ライフサイエンスコーパス: recording of

1 Recordings of 10 seconds of AF were analyzed to determin

2 Based on single-cell recordings of 156 photoreceptors, the presence of three

3 al, retrospective study, we analysed the ECG recordings of 185 people with refractory epilepsy and 17

4 We obtained stable recordings of 186 C nociceptors in the fibromyalgia grou

5 three predictions that were validated in EEG recordings of 48 convulsive seizures from 48 subjects wi

6 Extracellular electrophysiological recordings of 5-HT neurons revealed that, while alpha1-a

7 r-reconstructed source time courses from MEG recordings of 52 human subjects during the baseline of a

8 We analysed ECG recordings of 52 patients with alternating hemiplegia fr

9 pable of high-precision electrophysiological recording of a large network of electrogenic cells has l

10 s were followed up from 1999 until the first recording of a PD diagnosis, end of observation in the d

11 Assessments included an audio recording of a radiotherapy planning session to assess t

12 This technique involves the recording of a stack of TIRF images, by gradually increa

13 nal networks inferred from resting state EEG recordings of a cohort of 35 adults with heterogeneous i

14 t monobody-binding assays and single-channel recordings of a Fluc channel homolog to reveal a novel t

15 When fit to recordings of a local population of mouse layer 2/3 V1 n

16 e intracranial electroencephalography (IEEG) recordings of a seizure episode from a epilepsy patient

17 e a new ultradense corpus of audio and video recordings of a single child's life that allows us to me

18 ire electrode that allows in vivo concurrent recordings of a substantially greater number of motor un

19 g confined emission and electrophysiological recording of action potentials and local field activity.

20 ction potential, as determined by whole-cell recordings of action potentials on isolated mouse ventri

21 brane potential recordings and silicon probe recordings of action potentials reveal layer-specific ne

22 ly distinguish cell classes in extracellular recordings of action potentials.

23 Electrophysiological recordings of acutely dissociated neurons revealed that

24 , hepatic, and haematological monitoring and recording of adverse events.

25 The main limitation of the study was under-recording of adversity-related injuries and misclassific

26 e of MD change before and at the time of CLS recording of all patients, the average slope was -0.05 d

27 design of the outcome measure and the actual recording of all the measure's elements.

28 movement, and simultaneous electrophysiology recordings of all motor commands are typically not avail

29 The serendipitous recording of an earthquake swarm near the Indian Ocean t

30 We investigate this phenomenon in recordings of approximately 150 retinal ganglion cells,

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

32 In vivo microelectrode recordings of basal activity, as well as responses to af

33 naptic plasticity using electrophysiological recordings of basal transmission, paired pulse facilitat

34 As they rely on echolocation, audio recordings of bats allow tapping into their sensory acqu

35 ance imaging paradigm with synchronous video-recording of behavioural avoidance responses.

36 on of the full deflection profile from video recordings of bending tests, (ii) an optimisation algori

37 We report here a serendipitous recording of bidirectional lightning initiation in virgi

38 We used in vivo patch-clamp recordings of binaural neurons in the Mongolian gerbil a

39 Using electrical recording of bipolar cells under experimental conditions

40 However, there have only been very few recordings of bleaching within the Red Sea despite cover

41 d with multitaper spectral methods and video recording of body movement to characterize the spatio-te

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

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

44 hip fabrication methods opens a path towards recording of brain-wide neural activity during behaviour

45 ng rTMS interference in conjunction with EEG recordings of brain rhythms during the presentation of c

46 We used optical recording of Ca(2+) influx through TRPV1 to measure acti

47 Using optical recordings of Ca(2+) and membrane voltage, we demonstrat

48 hile performing whole-cell and juxtacellular recordings of CA3 neurons in vivo In CA3 pyramidal cells

49 This enabled in vivo recording of calcium dynamics of several thousand neuron

50 Additionally, recordings of calcium current in response to a command w

51 Single-cell recordings of cardiomyocytes isolated from HFpEF rats co

52 Whole-cell electrophysiological recordings of Cav1.233L channels expressed in HEK 293 ce

53 Extracellular single-unit recordings of CeA neurons in anesthetized rats showed th

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

55 ly selective methodologies to enable in vivo recording of chemical signals is of great importance for

56 Recording of circadian behavior in vivo alongside cellul

57 Bioluminescent recording of circadian clock protein (PERIOD2) output fr

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

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

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

61 t was investigated with targeted patch-clamp recordings of DA amacrine cells in TH-RFP mice and M1 ip

62 Electrophysiological recordings of DA neurons reveal that both the applicatio

63 n data on the case report form as opposed to recording of data as part of routine clinical care.

