ライフサイエンスコーパス: by recording

1 s (baseline) and at 1 month postoperatively, by recording 1-hour bilateral middle cerebral artery (MC

2 We demonstrate the flexibility of the device by recording (13)C signal decay due to longitudinal rela

3 We tested this assertion by recording 184 eyelid PCs and 240 non-eyelid PCs durin

4 mission hypothesis in mouse DRN brain slices by recording 5-HT1A receptor-mediated inhibitory postsyn

5 g of grain boundaries in CVD-grown graphene, by recording 65 kilopixel near-field images in 26 s and

6 By recording a large number of annotations on samples an

7 nd clearance kinetics were monitored in situ by recording a series of heteronuclear (1)H-(15)N correl

8 he energetics of macromolecular interactions by recording a thermogram of differential heating power

9 zation reaction was simultaneously monitored by recording absorption intensity changes of SNS specifi

10 This hypothesis was tested by recording action potentials and local field potential

11 Safety was assessed by recording adverse events and by electrocardiography,

12 Safety was assessed by recording adverse events.

13 nity cohort of 1,191 adults aged 25-75 years by recording all new BCCs and SCCs for 16 years in peopl

14 omisation, and safety was assessed primarily by recording all serious adverse events, including serio

15 By recording and analysing the interference patterns, we

16 has been probed at the single-molecule level by recording and analyzing photon-to-photon pair times o

17 In our experiment, we resolve this issue by recording and analyzing spectra that sample all the b

18 By recording and labeling individual neurons in behaving

19 genetic methods to test these classic ideas by recording and manipulating identified cell types with

20 control systems that interact with the brain by recording and modulating neural activity and aim to r

21 We examined the BF circuit by recording and optogenetically perturbing the activity

22 By recording and playing back the light-driven membrane

23 Here we address this question by recording and reversibly inactivating the lateral int

24 The approach was validated by recording and sampling from glutamatergic thalamocort

25 component (BIC), which is obtained typically by recording auditory brainstem responses (ABRs)-the BIC

26 aluated age-related changes in mouse hearing by recording auditory brainstem responses before and fol

27 By recording backscattered electrons, diffraction patter

28 betes and its temporal sequence over 5 years by recording beat-to-beat blood pressure and R-R interva

29 phage and antibiotic treatment were assessed by recording bioluminescence for short-time periods and

30 g bioluminescence for short-time periods and by recording body weight and survival of mice for longer

31 By recording both firing in GABAergic interneurons and t

32 By recording both the images and emission spectra of tho

33 By recording brain and spinal cord activity in the same

34 possible relationship between ICC-IM and SWs by recording Ca(2+) transients in mice expressing a gene

35 353 for P2X3-containing receptors was tested by recording Ca(2+) transients to exogenously applied AT

36 we assessed the regulation of TMEM16A gating by recording Ca(2+)-evoked Cl(-) currents conducted by e

37 In addition, by recording CatSper currents from human epididymal and

38 of binding of the DNA with RRM1 was explored by recording CD spectra at predetermined times following

39 We studied this issue by recording cell activity simultaneously from dorsal pr

40 intersubject motor coordination were studied by recording cell activity simultaneously from the front

41 By recording changes in the cell-substrate separation, t

42 SE, and clonal expansion has been documented by recording changes in the population densities of anti

43 eness of the LTP probe has been demonstrated by recording characteristic mass spectra and tandem mass

44 By recording chronoamperograms at room temperature and v

45 of the colloid system can then be monitored by recording corresponding UV-vis spectrum and initial m

46 Here, we show by recording cortical and striatal ongoing population ac

47 We tested this by recording CST-evoked focal synaptic potentials, extra

48 f the complete system have been demonstrated by recording current changes upon nanowire exposure to s

49 surized without flow for functional analysis by recording diameter changes using videomicroscopic tec

50 erface of CAP-Gly with microtubules, derived by recording direct dipolar contacts between CAP-Gly and

