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

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

13 examined how the brain mediates this process by recording amygdala neural activity while monkeys perf

14 ded DNA target of the HhaI methyltransferase by recording an extensive set of (13)C NMR relaxation pa

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

20 By recording and playing back the light-driven membrane

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

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

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

24 By recording backscattered electrons, diffraction patter

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

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

27 By recording both firing in GABAergic interneurons and t

28 By recording both the images and emission spectra of tho

29 By recording brain and spinal cord activity in the same

30 353 for P2X3-containing receptors was tested by recording Ca(2+) transients to exogenously applied AT

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

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

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

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

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

36 By recording chronoamperograms at room temperature and v

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

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

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

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

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

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

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

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

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

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

47 By recording electrical activity directly from the corti

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

49 By recording electrically from oligodendrocytes and imag

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

51 We addressed this discrepancy by recording electrocorticographic activity from neurosu

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

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

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

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

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

57 By recording en passant from the segmental nerves, we in

58 By recording endogenous GABA receptor currents directly

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

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

61 e course of item and source memory retrieval by recording event-related potentials (ERPs) in patients

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

63 external events in the brain is achieved not by recording exact details of those events, but rather b

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

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

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

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

68 By recording fluorescence lifetime imaging microscopy (F

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

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

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

72 s examined in the turtle brainstem in vitro, by recording from accessory optic system neurons that re

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

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

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

76 By recording from both hemispheres simultaneously, we in

77 By recording from CA1 pyramidal cells in acute hippocamp

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

79 By recording from cone-bipolar cell pairs in the retina

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

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

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

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

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

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

86 By recording from monosynaptically connected pairs of re

87 We have directly verified this assumption by recording from MSTd neurons after bilateral labyrinth

88 By recording from multiple molecular layer interneurons

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

90 We tested this hypothesis by recording from neuronal ensembles in rodent dorsomedi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

105 separate inhibitory pathways can be assayed by recording from rod bipolar cells that possess distinc

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

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

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

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

110 We examined these questions by recording from synaptically coupled pairs of cartwhee

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

112 By recording from the ACC and hippocampal CA1 simultaneo

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

114 By recording from the C. elegans thermosensory neurons A

115 By recording from the cortex of freely moving animals en

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

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

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

119 By recording from ventral hippocampal CA1 neurons in rat

120 Here, by recording fusion pore kinetics during single vesicle

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

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

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

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

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

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

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

128 own by simulating the summation of IPSCs and by recordings in knockout mice devoid of tonic inhibitor

129 TTX sensitivity) in rat ventricular myocytes by recording INa in control and detubulated myocytes.

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

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

132 this object motion sensitive (OMS) response by recording intracellularly from all classes of retinal

133 By recording intracellularly from dissociated neurons an

134 Here, by recording intracellularly from Purkinje neurons in un

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

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

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

138 Here, by recording iSC activity during reversible cryogenic in

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

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

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

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

143 tory inputs affected rod bipolar cell output by recording light-evoked excitatory postsynaptic curren

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

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

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

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

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

149 ity in acute medial PFC slices of adult rats by recording local field potentials (LFPs) with microele

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

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

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

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

154 sed in human embryonic kidney (HEK293) cells by recording macroscopic currents elicited by rapid glyc

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

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

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

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

159 By recording miniature EPSCs (mEPSCs) from frontal corte

160 By recording motor- and somatosensory-evoked potentials

161 By recording multiple parameters, a detailed discriminat

162 on estimation, has been directly tested here by recording neural activities before and after inactiva

163 This was achieved by recording neural activity in GC while rats licked fou

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

165 We tested these predictions by recording neural ensembles and LFPs from rats running

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

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

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

169 We tested this proposal by recording neuronal activity and length tuning in neur

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

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

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

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

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

175 perceived location of this "flashed" element by recording neuronal responses while monkeys viewed the

176 By recording neurons from the feeding and withdrawal net

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

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

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

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

181 Furthermore, by recording NMDA-receptor-mediated currents (I(NMDA)) a

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

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

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

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

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

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

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

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

190 By recording optogenetically tagged interneurons of spec

191 Spatial frequency was measured by recording optomotor responses at P100 and P150, and l

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

193 Functional restoration was determined by recording pinacidil-based KATP current by whole cell

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

195 By recording population activity with fMRI during the oc

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 roduced at a generator electrode is measured by recording potential-time transients with Ag, Ag/AgCl,

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

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

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

207 By recording responses in cells isolated from taste buds

208 By recording responses of neural ensembles to mixtures o

209 By recording responses to pairs of sinusoidally amplitud

210 re, we investigate resolution within the TWI by recording responses to tones containing silent gaps (

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 By recording simultaneously from a large number of singl

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

216 5- to 6-d-old rats, we test this hypothesis by recording simultaneously from forelimb and barrel reg

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

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

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

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

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

222 d by measuring retGC activity biochemically, by recording single rod and electroretinogram (ERG) resp

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

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

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

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

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

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

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

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

235 By recording spindle afferent responses from alert human

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

237 ion in film composition can then be built up by recording such diffraction patterns at regular interv

238 tin lipids, and binding curves was generated by recording surface fluorescence versus increasing conc

239 r motoneurons synapses in spinal cord slices by recording synaptic currents in the presence of a low-

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

256 st excitability of CTS pathways was measured by recording the EMG response evoked in the first dorsal

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

258 onset of vascular permeability was monitored by recording the extravasation kinetics of FITC-labeled

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

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

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

262 By recording the full fluorescence spectra and super-res

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

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

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

266 By recording the locomotive motor activities, we further

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

268 in liquids and solids is primarily detected by recording the net dipolar magnetic field outside the

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

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

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

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

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

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

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

276 We examined this possibility directly by recording the preparatory activity of single cortical

277 The MEDS score was calculated by recording the presence of terminal illness, tachypnea

278 By recording the presynaptic capacitance changes and the

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

280 ecular mechanisms of carotid body pH sensing by recording the responses of glomus cells isolated from

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

282 transmission is regulated in the macaque LGN by recording the retinal input to a single LGN neuron wh

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

284 in the POAH was tested in the present study by recording the single-unit activity of POAH neurons in

285 We do this by recording the spikes of CTect neurons and the field p

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

287 Uptake by PCs can be monitored by recording the synaptic transport current (STC) mediat

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

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

290 were administered before lights off followed by recording throughout the 12-h dark period and followi

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

292 By recording ultrasonic vocalizations (USV) produced by

293 target the output neurons of the neocortex, by recording unitary EPSPs from layer 5 pyramidal neuron

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 By recording visual event-related potentials (ERPs) elic

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

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