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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  (LTCC) current (I(Ca,L)) was measured using whole-cell recording.
6 with recent experimental data obtained using whole-cell recordings.
7 ulnerable and resilient rats, using in vitro whole-cell recordings.
8 iability, yield and quality of freely moving whole-cell recordings.
9 ry, retrograde tracing, calcium imaging, and whole-cell recordings.
10 RAC) activity was assessed from conventional whole-cell recordings.
11 activity were determined by perforated patch whole-cell recordings.
12 rated whole-cell desensitization observed in 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                    To this end, we performed whole-cell recording and biocytin labeling of PrS neuron
16                                        Using whole-cell recording and calcium imaging in rat slices,
17                                        Using whole-cell recording and cerebellar slices, we found tha
18   To answer these questions, we use in vitro whole-cell recording and dynamic-clamp somatic current i
19                         By combining in vivo whole-cell recording and pharmacological silencing of co
20                          Here we use in vivo whole-cell recording and two-photon Ca(2+) imaging in aw
21 uced into neocortical pyramidal cells during whole-cell recording and, using a combination of experim
22                                 Furthermore, whole-cell recordings and biochemical experiments reveal
23                                     In vitro whole-cell recordings and biocytin staining demonstrated
24   We investigated this idea using multisite, whole-cell recordings and Ca2+ imaging and found that pr
25 o have resonant properties and, based on our whole-cell recordings and computational modeling, that a
26                                        Using whole-cell recordings and direct measures of postsynapti
27                                              Whole-cell recordings and dye filling revealed a nucleus
28                                           In whole-cell recordings and inside-out patches, H(2)O(2) o
29      To address this, we established in vivo whole-cell recordings and obtained over 100 spontaneousl
30                         Here, we used paired whole-cell recordings and optogenetic approaches in mous
31 vitro ischaemia, using pre- and postsynaptic whole-cell recordings and presynaptic Ca(2+) imaging at
32 pal CA1 region of murine brain slices, using whole-cell recordings and single-cell Ca(2+) imaging.
33                                        Using whole-cell recordings and two-photon microscopy, we show
34           Channel function was determined by whole cell recordings, and subunits trafficking and cell
35  We then used two-photon glutamate uncaging, whole-cell recording, and Ca(2+) imaging to analyze the
36 ous activity patterns using calcium imaging, whole-cell recording, and multielectrode array recording
37             Amphetamine self-administration, whole-cell recordings, and electron microscopy were perf
38 itro; further analysis with genetic markers, whole-cell recordings, and single-cell transcriptomics v
39                                           In whole-cell recordings, application of a high-affinity Y(
40                 Using homologous binding and whole-cell recording assays, we found that an RNA aptame
41  range nearly identical to the I(h) found in whole-cell recordings before hearing onset.
42 or no effect when applied intracellularly in whole-cell recording, but blocks effectively and rapidly
43 ory bulb of adult zebrafish by pharmacology, whole-cell recordings, calcium imaging, and optogenetics
44 ddress this issue, we used single and paired whole-cell recordings combined with stimulation of corti
45                Using simultaneous multi-site whole-cell recordings complemented by computational mode
46                              Third, in vitro whole-cell recordings demonstrate that 50% (18/36) of OV
47                                     In vitro whole-cell recordings demonstrate the majority of OVLT n
48                                              Whole cell recordings demonstrated that elevated CO(2) r
49 onosynaptic tracing and electrophysiological whole-cell recordings demonstrated that DLS somatostatin
50                        Using nTS as a model, whole-cell recordings demonstrated that increased Fos ex
51                                              Whole-cell recordings demonstrated that neurons with dem
52                                     Based on whole-cell recording electrophysiology in brain slices,
53 t silencing of STN neurons as measured using whole-cell recording ex vivo.