51 tial attention as a function of WMC and WML, by recording distractibility across several target-to-di

52 ntration timecourses can be greatly improved by recording DOSY (diffusion-ordered spectroscopy) data

53 performance and first-order task performance by recording EEG signals while participants were asked t

54 By recording EEGs, we were able to determine whether thi

55 By recording electrical activity directly from the corti

56 In this study, we examined the role of Grb14 by recording electrical responses from rods in which the

57 By recording electrically from oligodendrocytes and imag

58 measurements in the SECCM imaging protocol, by recording electrochemical currents in a wide potentia

59 We addressed this discrepancy by recording electrocorticographic activity from neurosu

60 ial attention on a fine spatiotemporal scale by recording electrocorticography (ECoG) signals measure

61 Here, we addressed this deficit by recording electrophysiological activity in the mouse

62 , sunflower, linden, meadow, and fake honey) by recording emission from 270 to 640 nm with excitation

63 the fusion protein substrates were monitored by recording emission spectra and plotting the change in

64 cted through formation of CdS QDs, monitored by recording emission spectra at lambdaex = 290 nm.

65 studies typically assess foraging strategies by recording energy intake rates rather than realized re

66 lus-driven and internally generated activity by recording ensembles of HD neurons in the antero-dorsa

67 By recording entropy-driven changes in the directed net

68 ntion is shifted during such cuing paradigms by recording event-related potentials (ERPs).

69 then measured corollary discharge inhibition by recording evoked potentials from midbrain electrosens

70 ndividual synapses to sensory representation by recording excitatory postsynaptic currents (EPSCs) in

71 to the PCRt and dm-Vsp neurons were verified by recording extracellular responses to electrical stimu

72 ored functional plasticity in the AF pathway by recording extracellularly from individual M/T cells a

73 r these state-dependent vestibular behaviors by recording extracellularly from neurons in the vestibu

74 ferent neurons, which are frequently studied by recording extracellularly with penetrating microelect

75 ynaptic effects of (2R,6R)-HNK were examined by recording field excitatory postsynaptic potentials (f

76 By recording fluorescence lifetime imaging microscopy (F

77 We addressed this problem by recording fMRI data from human subjects performing a

78 By recording from >3000 ganglion cells in guinea pig, we

79 -invasive method for measuring these signals by recording from a central neuron that is electrically

80 We tested for cone-cone glutamate diffusion by recording from adjacent cone pairs in the ground squi

81 Yet by recording from axons of cerebellar stellate cell (SC)

82 tegorization-related activity in PFC and ITC by recording from both areas as monkeys alternated betwe

83 By recording from both hemispheres simultaneously, we in

84 We tested these predictions by recording from CA1 pyramidal cells in freely moving r

85 odulated by the cost paid to obtain rewards, by recording from dopamine neurons in awake behaving mon

86 we reexamined the contribution of ITC to VWM by recording from highly selective individual ITC neuron

87 Here we tested this idea by recording from hippocampal and entorhinal neurons dur

88 performed a critical test of this hypothesis by recording from identified F- and S-type motoneurons i

89 We tested this hypothesis by recording from IN neurons in alert squirrel monkeys d

90 ates disparate task-relevant visual features by recording from LIP neurons in monkeys trained to iden

91 By recording from MEC cell ensembles during navigation a

92 ain do not express functional NMDA receptors by recording from microglia cultured from adult brain.

