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1 r s at 5 Hz and 27 vesicles per s at 200 Hz (perforated patch recordings).
2 this was not different during whole-cell or perforated patch recording.
3 y) in mouse cartwheel cells using gramicidin perforated-patch recording.
4 n variants were obtained with whole-cell and perforated-patch recording.
5 eurons was investigated using whole-cell and perforated-patch recording.
6 those of the endogenous buffer assayed with perforated-patch recording.
7 ulation of AHP currents using whole-cell and perforated patch recordings.
8 pauses were studied in striatal slices using perforated patch recordings.
9 exposure to 110 mM BaCl(2) in whole-cell and perforated patch recordings.
10 zing) current, as determined with gramicidin-perforated patch recordings.
11 kinin, and 1 histamine) using whole-cell and perforated-patch recordings.
12 s was investigated by performing gramicidine perforated-patch recordings.
13 ndard whole-cell recordings and amphotericin perforated-patch recordings.
14 ffin cells using whole-cell voltage clamp in perforated-patch recordings.
15 cytes, a sizable IKs could be measured using perforated-patch recordings (8.0 +/- 1.6 pA pF-1, n = 13
17 s from a single case of TSC were measured by perforated patch recording and compared to normal-appear
29 rtual synaptic activity using dynamic clamp, perforated-patch recordings from dissociated bullfrog sy
30 ification in the ear, we made whole-cell and perforated-patch recordings from hair cells and postsyna
31 o move toward resolution of these questions, perforated-patch recordings from medium spiny neurons in
33 re assessed using trypan blue dye exclusion, perforated-patch recordings, fura-2 fluorescence, and ti
34 BAPTA concentrations with values measured in perforated-patch recordings gave the endogenous calcium
35 re simultaneously recorded using whole-cell, perforated patch recording in freshly dissociated guinea
36 nique was developed that involves the use of perforated patch recordings in combination with fluoresc
47 nt of single-cell fura-2 fluorescence during perforated-patch recording of TRPC6 currents showed that
56 and Bengalese finches, using whole-cell and perforated-patch recording techniques in current-clamp c
57 annel were investigated using whole-cell and perforated-patch recording techniques in NG108-15 cells.
63 ersal potential was determined by gramicidin perforated patch recordings to be -65.3 +/- 5.0 mV, lyin
72 ing unitary field potential and gramicidin D perforated-patch recordings, we provide evidence that th
75 ) receptor activation on membrane potential, perforated patch recordings were obtained from NG2 cells
78 ding but enhanced current amplitude in those perforated-patch recordings where little current was evi
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