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1 und decrease in the cardiac action potential half-width.
2 th in amplitude, failure rate, rise time and half-width.
3  an action potential waveform with a shorter half-width.
4 ance in association with an increase in EPSP half-width.
5 erhyperpolarization and a reduction in spike half-width.
6  on DIPI ratio and 0.802 (SD, 0.093) for gap half-width.
7 dplate currents (mepcs) with abnormally long half-widths.
8 (i), increased Kv3 currents and shortened AP half-widths.
9                             MNTB neuron APs (half-width 0.31 +/- 0.08 ms, n = 25) were fast, reliable
10 ired Kv3.3 subunits for fast repolarization (half-widths: 0.25 +/- 0.08 ms, n = 19 wild-type, 0.60 +/
11 .8% modulation percentage and a primary peak half-width 1.7 times wider than the modulation time, the
12 han in basket cells (rise times, 0.4-1.6 ms; half-widths, 2.2-9.7 ms).
13  spiking interneurone IPSPs had intermediate half-widths (27.3 +/- 3.68 ms, n = 3).
14 n be described by a pair of Gaussians of 1/e half-width A(Br) located at z = +Z(Br) relative to the b
15    Plots of the differential melt curve peak half-widths, a measure of cooperativity, versus d(TG4) c
16 or could not be determined, because the peak half-widths after suppression were paradoxically less th
17 murine cerebellar granule cells increased in half-width and amplitude following application of the be
18  Ca(2+) currents, increased action potential half-width and decreased spike threshold.
19 is partially responsible for determining the half-width and duration of the AP and thus Ca(2+) influx
20  was a positive correlation between the EPSP half-width and EPSP rise time.
21  morphology revealed that METH increased the half-width and produced larger coefficients of variation
22 ) currents, increasing action potential (AP) half-width and reducing repetitive firing.
23           Exogenous enzyme curtailed the ADP half-width and voltage integral by 20 and 25%, respectiv
24  faster AP repolarization (i.e., narrower AP half-widths and enlarged fast afterhyperpolarization).
25 es are chaotic for a range of their temporal half-widths and the probability density function (PDF) o
26 d latency to first spike, an increased spike half-width, and an overall increase in spike number with
27                       The rise times, areas, half-widths, and decay times of sEPSCs and emEPSCs and i
28 transition in GUVs and LUVs is much broader (half-width approximately 1.5 degrees C) than in MLVs ( a
29                Cholinergic release is brief (half-width approximately 200 ms), even in response to a
30 ease in pixel intensity (DIPI) ratio and gap half-width, are diagnostic metrics of SLS: i.e., the max
31 including shorter rise time, decay time, and half-width as compared to a bare carbon fiber electrode
32 eneration with larger amplitudes and shorter half-widths associated with SGCE mutations.
33 hes was estimated to be about 30 kilometres (half-width at half-maximum intensity, HWHM), but the cam
34 itonic absorption peaks as narrow as 50 meV (half-width at half-maximum) and peak-to-valley ratios (a
35 the occurrence of mEPCs with abnormally long half-widths at the neuromuscular junctions of Rab3A(-/-)
36 xpressing SERCA1 were reduced by 30-40 % and half-widths by 10-15 % compared to controls.
37                                  In a 0.6-ms half-width Ca2+ transient, Ca2+ occupied > 70% of the N-
38 , and enabled accurate measurements of spike half-widths characteristic of each cell type.
39 tenfold greater amplitude and twofold longer half-width compared to optical voltage transients (ArcLi
40 ion potential amplitude is increased and its half-width decreased, and a late depolarizing potential
41 on, generated the fastest impulse responses (half-width, Deltat = 7.9 +/- 1.1 ms).
