ライフサイエンスコーパス: recording

1 cal judgment, and the intermittent nature of recording.

2 muli while undergoing magnetoencephalography recording.

3 se patients compared with ankle pulse volume recording.

4 neurons when measured using whole-cell patch recording.

5 8 months (older) of age using infrared video recording.

6 after photobleach during intracellular [Ca] recording.

7 ATOM40 were detected in electrophysiological recordings.

8 ctional Source Separation (FSS) to their EEG recordings.

9 context of neurophysiological and behavioral recordings.

10 of new and existing models and experimental recordings.

11 lized seizures in the 3-5 days preceding the recordings.

12 which we confirmed via electrophysiological recordings.

13 s had more than 6 hours of uninterrupted EEG recordings.

14 l as observed by single-cell suction pipette recordings.

15 presentations that better match human neural recordings.

16 ous Parkinson's disease and essential tremor recordings.

17 pertly annotated seizure data from prolonged recordings.

18 enomena and highly multivariate experimental recordings.

19 versatility and mostly, automation of force recordings.

20 this, we performed high-temperature in vitro recordings.

21 correlative measures such as neural activity recordings.

22 chanism; however, many relied on single-unit recordings.

23 ful improvements were also captured by video recordings.

24 ce during two random days of each month with recordings.

25 e not caused by seizures as indicated by EEG recordings.

26 n of peripheral nerve slices for patch-clamp recordings.

27 cted by frequency changes in electrocerebral recordings.

28 solution(<30 min) and high fidelity rainfall recordings.

29 ms were annotated based on the accurate mass recordings (1.5 ppm tolerance) of the LC-MS data set and

30 emonstrate with large-scale spiking activity recordings a concurrent deregulation of the spontaneous

31 entrant activity just in atrial fibrillation recordings accounting for approximately 80% of time.

32 ral measurements, genetic manipulations, and recording and manipulation of neural activity noninvasiv

33 We then use the normalization model and recording and microstimulation experiments to show that

34 erwent continuous surface (scalp) EEG (sEEG) recording and multimodality monitoring, including invasi

35 and provides a framework for using multiarea recording and stimulation to probe the neural mechanisms

36 5] years), 32 (36%) had PDs on sEEG and dEEG recordings and 21 (23%) on dEEG recordings only.

37 Using dual intracellular recordings and a custom-built loose-patch amplifier, we

38 However, by performing perforated patch recordings and calcium imaging experiments in rats (male

39 No association was found between the ffERG recordings and gestational age or retinopathy of prematu

40 Targeted recordings and in vivo calcium imaging further revealed

41 te" datasets (electroencephalography surface recordings and magnetoencephalography source reconstruct

42 Using slice recordings and modeling of synaptic activity at cerebell

43 Electrophysiological recordings and multistate modelling analysis were implem

44 Using high-density electrode recordings and novel model-based analysis, we found seve

45 Follow-up included 3-day Holter ECG recordings and office visits at 3, 6, and 12 months.

46 ue visual cortex, using electrophysiological recordings and pharmacological manipulations.

47 Finally, by combining recordings and pharmacology in vivo, in slices, and in h

48 ou et al. manually annotated a subset of our recordings and reported that two strains displayed rhyth

49 Using intracellular recordings and structure-function analyses, we examined

50 arations based on paired extracellular nerve recordings and videography to identify central and perip

51 Here, we used human intracranial recordings and visual word-by-word presentation of sente

52 croscopy with time-of-flight parallel energy recording) and the high brilliance of the soft X-rays us

53 of cholinergic signaling, neurophysiological recordings, and cholinergic receptor blockade to delinea

54 ap, widely available and non-invasive tremor recordings, and is independent of operator or postural c

55 rograde virus, targeted electrophysiological recordings, and optogenetic manipulations, we show that

56 ns combined with immunocytochemistry, paired recordings, and two-photon Ca(2+) imaging, we analyzed e

57 a conceptually novel auto-cycling proximity recording (APR) mechanism, it continuously and repeatedl

58 ur data suggests that mouse behavior and EEG recordings are not sensitive to decreased Chrna7 copy nu

59 mics (using repeated electroencephalographic recordings) as an epilepsy biomarker in brain injury pat

60 Using homologous binding and whole-cell recording assays, we found that an RNA aptamer most like

61 siological imager for parallel intracellular recording at the network level.

