murine LGN during
186 e membrane potential responses, observed via
whole-cell recordings in vivo, of primary visual cortex
187 We examined field EPSPs and
whole-cell recordings in wild-type mouse hippocampal sli
188 By juxtacellular and
whole-cell-recordings in awake mice, we show here that i
189 Using gramicidin-perforated patch
whole cell recordings,
intracellular recordings and spec
190 i ring to step current injection observed in
whole-cell recordings is not a cellular property but a d
191 Omitting VX-809 during
whole-cell recordings led to a spontaneous decline of th
192 Whole-cell recordings made in dopamine neurons revealed
193 l surface biotinylation assays and also with
whole-cell recordings made under conditions designed to
194 Fmr1(-/-) mice than in wild-type mice during
whole-cell recordings manifesting Up/Down states (slow-w
195 lice electrophysiological (intracellular and
whole-cell recordings)
methods to assess whether differe
196 Whole-cell recordings obtained in vivo suggest that this
197 tions of the group II mGluR agonist APDC and
whole cell recordings of excitatory currents in identifi
198 Whole-cell recording of GABA neurons in nigral slices co
199 sis of the subunit nonlinearity by combining
whole-cell recording of mouse Y-type ganglion cells with
200 Here, by
whole-cell recording of synaptic responses in MeCP2 muta
201 on of the action potential, as determined by
whole-cell recordings of action potentials on isolated m
202 In this study, we performed
whole-cell recordings of cultured hippocampal neurons an
203 Targeted
whole-cell recordings of fluorescently labeled VIP+ cell
204 Whole-cell recordings of fluorescently tagged transfecte
205 We used
whole-cell recordings of human embryonic kidney cells he
206 Here, we made
whole-cell recordings of human pyramidal neurons in slic
207 Using
whole-cell recordings of layer V pyramidal neurons in an
208 We made
whole-cell recordings of membrane current in guinea pig
209 Here we addressed this by combining
whole-cell recordings of miniature IPSCs (mIPSCs) and qu
210 atergic synapses during development, we made
whole-cell recordings of NMDAR-mediated responses, in vi
211 Whole-cell recordings of NTS second-order neurons identi
212 Here we find, from
whole-cell recordings of photoreceptors in macaque monke
213 Whole-cell recordings of potassium currents were made fr
214 We performed
whole-cell recordings of pyramidal neurons in the PAM(+/
215 Whole-cell recordings of sperm Slo3 currents or of Slo3
216 Whole-cell recordings of the large ventral lateral neuro
217 Whole-cell recordings of the retrogradely labeled pTRG n
218 Using
whole-cell recording on a large number of neurons (n = 4
219 ctions between the mouse mPFC and BLA, using
whole-cell recordings,
optogenetics, and two-photon micr
220 eir lack of effect with internal dialysis in
whole-cell recording reflects rapid exit through membran
221 Whole-cell recordings reveal EPSCs following stimulation
222 In young Xenopus tadpoles, paired
whole-cell recordings reveal reticulospinal neurons that
223 In vivo
whole-cell recordings reveal that nearly every action po
224 Second, simultaneous outside-out patch and
whole-cell recordings reveal that retinal waves are acco
225 In vivo
whole-cell recordings reveal that the binocular integrat
226 Whole cell recordings revealed that the isoflurane-activ
227 Whole-cell recording revealed enhanced electrophysiologi
228 Whole-cell recording revealed that hippocampal pyramidal
229 AD-transgenic mice compared with wild type,
whole-cell recordings revealed excessive tonic eNMDAR ac
230 Confirming our previous results,
whole-cell recordings revealed inwardly rectifying AMPAR
231 Whole-cell recordings revealed synaptic currents that de
232 Cell-attached and
whole-cell recordings revealed that excitatory neuron fi
233 In vitro
whole-cell recordings revealed that specific optogenetic
234 Whole-cell recordings revealed that striatal inputs to t
235 Electrophysiological
whole-cell recordings revealed that the block was mostly
236 Whole-cell recordings revealed the presence of miniature
237 Whole cell recording showed that blue light (470 nm) eli
238 Whole-cell recordings showed that excitatory inputs were
239 Whole-cell recordings showed that fast EPSCs typically p
240 In fact, two-photon targeted, dual
whole-cell recordings showed that principal whisker stim
241 Paired
whole-cell recordings showed that tINs produce small ( a
242 orsal raphe nucleus (DRN) were examined with
whole-cell recording,
somatodendritic three-dimensional
243 Combining knock-out mice,
whole-cell recordings,
spine analysis, and translation p
244 dies employing fluorescence spectroscopy and