64 ion criteria were as follows: (i) systematic recording of diet during the gestational period and (ii)

65 lamus and cortex, we achieved the first dual recordings of directly connected thalamic and cortical n

66 ectrode array for high-throughput electrical recording of DNA synthesis.

67 self-administration and ex vivo voltammetric recording of dopamine signaling in the core of the nucle

68 Here, we analyzed voltammetry recordings of dopamine levels in the nucleus accumbens (

69 ential recording in patients, and multi-unit recording of dura- and light-sensitive thalamic neurons

70 minute hypoxia exercise test with continuous recording of ECG and physiological measurements before a

71 ered sinus arrhythmia [ETA]) from short-term recordings of electrocardiogram and respiratory chest ex

72 ardial infarction (N = 941) underwent 30-min recordings of electrocardiogram and respiratory chest ex

73 formance monitoring in OCD with simultaneous recording of electroencephalography (EEG) and functional

74 We performed simultaneous recordings of electroencephalography (EEG) from multiple

75 Recordings of electroretinogram (ERG) oscillatory potent

76 r, blinded review and ratings of taped video recordings of elliptical excisions performed by senior d

77 e can be non-locally observed by coincidence recording of entangled photon pairs.

78 Electrocorticographic or intrahippocampal recordings of epileptogenesis (from the insult to the fi

79 ptic activity, designed to replicate in vivo recordings of EPSPs in muscle vasoconstrictor neurons, p

80 Intracortical microstimulation (ICMS) and recording of evoked jaw and tongue electromyographic res

81 Here, in vivo whole-cell patch-clamp recording of excitatory neurons revealed variation in th

82 Patch-clamp recordings of excitatory and inhibitory currents were pe

83 icity were measured via electrophysiological recordings of excitatory postsynaptic currents and hippo

84 ity were measured using electrophysiological recordings of excitatory postsynaptic currents and long-

85 Furthermore, recordings of excitatory postsynaptic potential-to-spike

86 e description of the recurrent circuit using recordings of excitatory synapses between identified mot

87 ed from exercise logs, ambulatory heart rate recordings of exercise, and weekly telephone contacts.

88 nce, two-dimensional electrochemical imaging recording of exocytosis release between the electrodes w

89 We present non-faradaic electrochemical recordings of exocytosis from populations of mast and ch

90 ing long-term, high-resolution, longitudinal recordings of feeding dynamics under defined conditions,

91 a random sub-sample of participants and the recording of field notes.

92 The recordings of field excitatory post-synaptic potentials

93 ified neuronal populations and artifact-free recording of firing activity.

94 Here, single-molecule recordings of fluorescently labeled MMPs reveal cleavage

95 Targeted whole-cell recordings of fluorescently labeled VIP+ cells revealed

96 idate it as an adequate model using clinical recordings of focal seizures.

97 t path reconstructions and audio-video field recordings of foraging bats (Tadarida brasiliensis) reve

98 Recording of free-field cortical auditory evoked potenti

99 el system that enables full night ultrasonic recording of freely foraging bats, in addition to GPS tr

100 e combined behavior and electrophysiological recordings of frequency-tagged potentials in human obser

101 Additional recordings of GABA-A IPSCs showed CRF-R2 activation-faci

102 Physiological recordings of ganglion cell activity using microelectrod

103 We show in cut-open oocyte voltage-clamp recordings of gating and ionic currents of the Shaker Kv

104 ntitative RT-PCR, and whole cell patch clamp recordings of GFP-encoding Mus musculus nAChRs transfect

105 Here, using electroencephalogram recordings of great frigatebirds (Fregata minor) flying

106 by making use of longitudinal wrist movement recordings of >16,000 sleep bouts from 573 subjects.

107 During paired recordings of hair cells and afferent fibers, L-type vol

108 identified in the dental office by chairside recordings of HbA1c levels.

109 We used high-resolution recordings of head and eye movements in a natural viewin

110 tion of myocardial ischaemia and enables the recording of heart rate variability in non-resting condi

111 Applying whole-cell patch-clamp recording of HEK cells, we found that wild-type but not

112 In whole cell voltage clamp recordings of HEK293 cells, wild-type but not D757R Slo2

113 gical procedures were confirmed by real-time recording of hemodynamic parameters [pulsatile arterial

114 Single-channel electrophysiological recordings of heterologously expressed and purified Anop

115 chrony in: 1) simulated neurons, 2) in vitro recordings of hippocampal CA1 pyramidal cells, and 3) in

116 We performed whole cell patch clamp recordings of hippocampal neurons to determine the impac

117 take a novel approach exploiting noninvasive recordings of human brain activity to reveal the cortica

118 ngle muscle fibres, we demonstrate automated recordings of (i) caffeine-induced-, (ii) electrical fie

119 ovide the first in vivo electrophysiological recordings of identified CR+ interneurons, all of which

120 Intracellular recordings of identified interneurons revealed two mecha

121 In addition, in vivo recordings of identified substantia nigra pars compacta

122 as evaluated using single-unit extracellular recordings of identified VTA dopamine neurons.