62 Using slice recordings before hearing onset and in vivo recordings w

63 Here we perform in vivo paired recordings between identified spinal motoneurons and ske

64 In human scalp EEG recordings, both sustained potentials and alpha-band osc

65 rication can yield large-scale, high-density recording but face challenges of chronic gliosis and ins

66 ibe the construction and use of the Activity Recording Capillary Feeder or CAFE (ARC), a machine-visi

67 The apparent mode-shift depended greatly on recording conditions.

68 Glial recordings confirmed EAAT2 is functional on nTS astrocyt

69 Cell-attached patch clamp recordings confirmed that perisomatic Ih was increased i

70 Electrophysiological recordings confirmed this prediction and also showed gat

71 we show that sustained voltages in human EEG recordings contain fine-grained information about the or

72 ferents were present and attended to in home recordings) correlated with in-lab comprehension.

73 copy (fNIRS), an emerging optical method for recording cortical hemodynamics, to perform neuroimaging

74 In vitro whole-cell recordings demonstrate the majority of OVLT neurons are

75 Biosensor recordings demonstrated that HE is associated with a sig

76 Using intracranial electrophysiological recordings during an attentional blink task, we tested t

77 However, intra-hippocampus EEG recordings during virtual navigation in humans have cons

78 formance and first-order task performance by recording EEG signals while participants were asked to m

79 ct the synaptic currents of neurons near the recording electrode, due to the use of a distant referen

80 perimposed upon that of neurons close to the recording electrode.

81 dout (MEMOIR), is based on a set of barcoded recording elements termed scratchpads.

82 niques in sedated female cebus monkeys while recording EMG signals from intrinsic hand and forearm mu

83 In particular, microelectrode recordings enable the delineation of neuroanatomic struc

84 ceptually similar to an "attentional habit." Recording event-related potentials in humans during a re

85 of STN neurons as measured using whole-cell recording ex vivo.

86 erent systems: a music-playing flag, a sound recording film and a flexible microphone for security ap

87 w power wireless system allowing 72-hours of recording from 16 channels sampled at 19.5 KHz (9.7 KHz

88 Here we tested this idea by recording from hippocampal and entorhinal neurons during

89 ly, an electrical probe should be capable of recording from large numbers of neurons across multiple

90 We tested this prediction by recording from neurons in macaque area MSTd that integra

91 Our model allowed the long-term multisite recording from pure axonal branches in a microscopy-comp

92 Exceptional progress has been made by recording from single neurons in the cortex of the macaq

93 nalysis of simultaneous multiple patch-clamp recordings from 6068 pairs of rat neurons with validatio

94 st this voltage-clamp-artifact hypothesis in recordings from 62 ON-OFF DSGCs in the rabbit retina.

95 our approach by analysing intra-cranial EEG recordings from a database comprising 16 patients who ha

96 ed 21,912 hours of routine electrocardiogram recordings from a heterogenous group of 70 adult ICU pat

97 nstrate platform validation with patch-clamp recordings from a variety of cells in the mouse neocorte

98 Paired recordings from adult bullfrog auditory synapses demonst

99 Using extracellular electrophysiological recordings from anaesthetized mice we first show that si

100 Held was assessed by whole-cell patch clamp recordings from auditory neurons in mature (2-4 months)

101 n these mechanisms, we performed patch-clamp recordings from basal amygdala (BA) neurons in brain sli

102 We obtained dynamic PET recordings from brain of Spraque Dawley rats at baseline

103 s and intrinsic structure and multielectrode recordings from brain slices to explore intrinsic excita