54                          Simultaneous paired whole cell recordings from amphibian cones and horizonta
55 t responses of cones and by obtaining paired whole cell recordings from cones and HCs in salamander r
56 he photoresponses of all five cell types, by whole-cell recording from fluorescently labelled ipRGCs
57                                 By combining whole-cell recording from identified L6 principal cells
58                                  We combined whole-cell recording from individual thalamocortical neu
59 ighly synchronized activity as assessed with whole-cell recording from pairs of mitral cells.
60      To test this idea, we performed in vivo whole-cell recordings from antennal lobe neurons misexpr
61 ned the cellular basis for this rescue using whole-cell recordings from CA1 hippocampal pyramidal cel
62                                        Using whole-cell recordings from CA1 pyramidal cells and field
63                                Here, we made whole-cell recordings from calyceal terminals in newborn
64                                 Simultaneous whole-cell recordings from characterized neurones establ
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                       Using in vivo targeted whole-cell recordings from excitatory and inhibitory neu
69                                  We obtained whole-cell recordings from excitatory neurons and somato
70                                              Whole-cell recordings from GoCs revealed a role for the
71                                      We used whole-cell recordings from granule cells in acute slices
72                                              Whole-cell recordings from HEK293 cells showed the mutat
73                                 We conducted whole-cell recordings from HEK293 cells transiently tran
74                                       During whole-cell recordings from hippocampal and neocortical s
75 tergic transmission in the hippocampus using whole-cell recordings from hippocampal slices.
76           We conducted our experiments using whole-cell recordings from identified gastric-projecting
77                                              Whole-cell recordings from identified layer 1 interneuro
78 t methods were involved in our approach: (i) whole-cell recordings from identified retinal ganglion c
79          Here we present the results of dual whole-cell recordings from identified, synaptically conn
80                                      We used whole-cell recordings from Im neurons in acute slices of
81 tance changes: DeltaC(m)) were measured with whole-cell recordings from immature gerbil hair cells us
82 populations of retinal neurons and by making whole-cell recordings from individual AIIs and alpha-RGC
83                                           In whole-cell recordings from L2/3 neurons in vivo, brief d
84 cerebellar activity during learning, we made whole-cell recordings from larval zebrafish Purkinje cel
85                                 We performed whole-cell recordings from layer 2/3 and layer 4 visual
86              By performing two-photon guided whole-cell recordings from layer 2/3 excitatory and inhi
87          In this study, we performed in vivo whole-cell recordings from layer 5 (L5) pyramidal neuron
88                                              Whole-cell recordings from layer V medial PFC pyramidal
89                                              Whole-cell recordings from locus coeruleus neurons were
90 wing action potentials (APs), as measured in whole-cell recordings from male mice running in virtual
91                                              Whole-cell recordings from mPFC layer V pyramidal neuron
92 the dendrites, we made dendritic and somatic whole-cell recordings from MSO principal neurons in brai
93                                By performing whole-cell recordings from multiple cell types identifie
94                        We performed multiple whole-cell recordings from neurons in layer 5 (L5) of th
95                           Here, we performed whole-cell recordings from neurons in upper-layer primar
96                                 Simultaneous whole-cell recordings from pairs of cells show that the
97                                              Whole-cell recordings from principal cells of rat cortic
98                   Here, we performed in vivo whole-cell recordings from pyramidal neurons in the rat
99                                Here, in vivo whole-cell recordings from rat auditory cortical neurons
100                                      We made whole-cell recordings from rat locus coeruleus and prima
101                       Using a combination of whole-cell recordings from rat neocortical neurons and c
102 dy used the combination of intracellular and whole-cell recordings from rats and mice, as well as liv
103                               We made paired whole-cell recordings from rod bipolar (RB) and AII amac
104                                              Whole-cell recordings from SOM-INs revealed that both ex
105                                              Whole-cell recordings from SRKO retinal ganglion cells s
