1 directly upon GABA receptors of the neurons
being recorded from.
2 ion of serotonin in the vicinity of the cell
being recorded from.
3 Simultaneous core temperatures
were recorded from 1 to 5 days.
4 operative, and 10 postoperative risk factors
were recorded from 1,965 patients undergoing restorative
5 he vermillion and/or mucosal part of the lip
were recorded from 10 patients with clinically normal li
6 Light-adapted, full-field ERGs
were recorded from 10 XLRP carriers and 12 visually norm
7 At each time, mfERGs
were recorded from 103 retinal locations, and fundus pho
8 Resting-state EEG
was recorded from 12 TRD patients at pre-treatment basel
9 Magneto-encephalographic (MEG) data
were recorded from 13 adult human participants with ASD
10 elivered mild and moderate rectal distention
was recorded from 14 female IBS patients and 12 healthy
11 Precordial ECGs
were recorded from 15 ischemic cardiomyopathy and 15 Bru
12 ntials to reversing checkerboard stimulation
were recorded from 15 older controls and 15 amnestic MCI
13 Event-related potentials
were recorded from 15 patients with DSM-IV schizophrenia
14 Pallidal oscillations
were recorded from 153 contact pairs in 27 patients.
15 Therefore, local field potentials
were recorded from 16 hemispheres in 12 patients undergo
16 e electromyographic activity (EMG) and force
were recorded from 17 paralysed motor units (n = 7 subje
17 match) and unprimed (remotely related) words
were recorded from 18 healthy control subjects and 18 pa
18 The electroencephalogram (EEG)
was recorded from 19 scalp locations from 371 subjects r
19 Electroencephalographic data
were recorded from 19 SZ and 22 healthy control (HC) sub
20 A total of 268 cases of PCLPD
were recorded from 1973 to 2004.
21 or PRP for type 1 ROP between 2008 and 2012
were recorded from 2 medical centers in Atlanta, Georgia
22 Dark-adapted ERGs
were recorded from 2- to 4-month-old C57BL/6 and 7.5-mon
23 These
were recorded from 20 diabetic patients without retinopa
24 Neuromagnetic signals
were recorded from 20 right-handed healthy adult humans
25 Responses
were recorded from 210 participants in total (59 monozyg
26 ce, serum creatinine level, and measured GFR
were recorded from 244 individuals who underwent renal d
27 -stimulus pacing while unipolar electrograms
were recorded from 250 sites.
28 A total of 376 CP
were recorded from 26 807 CTO-PCI interventions (inciden
29 ity 129-channel event-related potential data
were recorded from 26 participants.
30 n who were eligible to participate, and data
were recorded from 2899 (87%) of these children.
31 Monocular torsional eye movements
were recorded from 30 subjects between 19 and 72 years o
32 Event-related potentials
were recorded from 32 scalp electrodes while participant
33 The ERN and the error positivity (Pe)
were recorded from 33 individuals with schizophrenia, 45
34 ull-field scotopic electroretinograms (ERGs)
were recorded from 44 male hemizygous Rs1h-KO and 44 mal
35 logical indicators of performance monitoring
were recorded from 45 OCD patients and 39 healthy compar
36 Ventricular epicardial electrograms
were recorded from 5 anesthetized pigs with a 127-electr
37 A total of 1193 head impacts
were recorded from 5 training camp practices in the 29 c
38 s/m(2)) on a rod-saturating blue background
were recorded from 51 MS patients and 33 age-matched con
39 METHOD: P50
was recorded from 52 patients with schizophrenia and 41
40 In total, 1762 CPs
were recorded from 527 121 PCI procedures (incidence of
41 PERGs
were recorded from 56 undilated eyes of 28 anesthetized
42 The EEG
was recorded from 57 rigorously screened adolescents (12
43 A total of 109 sponge species
was recorded from 69 sites, with the 10 most common spec
44 Data
were recorded from 69 macaque retinal ganglion cells, by
45 Extracellular action potentials
were recorded from 73 C1-C2 neurons whose axons were ant
46 Cytological diagnoses from EBUS-TBNA
were recorded from 774 patients with known or suspected
47 PR-VEP responses
were recorded from 81 adults and 137 infants (ages 3.6-7
48 ntanoic acid (D-AP5), a small EPSC component
was recorded from 90 % of neurones tested.
49 Overall, 521 reportable events
were recorded from 94 patients (93.1%).
50 3), 2,179 operational taxonomic units (OTUs)
were recorded from 983,056 sequences.
