ライフサイエンスコーパス: presynaptic action

1 ard oil (allyl isothiocyanate), indicating a presynaptic action.

2 e amplitude of miniature IPSCs, suggesting a presynaptic action.

3 Cs in a concentration-dependent manner via a presynaptic action.

4 ase in paired-pulse depression, indicating a presynaptic action.

5 motility, principally via prejunctional and presynaptic actions.

6 ampal information processing through several presynaptic actions.

7 tic plasticity are well established, but its presynaptic actions are poorly defined.

8 fect on amplitude, suggesting a facilitative presynaptic action at alpha1 receptors on GABAergic axon

9 mission exhibited properties associated with presynaptic action at D(1) receptors that were not evide

10 NPY) agonists inhibit glutamate release by a presynaptic action at the CA3-CA1 synapse of rat hippoca

11 In the presence of tetrodotoxin to minimize presynaptic actions, leptin also potentiated the postsyn

12 The presynaptic action of 3,4 diaminopyridine was not benefi

13 from GABAergic neurons, suggesting that the presynaptic action of acetylcholine via M(2) receptors w

14 This presynaptic action of CDK5 also regulates glutamatergic

15 Hence, the overall effect of the presynaptic action of glycine is to enhance the firing o

16 postsynaptic target cell endows a localized presynaptic action of neurotrophins.

17 The presynaptic action of PKC theta implied by this observat

18 ariation of the amplitude of EPSPs suggest a presynaptic action of serotonin.

19 n of nicotine and NS1738, suggesting again a presynaptic action of the alpha7 nAChRs.

20 time of SSCs were not affected, indicating a presynaptic action of the conditioned medium.

21 this effect and its duration suggest a novel presynaptic action of the neurosteroid PS on GABAergic i

22 s in MPSC frequency are exclusively due to a presynaptic action of this heavy metal.

23 al MVR and low receptor saturation allow the presynaptic actions of a neuromodulator to control the e

24 These presynaptic actions of FMRP are translation independent

25 l role of mGluR1alpha and mGluR5 in post-and presynaptic actions of glutamate in primate prefrontal c

26 genetic and pharmacological dissections for presynaptic actions of K+ channels in Drosophila neuromu

27 Finally, new evidence for novel presynaptic actions of kappa-opioids on LC afferents is

28 We postulate that presynaptic actions of neurosteroids have a role in the

29 ere unaffected by the peptides, indicating a presynaptic action on glutamate release.

30 Our results indicate that increased presynaptic action onto LHb neurons contributes to the r

31 ore, mutant FMRP loses the ability to rescue presynaptic action potential (AP) broadening in Fmr1 KO

32 The shape of the presynaptic action potential (AP) has a strong impact on

33 The presynaptic action potential (AP) is required to drive c

34 more mature synapses is not a consequence of presynaptic action potential (AP) speeding.

35 mp recording from the calyx showed that each presynaptic action potential (AP) was followed by a depo

36 transmission are determined, in part, by the presynaptic action potential (AP) waveform at the nerve

37 ever, the role of the electrical signal, the presynaptic action potential (AP), in modulating synapti

38 P decrease was accompanied by effects on the presynaptic action potential (AP), reducing AP duration

39 ) channels, resulting in prolongation of the presynaptic action potential (AP).

40 ) channels constrain the peak voltage of the presynaptic action potential (APSYN) to values much lowe

41 An important issue is whether a presynaptic action potential causes, at most, a single v

42 so unaltered, indicating that changes in the presynaptic action potential did not contribute to synap

43 release during prolonged, complex trains of presynaptic action potential firing (mean frequency, 48

44 Increases in presynaptic action potential frequency caused attenuatio

45 Presynaptic action potential generation was necessary fo

46 s underlying transmitter release evoked by a presynaptic action potential has been gathered indirectl

47 Repolarization of the presynaptic action potential is essential for transmitte

48 Thus, any presynaptic action potential may elicit temporally highl

49 The effect of changes in the shape of the presynaptic action potential on neurotransmission was ex

50 racellular electrode, but did not affect the presynaptic action potential or currents elicited by dir

51 Thus, rather than narrowing the presynaptic action potential or exclusively modulating N

52 synaptic transmission without affecting the presynaptic action potential or the presynaptic calcium

53 nts in OPCs, which amplitude correlates with presynaptic action potential rate.

