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1 nstant of repolarisation of the conditioning endplate potential.
2 s determined by micro-electrode recording of endplate potentials.
3 frequency but not the amplitude of miniature endplate potentials.
4 aracterized by a reduction in both miniature endplate potential amplitude and AChR abundance accompan
5                                    Miniature endplate potential amplitude was reduced 3 d after SC ab
6                                    Miniature endplate potential amplitude, but not frequency, was red
7 s muscle biopsy revealed decreased miniature endplate potential amplitudes, reduced endplate size and
8 t decrease of the amplitude of the miniature endplate potential and no deficiency of the ACh receptor
9  the mean amplitude of spontaneous miniature endplate potentials and bungarotoxin binding.
10 fatigable muscle weakness, reduced miniature endplate potentials and endplate potentials, reduced mot
11 el kinetics, or endplate ultrastructure, but endplate potentials depolarizing the resting potential t
12 or DuP 697, prevents the delayed increase in endplate potential (EPP) amplitude normally produced by
13 n the kinetics of stretch-induced changes in endplate potential (EPP) amplitude or miniature EPP (mEP
14              Cyclohexanol (10-25 mM) reduced endplate potential (EPP) amplitudes by 10-40% and enhanc
15 ontrol solution), the quantal content of the endplate potential (EPP) depressed more rapidly (approxi
16 nse to nerve stimulation was determined from endplate potentials (EPPs) and endplate currents (EPCs)
17                                   Similarly, endplate potentials (EPPs) evoked at low frequency were
18 ality between staining/destaining and summed endplate potentials (EPPs) representing total transmitte
19             Spontaneous MEPPs and uniquantal endplate potentials (EPPs) were released over the same l
20 mplitude; extracellular stimulation elicited endplate potentials (EPPs) which resembled MEPPs.
21 uires cholinergic signaling, which generates endplate potentials (EPPs), and excitation, the amplific
22 ll partially or fully occupied and expressed endplate potentials (EPPs).
23 ological measurements of ACh secretion (i.e. endplate potentials, EPPs) and the component of the prej
24 ed acetylcholine (ACh) release (reflected as endplate potentials, EPPs) is well described by a simple
25 tosolic [Ca2+], and reduced the amplitude of endplate potentials evoked after the end of a stimulus t
26 oved synergistic in restoring suprathreshold endplate potentials in mouse diaphragms fully intoxicate
27 depressed nerve control, increased miniature endplate potential (MEPP) amplitude, decreased MEPP freq
28 monstrate an increased spontaneous miniature endplate potential (mEPP) frequency in Nedd4 mutants.
29 ncreases evoked quantal output and miniature endplate potential (MEPP) frequency, again by activating
30                    The size of the miniature endplate potential (MEPP) increased 3- or 4-fold in prep
31  measuring the relative changes of miniature endplate potentials (mEPPs) and voltage responses to ste
32           Intervals of spontaneous miniature endplate potentials (MEPPs) are usually thought to follo
33       Boutons produced spontaneous miniature endplate potentials (MEPPs) of nearly normal amplitude;
34 C on neurosecretion in the form of miniature endplate potentials (MEPPs) were assessed.
35                                    Miniature endplate potentials (MEPPs) were more frequent near the
36 f spontaneous transmitter release (miniature endplate potentials (MEPPs)) from motor nerve terminals
37 tude or time course of spontaneous miniature endplate potentials (MEPPs).
38 tudy also showed a striking reduction of the endplate potential quantal content, consistent with addi
39 s, reduced miniature endplate potentials and endplate potentials, reduced motor endplate AChR number
40               Similar decreases in miniature endplate potential size ([integral]MEPP) followed repeti
41 ing continued, the fraction of the miniature endplate potential voltage-time integrals ( MEPPs) in th
42 the other hand, the mean amplitude of evoked endplate potentials was not decreased, due to an increas
43     The amplitude and rise time of miniature endplate potentials were also increased, but these chang
44                       On average, 63% of the endplate potentials were also seen in both recordings.
45     The amplitude and frequency of miniature endplate potentials were reduced, indicating impaired ne