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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

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