123 Patch-clamp recordings of Ih currents in cells expressing wild-type

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

125 the function of dopamine neurons comes from recordings of individual cells in behaving animals; howe

126 of the information that can be learned from recordings of individual dopamine and non-dopamine neuro

127 tential for unmeasured confounders and under-recording of induction of labour or perinatal death in t

128 following stress, and whole-cell patch clamp recordings of inhibitory postsynaptic currents were perf

129 tic measurements in whole cell voltage clamp recordings of inspiratory neurons revealed no changes in

130 Audio recordings of interviews were transcribed, iteratively a

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

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

133 s in large-scale high-density multielectrode recordings of isolated macaque retina.

134 Patch clamp recordings of isolated rat vagal neurons show that ghrel

135 tions with cholesterol was determined by the recording of isotherms of compression of Langmuir films

136 New experimental techniques now permit the recording of large amounts of individual trajectories, e

137 ctical, stable interface for stimulation and recording of large-scale cortical circuits.

138 dular approach for analyzing calcium imaging recordings of large neuronal ensembles.

139 Here we carried out recordings of large populations of HVC neurons in singin

140 Using whole-cell recordings of layer V pyramidal neurons in an ex vivo br

141 functional Magnetic Resonance Imaging (fMRI) recordings of listeners comprehending the same story and

142 Recordings of living humpback whales were searched for o

143 MEAs) to perform high-frequency amperometric recording of local pO2 and local field potential (LFP)-r

144 We applied electrophysiological recordings of local field potential and extracellular K(

145 Assisted by multisite recordings of local field potentials (LFPs) and layer-sp

146 Using extracellular recordings of local field potentials (LFPs) and multiuni

147 We used optic fiber-based calcium recordings of local neural populations in cortex and tha

148 adult Fmr1 KO mice as shown with single-unit recordings of LSO neurons.

149 he prokaryotic homolog GltPh and patch-clamp recordings of mammalian EAATs to determine how these tra

150 ive auditory enrichment in the form of audio recordings of maternal sounds (including their mother's

151 olfactory bulb (AOB) using targeted ex vivo recordings of mating-activated neurons tagged with a flu

152 Combined with high-speed optical recordings of MB displacement and ultra-high-speed recor

153 ings of MB displacement and ultra-high-speed recordings of MB oscillation, we aimed to identify diffe

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

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

156 Whole-cell voltage-clamp recordings of mEPSCs in CA1 pyramidal neurons showed tha

157 te were determined from continuous heat-flow recordings of metabolic activity.

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

159 In physiological recordings of midbrain neurons sensitive to interaural d

160 Voltage-clamp recordings of miniature EPSCs (mEPSCs) from NST neurons

161 A recent study using whole-cell patch clamp recording of MNs in acute spinal cord slices from sympto

162 tained analog memory device for longitudinal recording of molecular stimuli into DNA mutations in hum

163 Perforated patch-clamp recordings of MOPr-mediated activation of G-protein-acti

164 Through recordings of motoneurons, inhibitory interneurons, and

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

166 processes information require high-fidelity recordings of multiple different forms of neural activit

167 his cell-based reporter allows for real-time recordings of mutually exclusive PPIs of PKA upon activa

168 Here, we used in situ patch-clamp recording of myenteric neurons from mice to define funct

169 Recording of Na currents revealed proexcitatory increase

170 Simultaneous cell-attached loose-patch recordings of Na(+) currents on each membrane revealed t

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

172 mical and functional data from intracerebral recordings of nearly 100 patients, to generate highly re

173 Electromyographic recordings of neck and hand muscles during scanning ensu

174 Here, we obtained dual patch-clamp recordings of neighboring IO neurons from young adult ma

175 pocampal CA1 pyramidal cells, and 3) in vivo recordings of neocortical V4 neurons.