104 Here, we made whole-cell recordings from calyceal terminals in newborn rat pups.

105 In addition, using recordings from gerbil, mouse, and bullfrog auditory org

106 In addition, in vivo electrophysiological recordings from GPe showed that ethanol decreased the fi

107 Strikingly, electrophysiological recordings from hippocampal slices of mice lacking PRMT8

108 CANCE STATEMENT Using magnetoencephalography recordings from human listeners in a simulated cocktail

109 Our work suggests that LFP recordings from human STN differentiate between sleep cy

110 activity during learning, we made whole-cell recordings from larval zebrafish Purkinje cells while mo

111 By performing two-photon guided whole-cell recordings from layer 2/3 excitatory and inhibitory neur

112 Months-long recordings from motor cortex and striatum made and analy

113 hannel local field potential and single-unit recordings from multiple brain regions in awake restrain

114 We used simultaneous recordings from multiple neurons in the hippocampus and

115 Using recordings from neurosurgical epilepsy patients with int

116 hy basal ganglia, constrained by single unit recordings from non-human primates.

117 persistent activity by examining population recordings from posterior parietal (PPC) and prefrontal

118 we performed two-photon guided whole-cell Vm recordings from primary visual cortex layer 2/3 excitato

119 g during in vivo loose-patch (juxtacellular) recordings from principal neurons of the MSO of anesthet

120 Using intracranial EEG recordings from rare patients with medically resistant e

121 sue, we made two-photon targeted patch-clamp recordings from rat TC and TRN neuron dendrites to measu

122 Consistently, patch-clamp recordings from retrovirally labeled new granule cells a

123 Fbxl3(Afh) mutation and perform patch-clamp recordings from SCN brain slices across the projected da

124 Recordings from small invertebrates like C. elegans are

125 on distance is revealed in a new analysis of recordings from superficial layers of macaque primary vi

126 -30 nm) to establish the first intracellular recordings from targeted spine heads under two-photon vi

127 In vivo recordings from the DANA platform in anesthetized rats d

128 ssed with concurrent polysomnography and LFP recordings from the DBS electrodes, for an average of 7.

129 Electroencephalographic recordings from the developing human brain are character

130 Here, using intracranial recordings from the human hippocampus we found more powe

131 Coherence between paired EMG recordings from tibialis anterior muscle in the 20-40 Hz

132 Here, we used dual patch-clamp recordings from turtle vestibular hair cells and their a

133 hnique to dual micro-electrode array in vivo recordings from two distinct regions: olfactory bulb (OB

134 hat were being generated using intracortical recordings from two people with tetraplegia.

135 In long-term bioluminescence recordings, GABAA receptor blockade desynchronized the F

136 miological analysis of an all-payer database recording hospitalizations during 2013 in the United Sta

137 age, sex, general practice, date of cataract recording (i.e., index date), and years of history in th

138 s technology is still too heavy for extended recording in mice.

139 lectrical microstimulation in V1 paired with recording in MT to provide causal evidence that the rela

140 drive to PV+ INs using targeted patch-clamp recording in spinal cord slices from adult transgenic mi

141 After the inclusion of CAEP recording in the infant pathways, it was 3.9 months.

142 Further, single-unit recording in the MeA uncovered significant changes in th

143 tudy demonstrates that the inclusion of CAEP recording in the pathway facilitated earlier hearing aid

144 genetic activation of DG granule cells while recording in whole-cell patch-clamp and juxtacellular co

145 ilized the broad anatomical coverage of iEEG recordings in 12 eye-tracked neurosurgical patients to t

146 via full-field electroretinographic (ffERG) recordings in 6.5-year-old children born extremely prete

147 ging of 19 healthy adults, and single-neuron recordings in 9 neurosurgical patients.

148 ole-brain fMRI with longitudinal single-unit recordings in a local population (<1 mm(3)).

149 t analysis and cell type-specific deep-brain recordings in behaving mice, we show that orexin cell ac

150 ally show strong depression in voltage-clamp recordings in brain slices.