106 ribute to this imbalance, we obtained paired whole-cell recordings from striatal direct- and indirect
107                        Using triple and dual whole-cell recordings from synaptically connected human
108 o address this question, we performed paired whole-cell recordings from synaptically coupled nRT and
109                      In contrast, using dual whole-cell recordings from the apical dendrite and soma
110                                              Whole-cell recordings from the CA1 neurons showed that D
111 otentials) and outputs (spikes) with in vivo whole-cell recordings from the IC of awake Mexican free-
112 ated FM directional selectivity with in vivo whole-cell recordings from the inferior colliculus of aw
113                                   Using dual whole-cell recordings from the IO of young adult rhesus
114                                         Dual whole-cell recordings from the soma and distal apical de
115 present work addresses these questions using whole-cell recordings from the spiral process of type II
116 naptic inputs and intrinsic properties using whole-cell recordings from V1 neurons of awake, fixating
117 (Tadarida brasilensis mexicana) with in vivo whole-cell recordings from which we derived excitatory a
118                                              Whole-cell recordings further revealed that the silencin
119                                              Whole-cell recordings further showed that synaptically r
120                                           In whole-cell recordings, G2019S SPNs exhibited a fourfold
121                                Using in vivo whole-cell recordings, I show (1) that a subset of GCs i
122                                           In whole-cell recordings, IgG-IC induced a nonselective cat
123 ecorded postsynaptic currents using in vitro whole cell recordings in acute slices and measured cysti
124                                        Using whole cell recordings in coronal hypothalamic slices fro
125 fy the conductance activated by leptin using whole-cell recording in EGFP-POMC neurons from transgeni
126                                        Using whole-cell recording in ex vivo brain slices from cocain
127 ulvinar nucleus relay neurons using in vitro whole-cell recording in juvenile and adult tree shrew (T
128 ory cortex using variance analysis of paired whole-cell recording in olfactory cortex slices.
129 RNA sequencing, ultrastructural imaging, and whole-cell recording in wild-type mice suggest that cont
130 g its postsynaptic neuron, we performed dual whole-cell recordings in acute brain slices from rats an
131                                        Using whole-cell recordings in acute cortical slices, we inves
132                          Using voltage-clamp whole-cell recordings in acute thalamocortical brain sli
133                We used simultaneous targeted whole-cell recordings in an active slice preparation and
134                                              Whole-cell recordings in basolateral amygdala (BLA) slic
135                                              Whole-cell recordings in BDNF mutant VMH neurons reveale
136                                              Whole-cell recordings in BLA pyramidal neurons revealed
137                       Using optogenetics and whole-cell recordings in brain slices, we find that a la
138                                        Using whole-cell recordings in brain slices, we found that dyn
139                                        Using whole-cell recordings in brain slices, we identified a t
140                                              Whole-cell recordings in cortical slices from NrCAM-null
141                                              Whole-cell recordings in freely moving animals can be ob
142 nces between place and silent cells by using whole-cell recordings in freely moving rats.
143                                              Whole-cell recordings in intact and hemisected spinal co
144 ac effects of Rgs6 ablation were analyzed by whole-cell recordings in isolated cardiomyocytes and ECG
145                                              Whole-cell recordings in L2/3 of awake mice revealed tha
146 smission in the rat PL were determined using whole-cell recordings in layer V pyramidal neurons.
147      Using a combination of optogenetics and whole-cell recordings in mice, we now provide physiologi
148                                 We used dual whole-cell recordings in mouse brain slices to study the
149 sured using fast-scan cyclic voltammetry and whole-cell recordings in mouse brain slices.
150 ivity and spike synchrony, we performed dual whole-cell recordings in mouse entorhinal cortical slice
151                                        Here, whole-cell recordings in mouse retina showed that cholin
152 putations underlying predictive coding using whole-cell recordings in mouse visual cortex.
153                                        Using whole-cell recordings in parasagittal rat brain slices t
154 ection of rat hippocampal slice cultures and whole-cell recordings in pyramidal neurons.
