ライフサイエンスコーパス: recording

1 r concurrent voltage application and current recording).

2 he number of detectable NMJs during endplate recording.

3 s to achieve improved functionally selective recording.

4 atial extent, recording potential and rarity recording.

5 lectrophysiological technique of patch clamp recording.

6 r time, and factors associated with accurate recording.

7 g narrative context ("anomalous") during EEG recording.

8 g molecular markers and electrophysiological recording.

9 s information in high-dimensional population recordings.

10 ic TREK-1 currents in whole-cell patch-clamp recordings.

11 ar recordings and state-of-the-art simulated recordings.

12 through GABA(A)R activity, based on in vitro recordings.

13 ransmission was analyzed using cell-attached recordings.

14 t rates of current rundown in ruptured patch recordings.

15 icity were monitored using electromyographic recordings.

16 chanism with low spatial resolution clinical recordings.

17 etry results, and with normal full-field ERG recordings.

18 alidated using multiple electrophysiological recordings.

19 ypothesis using human electroencephalography recordings.

20 -cell desensitization observed in whole-cell recordings.

21 tion intensity using wireless electromyogram recordings.

22 in vivo, anesthetized, electrophysiological recordings.

23 nd compared the outcomes to in vitro optical recordings.

24 ace for in-vivo intraneural action potential recordings.

25 ations on m7G status, and the first database recording 1218 disease-associated genetic mutations that

26 ntified fossils from 32 sites on 15 islands (recording 137 species of resident and migratory birds),

27 date our findings with two external datasets recording 42,151 additional NPIs from 226 countries.

28 clinical factors associated with psychiatric recording accuracy, with multiple imputation for missing

29 In LFP recordings along the dorsal CA1-DG axis from sleeping ma

30 rt and attenuate the signal that reaches the recording amplifier.

31 can lead to a better design for electrodes, recording amplifiers, and experimental setups.

32 EPA benefits from a precise signal recording and analysis method which leads to the detecti

33 ammable intracranial electroencephalographic recording and electrical stimulation integrated and sync

34 The combination of in vivo extracellular recording and genetic-engineering-assisted optical stimu

35 defining cell type-specific TF profiles and recording and integrating TF-binding events across time.

36 In the present study, by juxtacellularly recording and labeling single CA2/CA3 neurons in freely-

37 A future that involves recording and modulating neural activity with such syste

38 he application of our probes in simultaneous recording and optical/chemical modulation of brain activ

39 rphologically characterized by intracellular recording and staining in the optic lobe of intact anima

40 We developed a mobile deep brain recording and stimulation (Mo-DBRS) platform that enable

41 ent investigation used multichannel neuronal recording and tract tracing methods to examine the ferre

42 Future studies involving EEG recordings and chronic cranial windows must consider the

43 Striatal field recordings and electrical stimulation of corticostriatal

44 ng, in vitro brain slice whole-cell patching recordings and in vivo stereotaxic hippocampal injection

45 techniques ranging from electrophysiological recordings and molecular biology to confocal microscopy

46 addressed this issue by using extracellular recordings and optogenetic stimulations in mice across p

47 Using perforated patch recordings and optogenetics, they show that dopamine rel

48 tients with epilepsy undergoing intracranial recordings and participating in a goal-conflict task whe

49 neurons, we performed multi-cell patch clamp recordings and Patch-seq on neurons derived from Nestin-

50 a include paired intracellular/extracellular recordings and state-of-the-art simulated recordings.