176 ew genetic targeting strategies with optical recording of neural activity during behaviour in this mo

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

178 automated platform for continuous long-term recordings of neural activity and behavior in freely mov

179 tinnitus perception) requires high-precision recordings of neural activity combined with a behavioral

180 or prehensile actions.SIGNIFICANCE STATEMENT Recordings of neural activity from nonhuman primate fron

181 mined gamma- and theta-frequency activity in recordings of neural activity from the BLA-HPC-mPFC circ

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

183 eating improved technologies for large-scale recordings of neural activity in the live brain is a cru

184 Optical recordings of neural activity offer the promise of rapid

185 multiunit activity and local field potential recordings of neural activity were performed concurrentl

186 g concurrent magnetoencephalographic and EEG recordings of neural responses evoked by degraded speech

187 Video recordings of neurological examinations, including the M

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

189 croelectrode array that enables simultaneous recording of neuronal firing and local dopamine receptor

190 an effective method for large-scale, stable recording of neuronal spikes in concert with local popul

191 rpose, we combined optic-fiber-based calcium recordings of neuronal activity and cortical microstimul

192 ep brain stimulation (DBS) allows for direct recordings of neuronal activity from the human basal gan

193 The ability to acquire large-scale recordings of neuronal activity in awake and unrestraine

194 tionized neuroscience by enabling systematic recordings of neuronal circuits in living animals.

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

196 brief epochs, and applied it to simultaneous recordings of neuronal populations in cortical areas V1

197 Large-scale recordings of neuronal spiking combined with optogenetic

198 Simultaneous recordings of neurons in singing finches reveal that neu

199 and ex vivo and in vivo electrophysiological recordings of nicotine-elicited DA cell activation.

200 Using multi-electrode array recordings of odor responses in the olfactory bulb, we f

201 Using patch clamp recording of olfactory bulb slices in the whole-cell con

202 on of neural activity, and optophysiological recording of olfactory circuits in the bee brain to dete

203 We present the first demonstration of the recording of optically encoded audio onto a plasmonic na

204 Audio recordings of out-of-hospital cardiac arrest calls were

205 We used whole-cell patch-clamp recordings of over 460 neurons to characterize neurons d

206 a at least 3,000 years before any historical recordings of pandemics.

207 ivity matrix from non-seizure electrographic recordings of patients and use these connectivity matric

208 initially arose from objective eye movement recordings of patients with nystagmus and an eccentric f

209 assessed in both hemispheres by intraluminal recordings of pharyngeal motor-evoked responses (PMEPs)

210 Recordings of phrenic nerve activity in female Sprague D

211 to impulsive additional noise (playbacks of recordings of pile-driving and seismic surveys), but not

212 The simultaneous recording of PKA and ERK1&2 kinase activities reveals co

213 rd-directed behaviors are ambiguous, and few recordings of PL/IL activity have been performed to demo

214 Recordings of plaque, bleeding on probing, probing depth

215 tal techniques have allowed the simultaneous recordings of populations of hundreds of neurons, foster

216 is traditionally studied using intracellular recordings of postsynaptic potentials or currents evoked

217 -energy X-rays of the synchrotron permit the recording of powder diffraction patterns in as little as

218 ld nerve terminals, which allow simultaneous recording of presynaptic calcium currents and postsynapt

219 d sensory-evoked activity with extracellular recordings of primary visual cortex (V1) in nonanestheti

220 Using optophysiological recordings of projection neurons, we compared the respon

221 Electrophysiological recordings of PVT-to-NAc neurons revealed that GLP-1R ac

222 power of low-frequency oscillations in ECoG recordings of R6/2 mice is diminished while the spectral

223 Simultaneous recording of rapid voltage changes in multiple neurons w

224 ve Pavlovian discrimination and voltammetric recordings of real-time DA release were taken in either

225 Systematic recording of relevant clinical data, curation of a gene-

226 Inadequate emphasis is placed on recording of research decisions and on reproducibility o

227 Intracellular electrophysiological recordings of responses to light stimulation of the tran

228 In the blind rd1 mouse, multielectrode array recordings of retinal explants revealed robust and unifo

229 prediction violation by performing combined recordings of saccadic eye movements and fast event-rela

230 Loose-patch electrophysiological recordings of SCN neurons revealed a significant reducti

231 Simultaneous recording of sensor response over the range of temperatu

232 od on neural activity, we performed in vitro recordings of SGNs in culture.

233 inuous additional noise source (playbacks of recordings of ship passes).

234 la) exposed to additional noise (playback of recordings of ships passing through harbours), rather th

235 Microelectrode recording of SHR hearts showed that VT was initiated by

236 Due to small diameters of axons, direct recording of single AP transmission is challenging.

237 small conductance that has precluded direct recording of single-channel currents.