54 ime course of vesicle release triggered by a presynaptic action potential suggests that the homeostat

55 influx, changes that are independent of the presynaptic action potential waveform.

56 HPG, with no significant modification of the presynaptic action potential waveform.

57 els, which was manipulated by prolonging the presynaptic action potential with the K+ channel blocker

58 Analysis of the presynaptic action potential's (AP(syn)) role in synapti

59 ant calcium entry during the upstroke of the presynaptic action potential, and extremely fast calcium

60 controlling neurotransmitter release is the presynaptic action potential, but its amplitude and dura

61 r of quanta released in response to a single presynaptic action potential, possibly due to an increas

62 Because Na(+) channels also underlie the presynaptic action potential, we conclude that their act

63 Activation of CaMKII is required to drive presynaptic action potential-independent transmission at

64 Presynaptic action potential-independent transmitter rel

65 ulating potassium channels and narrowing the presynaptic action potential.

66 amount of neurotransmitter released after a presynaptic action potential.

67 mally, more than one vesicle is released per presynaptic action potential.

68 an number of transmitter quanta released per presynaptic action potential.

69 tetraethylammonium were used to broaden the presynaptic action potential.

70 mence just 150 micros after the start of the presynaptic action potential.

71 ws vesicles to fuse with short delay after a presynaptic action potential.

72 presynaptic calcium entry following a single presynaptic action potential.

73 occur at single release sites following one presynaptic action potential?

74 At chemical synapses, presynaptic action potentials (APs) activate voltage-gat

75 The waveform of presynaptic action potentials (APs) regulates the magnit

76 ansmitter release that occurs independent of presynaptic action potentials (APs) shows significant se

77 The shape of presynaptic action potentials (APs), particularly the fa

78 esicles release their content independent of presynaptic action potentials (APs).

79 initial release probability, closely spaced presynaptic action potentials can result in facilitation

80 dampen connection strength selectively when presynaptic action potentials fire at low frequency.

81 The presynaptic action potentials had large overshoots to ~2

82 Presynaptic action potentials have so far been measured

83 tibular hair cells) modifies the kinetics of presynaptic action potentials in the B photoreceptor in

84 transmission is mediated by large and rapid presynaptic action potentials in the human brain.

85 Presynaptic action potentials of small inhibitory termin

86 imulation-dependent manner without affecting presynaptic action potentials or inward Ca(2+) current.

87 These results demonstrate that presynaptic action potentials rapidly and reversibly reg

88 ell pairs, closely timed (10-50 ms) pairs of presynaptic action potentials resulted in statistically

89 uickly, enabling the synapse to discriminate presynaptic action potentials that are spaced closely in

90 Rate-invariant transmission relies on brief presynaptic action potentials that delimit calcium influ

91 nreliable at signaling the arrival of single presynaptic action potentials to the postsynaptic neuron

92 quisite for reliability' (E.W. Dijkstra [1]) Presynaptic action potentials trigger the fusion of vesi

93 ry postsynaptic potentials (EPSPs) evoked by presynaptic action potentials were not affected by presy

94 nergy budget in which 11% of O(2) use was on presynaptic action potentials, 17% was on presynaptic Ca

95 with increasing frequency and broadening of presynaptic action potentials, and depended on the sensi

96 Loss of function of Itsn1 did not alter presynaptic action potentials, Ca(2+) entry via voltage-

97 nce that endogenous zinc, released by single presynaptic action potentials, inhibits synaptic AMPA cu

98 To uncover properties of human presynaptic action potentials, we exploited recently dev

99 tems in part from a remarkable shortening of presynaptic action potentials, which may lead to a lower

100 se from the postsynaptic responses to evoked presynaptic action potentials.

101 nsient components which were coincident with presynaptic action potentials.

102 he postsynaptic response to a 20 Hz train of presynaptic action potentials.

103 e not fully functional and respond poorly to presynaptic action potentials.

104 al synapses is synchronized to the timing of presynaptic action potentials.

105 imizing the consequences of random timing of presynaptic action potentials.

106 terminals release transmitter in response to presynaptic action potentials.

107 SCs that TTX blocked, presumably by blocking presynaptic action potentials.

108 stsynaptic response to an arbitrary train of presynaptic action potentials.

109 The presynaptic action resulted in more vesicles being relea