93 By recording from monosynaptically connected pairs of re

94 By recording from multiple molecular layer interneurons

95 d the outside world either by stimulating or by recording from neural tissue to treat or assist peopl

96 We investigated these issues by recording from neuronal populations in areas V1 and V

97 mechanisms underlying this useful adaptation by recording from neurons as they responded to stimuli m

98 esponsible for working memory can be gleaned by recording from neurons during the performance of a de

99 We tested this prediction by recording from neurons in macaque area MSTd that inte

100 Moreover, by recording from neurons in vivo, we found that primary

101 We investigated these questions by recording from over 200 single neurons in the amygdal

102 We tested for electrical synapses by recording from pairs of relay neurons in acute slices

103 By recording from pairs of rods and Off cone bipolar cel

104 by a diurnal-to-nocturnal shift in behavior, by recording from photoreceptors of first instar nymphs

105 We addressed these questions by recording from primary motor (M1) and premotor cortic

106 signals that this pathway conveys to cortex by recording from pulvinar neurons that we identified by

107 Here we tested this hypothesis by recording from putative dopamine neurons in the VTA o

108 potential effects of CNIHs on native AMPARs by recording from rat optic nerve oligodendrocyte precur

109 us of the amygdala (CeA) in brainstem slices by recording from retrogradely labelled NTS projection n

110 Exceptional progress has been made by recording from single neurons in the cortex of the ma

111 addressed this fundamental question directly by recording from single otolith afferents in monkeys du

112 he nature and origin of choice probabilities by recording from subcortical (brainstem and cerebellar)

113 Here, we address this question by recording from subjects selectively listening to one

114 we apply an SDT framework to a motor system by recording from superior colliculus (SC) neurons durin

115 We addressed these issues by recording from synaptically coupled pairs of glycine/

116 By recording from the ACC and hippocampal CA1 simultaneo

117 We circumvented these difficulties by recording from the axons of MSO neurons in the latera

118 By recording from the cortex of freely moving animals en

119 d spatial information.SIGNIFICANCE STATEMENT By recording from the human medial temporal lobe (MTL) w

120 We examined this hypothesis by recording from the PFC of monkeys comparing direction

121 We investigated this question by recording from the supplementary eye field (SEF) of m

122 sentations in cortico-basal ganglia circuits by recording from thousands of neurons in the prefrontal

123 the current study, we addressed these issues by recording from V1 of awake monkeys implanted with an

124 By recording from ventral hippocampal CA1 neurons in rat

125 sory inputs required to sustain grid firing, by recording grid cells as mice explore familiar environ

126 Here, we investigated this role by recording HD cells in the anterior thalamus after eit

127 present study was to address this challenge by recording high-density electroencephalography (HD-EEG

128 tivity in regions of this "default network," by recording high-frequency power (76-200 Hz) electrical

129 arge-scale structure of place field activity by recording hippocampal neurons in rats exploring a pre

130 By recording how many coat proteins bind to each of many

131 perience-or adaptation-are typically assayed by recording in a relevant subcortical or cortical netwo

132 We tested this coordination hypothesis by recording in macaque ACC/PFC during the covert utiliz

133 ma and their associated sources were studied by recording in situ bottom temperatures and sea levels

134 as measured by clamping voltage near 0 mV or by recording in the presence of ionotropic glutamate rec

135 e retina of the guinea pig (Cavia porcellus) by recording inhibitory currents from RGCs in the presen

136 e retina of the guinea pig (Cavia porcellus) by recording inhibitory currents from RGCs in the presen

137 Here we evaluated the differential circuitry by recording inputs (postsynaptic potentials) and output

138 By recording intracellularly from dissociated neurons an

139 Here, by recording intracellularly from Purkinje neurons in un

140 tection modulates visual recognition signals by recording intracranial field potential responses from

141 We studied non-motor decision making by recording intraoperative STN and prefrontal cortex (P

142 Here, by recording ionic currents from spermatozoa of an infer

143 Here, by recording iSC activity during reversible cryogenic in

144 trasted how well different areas encode time by recording large numbers of units simultaneously from

145 Accordingly, by recording LFP activity from the STN in parkinsonian p

146 We investigated these interactions by recording LFPs and single-unit activity using multipl

147 We addressed this issue by recording LFPs from multielectrode arrays implanted i

148 By recording light-evoked synaptic currents from GCs, we

149 vity at multiple spatial and temporal scales by recording local field potentials (LFPs) and action po