155                         Here, we show, using whole-cell recordings in rat hippocampal slices, that gr
156                            We therefore used whole-cell recordings in rat midbrain slices to investig
157 synaptic inputs to dorsal horn neurons using whole-cell recordings in rat spinal cord slices.
158                                              Whole-cell recordings in rhythmically active newborn mou
159                           Here, using paired whole-cell recordings in rodent hippocampal slices, we r
160 ing mice and concomitant field potential and whole-cell recordings in slice preparations we found tha
161                                Here, we used whole-cell recordings in slices from bacterial artificia
162                                              Whole-cell recordings in striatal slices demonstrated th
163                                      In vivo whole-cell recordings in the hypothalamus confirmed near
164                            We employ in vivo whole-cell recordings in the mouse primary auditory cort
165                                Here, in vivo whole-cell recordings in the mouse V1 revealed that simp
166 imulation of two sites along each branch and whole-cell recordings in the parent neurons.
167     TRPV2 desensitization was not altered in whole-cell recordings in the presence of calmodulin inhi
168                                              Whole-cell recordings in vitro showed that AIA enhanced
169                                              Whole-cell recordings in vitro showed that both MRGPRA3+
170              Here, we used cell-attached and whole-cell recordings in vitro to study activity of pyra
171 ween V1 L2/3 neurons assayed by simultaneous whole-cell recordings in vitro to their response propert
172 to glycinergic afferents in the ICC and made whole-cell recordings in vitro while exciting glycinergi
173 ergic neurons using immunohistochemistry and whole-cell recordings in vitro.
174 -photon calcium imaging in vivo and multiple whole-cell recordings in vitro.
175 c basis for orientation selectivity, we made whole-cell recordings in vivo from mouse V1 neurons, com
176 synaptic integration across species, we made whole-cell recordings in vivo from the murine LGN during
177 e membrane potential responses, observed via whole-cell recordings in vivo, of primary visual cortex
178                  We examined field EPSPs and whole-cell recordings in wild-type mouse hippocampal sli
179                         By juxtacellular and whole-cell-recordings in awake mice, we show here that i
180            Using gramicidin-perforated patch whole cell recordings, intracellular recordings and spec
181 i ring to step current injection observed in whole-cell recordings is not a cellular property but a d
182                       Omitting VX-809 during whole-cell recordings led to a spontaneous decline of th
183                                              Whole-cell recordings made in dopamine neurons revealed
184 l surface biotinylation assays and also with whole-cell recordings made under conditions designed to
185 Fmr1(-/-) mice than in wild-type mice during whole-cell recordings manifesting Up/Down states (slow-w
186 lice electrophysiological (intracellular and whole-cell recordings) methods to assess whether differe
187                                              Whole-cell recordings obtained in vivo suggest that this
188 tions of the group II mGluR agonist APDC and whole cell recordings of excitatory currents in identifi
189                                              Whole-cell recording of GABA neurons in nigral slices co
190 sis of the subunit nonlinearity by combining whole-cell recording of mouse Y-type ganglion cells with
191                                     Here, by whole-cell recording of synaptic responses in MeCP2 muta
192 on of the action potential, as determined by whole-cell recordings of action potentials on isolated m
193                                              Whole-cell recordings of adjacent newly generated neuron
194                                              Whole-cell recordings of arcuate kisspeptin neurons in b
195                                     Targeted whole-cell recordings of fluorescently labeled VIP+ cell
196                                      We used whole-cell recordings of human embryonic kidney cells he
197                                Here, we made whole-cell recordings of human pyramidal neurons in slic
198                                  Patch-clamp whole-cell recordings of KCNN3 channel-expressing CHO ce
199                                        Using whole-cell recordings of layer V pyramidal neurons in an
200          Here we addressed this by combining whole-cell recordings of miniature IPSCs (mIPSCs) and qu
201 atergic synapses during development, we made whole-cell recordings of NMDAR-mediated responses, in vi
202                                        Using whole-cell recordings of NTS neurons, from horizontal br
203                                              Whole-cell recordings of NTS second-order neurons identi
