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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.
6 tic plasticity are well established, but its presynaptic actions are poorly defined.
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
11                                          The presynaptic action of 3,4 diaminopyridine was not benefi
12  from GABAergic neurons, suggesting that the presynaptic action of acetylcholine via M(2) receptors w
13                                         This presynaptic action of CDK5 also regulates glutamatergic
14             Hence, the overall effect of the presynaptic action of glycine is to enhance the firing o
15  postsynaptic target cell endows a localized presynaptic action of neurotrophins.
16                                          The presynaptic action of PKC theta implied by this observat
17 ariation of the amplitude of EPSPs suggest a presynaptic action of serotonin.
18 n of nicotine and NS1738, suggesting again a presynaptic action of the alpha7 nAChRs.
19 time of SSCs were not affected, indicating a presynaptic action of the conditioned medium.
20 this effect and its duration suggest a novel presynaptic action of the neurosteroid PS on GABAergic i
21 s in MPSC frequency are exclusively due to a presynaptic action of this heavy metal.
22 al MVR and low receptor saturation allow the presynaptic actions of a neuromodulator to control the e
23                                        These presynaptic actions of FMRP are translation independent
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
26              Finally, new evidence for novel presynaptic actions of kappa-opioids on LC afferents is
27                            We postulate that presynaptic actions of neurosteroids have a role in the
28 ere unaffected by the peptides, indicating a presynaptic action on glutamate release.
29          Our results indicate that increased presynaptic action onto LHb neurons contributes to the r
30 ore, mutant FMRP loses the ability to rescue presynaptic action potential (AP) broadening in Fmr1 KO
31                             The shape of the presynaptic action potential (AP) has a strong impact on
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
37              An important issue is whether a presynaptic action potential causes, at most, a single v
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
40                                 Increases in presynaptic action potential frequency caused attenuatio
41                                              Presynaptic action potential generation was necessary fo
42 s underlying transmitter release evoked by a presynaptic action potential has been gathered indirectl
43                        Repolarization of the presynaptic action potential is essential for transmitte
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
46              Thus, rather than narrowing the presynaptic action potential or exclusively modulating N
47  synaptic transmission without affecting the presynaptic action potential or the presynaptic calcium
48 nts in OPCs, which amplitude correlates with presynaptic action potential rate.
49 ime course of vesicle release triggered by a presynaptic action potential suggests that the homeostat
50 HPG, with no significant modification of the presynaptic action potential waveform.
51  influx, changes that are independent of the presynaptic action potential waveform.
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
57                                              Presynaptic action potential-independent transmitter rel
58 ulating potassium channels and narrowing the presynaptic action potential.
59  amount of neurotransmitter released after a presynaptic action potential.
60 mally, more than one vesicle is released per presynaptic action potential.
61 an number of transmitter quanta released per presynaptic action potential.
62  tetraethylammonium were used to broaden the presynaptic action potential.
63 mence just 150 micros after the start of the presynaptic action potential.
64 ws vesicles to fuse with short delay after a presynaptic action potential.
65  occur at single release sites following one presynaptic action potential?
66                        At chemical synapses, presynaptic action potentials (APs) activate voltage-gat
67                                 The shape of presynaptic action potentials (APs), particularly the fa
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
70                                              Presynaptic action potentials of small inhibitory termin
71 imulation-dependent manner without affecting presynaptic action potentials or inward Ca(2+) current.
72               These results demonstrate that presynaptic action potentials rapidly and reversibly reg
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
83 nsient components which were coincident with presynaptic action potentials.
84 he postsynaptic response to a 20 Hz train of presynaptic action potentials.
85 e not fully functional and respond poorly to presynaptic action potentials.
86 al synapses is synchronized to the timing of presynaptic action potentials.
87 imizing the consequences of random timing of presynaptic action potentials.
88 terminals release transmitter in response to presynaptic action potentials.
89 SCs that TTX blocked, presumably by blocking presynaptic action potentials.
90 stsynaptic response to an arbitrary train of presynaptic action potentials.
91                                          The presynaptic action resulted in more vesicles being relea

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