51 Embryonic transcription of each phosphatase
was recorded from a high-density oligonucleotide tiling
52 Primary afferent firing
was recorded from a mesenteric nerve bundle supplying a
53 ng nonresonant excitation, whereas no signal
was recorded from a monolayer at the sapphire interface.
54 Blood pressure
was recorded from a radial artery catheter kept at the s
55 In a porcine model (n=8), neuronal activity
was recorded from a ventricular ganglion using a microel
56 Electrograms
were recorded from a 36-electrode catheter in the left v
57 Motor-evoked potentials
were recorded from a hand muscle in 12 patients with PD
58 CCEPs
were recorded from a larger area than the posterior lang
59 Monophasic action potentials
were recorded from a left ventricular epicardial site on
60 preoperative risk factors, including ASA PS,
were recorded from a random sample of 5878 surgical pati
61 Fluorescence changes in patch-clamped cells
were recorded from a Shaker channel mutant (M356C) label
62 studies in which immediate reactions to GBCA
were recorded from a total of 716 978 administrations of
63 Auditory ERPs
were recorded from a wide range of horizontal locations
64 Electroretinographic (ERG) a-wave responses
were recorded from abcr-/- mice and two control strains.
65 The following parameters
were recorded from abdominopelvic CT study reports for t
66 at the wrist and compound action potentials
were recorded from abductor pollicis brevis muscle.
67 wrist and compound muscle action potentials
were recorded from abductor pollicis brevis.
68 resulting compound muscle action potentials
were recorded from abductor pollicis brevis.
69 eady-state visual evoked potentials (SSVEPs)
were recorded from action videogame players (VGPs) and f
70 microA while evoked field potentials (EFPs)
were recorded from adjacent and more distant HF areas re
71 on, infections, interventions, and mortality
were recorded from admission through PICU death or disch
72 ERGs
were recorded from adult wild-type C57/BL6 mice anaesthe
73 Surface EMG signals
were recorded from all participants and decoded using a
74 otentials of different amplitudes and shapes
were recorded from all the four recording sites, suggest
75 Single-channel clusters
were recorded from alpha4beta2gamma2 receptors in the pr
76 ERGs
were recorded from anaesthetized Brown Norway rats in re
77 lopmental stage of a neuron or glial cell is
being recorded from,
and to attribute measured membrane
78 Photopic slow-sequence mfERGs
were recorded from anesthetized adult macaque monkeys an
79 Retinal intrinsic optical signals
were recorded from anesthetized cats with a modified fun
80 Photopic full-field flash ERGs
were recorded from anesthetized macaque monkeys before a
81 hemical (0.2 ml algogenic chemicals) stimuli
were recorded from antidromically activated PSDC and VLF
82 licker at 0.5, 1, 2, 4, 8, 16, 32, and 64 Hz
were recorded from areas V1, V2/V3, motion-sensitive are
83 Unipolar electrograms
were recorded from as many as 98 epicardial and 144 intr
84 Here, STCs
were recorded from astrocytes in rat hippocampal slices
85 Single units
were recorded from auditory thalamus [medial geniculate
86 ng pregnancy, and childhood malaria episodes
were recorded from birth to age 5 years.
87 of the photorefractor and allow responses to
be recorded from both eyes.
88 mfVEP
was recorded from both eyes of 12 patients with ON/MS.
89 The PERG
was recorded from both eyes of 14 normal subjects in res
90 During AF, electrograms
were recorded from both atria simultaneously for 1 to 5
91 Findings
were recorded from both colonoscopy reports and correspo
92 Full-field electroretinograms (ERGs)
were recorded from both eyes at 2, 3, 4, and 5 months af
93 d ankle joints and activity from six muscles
were recorded from both legs.
94 Evoked EPSCs (eEPSCs)
were recorded from both types of neurons by stimulating
95 Brain lesion count
was recorded from brain magnetic resonance (MR) imaging
96 Respiratory neural activity
was recorded from brainstem-spinal cord in vitro perinat
97 Neuronal activity
was recorded from CA1 pyramidal cells, and in both young
98 AMPAR-mediated currents
were recorded from CA1 pyramidal neurons and dentate gra
99 Current-clamp responses
were recorded from CA1 pyramidal neurons in wild-type (W
100 re excitatory postsynaptic currents (mEPSCs)
were recorded from CA1 pyramidal neurons.