204 erformed calcium imaging, cell-attached, and whole-cell recordings of PC and PV cells within the CA1
205                                              Whole-cell recordings of PCs from acute cerebellar slice
206                           Here we find, from whole-cell recordings of photoreceptors in macaque monke
207 siological parameters were derived from dual whole-cell recordings of pyramidal cells in organotypic
208                                 We performed whole-cell recordings of pyramidal neurons in the PAM(+/
209                                              Whole-cell recordings of sperm Slo3 currents or of Slo3
210                                 Here we used whole-cell recordings of T5 neurons and found a similar
211                                              Whole-cell recordings of the large ventral lateral neuro
212                                              Whole-cell recordings of the retrogradely labeled pTRG n
213                                        Using whole-cell recording on a large number of neurons (n = 4
214 d Ca(2+) imaging on mice from both sexes and whole-cell recordings on female mouse TIDA neurons in vi
215 ctions between the mouse mPFC and BLA, using whole-cell recordings, optogenetics, and two-photon micr
216                        By combining imaging, whole-cell recording, pharmacology, and anatomical techn
217 llular application of apamin via the somatic whole-cell recording pipette reduced the medium afterhyp
218 eir lack of effect with internal dialysis in whole-cell recording reflects rapid exit through membran
219                                              Whole-cell recordings reveal EPSCs following stimulation
220                                      In vivo whole-cell recordings reveal that mechanisms contributin
221                                      In vivo whole-cell recordings reveal that nearly every action po
222                                      In vivo whole-cell recordings reveal that the binocular integrat
223                                              Whole cell recordings revealed that the isoflurane-activ
224                                              Whole-cell recording revealed enhanced electrophysiologi
225                                              Whole-cell recording revealed that hippocampal pyramidal
226  AD-transgenic mice compared with wild type, whole-cell recordings revealed excessive tonic eNMDAR ac
227             Confirming our previous results, whole-cell recordings revealed inwardly rectifying AMPAR
228                                              Whole-cell recordings revealed synaptic currents that de
229                            Cell-attached and whole-cell recordings revealed that excitatory neuron fi
230                                     In vitro whole-cell recordings revealed that specific optogenetic
231                                              Whole-cell recordings revealed that striatal inputs to t
232                         Electrophysiological whole-cell recordings revealed that the block was mostly
233                                              Whole-cell recordings revealed the presence of miniature
234                                              Whole cell recording showed that blue light (470 nm) eli
235                                              Whole-cell recordings showed that excitatory inputs were
236                                              Whole-cell recordings showed that fast EPSCs typically p
237           In fact, two-photon targeted, dual whole-cell recordings showed that principal whisker stim
238                                              Whole-cell recordings showed that small-diameter Vglut3(
239                                       Paired whole-cell recordings showed that tINs produce small ( a
240 orsal raphe nucleus (DRN) were examined with whole-cell recording, somatodendritic three-dimensional
241                    Combining knock-out mice, whole-cell recordings, spine analysis, and translation p
242 dies employing fluorescence spectroscopy and whole cell recording suggest that agonist binding is fol
243                                      In vivo whole cell recordings suggest that feedforward inhibitio
244 ocytosis, we used the compensated tight-seal whole-cell recording technique to monitor depolarization
245              We tested this hypothesis using whole-cell recording techniques in genetically identifie
246                                        Using whole-cell recording techniques in rat brain slices, we
247                                        Using whole-cell recording techniques, we investigated the eff
248 alcium imaging, ex vivo calcium imaging, and whole-cell recordings that this pairing-induced potentia
249 d that neurons remained intact after 'blind' whole-cell recording, that DNA vectors could be delivere
250 ing immunohistochemistry, tract tracing, and whole-cell recordings, that homologs of the SNr and PPN
251                                          LNv whole-cell recordings then show that changes in Shaw and
252                                           By whole cell recording, these fusions are fully functional