150 predominantly represented in auditory cortex by recording local field potentials (LFPs) and multiunit

151 t shifts in cortical functional connectivity by recording local field potentials (LFPs) during sponta

152 of the spatial spread of cochlear excitation by recording local field potentials (LFPs) in the inferi

153 intracranial electrophysiology (ICE), namely by recording local field potentials from populations of

154 We addressed this question by recording local field potentials in the Drosophila ce

155 We tested this prediction by recording local field potentials in two ferrets after

156 Identification of areas was confirmed by recording local-field potentials from the electrode,

157 the levels of synaptic activity as inferred by recording long-term potentiation generated at both co

158 an FES system in primates that is controlled by recordings made from microelectrodes permanently impl

159 By recording mass spectra of individual ions via charge

160 cetylglucosamine (UDP-GlcNAc), was monitored by recording mass spectra with characteristic isotopic p

161 We tested these ideas by recording medial entorhinal cortex (MEC) head-directi

162 zed whether microglial cells might sense CSD by recording membrane currents from microglia in acutely

163 eurons have been assessed one cell at a time by recording membrane currents in response to applicatio

164 By recording miniature EPSCs (mEPSCs) from frontal corte

165 By recording motor- and somatosensory-evoked potentials

166 By recording multiple parameters, a detailed discriminat

167 across the different layers of visual cortex by recording multiunit (defined as high-frequency power

168 Here we addressed this issue by recording neural activity in hippocampal region CA1 w

169 ead of neural activation to intracochlear ES by recording neural responses across the cochleotopicall

170 We test this hypothesis by recording neural responses in the visual cortex of rh

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

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

173 sured representations of magnitude in humans by recording neural signals whilst they viewed symbolic

174 coding across the human medial temporal lobe by recording neuronal activity during virtual navigation

175 We studied this evaluation process by recording neuronal activity in the supplementary eye

176 edforward pathways to decision signals in MT by recording neuronal activity while monkeys performed m

177 ng the sequential features of complex sounds by recording neuronal responses bilaterally in the audit

178 We explored this issue by recording neuronal responses in the right dlPFC of tw

179 By recording neurons from the feeding and withdrawal net

180 Here we show, by recording neurons in attending macaque monkeys (Macac

181 saccades in frontal cortex was investigated by recording neurons in monkey frontal eye field (FEF) d

182 We studied these two questions by recording neurons in primary somatosensory (S1) and d

183 ay information about the UCS to the amygdala by recording neurons in the amygdala and periaqueductal

184 ted the contribution of D-serine and glycine by recording NMDAR-mediated responses at hippocampal Sch

185 arameters for 130 locked nucleic acid probes by recording nucleic acid melting temperature during ISH

186 Rutin oxidation reaction was followed by recording of spectral changes over the time at 360 nm

187 we detected first spiking activity followed by recording of synaptic currents in distinct types of a

188 a [Ru(bpy)(3)](2+) visible light sensitizer by recording of the OO vibrational mode at 830 cm(-1).

189 Sound coding in SGN, assessed by recordings of single auditory nerve fibers and their

190 ivated the auditory pathway, as demonstrated by recordings of single neuron and neuronal population r

191 ocessing in early visual cortex was assessed by recordings of steady-state visual evoked potentials (

192 By recording optogenetically tagged interneurons of spec

193 By recording over 250,000 daily measurements for up to 4

194 of the space segregated by these boundaries, by recording place cell activity from CA1 and CA3 while

195 Here we examined this question by recording population activity at the cellular level f

196 By recording population spikes simultaneously throughout

197 lations affect neocortical assembly patterns by recording populations of single cells and transient g

198 Synaptic release from cones was measured by recording postsynaptic currents in Ambystoma tigrinum

199 om POMC neuron terminals, which was detected by recording postsynaptic currents in downstream neurons

200 and successful ablation sites can be guided by recording potentials within or near the CS os.