101 lar excitatory postsynaptic field potentials
were recorded from CA3-CA1 synaptic contacts from hippoc
102 Chick-a-dee calls
were recorded from Carolina chickadees in a naturalistic
103 Sensory activity
was recorded from carotid bodies ex vivo.
104 Basal KNa channel activity could
be recorded from cell-attached patches of acutely dissoc
105 altering tonic VIIIth nerve input, ADN cells
were recorded from chinchillas after bilateral semicircu
106 Brainstem responses
were recorded from Chinese and English participants in r
107 al field potentials and multiunit discharges
were recorded from chronically implanted electrodes.
108 ts, auditory event related potentials (ERPs)
were recorded from chronically implanted intracranial el
109 injections of BMI (25 ng/side) into the PVN
were recorded from conscious rats to avoid the complicat
110 Motor evoked potentials (MEPs)
were recorded from contralateral (cMM) and ipsilateral (
111 EPSCs
were recorded from cultured hippocampal neurons and DSE
112 methyl-D-aspartate (NMDA)-activated currents
were recorded from cultured rat cortical neurons.
113 When whole-cell responses
were recorded from current-clamped neurones using the gr
114 raphic (ERG) responses to full-field stimuli
were recorded from dark-adapted rats at ages 18 and 31 d
115 iques, substantially higher signal intensity
was recorded from developed platform in comparison to th
116 GABA-mediated postsynaptic currents (IPSCs)
were recorded from dopaminergic (DA) neurons of the vent
117 (A)R)-mediated postsynaptic currents (IPSCs)
were recorded from dopaminergic neurons of the ventral t
118 al-arm maze task, and local field potentials
were recorded from dorsal hippocampus and prefrontal cor
119 PERGs and FERGs
were recorded from each eye in 32 C57BL/6J mice using co
120 s aged 13 to 17 years, longitudinal DTI data
were recorded from each subject at two time points that
121 Vitreal and intraretinal ERGs
were recorded from eight dark-adapted, anesthetized Abys
122 64-channel scalp EEG data
were recorded from eight healthy subjects in two tasks:
123 excitatory postsynaptic potentials (fEPSPs)
were recorded from either the dentate gyrus (DG) or CA1
124 Monophasic action potentials (MAPs)
were recorded from epicardial and endocardial surfaces o
125 High-resolution optical action potentials
were recorded from epicardial and endocardial surfaces o
126 Whole-cell currents
were recorded from epicardial and M myocytes.
127 trically evoked auditory brainstem responses
were recorded from ES-treated animals at the start and e
128 ard current during a step hyperpolarization,
was recorded from every labeled, medium-sized neuron and
129 evoked potentials (MEPs) and motor threshold
were recorded from extensor carpi radialis using transcr
130 Test and conditioned responses
were recorded from flexor carpi radialis (FCR) when the
131 Motor activity
was recorded from four dogs during fasting and after fee
132 Electromyograms (EMGs)
were recorded from four hand muscles, and reflexes were
133 ing the random split-mouth method, PD and AL
were recorded from four sites per tooth: mesial-buccal,
134 ERGs
were recorded from four trichromatic and two dichromatic
135 IKs
was recorded from freshly isolated rabbit ventricular my
136 Em and currents
were recorded from freshly isolated PASMCs using the per
137 le-cell currents induced by glycine (I(Gly))
were recorded from freshly isolated PFC neurons of Sprag
138 selective electrical vagal stimulation (EVS)
were recorded from gastric fundus and antral regions of
139 s, calcium-dependent fluorescence transients
were recorded from GCaMP-labeled cortical neurons.
140 I(Ca)
was recorded from gerbil IHCs maintained near physiologi
141 Cs), both of which can excite these neurons,
were recorded from GnRH neurons in brain slices from adu
142 In the present experiment, ERPs
were recorded from healthy young adults (N=24) while the
143 Glutamate-gated currents can
be recorded from heterologous cells that express vertebr
144 Interictal HFOs
were recorded from hippocampal microelectrodes in 10 pat
145 Spontaneous field potentials
were recorded from hippocampus of pre-pubertal (~28-32 P
146 Scotopic and photopic Ganzfeld ERGs
were recorded from homozygous Pcdh15av-5J and Pcdh15av-J
147 al health data including laboratory findings
were recorded from hospital records, and the periodontal
148 No calcium currents
are recorded from human embryonic kidney 293 cells coexp
149 High-density electroencephalography
was recorded from human subjects during a 160 min contin
150 Isometric force and surface EMG signals
were recorded from human adductor pollicis muscles in re
151 channel currents elicited by 0.1 or 1 mM ACh
were recorded from human embryonic kidney (HEK) cells th
152 Responses to acoustic input
were recorded from human temporal cortex using subdural
153 he periaqueductal grey (PAG), which have now
been recorded from in humans during exercise.