151 Here we show with in vivo intracellular recordings in cats that while excitation is restricted t

152 t Parkinson's disease and 20 postural tremor recordings in essential tremor, and validated on a secon

153 Patch clamp recordings in GCs reveal that movement is accompanied by

154 urrent-flow models with in vivo intracranial recordings in humans, providing a solid foundation to ta

155 Whole-cell recordings in L2/3 of awake mice revealed that the E/I r

156 the rat PL were determined using whole-cell recordings in layer V pyramidal neurons.

157 We used long-term photometric recordings in mice to study a population of dorsal raphe

158 Telemetric electrocardiogram recordings in Mybphl mice revealed cardiac conduction sy

159 We studied local field potential (LFP) recordings in PD subjects undergoing STN-DBS over the co

160 Using whole-cell patch-clamp recordings in posthearing mice, we show that only a prop

161 We used intracellular recordings in rat (both sexes) neocortical brain slices

162 Using noninvasive human MEG recordings in subjects performing a visuospatial attenti

163 ons, we collected genetic markers and speech recordings in the admixed creole-speaking population of

164 We used direct recordings in the amygdala and hippocampus from human ep

165 Temperature recordings in the NAc, muscle, and skin showed that fent

166 e the underlying neural dynamics, we conduct recordings in the orbitofrontal cortex (OFC).

167 ted in both real and simulated 512-electrode recordings in the peripheral primate retina with single-

168 Here, we performed large-scale extracellular recordings in the striatum and orbitofrontal cortex of m

169 d in a test cohort comprising 16 rest tremor recordings in tremor-dominant Parkinson's disease and 20

170 t-term plasticity from multi-electrode spike recordings in vivo.

171 Using electrophysiological recordings in young ferrets, we show that auditory corte

172 rvalbumin neurons, as well as single channel recordings, indicates that heteromeric alpha/beta subuni

173 etina of the guinea pig (Cavia porcellus) by recording inhibitory currents from RGCs in the presence

174 We studied non-motor decision making by recording intraoperative STN and prefrontal cortex (PFC)

175 Targeted patch-clamp recording is a powerful method for characterizing visual

176 bral blood flow (CBF) and neurophysiological recordings (local field potentials, LFPs).

177 roughput fabrication techniques and low-cost recording media.

178 Using multielectrode recording methods and white noise stimuli, we recorded n

179 g techniques and high-density multi-cellular recording methods with poor anatomical correlations.

180 After recordings, microstimulation was applied to compare sens

181 mass spectrometry, single-channel electrical recording, molecular simulations and circular dichroism

182 lanted DBS electrodes, whilst simultaneously recording muscle activity of the affected limbs.

183 Caudate neural recordings (n = 1) show that changes in value-coding neu

184 Recording nanobody-labeled nuclear pore complexes in Xen

185 Here, we tested the PS model by recording neural responses to alternating (ALT) and sync

186 Here, we analyzed iEEG recordings obtained from 215 epilepsy patients as they p

187 Using electrical recording of bipolar cells under experimental conditions

188 action recognition requires tasks that allow recording of brain activity or perturbing brain regions

189 tion of temperature through the simultaneous recording of images, quantitative color changes, and mas

190 ar uptake in BON cells, electrophysiological recording of isolated neurons, and its ability to stimul

191 ouble-sided VSD imaging enabled simultaneous recording of membrane potential events from almost all o

192 microtubules at high density, enabling video recording of microtubule dynamics in interphase and mito

193 Recording of Na currents revealed proexcitatory increase

194 a widely used imaging method for large-scale recording of neural activity in vivo.

195 method creates opportunities for noninvasive recording of neuronal activity with high spatial and tem

196 By direct recording of synaptic currents, we also show that motone

197 all the available information from the video recording of the tests.