whole cell recording suggest that agonist binding is fol
245 In vivo
whole cell recordings suggest that feedforward inhibitio
246 ocytosis, we used the compensated tight-seal
whole-cell recording technique to monitor depolarization
247 Using
whole cell recording techniques in in vitro thalamic sli
248 We tested this hypothesis using
whole-cell recording techniques in genetically identifie
249 Using
whole-cell recording techniques in rat brain slices, we
250 Using
whole-cell recording techniques, we investigated the eff
251 alcium imaging, ex vivo calcium imaging, and
whole-cell recordings that this pairing-induced potentia
252 d that neurons remained intact after 'blind'
whole-cell recording,
that DNA vectors could be delivere
253 ing immunohistochemistry, tract tracing, and
whole-cell recordings,
that homologs of the SNr and PPN
254 By
whole cell recording,
these fusions are fully functional
255 ted possible retinal mechanisms using paired
whole cell recordings to examine effects of these compou
256 ning photostimulation of caged glutamate and
whole cell recordings to map excitatory and inhibitory s
257 microscopy with glutamate photo-uncaging and
whole-cell recording to examine synaptic strength at ind
258 hoton laser scanning microscopy coupled with
whole-cell recordings to examine calcium dynamics in the
259 We used
whole-cell recordings to investigate how SP affects MSNs
260 We performed dual dendritic and somatic
whole-cell recordings to measure spontaneous EPSPs using
261 We used in vivo
whole-cell recordings to measure the synaptic inhibition
262 lycemia-induced changes in cytosolic ROS and
whole-cell recordings to measure the use-dependent rundo
263 We used
whole-cell recordings to show that pharmacological inhib
264 to adult mice of either sex a combination of
whole-cell recording,
two-photon microscopy, and spine m
265 sound-evoked responses in the mouse ACx and
whole-cell recordings,
two-photon calcium imaging in pre
266 Here we use
whole-cell recordings,
two-photon microscopy, GABA uncag
267 Here we used
whole-cell recordings,
two-photon microscopy, optogeneti
268 Using
whole-cell recording,
we examined the spontaneous, subth
269 er-pulse photolysis technique, combined with
whole-cell recording,
we measured the rate of channel op
270 e dBest1 activates slowly after establishing
whole-cell recording,
we tested the hypothesis that the
271 From the
whole-cell recordings,
we derived synaptic conductance w
272 Using in vivo
whole-cell recordings,
we examine the mechanisms underly
273 Using blind
whole-cell recordings,
we found 33% of M/TCs to be 'sile
274 Here, by combining in vivo loose-patch and
whole-cell recordings,
we found that complex cells, iden
275 Using
whole-cell recordings,
we found that preGlyRs facilitate
276 quadruple-octuple in vitro and dual in vivo
whole-cell recordings,
we found two previously unknown i
277 From
whole-cell recordings,
we identified three subthreshold
278 Using in vivo and in vitro
whole-cell recordings,
we identify the underlying mechan
279 Using paired
whole-cell recordings,
we measured the behaviour of the
280 Using paired
whole-cell recordings,
we show that activation of Group
281 Using in vivo
whole-cell recordings,
we show that the timing of an LN'
282 Here, using in vivo
whole-cell recordings,
we tested these models by directl
283 Whole cell recordings were used to examine effects of vo
284 Whole-cell recordings were collected from medium spiny n
285 Whole-cell recordings were conducted in male offspring b
286 Whole-cell recordings were made from GFP (Renilla)-tagge
287 Intracellular and
whole-cell recordings were made from locus ceruleus neur
288 Here,
whole-cell recordings were made from proopiomelanocortin
289 protein expression in GABAergic neurons and
whole-cell recordings were made from these fluorescent n
290 In the present study,
whole-cell recordings were made in POMC cells in mouse b
291 Whole-cell recordings were made of GnRH neurons in brain
292 Whole-cell recordings were obtained from tyrosine hydrox
293 Whole-cell recordings were performed on slices of the ra
294 Whole-cell recordings were performed to measure intrinsi
295 Multiple-electrode
whole-cell recordings were performed to probe synapse fo
296 In the present study, we combined
whole cell recordings with laser scanning photostimulati
297 dynamics of place cells by combining in vivo
whole-cell recordings with a virtual-reality system.
298 By combining octuple
whole-cell recordings with an optimized avidin-biotin-pe
299 In this study we combined multineuron
whole-cell recordings with optogenetics to determine the
300 Whole-cell recordings yielded results similar to patches