154 Loss of function in all missense variants
was recorded from in-vitro functional studies, and was s
155 n region, where abnormal electrical activity
was recorded from individuals with schizophrenia many ye
156 o address these issues, macroscopic currents
were recorded from inside-out giant patches from Xenopus
157 s and single channel or macroscopic currents
were recorded from inside-out patches.
158 During a terminal experiment, H-reflexes
were recorded from interosseus muscles after stimulation
159 responses to afferent and efferent stimuli,
were recorded from intrinsic cardiac neurons.
160 ICa
was recorded from isolated ventricular cardiomyocytes.
161 Fluorescent Ca2+ or voltage signals
were recorded from isolated adult rat ventricular myocyt
162 als and cell shortening or Ca(2+) transients
were recorded from isolated canine left ventricular myoc
163 Whole-cell currents
were recorded from isolated CCSM cells of Slo+/+ and Slo
164 Results: A total of 80412524 deaths
were recorded from January 1, 1980, through December 31,
165 voked excitatory synaptic potentials (EPSPs)
were recorded from L5 neurons by using a whole-cell curr
166 TMRM fluorescence (FTMRM)
was recorded from Langendorff-perfused rabbit hearts imm
167 enerated, and inhibitory synaptic properties
were recorded from layer 2/3 pyramidal neurons.
168 al magnetic stimulation (TMS) and H-reflexes
were recorded from left hand muscles during choice react
169 es in the intermediate/deep layers of the OT
were recorded from lightly anesthetized owls confronted
170 Slow waves (slow wavesSMC)
were recorded from LSMCs and CSMCs.
171 Rhythmic locomotor-like activity
was recorded from lumbar ventral roots after short train
172 ysed auditory evoked potentials (AEPs) which
were recorded from medical students while they diagnosed
173 In this study, single-unit activity
was recorded from monkeys while they performed a "center
174 Electroretinogram (ERG)
was recorded from MPS IIIB and wild-type (WT) mice at th
175 lation (VF), transmembrane potentials (V(m))
were recorded from multiple sites of perfused rabbit hea
176 GABAergic, and glycinergic synaptic currents
are recorded from muscle cells, demonstrating that activ
177 ainstem frequency-following responses (FFRs)
were recorded from musicians and non-musician controls i
178 ical activity from face and scalp electrodes
was recorded from neonates during an eye movement condit
179 ) and miniature end-plate potentials (MEPPs)
were recorded from neuromuscular junctions in the hemidi
180 In each environment, activity
was recorded from neuronal ensembles in hippocampal area
181 rat hypothalamic slices, electrical activity
was recorded from neurons in the ventrolateral VMN, the
182 Na(+) currents
were recorded from neurons in brain slices obtained from
183 Burst-tonic activity
was recorded from oculomotor nucleus neurons in three an
184 Bronchoconstrictor responses
were recorded from offspring bronchial segments.
185 Responses
were recorded from one eye of each subject using a bipol
186 ata, and donor and recipient characteristics
were recorded from our prospective cohort from the Singa
187 data and donor and recipient characteristics
were recorded from our prospective cohort from the Singa
188 data and donor and recipient characteristics
were recorded from our prospective cohort from the Singa
189 activity during horizontal sinusoidal motion
was recorded from pairs of oculomotor, trochlear, or abd
190 Complications
were recorded from patient records; preventability was b
191 equivalent in millirems (1 mrem = 0.01 mSv)
was recorded from personal dosimeters worn on laboratory
192 s region, whereas a robust somatosensory MMN
was recorded from postcentral gyrus in the absence of an
193 4 days, and voltage-gated potassium currents
were recorded from presumptive CA3 pyramidal neurones.
194 Electrophysiological activity
was recorded from primary cultures of dissociated rat co
195 field and auditory-evoked potentials (AEPs)
were recorded from primary auditory cortex and hippocamp
196 LFPs and 918 single units
were recorded from primary motor cortex (M1), primary so
197 y afferent neurones innervating the duodenum
were recorded from rat nodose ganglia.