42  range of 250000-400000 plates/m (2-3-s band half-width), demonstrating the high separation efficienc
43 esidence time: (i) measuring twice the front half-width for standard TDA, (ii) fitting a Gaussian cur
44  show that one such gene, Kv4.2, controls AP half-width, frequency-dependent AP broadening and dendri
45 , for which the durations at half-amplitude (half-widths) from internal nerve pairs in adjacent segme
46  any motoneurone synchronization peak with a half-width greater than about 2.2 ms should be assumed t
47 ral precision compared with cells with slow (half width, >100 msec) EPSPs.
48 erage distance (Rav) of less than 21 A and a half-width (HW) of 36 A.
49                       In both WT and KO, the half-width (HW) of the test response, and its number of
50 sients (ACTs) of varying duration (0.1-50 ms half-widths (hws)) and amplitude can be generated.
51                During LTS bursts, somatic AP half-width increases progressively with increasing spike
52                                          Its half-width is determined by the helical coherence length
53 nse rate can be estimated with a 95% CI with half width less than 20%.
54  vacancies near the grain-boundary core with half-width < 0.6 nm.
55          Typically, a very narrow peak (mean half-width <4 msec) near zero lag was observed.
56 row pass bands that shift by less than their half width (< 15 nm) even at extreme angles.
57                      Interneurons with fast (half width, <100 msec) EPSPs fired after short EPSP-spik
58 ts our interpretation that slow rising, long half-width mEPCs are caused by reduced diameter fusion p
59 tz spectrum with peak frequency omega(1) and half-width mu(1); its susceptibility with respect to a w
60 al model incorporating AP peak latencies and half-widths obtained from the apical, oblique and basal
61 centrally located and had defined horizontal half widths of 1, 2, and 3 degrees .
62 epths (h) of 27, 54, and 108 nm and the same half-width of 265 nm.
63 e was well approximated by a Gaussian with a half-width of 650 micros at 24 degrees C and 340 micros
64 als for these mean differences had a maximum half-width of about 5.6% across the SUV parameters asses
65 umps averaged 10 pA in peak amplitude with a half-width of ca 20 ms, representing simultaneous activa
66 -vertical incidence and is consistent with a half-width of mantle upwelling of about 100 km.
67 cts is based on a specified margin of error (half-width of the 95% confidence interval [CI]) of the p
68 mean value of -2.9 prism diopters (PD) and a half-width of the 95% limit of agreement of +/-11.4 PD.
69 ite below the surface is proportional to the half-width of the contact.
70      The phosphorylation of cTnI reduced the half-width of the distribution from 9.5 to 3.7 A.
71 between the fluorophores was 16.0 A, but the half-width of the distribution was large (17.9 A), which
72 noxolone suppressed amplitude, frequency and half-width of the epileptiform currents both in wild-typ
73 lecting mirror convolutes with the intrinsic half-width of the marker atom distribution in the membra
74 0.05 ms time to peak, n = 16) functions with half-widths of 0.38 +/- 0.10 ms, which declined to plate
75                                          The half-widths of the confidence intervals for relative dev
76                   Intrascanner repeatability half-widths of the confidence intervals for relative dev
77                                          The half-widths of the normal distribution curves range from
78 a(V)1.8 current density and action potential half-width, overshoot, and repetitive firing.
79 strate a correlation between the vibrational half-width parameter of the protein alpha-helical amide
80 PSP amplitudes, frequencies, rise-times, and half-widths preferentially in PT neurons.
81 e, sigma(in), and contributes to an apparent half-width, sigma, which is measured in the XSW experime
82 f U6 on the latency to first spike and spike half-width suggesting that these effects are mediated th
83            Tonic spikes have similar somatic half-widths to late burst spikes and undergo similar den
84 ribution function yields significantly small half-width values of 5.6 and 3.7 A, respectively, sugges
85 ption of peak asymmetry via leading/trailing half-widths vs relative height (fraction of maximum heig
86                          The increase in the half-width was much greater than that in the amplitude.
87                                       LSO AP half-widths were also fast, but absolutely required Kv3.
88 Similar but less pronounced decreases of the half-widths were also observed with the phosphorylated c
89 rdings revealed increased amperometric spike half-widths without change in quantal size after either