198 MetS and 226 healthy controls underwent ECG recordings of at least 4 hours starting in the morning w

199 nology, we have made the first extracellular recordings of body-wall muscle electrophysiology inside

200 hod alone.SIGNIFICANCE STATEMENT Noninvasive recordings of changes in the brain's blood flow using fu

201 Applying DART to 1,486 recordings of class sessions from 67 courses, a total of

202 In paired recordings of cones and horizontal cells, L-AP4 slightly

203 METHODS AND Patch-clamp recordings of cultured neonatal rat ventricular myofibro

204 ecreased frequency in cardiomyocytes through recordings of intracellular Ca(2+) dynamics.

205 PCR (q-PCR), immunostaining and patch clamp recordings of membrane current and voltage, we identifie

206 idual motors via analysis of high-resolution recordings of motor speed, while dynamically varying the

207 speed using an adaptation paradigm and video recordings of natural human locomotion.

208 Furthermore, recordings of neural activity from the guinea pig inferi

209 Here, we show direct plasticity in recordings of neuronal populations in awake, behaving no

210 Simultaneous recordings of neurons in singing finches reveal that neu

211 Recordings of phrenic nerve activity in female Sprague D

212 s relationship, we analyzed eight multiscale recordings of spontaneous seizures from four patients wi

213 roughput calcium-flux assays and patch clamp recordings of transiently transfected HEK-293 cells for

214 l assessments and electroencephalogram (EEG) recordings on freely-moving mice.

215 EEG and dEEG recordings and 21 (23%) on dEEG recordings only.

216 dataset also may be incomplete in TBI death recording or contain misclassification of mortality data

217 bolites to differentiate goldenberry fruits, recording organic fruits higher amounts of these compoun

218 By recording over 250,000 daily measurements for up to 43 i

219 particles can retain their primary magnetic recording over billions of years.

220 several critical problems with the molecular recording paradigm: determining recording start times an

221 using pretreatment Periodontal Screening and Recording (PSR) index sextant scores to estimate periodo

222 Intracellular recording revealed a resting membrane potential of appro

223 Whole-cell electrophysiological recordings revealed altered intrinsic membrane propertie

224 Afferent neuron recordings revealed that hair cells with enlarged ribbon

225 EEG and EMG recordings revealed that ppDIO increases sleep during th

226 Recordings revealed that sensory and motor neurons comin

227 Whole cell recordings revealed that the isoflurane-activated backgr

228 Simultaneous fMRI recordings revealed that the same subjects also exhibite

229 Single channel recordings revealed the conductance of the channels to b

230 , single-trial hybrid optical voltage sensor recordings revealed voltage changes with submillisecond

231 Electrode array recordings show that early auditory responses demonstrat

232 Electrophysiological recordings show that natural variations in TRP-4 reduce

233 timulation coupled with electrophysiological recordings show that Sema-1a-dependent R axon lamination

234 The recordings show the strikingly stereotyped spatio-tempor

235 Interestingly, our recordings showed also cross-modal dendritic interaction

236 es with a wide range of sensing, monitoring, recording, signal-processing and actuation capabilities.

237 eos time-locked with whole-animal electrical recordings, simultaneous measurement of behavioural kine

238 By recording simultaneously from a large number of single n

239 ity in the visual cortex of adult rats while recording single unit and population activity, we demons

240 fair-weather convective cells pass over the recording site in Oklahoma, USA.

241 nged between 100-800 microm from the somatic recording site.

242 tation of neuronal activity through multiple recording sites and at high sampling rates.

243 power are seen across lateral temporal lobe recording sites and persist throughout the remainder of

244 xhibit promising chronic tissue response and recording stability.

245 he molecular recording paradigm: determining recording start times and coping with DNA polymerase pau

246 elates of such speed-accuracy adjustments by recording subthalamic nucleus (STN) activity and electro

247 Recordings suggest that both excitation and inhibition a

248 ing the brain slice preparation for cellular recordings, superfusion of DynA onto pPVT neurons decrea

249 , to quantitatively demonstrate how acoustic recordings supported by spatio-temporal metadata enable

250 unwanted electrical pickup between probe and recording system.