198 Multi-unit activity
was recorded from rats doing an working memory task in c
199 responses to intraorally delivered tastants
were recorded from rats implanted with bundles of electr
200 , ensembles of medial frontal cortex neurons
were recorded from rats trained to perform three differe
201 ty status (Expanded Disability Status Scale)
was recorded from records and questionnaires.
202 the mammalian retina and excitatory currents
were recorded from retinal ganglion cells under whole-ce
203 Hemodynamic responses
were recorded from right and left occipital sites using
204 Monophasic action potentials
were recorded from right and left ventricular endocardiu
205 r electrograms as a surrogate for APD (n=19)
were recorded from right and left ventricular endocardiu
206 Transmembrane potentials
were recorded from right ventricular endocardial tissue
207 by the normal transduction cascade, since it
was recorded from rods lacking transducin.
208 At 3.5 gigapascals, acoustic emissions
are recorded from samples with up to 50 vol% of antigori
209 Whole cell Ba(2+) currents
were recorded from SAN cells from mice carrying a point
210 An electroencephalogram
was recorded from scalp electrodes of 10 PLS patients an
211 Electromyographic (EMG) activity
was recorded from selected hindlimb muscles during linea
212 ts target region in the dorsal striatum (DS)
were recorded from simultaneously as rats performed diff
213 Electrophysiological activity
was recorded from single neurons (units) in the hippocam
214 Cytosolic Ca2+ oscillations
were recorded from single aequorin-injected hepatocytes.
215 taste buds on the caudal 1/3 of the tongue)
were recorded from single cells in the rostral nucleus o
216 Spike trains
were recorded from single units in the ventral cochlear
217 Single-cell neural activity
was recorded from SOA neurons in two monkeys with exotro
218 notochord was used, and responses to bending
were recorded from SRNs, as well as from motoneurons inn
219 Excitatory postsynaptic currents (EPSCs)
were recorded from superficial dorsal horn neurons of sp
220 Action potentials (APs)
were recorded from superfused SVC and PV sleeves using m
221 Surgical and tumor factors
were recorded from surgical and pathologic reports from
222 anial somatosensory event-related potentials
were recorded from temporal, parietal, and frontal lobe
223 Neuronal activity
was recorded from tetrodes within the anterior interposi
224 bthreshold A-type K(+) currents (ISA s) have
been recorded from the cell bodies of hippocampal and ne
225 bthreshold A-type K(+) currents (ISA s) have
been recorded from the somata of nociceptors and spinal
226 g this central crease; the analytical signal
is recorded from the folded configuration.
227 eplicated runs and low variation in the runs
was recorded from the AUC values.
228 ons, and multichannel single-neuron activity
was recorded from the caudal supplementary motor area.
229 Cochlear microphonic potential (CM)
was recorded from the CF2 region and the sparsely innerv
230 cal response to phrenic afferent stimulation
was recorded from the cortical surface, contralateral to
231 discharge of duodenal vagal afferent fibres
was recorded from the dorsal abdominal vagus nerve in an
232 Electrical activity
was recorded from the fourth cervical ventral root (C4 V
233 Rhythmic inspiratory-related activity
was recorded from the hypoglossal rootlet of 700- to 800
234 ve activity of single-unit cardiac afferents
was recorded from the left sympathetic chain (T2-T5) in
235 of single unit cardiac sympathetic afferents
was recorded from the left sympathetic chain or rami com
236 of single unit cardiac sympathetic afferents
was recorded from the left sympathetic chain or rami com
237 Single-unit cardiac afferent activity
was recorded from the left sympathetic chain or rami com
238 In the current study, spiking activity
was recorded from the medial PFC of rats performing a de
239 Single neuron activity
was recorded from the prelimbic and infralimbic areas of
240 digenous children while the lowest diversity
was recorded from the relatively wealthy Chinese childre
241 Electrical brain activity
was recorded from the scalps of healthy men and women wh
242 Single-unit activity of cardiac afferents
was recorded from the sympathetic chain of anesthetized
243 Extracellular single unit activity
was recorded from the urethane-anesthetized hamster.
244 Both surface EMG and SMU activity
were recorded from the 1DI muscle.
245 d to magnesium sulphate treatment, no events
were recorded from the 2 trials providing data.
246 acid administration through the gastrostomy
were recorded from the acromiotrapezius muscle.