51 are computed between macaque visual cortical recordings and their correlation with task performance i

52 rformed optogenetically targeted single-unit recordings and two-photon imaging of Ntsr1-Cre+ L6 CT ne

53 activity (MSNA; microneurography, 12 paired recordings), and beat-to-beat blood pressure (BP; photop

54 elocity fractionation software, conventional recording, and anatomic localization of the ganglionated

55 ecorders were used to collect day-long audio recordings, and infant speech-related and adult vocalisa

56 e-cell patch recordings, in vivo single-unit recordings, and optogenetic manipulation of OVLT neurons

57 the reason it is so different from unipolar recordings are not completely known and are a matter of

58 Rats were implanted with recording arrays in the BLA and, after recovery from sur

59 ows efficient classification of electrograms recordings as AF driver or nondriver compared with the N

60 s together with neuronal electrical activity recording at the submillisecond time scale, enabling the

61 ectroencephalography (vEEG)/electromyography recordings at advancing ages.

62 t/activity patterns derived from actigraphic recordings at baseline predicts incident heart failure i

63 human seizures, using invasive brain voltage recordings at seizure onset.

64 adcopter (DJI Phantom 3), while concurrently recording behavioural reactions on video.

65 we used Patch-seq(8) to combine patch-clamp recording, biocytin staining, and single-cell RNA sequen

66 e, multi-region, and multi-probe Neuropixels recordings can be carried out with high yields over mult

67 The instability of neural recordings can render clinical brain-computer interfaces

68 Instead of the usual mode of recording cantilever deflection driven by sample expansi

69 ptor antagonist bicuculline methiodide while recording cellular activity in PFC of male rhesus monkey

70 Recording clearly distinctive physiological neural signa

71 In vivo recording combined with optogenetics in mice revealed th

72 Under near-physiological recording conditions we found that, similar to IHCs, imm

73 ty and difficulties in maintaining long-term recording conditions.

74 A dual extracellular recording configuration revealed that the presynaptic ef

75 Fast-scan cyclic voltammetry recordings confirmed that presynaptic inhibition of dopa

76 ntial monitoring periods included often many recording days with low pollen exposure (max.

77 Whole-cell patch-clamp recordings demonstrate that loss of SIRT1 decreases intr

78 lity, and a death event captured during vEEG recording demonstrated severe bradycardia prior to death

79 Whole cell recordings demonstrated that elevated CO(2) reduced the

80 on barriers in applications such as magnetic recording devices and flexible electronics.

81 typic ganglion cells in multielectrode array recordings during light stimulation in retinas of adult

82 trual cycle of the mother) from longitudinal recordings during the baby's stay in the Neonatal Intens

83 using in vivo wireless local field potential recordings during working memory processing, in vitro br

84 signals captured across scales by different recording electrodes are regularly used for Brain Machin

85 of multiple cellular-size light sources and recording electrodes.

86 n measured corollary discharge inhibition by recording evoked potentials from midbrain electrosensory

87 Here, however, in awake monkey recording experiments, we found that roughly half of V4

88 etween one, four and seven digits, where EEG recordings for working memory load estimation were taken

89 ered rodents due to technical limitations of recording from larger freely-moving animals for several

90 tem with micro-drives or flex-PCB cables for recording from multiple brain regions, as well as a faci

91 This question cannot be answered by simply recording from multiple brains (hyperscanning).

92 ay facilitate the standardization of chronic recording from Neuropixels probes in freely moving anima

93 patial information.SIGNIFICANCE STATEMENT By recording from the human medial temporal lobe (MTL) whil

94 We demonstrate simultaneous recordings from 20 sensors in parallel in human embryoni

95 ultaneous intracranial stereoencephalography recordings from across the brain revealed a similarly lo

96 Furthermore, dense extracellular recordings from awake mice reveal changes of both single

97 Whole-cell patch recordings from brainstem slices of mice of both sexes w

98 Recordings from cell pairs revealed the synchronized occ

99 We obtained direct neural recordings from electrodes implanted in human subjects a

100 Here, we report electrophysiological recordings from ENs of larval zebrafish that directly il

101 Optical in vivo recordings from freely walking Drosophila are currently

102 Our patch-clamp recordings from heterologously expressed GlyRs character

103 However, recordings from humans have indicated that hippocampal t

104 Here we use patch-clamp electrophysiological recordings from identified MOC neurons in brainstem slic

105 In vitro patch-clamp recordings from L5B pyramidal output neurons showed age-

106 Electrophysiological recordings from medial habenular neurons revealed that G

107 Extracellular recordings from mice exploring real 2D arenas demonstrat

108 Recordings from mice lacking Regulator of G protein Sign

109 reliably perform simultaneous intracellular recordings from more than a few tens of neurons.

