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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 ampal information processing through several presynaptic actions.
7 fect on amplitude, suggesting a facilitative presynaptic action at alpha1 receptors on GABAergic axon
8 mission exhibited properties associated with presynaptic action at D(1) receptors that were not evide
9 NPY) agonists inhibit glutamate release by a presynaptic action at the CA3-CA1 synapse of rat hippoca
10 In the presence of tetrodotoxin to minimize presynaptic actions, leptin also potentiated the postsyn
12 from GABAergic neurons, suggesting that the presynaptic action of acetylcholine via M(2) receptors w
20 this effect and its duration suggest a novel presynaptic action of the neurosteroid PS on GABAergic i
22 al MVR and low receptor saturation allow the presynaptic actions of a neuromodulator to control the e
24 l role of mGluR1alpha and mGluR5 in post-and presynaptic actions of glutamate in primate prefrontal c
25 genetic and pharmacological dissections for presynaptic actions of K+ channels in Drosophila neuromu
30 ore, mutant FMRP loses the ability to rescue presynaptic action potential (AP) broadening in Fmr1 KO
32 mp recording from the calyx showed that each presynaptic action potential (AP) was followed by a depo
33 transmission are determined, in part, by the presynaptic action potential (AP) waveform at the nerve
34 ever, the role of the electrical signal, the presynaptic action potential (AP), in modulating synapti
35 P decrease was accompanied by effects on the presynaptic action potential (AP), reducing AP duration
36 ) channels constrain the peak voltage of the presynaptic action potential (APSYN) to values much lowe
38 so unaltered, indicating that changes in the presynaptic action potential did not contribute to synap
39 release during prolonged, complex trains of presynaptic action potential firing (mean frequency, 48
42 s underlying transmitter release evoked by a presynaptic action potential has been gathered indirectl
44 The effect of changes in the shape of the presynaptic action potential on neurotransmission was ex
45 racellular electrode, but did not affect the presynaptic action potential or currents elicited by dir
47 synaptic transmission without affecting the presynaptic action potential or the presynaptic calcium
49 ime course of vesicle release triggered by a presynaptic action potential suggests that the homeostat
52 els, which was manipulated by prolonging the presynaptic action potential with the K+ channel blocker
53 ant calcium entry during the upstroke of the presynaptic action potential, and extremely fast calcium
54 r of quanta released in response to a single presynaptic action potential, possibly due to an increas
55 Because Na(+) channels also underlie the presynaptic action potential, we conclude that their act
56 Activation of CaMKII is required to drive presynaptic action potential-independent transmission at
68 initial release probability, closely spaced presynaptic action potentials can result in facilitation
69 tibular hair cells) modifies the kinetics of presynaptic action potentials in the B photoreceptor in
71 imulation-dependent manner without affecting presynaptic action potentials or inward Ca(2+) current.
73 ell pairs, closely timed (10-50 ms) pairs of presynaptic action potentials resulted in statistically
74 uickly, enabling the synapse to discriminate presynaptic action potentials that are spaced closely in
75 Rate-invariant transmission relies on brief presynaptic action potentials that delimit calcium influ
76 nreliable at signaling the arrival of single presynaptic action potentials to the postsynaptic neuron
77 quisite for reliability' (E.W. Dijkstra [1]) Presynaptic action potentials trigger the fusion of vesi
78 ry postsynaptic potentials (EPSPs) evoked by presynaptic action potentials were not affected by presy
79 nergy budget in which 11% of O(2) use was on presynaptic action potentials, 17% was on presynaptic Ca
80 with increasing frequency and broadening of presynaptic action potentials, and depended on the sensi
81 nce that endogenous zinc, released by single presynaptic action potentials, inhibits synaptic AMPA cu
82 tems in part from a remarkable shortening of presynaptic action potentials, which may lead to a lower
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