238 re activity in freely moving animals through recording of single-neuron activity, high-frequency loca

239 ts (many neurons encoding multiple objects), recordings of single neurons in the human medial tempora

240 Using electrophysiological recordings of single unmyelinated cutaneous fibres and t

241 These first recordings of single-channel Orai1 currents reveal unexp

242 Altogether, patch-clamp recordings of single-photon responses in mouse rods, tra

243 In vivo recording of SNA of the left efferent cardiac sympatheti

244 Our aim was to compare recording of specific targets for BP and BMI in individu

245 ties may be to use large-scale extracellular recording of spike trains and apply statistical methods

246 Multielectrode recordings of spike activity and field potentials were m

247 ly, sequential patterns were also present in recordings of spontaneous activity without any sensory s

248 novel biosensor opens the way for multisite recordings of spontaneous cholinergic dynamics in behavi

249 Whole-cell patch clamp recordings of spontaneous miniature postsynaptic current

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

251 The recording of starch grains attributable to Avena (oat) c

252 ssing in early visual cortex was assessed by recordings of steady-state visual evoked potentials (SSV

253 The enhanced fluctuations enable the recording of subtle deviations from a harmonic potential

254 ical fluorescence microscopy now permits the recording of such small cellular structures.

255 e skin for long-term wearable, high-fidelity recording of swallowing electromyograms on the chin.

256 te, plasma norepinephrine, microneurographic recording of sympathetic nerve traffic, and measurements

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

258 Here, by whole-cell recording of synaptic responses in MeCP2 mutant mice in

259 these differences using in vitro patch-clamp recordings of synaptic events and multiscale imaging of

260 Optical recording of synaptically mediated calcium responses ide

261 single NMDAR subtypes, kinetic modeling, and recordings of synaptically evoked NMDAR responses in acu

262 monstrate such an interaction in EEG and MEG recordings of task-free human brain activity.

263 Electrophysiological recordings of taste and taste + odor responses were cond

264 atural nucleotides and is based on real-time recording of the differential polymerase/DNA-binding kin

265 ndow for simultaneous optical and electrical recording of the ENS in vivo.

266 scalar coupling evolution delays within the recording of the FID (free induction decay), not only st

267 Continuous high-definition digital recording of the LED coordinates provides automatic trac

268 A 60-min dynamic PET recording of the liver was performed for 180 min with bl

269 Here, we report optical recording of the natural activity of two key cell types

270 electrophysiology methods allow longitudinal recording of the same neurons' functional properties and

271 e findings provide the first high-resolution recording of the subcellular Ca(2+) dynamics that contro

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

273 onal disconnections and electrophysiological recordings of the amygdalo-striatal networks in rats tra

274 Compound action potential recordings of the AN coupled to biophysical modeling dem

275 rect evidence available from spinal epidural recordings of the descending corticospinal volleys.

276 ient-centered communication coded from audio recordings of the first oncologist visit following patie

277 bited disrupted synaptic plasticity in slice recordings of the hippocampal CA1 region.

278 Whole-cell recordings of the large ventral lateral neurons (l-LNv)

279 Single-channel electrical recordings of the peptide alamethicin and of the proteol

280 This latter study employed extracellular recordings of the proximal negative field potential, pha

281 Immunohistochemistry and single-cell recordings of the retinas were also performed.

282 Ex vivo recordings of the SCN from these mice showed rapid desyn

283 ctional studies using single channel current recordings of the sensorless pore module reconstituted i

284 d novel approach for performing simultaneous recordings of the subthalamic nucleus and cortex using m

285 We analysed high-speed video recordings of the three-dimensional searching flights of

286 Audio recordings of the youth were transcribed and coded for t

287 cterization of the HD RGCs and physiological recordings of their light responses, receptive-field siz

288 stories and 15 listeners comprehending audio recordings of these stories.

289 d technological developments will soon allow recording of thousands or tens of thousands.

290 Despite their importance, no direct recordings of trans-plasma membrane electron currents ha

291 circadian reporters that permit single-cell recording of transcriptional and post-transcriptional rh

292 In whole-cell patch clamp recordings of transfected HEK293T cells, channels (Cav1.

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

294 or characterization measurements such as the recording of transmission matrix, and also able to keep

295 Using recordings of unit activity in the midbrain, we were abl

296 a multiwell plate, which allows simultaneous recording of up to 350 samples.

297 e prepared enabling simultaneous patch-clamp recordings of up to four labeled corticospinal neurons a

298 e probes in principle allow the simultaneous recording of very large numbers of neurons.

299 Here we report on population recordings of visual responses from neurons in the mouse

300 Two-electrode voltage-clamp recordings of Xenopus laevis oocytes expressing mutant K