201 ctrometer, and its performance was evaluated by recording product-ion spectra of doubly protonated su

202 Further, by recording Purkinje neuron membrane potential intracel

203 Here we addressed this question by recording putative CINs from the DMS in rats performi

204 ate optical photon generation from the qubit by recording quantum Rabi oscillations of the qubit thro

205 ses from ganglion and AII amacrine cells and by recording RB-mediated synaptic currents from AII amac

206 way to screen candidate drugs is established by recording real-time mass voltammograms, which allows

207 ntial-dependent product profile was obtained by recording real-time mass voltammograms.

208 effects of the stimuli (N=4) were identified by recording responses from the pharyngeal, laryngeal, a

209 By recording responses of neural ensembles to mixtures o

210 By recording responses to pairs of sinusoidally amplitud

211 1R1-TAS1R3 heteromer receptor in umami taste by recording responses, specifically to l-glutamate and

212 luated this conventional model of rod vision by recording rod-mediated light responses from ganglion

213 We addressed this hypothesis by recording scalp EEG during a stop task while modulati

214 This kinetic study is carried out by recording simultaneous cyclic voltammograms and voltf

215 By recording simultaneously from a large number of singl

216 on local and spatially separated populations by recording simultaneously from dozens of neurons in bo

217 5- to 6-d-old rats, we test this hypothesis by recording simultaneously from forelimb and barrel reg

218 Here we show that by recording simultaneously from hundreds of units in pr

219 between cortical areas on longer timescales by recording simultaneously from neurons in primary visu

220 ion in vivo in the cat primary visual cortex by recording simultaneously spikes of layer 4 simple cel

221 We investigated these issues by recording, simultaneously and with high spatiotempora

222 We addressed this problem by recording single neurons in the ventral posterior lat

223 rbitofrontal cortex during reversal learning by recording single unit activity from 180 control and 2

224 We tested this hypothesis by recording single unit activity of pre-Botzinger pre-I

225 asolateral amygdala conforms to this pattern by recording single units in a behavioral task in which

226 leading to propofol-induced unconsciousness by recording single-neuron activity and local field pote

227 ned memory-related changes in spatial tuning by recording single-neuron activity from neurosurgical p

228 an auditory spatial selective listening task by recording single-neuron activity in behaving monkeys

229 Here we evaluated this hypothesis by recording single-unit activity from BLA in rats durin

230 We addressed this question by recording single-unit activity from the dorsolateral

231 Here, we examined this by recording single-unit activity from the OFC in rats n

232 e test for neural correlates of this process by recording single-unit activity in the orbitofrontal c

233 ural basis of this psychophysical phenomenon by recording single-unit responses from the primary audi

234 is prediction in two healthy rhesus macaques by recording single-unit spiking activity from the globu

235 glutamatergic astrocyte-to-neuron signalling by recording slow outward currents (SOCs) and slow inwar

236 possibility was investigated systematically by recording spike times from chicken auditory nerve fib

237 We investigated this by recording spike trains from the olfactory bulb in awa

238 lion cells in the isolated salamander retina by recording spiking activity with extracellular electro

239 By recording spindle afferent responses from alert human

240 orrelates of such speed-accuracy adjustments by recording subthalamic nucleus (STN) activity and elec

241 aptations in dmPFC resulting from OF in mice by recording synaptic responses in dmPFC layer V pyramid

242 ific workflows are created within the system by recording tasks performed by the user.

