ライフサイエンスコーパス: perforated patch recording

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 in abGCs of adult male and female mice using perforated patch recordings.

12 of GPe neurons in male and female mice using perforated patch recordings.

13 kinin, and 1 histamine) using whole-cell and perforated-patch recordings.

14 s was investigated by performing gramicidine perforated-patch recordings.

15 ndard whole-cell recordings and amphotericin perforated-patch recordings.

16 ffin cells using whole-cell voltage clamp in perforated-patch recordings.

17 cytes, a sizable IKs could be measured using perforated-patch recordings (8.0 +/- 1.6 pA pF-1, n = 13

18 Using perforated-patch recording, a small proportion of the co

19 In perforated patch recordings, activation of GABAARs, eith

20 s from a single case of TSC were measured by perforated patch recording and compared to normal-appear

21 Perforated patch recording and whole-cell recording comb

22 However, by performing perforated patch recordings and calcium imaging experime

23 Using perforated patch recordings and optogenetics, they show

24 Perforated-patch recordings and two-photon calcium imagi

25 ore, they are present in both whole-cell and perforated-patch recording configurations.

26 ns under voltage clamp in the whole-cell and perforated-patch recording configurations.

27 Perforated patch recordings demonstrate that the reversa

28 With gramicidin-perforated patch recording, E(GABA) was -25 +/- 5 mV (me

29 In perforated patch recordings, EREV for RB cells was signi

30 Activation of the B cell receptor (BCR) in perforated-patch recordings evoked the same response.

31 Data obtained with whole-cell and perforated patch recordings from SNR neurons in slices i

32 Whole-cell perforated-patch recording from cultured CA1-CA3 pyramid

33 rain slices were prepared for whole-cell and perforated-patch recordings from CA1 hippocampal pyramid

34 rtual synaptic activity using dynamic clamp, perforated-patch recordings from dissociated bullfrog sy

35 ification in the ear, we made whole-cell and perforated-patch recordings from hair cells and postsyna

36 to closely mimic physiological conditions by perforated-patch recordings from IHCs kept at the physio

37 o move toward resolution of these questions, perforated-patch recordings from medium spiny neurons in

38 In perforated-patch recordings from rat utricular hair cell

39 re assessed using trypan blue dye exclusion, perforated-patch recordings, fura-2 fluorescence, and ti

40 BAPTA concentrations with values measured in perforated-patch recordings gave the endogenous calcium

41 re simultaneously recorded using whole-cell, perforated patch recording in freshly dissociated guinea

42 nique was developed that involves the use of perforated patch recordings in combination with fluoresc

43 Based on gramicidin-perforated patch recordings in hypothalamic slices from

44 Using perforated-patch recording in a mammalian synapse, we fo

45 Perforated patch recordings indicated that the efficacy

46 In perforated patch recordings, linopirdine, a specific M-c

47 The perforated patch recording method was employed in order

48 A perforated patch recording method was used to determine

49 Using both whole-cell and perforated patch recording methods, hypotonic solution c

50 capsaicin were examined using whole-cell and perforated patch recording methods.

51 The whole-cell perforated-patch recording mode was used to record a Ca2

52 Contrary to our expectations, nystatin-perforated patch recordings of whole-cell K+ currents re

53 nt of single-cell fura-2 fluorescence during perforated-patch recording of TRPC6 currents showed that

54 In perforated-patch recordings, phorbol 12-myristate 13-ace

55 Gramicidin perforated-patch recording revealed a GABA reversal pote

56 Perforated-patch recordings revealed changes in action p

57 Perforated-patch recordings revealed that oscillatory re

58 Perforated-patch recordings revealed that serum induced

59 In agreement, perforated-patch recordings show that intracellular Cl(-

60 Here, whole-cell patch clamp and perforated-patch recordings show that substrates of the

61 The perforated patch recording technique was used to investi

62 and Bengalese finches, using whole-cell and perforated-patch recording techniques in current-clamp c

63 annel were investigated using whole-cell and perforated-patch recording techniques in NG108-15 cells.

64 Here, we used whole-cell and perforated-patch recording techniques to elucidate the m

65 postnatal CR cells was studied directly with perforated-patch recording techniques.

66 In perforated-patch recordings, the rate of desensitization

67 In perforated-patch recordings, the rise in [Ca2+]i coincid

68 In whole-cell perforated-patch recordings, these cells responded to lo

69 ersal potential was determined by gramicidin perforated patch recordings to be -65.3 +/- 5.0 mV, lyin

70 We used gramicidin-perforated patch recordings to characterize Cl- transpor

71 We used perforated patch recordings to detect spontaneous local

72 Here, we use whole-cell and perforated-patch recordings to test for GABA-A receptors

73 The rebound of the current seen in perforated-patch recordings was blocked by the PI4-kinas

74 Next, using gramicidin-based perforated patch recordings, we found that the GABA reve

75 Using perforated-patch recording, we also found that K(ATP) ch

76 By using gramicidin perforated-patch recordings, we established that the pre

77 Using perforated-patch recordings, we found that individual ha

78 Using perforated-patch recordings, we have examined the part p

79 Using whole-cell and perforated-patch recordings, we have examined the part p

80 ing unitary field potential and gramicidin D perforated-patch recordings, we provide evidence that th

81 Perforated patch recordings were made from single mouse

82 Whole-cell and gramicidin-perforated patch recordings were obtained from inferior

83 ) receptor activation on membrane potential, perforated patch recordings were obtained from NG2 cells

84 Perforated patch recordings were used to determine how p

85 Whole-cell and perforated-patch recordings were made from neurons in ra

86 ding but enhanced current amplitude in those perforated-patch recordings where little current was evi

87 sion from CINs onto dopaminergic axons using perforated-patch recordings, which revealed rapid sponta