251 Traditional tethered recording systems restrict movement and limit the enviro

252 to a new multidimensional photoemission data-recording technique (combining full-field k-microscopy w

253 fs between anatomically-accurate single-cell recording techniques and high-density multi-cellular rec

254 otentially be tested with neurophysiological recording techniques.

255 blue whales (Balaenoptera musculus), and by recording the direction and size of their rolls during l

256 By recording the flight tones of multiple, tethered, male A

257 By recording the full fluorescence spectra and super-resolv

258 y well-dated annual glacial varve chronology recording the melting history of the Fennoscandian Ice S

259 gression models to routine surveillance data recording the presence of poliomyelitis associated with

260 icroarray immunoassay and LSPR measurements, recording the shift of the RP produced after the antibod

261 They allow for counting and recording thousands of input pulses and responding to pu

262 Following a 24 h recording to characterize basal sleep/wake parameters, m

263 high spatiotemporal resolution neuromagnetic recordings to examine how color selectivity emerges in t

264 We have used chronic electrophysiological recordings to investigate accompanying electrophysiologi

265 In this study, we relied on multielectrode recordings to investigate how single GC neurons respond

266 used near-threshold TMS with concurrent EEG recordings to measure how oscillatory brain dynamics cov

267 ed site-directed mutagenesis and patch-clamp recordings to probe the ion channel extracellular collar

268 tance for studies that seek to assign FP/LFP recordings to specific cortical layers.

269 We combine computational models and in vivo recordings to study the relationship between the spatial

270 hen leveraged the simultaneous nature of the recordings to test several hypotheses about the populati

271 ncy measurements (SFM) was assessed based on recording total impedance |Z| in different individual fr

272 e individual steps in the transport cycle by recording transporter-associated currents: the recovery

273 os of head-fixed larvae while simultaneously recording underlying field potentials.

274 Pulse volume recording was moderate to severely dampened in 54 of 119

275 By using single-channel current recording, we define discrete assembly intermediates and

276 Using multielectrode recording, we found a large fraction of neurons in early

277 Using whole-cell current clamp recording, we found that L2/3 pyramidal neurons in prefr

278 Here, using intracellular recording, we monitored inputs and plasticity-inducing c

279 From the video recordings, we collected 598 offshore calls from 10 indi

280 rmore, using confocal imaging and time-lapse recordings, we demonstrated "intracellular crawling" of

281 In eight of nine recordings, we discovered long (900 ms) reoccurring subt

282 tly, using gramicidin-perforated patch clamp recordings, we found that the GluK2-mediated increase in

283 Using bipolar depth recordings, we report here a sequence wherein: (1) conve

284 Here, using high-density EEG recordings, we show that 4- to 6-month-old infants displ

285 In controls, recordings were also obtained during Valsalva manoeuvre

286 Whole-cell recordings were conducted in male offspring between 4 an

287 EMG recordings were made from right ankle dorsiflexor and ri

288 A new study in which recordings were made from the retrosplenial cortex while

289 Adequate ffERG recordings were obtained from 52 preterm children (19 gi

290 fter toluene exposure were not observed when recordings were performed 7 days after the exposure.

291 troencephalographic and electrophysiological recordings were performed at day 5 and 2 months post-SE.

292 ntracellular current clamp and voltage clamp recordings were performed in muscle from a mouse model o

293 Electroencephalographic recordings were visually classified based on PD frequenc

294 articipated in three magnetoencephalographic recordings while first passively listening to recorded s

295 t combines large-scale micro-electrode array recordings with genetic identification and the anatomica

296 We combined electrophysiological recordings with infrared and UV-visible spectroscopic me

297 ombine intersection-based analysis of neural recordings with intervention on neural activity to deter

298 recordings before hearing onset and in vivo recordings with iontophoretic drug applications after he

299 We used in vitro whole-cell patch-clamp recordings with laser-scanning photostimulation and perf

300 een extensively characterized in single-unit recordings, yielding important insights into how individ