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1 e depolarizing GABA component underlying the post-tetanic depolarization.
2 d under control conditions was replaced by a post-tetanic depression with a slow time course of recov
3              The influence of latrunculin on post-tetanic EPPs depended on its concentration in the b
4 that a fast Na(+)/K(+)-ATPase (NKA)-mediated post-tetanic hyperpolarization (PTH) controls the probab
5               The HCNCs are activated by the post-tetanic hyperpolarization occurring during this tim
6  (SynI) phosphorylation in the expression of post-tetanic potentiation (PTP) and in its modulation by
7                                However, like post-tetanic potentiation (PTP) and long-term potentiati
8      Moreover, transmission augmentation and post-tetanic potentiation (PTP) are disrupted in the mut
9 entration ([Ca(2+)](i)) in the generation of post-tetanic potentiation (PTP) at crayfish neuromuscula
10 BSTRACT: High-frequency stimulation leads to post-tetanic potentiation (PTP) at many types of synapse
11          High-frequency stimulation leads to post-tetanic potentiation (PTP) at many types of synapse
12 irement for a form of short-term plasticity, post-tetanic potentiation (PTP) at sensory neuron (SN)-m
13 d by high-frequency stimulation and mediates post-tetanic potentiation (PTP) in the rat hippocampus.
14                                              Post-tetanic potentiation (PTP) is a form of short-term
15                                              Post-tetanic potentiation (PTP) is a widespread form of
16                                              Post-tetanic potentiation (PTP) is a widespread form of
17                                  KEY POINTS: Post-tetanic potentiation (PTP) is attributed mainly to
18                                              Post-tetanic potentiation (PTP) is attributed mainly to
19 igh-frequency action potential train induces post-tetanic potentiation (PTP) of transmission at many
20                         The mechanism of the post-tetanic potentiation (PTP) or edrophonium-induced f
21        Here, we identify a Ca(2+) sensor for post-tetanic potentiation (PTP), a form of plasticity th
22 r a prevalent form of short-term plasticity, post-tetanic potentiation (PTP), involves protein kinase
23 d short-term facilitation and uniquely large post-tetanic potentiation (PTP).
24 se to short-term enhancement of release like post-tetanic potentiation (PTP).
25 trigger Ca(2+)-dependent vesicle release and post-tetanic potentiation (PTP).
26 e amplitude or the time-constant of decay of post-tetanic potentiation (PTP).
27 es exhibit a form of intrinsic facilitation: post-tetanic potentiation (PTP).
28 ng facilitation (F2), augmentation (AUG) and post-tetanic potentiation (PTP).
29 d the magnitude of LTP without affecting the post-tetanic potentiation (PTP).
30 mobilization of reserve pool vesicles during post-tetanic potentiation (PTP).
31 aired-pulse facilitation (PPF) and increased post-tetanic potentiation (PTP); mice lacking synapsin I
32  homosynaptic plasticity induced by tetanus [post-tetanic potentiation (PTP)] or low-frequency stimul
33 st that exogenous adenosine can inhibit both post-tetanic potentiation and long-term potentiation in
34 yloid fragment augmented theta burst-induced post-tetanic potentiation and LTP in mouse hippocampal s
35 STE) such as facilitation, augmentation, and post-tetanic potentiation at central synapses in the sea
36 imately 3 min, with a time course similar to post-tetanic potentiation at chemical synapses.
37                           (2020) reveal that post-tetanic potentiation at dentate gyrus mossy fiber s
38 nt in the periphery (perhaps attributable to post-tetanic potentiation at the neuromuscular junction)
39 red-pulse inhibition and increased GABAergic post-tetanic potentiation in both striatal and hippocamp
40 ical array, revealing a structural basis for post-tetanic potentiation in isolated muscles.
41         Peptidergic vesicle mobilization and post-tetanic potentiation of neuropeptide release are su
42 dependent capture of transiting vesicles and post-tetanic potentiation of neuropeptide release.
43             RyR and CaMKII are essential for post-tetanic potentiation of neuropeptide secretion.
44     During mitochondrial depolarization, the post-tetanic potentiation of the EPP observed under cont
45 ssion of short-term homosynaptic plasticity [post-tetanic potentiation or homosynaptic depression (HS
46 al ganglionic transmission without affecting post-tetanic potentiation or long-term potentiation.
47 ansmission, had no significant effect on the post-tetanic potentiation or long-term potentiation.
48                      Mutant mice showed less post-tetanic potentiation than wild-type animals, and al
49 a small concentration (2 microM) blocked the post-tetanic potentiation without affecting long-term po
50 ter presynaptic activation (augmentation and post-tetanic potentiation), while leaving intact its cap
51 ity-induced synapse maturation and abolishes post-tetanic potentiation, a form of synaptic plasticity
52 rib mutants exhibit loss of facilitation and post-tetanic potentiation, and faster synaptic depressio
53 icity with decreased facilitation, decreased post-tetanic potentiation, and increased depression.
54 ent, such as facilitation, augmentation, and post-tetanic potentiation, are usually attributed to eff
55 thus, shares components of the mechanisms of post-tetanic potentiation, NMDA- and mGluR-dependent lon
56 aralleled by calcium/synaptotagmin-dependent post-tetanic potentiation.
57 trength and contributes to the generation of post-tetanic potentiation.
58 ity: short-term depression, facilitation and post-tetanic potentiation.
59 playing pronounced synaptic augmentation and post-tetanic potentiation.
60 paired-pulse facilitation, LTP induction, or post-tetanic potentiation.
61 ical manipulations implicate mitochondria in post-tetanic potentiation.
62 ission as well as long-term potentiation and post-tetanic potentiation.
63 ding reduced facilitation, augmentation, and post-tetanic potentiation.
64 ion in Sca1 null mice, whereas long-term and post-tetanic potentiations are normal.
65                                   By day 15, post-tetanic, short-term, and long-term potentiation wer
66 er HFS or TBS gave similar levels of LTP and post tetanic stimulation (PTP), suggesting that the resp
67 ntiation of excitatory transmission, and the post-tetanic time courses of decay of elevated [Ca(2+)](
68 rial Na+-Ca2+ exchanger and helps to sustain post-tetanic transmitter release at mouse neuromuscular