247 whereas responses to stimulation of the heel
were recorded from the ankle extensor medial gastrocnemi
248 ponses to electrical stimulation of the toes
were recorded from the ankle flexor tibialis anterior (T
249 HD cells
were recorded from the anterior dorsal thalamus of Long-
250 Electrograms
were recorded from the anterolateral right atrium, His b
251 M-mode images of the interventricular septum
were recorded from the apical 4-chamber view in 7 closed
252 ation-induced (MC-induced) unitary responses
were recorded from the basal ganglia of control and 6-hy
253 tentials (fEPSPs) or population spikes (PSs)
were recorded from the CA1 hippocampus following CA1 s.
254 Neural ensembles
were recorded from the CA3 region of rats running on T-b
255 Ultrasound and surface EMG
were recorded from the calf and tibialis anterior (TA) m
256 ology and Chronic Health Evaluation II score
were recorded from the case notes.
257 sh multifocal electroretinograms (sf-mfERGs)
were recorded from the central 45 degrees, and stereo fu
258 Full-thickness images
were recorded from the central and temporal cornea, and
259 Perinatal data
were recorded from the children's medical records or rep
260 Alarm notification data and response times
were recorded from the continuous capture of institution
261 Extracellular field potentials
were recorded from the deep-layer visual neocortex.
262 Optical signals
were recorded from the epicardium with a CCD video camer
263 H-reflex) and motor evoked potentials (MEPs)
were recorded from the gastrocnemius muscle.
264 d electroretinograms (flash and flicker ERG)
were recorded from the injured and control eyes before a
265 angiograms showing individual cell movement
were recorded from the intact eyes of four monkeys and t
266 Surface ECGs
were recorded from the limb leads, and VAQRS was calcula
267 Eighty-six single fibres
were recorded from the LSN.
268 The mapping of the data that
were recorded from the MEA revealed the transfer mode of
269 Mean skin temperatures
were recorded from the mouth and nose using infrared the
270 Additional responses to odors
were recorded from the neuron in Heliothis virescens.
271 ect and indirect pupil light reflexes (PLRs)
were recorded from the noninjured eye, and electroretino
272 Motor-evoked potentials
were recorded from the resting and active right FDI.
273 Motor-evoked potentials (MEPs)
were recorded from the right first dorsal interosseous i
274 trically-evoked responses in both structures
were recorded from the same slice.
275 No auditory or visual responses
were recorded from the SC, although neurons in the neigh
276 Cochlear microphonic potentials (CMs)
were recorded from the sharply tuned, strongly resonant
277 rical stimulation of the L4/L5 dorsal roots,
were recorded from the spinal cord above and below a les
278 Point-wise total deviation values
were recorded from the static automated perimetry (Swedi
279 Local field potentials
were recorded from the subthalamic nucleus of 12 patient
280 Local field potentials
were recorded from the subthalamic nucleus of eight Park
281 and P150, and luminance threshold responses
were recorded from the superior colliculus at P150.
282 -unit and discriminated single unit activity
were recorded from the surface of arterial vessels.This
283 (I.M.) and surface electromyographic signals
were recorded from the vastus lateralis (VL) during volu
284 Tidal volume and respiratory rate
were recorded from the ventilator.
285 Extracellular unit responses
were recorded from the vestibular nucleus (VN) and media
286 mpound action potentials to puretone stimuli
were recorded from the VIIIth craniofacial nerve at 4wee
287 ith timescales the order of milliseconds can
be recorded from these samples.
288 Three shapes of action potential (AP)
were recorded from these receptors: type 1 with no infle
289 s of sensory stimuli were presented and ERPs
were recorded from thirty-two scalp electrodes while par
290 Thirty-nine plant taxa
were recorded from three hives but only ten at greater t
291 us excitatory postsynaptic currents (sEPSCs)
were recorded from two different classes of neurons in t
292 Responses
were recorded from two intrinsic hand muscles.
293 tivity of 21 MRMNs in the oculomotor nucleus
were recorded from two monkeys with exotropia as they pe
294 Responses
were recorded from two normal subjects whose pupils were
295 Single-unit activity
was recorded from V6A in two Macaca fascicularis fixatin
296 ory postsynaptic currents (eEPSCs or sEPSCs)
were recorded from visualized, layer II/III pyramidal ce
297 Spontaneous phasic contractions
were recorded from W/Wv muscles in the absence of slow w
298 Full-field electroretinograms (ERGs)
were recorded from wild-type (C57BL/6; Rpe65(+/+)) and R
299 Although more contractions
were recorded from women who delivered before 35 weeks t
300 during which a total of 8259 and 7042 cells
were recorded from young and old rats, respectively.