110 Here, we review some contributions that recordings from neurons in humans implanted with electro

111 Our recordings from synapses, dendrites and large neuronal p

112 Intracellular neuronal recordings from the brain of awake nonhuman primates hav

113 Here, we combine stereoEEG recordings from the human cortex, with single-lead and t

114 Recordings from the medial temporal lobe, including the

115 reduction technique on single-trial ensemble recordings from the middle temporal (MT) area during per

116 We used electrocorticographic recordings from the sensorimotor cortex of people with r

117 Synaptic current recordings from these cells further reveal that this pre

118 that can simultaneously obtain intracellular recordings from thousands of connected mammalian neurons

119 However, without simultaneous recordings from thousands of cortical neurons with share

120 Intracranial electroencephalography (iEEG) recordings from three subjects suggested that high-frequ

121 Using ex-vivo patch-clamp recordings from up to 55 SCs per mouse, we found that in

122 d whether song traits were related to age at recording, future survival, longevity, and territory qua

123 ng the depth of cortex, electrophysiological recordings generated for the first time a continuous spa

124 (PFC; area 46) of two male macaque monkeys, recording >500 neurons simultaneously.

125 an average normalized fluorescence intensity recordings >1.40 for the calcium transients.

126 hat the circuit design parameters of current recording iBCIs can be relaxed considerably without loss

127 RETeval recordings identified significant OP implicit time delay

128 design and preparation of samples, (ii) data recording, (iii) software management with appropriate pa

129 While electrodes allow for recording in freely-behaving animals, they tend to be bu

130 Here, using single-channel electrical recording in planar lipid bilayers in conjunction with p

131 and their associated sources were studied by recording in situ bottom temperatures and sea levels obs

132 d RNA multiplexed activity) imaging based on recording in vivo single-neuron calcium dynamics followe

133 eters, respectively) derived from short-term recordings in a cohort of children with overweight/obesi

134 In this study, we performed extracellular recordings in adult female mice to monitor the activity

135 Whole-cell recordings in basolateral amygdala (BLA) slices from rat

136 Through single-cell recordings in behaving male and female C57BL/6 mice, we

137 In vivo optrode recordings in behaving mice showed that many VTA neurons

138 From electrophysiological recordings in cell cultures expressing Cx43 or Cx45, the

139 questions by carrying out high channel count recordings in dorsal-lateral prefrontal cortex (dlPFC; 7

140 Using intracranial and surface EEG recordings in four independent data sets, we demonstrate

141 alistic audiovisual speech with intracranial recordings in humans of both sexes, we find evidence for

142 postnatal weeks, using patch-clamp and field recordings in mouse brain slices (C57Bl/6, male and fema

143 Finally, patch recordings in nucleus accumbens (NAcc) medium spiny neur

144 Machine learning of action potential recordings in patients revealed novel phenotypes for lon

145 c implants allow for high-quality, long-term recordings in preclinical studies, the electrodes are fo

146 Local field potential recordings in rodent striatum show dopamine- and reward-

147 n important gap between electrophysiological recordings in single neurons at a micron scale and fMRI

148 n important gap between electrophysiological recordings in single neurons at the micron scale in nonh

149 Using in vitro electrophysiological recordings in the central nucleus of the amygdala (CeA),

150 Here, continuous oxygen microelectrode recordings in the coral diffusive boundary layer reveale

151 epeatedly and reliably perform intracellular recordings in the cortex of awake marmosets.

