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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
16                                        Using perforated-patch recording, a small proportion of the co
17 s from a single case of TSC were measured by perforated patch recording and compared to normal-appear
18                                              Perforated patch recording and whole-cell recording comb
19                       However, by performing perforated patch recordings and calcium imaging experime
20                                              Perforated-patch recordings and two-photon calcium imagi
21 ore, they are present in both whole-cell and perforated-patch recording configurations.
22 ns under voltage clamp in the whole-cell and perforated-patch recording configurations.
23                                              Perforated patch recordings demonstrate that the reversa
24                              With gramicidin-perforated patch recording, E(GABA) was -25 +/- 5 mV (me
25                                           In perforated patch recordings, EREV for RB cells was signi
26   Activation of the B cell receptor (BCR) in perforated-patch recordings evoked the same response.
27            Data obtained with whole-cell and perforated patch recordings from SNR neurons in slices i
28                                   Whole-cell perforated-patch recording from cultured CA1-CA3 pyramid
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
32                                           In perforated-patch recordings from rat utricular hair cell
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
37                          Based on gramicidin-perforated patch recordings in hypothalamic slices from
38                                        Using perforated-patch recording in a mammalian synapse, we fo
39                                              Perforated patch recordings indicated that the efficacy
40                                           In perforated patch recordings, linopirdine, a specific M-c
41                                          The perforated patch recording method was employed in order
42                                            A perforated patch recording method was used to determine
43                    Using both whole-cell and perforated patch recording methods, hypotonic solution c
44 capsaicin were examined using whole-cell and perforated patch recording methods.
45                               The whole-cell perforated-patch recording mode was used to record a Ca2
46       Contrary to our expectations, nystatin-perforated patch recordings of whole-cell K+ currents re
47 nt of single-cell fura-2 fluorescence during perforated-patch recording of TRPC6 currents showed that
48                                           In perforated-patch recordings, phorbol 12-myristate 13-ace
49                                   Gramicidin perforated-patch recording revealed a GABA reversal pote
50                                              Perforated-patch recordings revealed changes in action p
51                                              Perforated-patch recordings revealed that oscillatory re
52                                              Perforated-patch recordings revealed that serum induced
53                                In agreement, perforated-patch recordings show that intracellular Cl(-
54             Here, whole-cell patch clamp and perforated-patch recordings show that substrates of the
55                                          The perforated patch recording technique was used to investi
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.
58                 Here, we used whole-cell and perforated-patch recording techniques to elucidate the m
59 postnatal CR cells was studied directly with perforated-patch recording techniques.
60                                           In perforated-patch recordings, the rate of desensitization
61                                           In perforated-patch recordings, the rise in [Ca2+]i coincid
62                                In whole-cell perforated-patch recordings, these cells responded to lo
63 ersal potential was determined by gramicidin perforated patch recordings to be -65.3 +/- 5.0 mV, lyin
64                           We used gramicidin-perforated patch recordings to characterize Cl- transpor
65           The rebound of the current seen in perforated-patch recordings was blocked by the PI4-kinas
66                 Next, using gramicidin-based perforated patch recordings, we found that the GABA reve
67                                        Using perforated-patch recording, we also found that K(ATP) ch
68                          By using gramicidin perforated-patch recordings, we established that the pre
69                                        Using perforated-patch recordings, we found that individual ha
70                                        Using perforated-patch recordings, we have examined the part p
71                         Using whole-cell and perforated-patch recordings, we have examined the part p
72 ing unitary field potential and gramicidin D perforated-patch recordings, we provide evidence that th
73                                              Perforated patch recordings were made from single mouse
74                    Whole-cell and gramicidin-perforated patch recordings were obtained from inferior
75 ) receptor activation on membrane potential, perforated patch recordings were obtained from NG2 cells
76                                              Perforated patch recordings were used to determine how p
77                               Whole-cell and perforated-patch recordings were made from neurons in ra
78 ding but enhanced current amplitude in those perforated-patch recordings where little current was evi

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