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1  suitable for analyzing multiple miRNAs on a single electrode.
2 e through conventional electrochemistry on a single electrode.
3 n one neuron is believed to be recorded on a single electrode.
4 f activation relative to injection through a single electrode.
5 peripheral lesions (n = 3) were treated with single electrodes.
6 low-intensity pacing stimuli delivered via a single electrode and is effective for terminating slower
7 m and compared with that obtained by using a single electrode and otherwise similar technique.
8 el was between that for RF ablation with the single electrode and that for RF ablation with the elect
9 ion-modulated neural selectivity across both single-electrode and population-level cortical responses
10 rdings in the peripheral primate retina with single-electrode and several types of multi-electrode st
11 amplitude-modulation rate of pulse trains on single electrodes at the apex or middle of long electrod
12                   The computations determine single-electrode capacitances in the neighborhood of 80
13 ation was significantly larger than the mean single-electrode coagulation (minimum diameter, 2.8 vs 1
14 mented in either a two-electrode or bipolar (single-electrode) configuration.
15 on amplified the signal fourfold compared to single-electrode detection, and the recycling efficiency
16 tions (nLFP) consistently changed in rate at single electrodes during tasks.
17                                              Single-electrode extracellular recording was used to fin
18 tivity lasting > 70% of AF cycle length on a single electrode (fractionated activity) or multiple ele
19    Unlike conventional electrochemistry at a single electrode, however, the mass-transport-limited cu
20 x) experiments with charged Teflon used as a single electrode in solution causing various chemical re
21 activity of pairs of neurons recorded with a single electrode in visual cortical area MT while monkey
22    Lens voltage was monitored by inserting a single electrode into the intact human lens, and changes
23  the first study to demonstrate that, on the single-electrode level, retinal electrical stimulation i
24  either the high-gamma or mu/beta power at a single electrode located over the motor or premotor area
25                                  With 3.0-cm single electrodes, maximum coagulation (mean, 5.2 cm +/-
26 m(3)) was significantly larger than the mean single-electrode (minimum diameter, 1.7 cm; maximum diam
27                         Cortical activity at single electrodes over the human superior temporal gyrus
28                                              Single electrode patch clamp techniques were used in dis
29                          RF application to a single electrode produced maximal coagulation of 2.9 cm
30 sual field maps of LFP and MUA recorded at a single electrode site were very similar.
31 12 with cluster, and 12 with multiple [three single electrodes spaced 2 cm apart] electrodes) were cr
32                   Single percepts induced by single-electrode stimulation were relatively small, but
33                                         On a single electrode, the multi-layered immunosensor could b
34 s previously shown, current passed through a single electrode typically induced a single retinal gang
35 htness of electrically generated percepts on single electrodes using a variety of electrical stimulat
36 rp electrode current clamp and discontinuous single electrode voltage clamp recordings were made from
37                                              Single electrode voltage clamp studies demonstrated that
38                     Evoked IPSCs examined by single electrode voltage-clamp methods in granule cells
39                                  Recorded in single-electrode voltage clamp mode, clonidine decreased
40  the light-induced currents in discontinuous single-electrode voltage clamp mode.
41                                        Using single-electrode voltage clamp, we show that brief chang
42  were recorded in isolated cardiomyocytes by single-electrode voltage clamp; [Ca2+]i was measured usi
43 hese neurones as either 'phasic' or 'tonic', single-electrode voltage-clamp recordings of the inwardl
44                         An internally cooled single electrode was used in five sessions; an internall
45                                           At single electrodes, we found response selectivity to dist
46                                  The LFPs at single electrodes were characterized by sharp negative p
47  process can be repeated up to 19 times on a single electrode without loss of assay sensitivity, and

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