152 in humans, we performed direct intracranial recordings, in a large cohort of patients (n = 50), from

153 pproach, including in vitro whole-cell patch recordings, in vivo single-unit recordings, and optogene

154 Electromyogram recordings indicated that during training, muscle activa

155 scribe variation in participants' behaviour: recording intensity, spatial extent, recording potential

156 The improvement in recording is most dramatic in the hippocampus region, wh

157 e TBR estimation error variance with the CGM recording length.

158 Intracellular recordings linked propensity to cell excitability.

159 consciousness into consciousness by directly recording local field potentials and single neuron activ

160 addition to utilization of an intracochlear recording location to likely improve signal fidelity.

161 Here, we use optical recordings, manipulations, and computational modeling to

162 In brain slice recordings, many NPY neurons fired spontaneously, sugges

163 Modern recording methods enable sampling of thousands of neuron

164 ate positioning hardware provided a route to recording micro- and nanoscopic mapping of the topograph

165 tients using a proprietary electrocardiogram recording monitor for symptom-activated and 24-h AF auto

166 The arterial pulse recording morphology was compared against a volume clamp

167 Putamen recordings (n = 1) supported a cognition-action separati

168 ikely direction of visual moving dots, while recording neural activity with millisecond resolution us

169 We test this hypothesis by recording neural responses in the visual cortex of rhesu

170 xibility for choosing regions of interest in recording neuronal activities.

171 n of the critical MD relay by systematically recording neurons within a grid of penetrations.

172 in humans using intracranial microelectrode recordings obtained from 27 human epilepsy patients who

173 e locations was developed and applied to EEG recordings obtained from 293 healthy subjects and 427 sc

174 The shift to electronic recording of anthropometric measurements in electronic h

175 tick boxes or a prescriptive and structured recording of care.

176 neuECG, the simultaneous noninvasive recording of ECG and skin sympathetic nerve activity (SK

177 oscopy and polarimetry, SP-CUP enables video-recording of five photon tags (x, y, z: space; t: time o

178 ons of neurons rely on delivery of light and recording of fluorescent signals through optical fibers

179 Population-level recording of neuronal activity further revealed potentia

180 T neurons, we performed the first definitive recording of OT neurons in awake mice using two-photon c

181 Accurate recording of SMI during hospital admissions has the pote

182 on of acute perfusion changes as well as the recording of temporal response patterns and degrees of f

183 e potential for unique applications, such as recording of TF occupancy over time and cell type specif

184 No recording of the diastolic pathway of the clinical VT wa

185 Partial recording of the diastolic pathway of the clinical VT wa

186 Complete recording of the diastolic pathway was achieved in 36/85

187 The recording of triaxial acceleration by animal-attached de

188 With feedback control based on recordings of acoustic emissions, 98% of the sonication

189 An automated analysis of repeated 30 s recordings of beating atria in 381 live, intact zebrafis

190 by new evidence from real-time amperometric recordings of cholinergic signaling indicating a specifi

191 rod flash responses and recent voltage-clamp recordings of cone flash responses, using a model incorp

192 urther tested in previous VF optical mapping recordings of coronary perfused donor heart left ventric

193 ecruited an mPFC-DRN neural circuit, in vivo recordings of firing rate of DRN 5-HT neurons, cerebral

194 Here, using patch-clamp recordings of HEK293 cells heterologously co-expressing

195 Simultaneous recordings of intracellular Ca(2+) and APs allowed measu

196 a traveling wave, we performed extracellular recordings of local field potentials (LFP) and multi-uni

197 We performed whole-cell patch-clamp recordings of medium spiny neurons (MSNs) in the NAc and

198 Voltammetry recordings of mesolimbic dopamine levels demonstrated th

199 Recordings of monophasic action potentials in vivo revea

200 In electrophysiological recordings of mouse CA1 hippocampal pyramidal neurons, A

201 Multielectrode recordings of neuronal networks revealed hyperexcitabili

202 Whole-cell recordings of PCs from acute cerebellar slices revealed

203 vely studied and modeled using intracellular recordings of postsynaptic currents and potentials, infe