243 Exposure to temperature stress was measured by recording temperature in the understorey and across f

244 only measured electrophysiologically in vivo by recording the activity of individual wide-dynamic-ran

245 We investigated this question by recording the activity of saccade-related burst neuro

246 Here we addressed this by recording the activity of single neurons in the hippo

247 We tested this hypothesis directly by recording the activity of these motoneurons during se

248 ated with the cycling buffer, and quantified by recording the amount of fluorescent product generated

249 Hybridization was monitored by recording the amperometric responses measured at -0.1

250 -ATP exchange rates in isolated mitochondria by recording the changes in free extramitochondrial [Mg(

251 adsorption of H2O onto the GaN(0001) surface by recording the core-level photoemission spectra and ob

252 rane was optimized for voltage-clamped cells by recording the current induced by co-application of 30

253 us and semicrystalline phases of the polymer by recording the decay of elastically scattered helium a

254 romachined regions were measured immediately by recording the diffraction efficiency of inscribed gra

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

256 By recording the direction of the scattered particles af

257 We studied these mechanisms by recording the electrical activity of the human brain

258 at the photoreceptor-horizontal cell synapse by recording the electrical responses of photoreceptors

259 The binding of the Anti-IgY-HRP is detected by recording the electrocatalytic signal caused by addit

260 By recording the electroencephalogram in the two experim

261 s vs. CXCR4-non-expressing interneurons, and by recording the electrophysiological effects caused by

262 the fine-grained geometry of the face's DPPS by recording the enhancement of the blink reflex elicite

263 By recording the flight tones of multiple, tethered, mal

264 ction of nitrated ceruloplasmin was realized by recording the fluorescence intensity of quantum dots

265 The activity of each entity was documented by recording the following metrics of popularity: the nu

266 By recording the full fluorescence spectra and super-res

267 ortho-hydrogen ( o-H 2) was followed by NMR by recording the increase in the intensity of the signal

268 Quantitative detection could be realized by recording the intensity of the test line with the Ima

269 of characterization of autoantibody activity by recording the kinetics of their binding with free nat

270 intrinsic nature of sigma1 receptor ligands by recording the ligand-mediated conformational changes

271 Synaptic plasticity was assessed in vivo by recording the MeA evoked field potential responses to

272 Here we tested these contrasting hypotheses by recording the neuronal activity of the subthalamic nu

273 Safety of the procedure was assessed by recording the number of adverse events.

274 We demonstrate this by recording the oscillatory behavior of a Belousov-Zhab

275 f TENG array can be used for tracking motion by recording the output voltages signals in real-time to

276 entation of the myosin neck (containing LC1) by recording the parallel and perpendicular components o

277 We measured these fluctuations by recording the parallel and perpendicular components o

278 By recording the photoreceptor neuron ASJ in wild-type a

279 By recording the presynaptic capacitance changes and the

280 of solid AuQC piezoelectrodes was monitored by recording the resonance frequency shift and electroch

281 We fitted the parameters of the model by recording the responses of primary afferents to filte

282 Functional effects were evaluated by recording the scotopic threshold response (STR) and p

283 dLGN in the common pigmented C57/BL6 strain, by recording the synaptic responses evoked by electrical

284 Typically, these measurements are made by recording the temporal decay of a carrier-concentrati

285 Ulcer duration was determined by recording the time taken for ulcers to disappear.

286 The pH sensing is realized by recording the tip cyclic voltammetry and monitoring t

287 l window into conical intersections obtained by recording the transient wavepacket coherence during t

288 he PLA activity can be measured continuously by recording the variations with time of the UV absorpti

289 f different dimensionality reduction methods by recording their computational cost.

290 the individual steps in the transport cycle by recording transporter-associated currents: the recove

291 By recording ultrasonic vocalizations (USV) produced by

292 Here, by recording under a designed standardized scenario, the

293 We overcame this problem by recording unique tracks of green turtles (Chelonia my

294 neural encoding, and we test the hypothesis by recording, using MEG, the neural responses of human s

295 ibrium measured by flash photolysis followed by recording UV-vis spectra.

296 This hypothesis has never been tested by recording VF with electrodes spaced sufficiently clos

297 The released gas bubbles are documented by recording videos of the assay reservoir.

298 We tested this idea by recording vmPFC neurons while macaques performed a ga

299 e moreover assessed T-tubules sodium current by recording whole-cell sodium currents in control (N=5)

300 oplasmic domain has in MscS channel function by recording wild-type and mutant MscS single-channel ac