253 ted possible retinal mechanisms using paired whole cell recordings to examine effects of these compou
254 ning photostimulation of caged glutamate and whole cell recordings to map excitatory and inhibitory s
255 microscopy with glutamate photo-uncaging and whole-cell recording to examine synaptic strength at ind
256            Here, we combined optogenetic and whole-cell recordings to draw a functional portrait of e
257 hoton laser scanning microscopy coupled with whole-cell recordings to examine calcium dynamics in the
258      We performed dual dendritic and somatic whole-cell recordings to measure spontaneous EPSPs using
259                              We used in vivo whole-cell recordings to measure the synaptic inhibition
260 lycemia-induced changes in cytosolic ROS and whole-cell recordings to measure the use-dependent rundo
261 ions were discovered [15], we used quadruple whole-cell recordings to screen connectivity within the
262                                      We used whole-cell recordings to show that pharmacological inhib
263 to adult mice of either sex a combination of whole-cell recording, two-photon microscopy, and spine m
264  sound-evoked responses in the mouse ACx and whole-cell recordings, two-photon calcium imaging in pre
265                                  Here we use whole-cell recordings, two-photon microscopy, GABA uncag
266                                 Here we used whole-cell recordings, two-photon microscopy, optogeneti
267                                        Using whole-cell recording, we examined the spontaneous, subth
268 er-pulse photolysis technique, combined with whole-cell recording, we measured the rate of channel op
269 e dBest1 activates slowly after establishing whole-cell recording, we tested the hypothesis that the
270  (2-p) Calcium (Ca) imaging and 2-p targeted whole-cell recordings, we cell-type specifically investi
271                                     From the whole-cell recordings, we derived synaptic conductance w
272                                  Using blind whole-cell recordings, we found 33% of M/TCs to be 'sile
273   Here, by combining in vivo loose-patch and whole-cell recordings, we found that complex cells, iden
274                                        Using whole-cell recordings, we found that preGlyRs facilitate
275                                        Using whole-cell recordings, we found that the alpha3beta4* nA
276 th extracellular multiunit and intracellular whole-cell recordings, we found that the magnitude and r
277  quadruple-octuple in vitro and dual in vivo whole-cell recordings, we found two previously unknown i
278                          Here, using in vivo whole-cell recordings, we show that a visual cue can evo
279                                 Using paired whole-cell recordings, we show that activation of Group
280                                Using in vivo whole-cell recordings, we show that the timing of an LN'
281                          Here, using in vivo whole-cell recordings, we tested these models by directl
282                                              Whole cell recordings were used to examine effects of vo
283                                              Whole-cell recordings were collected from medium spiny n
284                                              Whole-cell recordings were conducted in male offspring b
285                                              Whole-cell recordings were made from GFP (Renilla)-tagge
286                            Intracellular and whole-cell recordings were made from locus ceruleus neur
287                                        Here, whole-cell recordings were made from proopiomelanocortin
288                        In the present study, whole-cell recordings were made in POMC cells in mouse b
289                                              Whole-cell recordings were obtained from tyrosine hydrox
290                                              Whole-cell recordings were performed on slices of the ra
291                                              Whole-cell recordings were performed to measure intrinsi
292                           Multiple-electrode whole-cell recordings were performed to probe synapse fo
293            In the present study, we combined whole cell recordings with laser scanning photostimulati
294 dynamics of place cells by combining in vivo whole-cell recordings with a virtual-reality system.
295                         By combining octuple whole-cell recordings with an optimized avidin-biotin-pe
296        Here we combine multiple simultaneous whole-cell recordings with extracellular stimulation and
297                                        Using whole-cell recordings with morphological recovery, we id
298        In this study we combined multineuron whole-cell recordings with optogenetics to determine the
299 s by comparing statistics from single-neuron whole-cell recordings with population statistics obtaine
300                                              Whole-cell recordings yielded results similar to patches

 
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