204 ease the activity of only one motoneuron and recordings of postsynaptic currents from inputs formed b

205 Using simultaneous recordings of rodent motor (M1) and premotor (M2) cortex

206 Here, we used electrophysiological recordings of single units in behaving male mice exposed

207 nal firing, we analyzed microelectrode array recordings of spontaneously occurring human seizures, an

208 Whole-cell patch-clamp recordings of striatal spiny projection neurons and hist

209 wireless iBCIs that provide the high-quality recordings of today's wired neural interfaces may lead t

210 Patch-clamp recordings of ventral CA1 pyramidal cells 24 h after a s

211 e compared to each other and to experimental recordings of visual-driven neural activity.

212 Electrophysiological recordings on acute hippocampal slices showed that exoge

213 Each subject took part in two recordings on different days, one with 19 dry electrodes

214 Effective use of either neural recording or stimulation technologies requires an approp

215 in the utilisation of prescribed methods of recording or tick boxes rather than relational, individu

216 for concurrent current injection and voltage recording) or into pseudovoltage-clamp mode (for concurr

217 ion to cells, ECORE allows long-term optical recording over multiple days.

218 oltage and extracellular glutamate transient recording over widespread regions of mice dorsal neocort

219 ge versus time traces collected from surface recordings over the heart(1).

220 it does not require dura removal, permitting recordings over weeks and months in a single animal.

221 Here we evaluated the chronic recording performance of L1-coated silicon based laminar

222 During extraoperative electrocorticography recordings performed as part of the presurgical evaluati

223 Here, we have combined electrophysiological recordings, pharmacological and optogenetic manipulation

224 personalised health monitoring to facilitate recording physiological signals, body motions, and analy

225 an NMDAR channel blocker applied through the recording pipette (MK-801).

226 Recording population calcium dynamics by fiber photometr

227 aviour: recording intensity, spatial extent, recording potential and rarity recording.

228 ate participants' noradrenergic system while recording pupillometry and EEG to infer its functional c

229 mmatory tissue response and improving neural recording quality and longevity.

230 optical photon generation from the qubit by recording quantum Rabi oscillations of the qubit through

231 We present optical recordings, receptive field maps, and sensitivity curves

232 Following 3 days of basal recordings, reserpine was administered on three consecut

233 nce of targets in a visual search task while recording response times (RTs) and event-related potenti

234 Whole-cell patch-clamp recordings reveal that detection inside the RF increases

235 We establish that whole-cell physiological recordings reveal tuning of individual vestibular affere

236 These recordings revealed a critical and selective role for K(

237 In vivo recordings revealed a strong role for hAPP/Abeta, but no

238 NAcC neuronal recordings revealed a stronger representation of incenti

239 These recordings revealed progressive phase shifts in activity

240 d on electroencephalogram and electromyogram recordings revealed that AIMD mice spent significantly l

241 -filled cells from both in vitro and in vivo recordings revealed that NaCl- and AngII-responsive neur

242 In vivo single-unit recordings revealed transient fast spiking responses to

243 18 humpback whales were equipped with depth-recording satellite tags (SPLASH10) to shed light on env

244 s and data scenarios (representing realistic recording schemes) were simulated to validate SIRE and t

245 sensory inference explicitly by behaviorally recording sensory statistical learning errors, and used

246 Mice underwent daily recording sessions of rest-task-rest while learning the

247 epresentations both within trials and across recording sessions.

248 icacy has not been possible due to different recording setups, tasks, species, etc.

249 Ex vivo electrophysiological recordings show that nesfatin-1 hyperpolarizes dopamine,

250 Moreover, extracellular recordings show that the digestion of PNNs induces a dec

251 Cerebellar surface recordings showed a functional perturbation of the later

252 In both experiments, EMG recordings showed larger activity at the ear on the side

253 ase mapping of prolonged human persistent AF recordings shows significant Endocardial-epicardial diss

254 tionnaires were sent to referring physicians recording site of recurrence and intended (Q1 to Q2 chan

255 ormidable technical challenges, such as poor recording stability and difficulties in maintaining long

256 umber of neuronal therapies including neural recording, stimulation and sensing of bioactive molecule

257 We found that HGT into the recording strain in human clinical fecal samples can be

258 In this system, an E. coli recording strain is exposed to a microbial sample and sp

259 Jointly, intracranial recording studies are starting to reveal aspects of the

260 First, even the highest quality single-cell recording studies find a fraction of the stimulus inform

261 The seamless genetic recording system described here provides an alternative

262 ble to those recorded using conventional EMG recording systems.

263 rade optogenetic excitation with single-cell recordings targeted to retrogradely labeled thalamocorti

264 To achieve these goals, we used single-unit recording techniques and an established animal model of

265 ncluding behavioral assays and multineuronal recording techniques, to investigate effects of imidaclo

266 scratching was assessed using a magnet-based recording technology.

267 nstrated that both techniques are capable of recording the early stage of uniaxial flow behaviour of

268 epinephrine (NE) release, while concurrently recording the EEG of male younger (N = 39; 25.2 +/- 3.2

269 By recording the electroencephalogram in the two experiment

270 mbedded within a Western tonal context while recording their cortical activity using magnetoencephalo

271 d in a 3-dimensional collagen matrix through recording their long-term trajectories.

272 aphy and video electroencephalography (vEEG) recordings throughout a 14-day monitoring period in an i

273 ourse of 1 year, comprising an overall video recording time of approximately 304.1 h.

274 ion of less than 90% for at least 30% of the recording time on nocturnal oximetry were assigned, in a

275 Here we used high-density EEG recordings to ask whether the underlying neural sources

276 ply this model to large-scale multielectrode recordings to illustrate how such an approach has the po

277 First, we used whole-cell patch-clamp recordings to measure the physiological changes in hippo

278 iscovered [15], we used quadruple whole-cell recordings to screen connectivity within the LH with sta

279 ntegrated than any current neural population recording tools (e.g. electrode arrays, fluorescence ima

280 limited, in part, by the invasive nature of recording tools.

281 We overcame this problem by recording unique tracks of green turtles (Chelonia mydas

282 Optical recording using voltage-sensitive fluorescent probes has

283 Using simultaneous video recording, we demonstrate that the learned lick behavior

284 y combined with in vivo electrophysiological recording, we demonstrated that regenerating corticospin

285 Using perforated patch-clamp recording, we found that optogenetic stimulation of nigr

286 sing Ca(2+) imaging and electrophysiological recordings, we demonstrate that bitter gustatory recepto

287 Using whole-cell recordings, we found that the alpha3beta4* nAChR-selecti

288 By paired patch-clamp recordings, we further demonstrate that acutely introduc

289 Here, using intracranial EEG recordings, we show that episodic memories formed after

290 Multielectrode recordings were analyzed in the time-frequency domain to

291 In this retrospective study ECG recordings were obtained during routine clinical work fr

292 Single-unit auditory nerve fiber recordings were obtained from 41 Mongolian gerbils of ei

293 Whole-cell patch-clamp recordings were obtained from Purkinje cells in cerebell

294 Ex vivo recordings were performed in NAcS D(1) receptor-expressi

295 The interview recordings were transcribed by the research team and ent

296 phic (EMG) and electroencephalographic (EEG) recordings were used to quantify physiological changes d

297 Improving chronic recording will benefit the brain-computer interface tech

298 elp to alleviate damage and allow for longer recording windows at 920 nm.

299 provide high-resolution electrophysiological recording with high signal-to-noise ratio.

300 aimed to investigate the sensitivity of SMI recording within general hospitals, changes in diagnosti

301 egion, where the control group showed severe recording yield decrease after one week, while the L1 im