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1 vesicles of the synaptic vesicle pool to the presynaptic membrane.
2 t did not label presynaptic terminals or the presynaptic membrane.
3 usion event that joins synaptic vesicles and presynaptic membrane.
4 gulate or facilitate vesicle delivery to the presynaptic membrane.
5 edistributed synaptic vesicles closer to the presynaptic membrane.
6 oteins to anchor active-zone proteins to the presynaptic membrane.
7 density in mitochondrial membrane facing the presynaptic membrane.
8 lieved to drive fusion of the vesicle to the presynaptic membrane.
9 cted eight-pass transmembrane protein in the presynaptic membrane.
10 ts by fusing to other vesicles docked at the presynaptic membrane.
11 t by flattening out and becoming part of the presynaptic membrane.
12 rs (SERT, NET, and DAT, respectively) in the presynaptic membrane.
13 s the collapse of synaptic vesicles into the presynaptic membrane.
14 n of neurotransmitter-filled vesicles at the presynaptic membrane.
15 fusion of neurotransmitter vesicles with the presynaptic membrane.
16 photoreceptors it attaches the ribbon to the presynaptic membrane.
17 whereas sGCbeta concentrates just inside the presynaptic membrane.
18 of proteins in the synaptic vesicles and the presynaptic membrane.
19 e machinery and morphological changes at the presynaptic membrane.
20 be explained solely by depolarization of the presynaptic membrane.
21 drolysis before they could be fused with the presynaptic membrane.
22 nct functions after vesicle docking with the presynaptic membrane.
23 d ultrastructural analysis of the effects on presynaptic membranes.
24 termine the resting electrical properties of presynaptic membranes.
25 Mpp4, PMCAs were lost from rod photoreceptor presynaptic membranes.
26 his ready supply of synaptic vesicles at the presynaptic membranes.
27 t realized through lateral inhibition across presynaptic membrane, (2) the constraint of a single rel
28 eurotransmitter-laden vesicles fuse with the presynaptic membrane and discharge their contents into t
31 a dense body, or ribbon, is anchored to the presynaptic membrane and tethers synaptic vesicles; func
32 ate the fusion of synaptic vesicles with the presynaptic membrane and the ensuing transmitter release
34 ity's base includes vesicles docked with the presynaptic membrane and thus presumably ready for relea
35 ld explain alpha-synuclein's localization to presynaptic membranes and raises the possibility that pe
36 defect is accompanied by an expansion of the presynaptic membrane, and a depletion of vesicles from t
37 es to each other, to calcium channels in the presynaptic membrane, and to synaptic vesicles docked on
38 are transported and primed to fuse with the presynaptic membrane are important to all chemical synap
39 rotransmitter-containing vesicles and on the presynaptic membrane are thought to underlie docking and
41 ors, even while moving en masse again to the presynaptic membrane as a prelude for another round of e
42 onnected to synaptic vesicles contacting the presynaptic membrane at sites where fusion does not occu
44 ble vesicles were not clustered close to the presynaptic membrane but instead were dispersed almost r
48 Here, we address this issue by performing presynaptic membrane capacitance measurements together w
50 eatment parallels the rapid expansion of the presynaptic membrane consequent to the massive vesicle f
51 icles may help account for a greater vesicle-presynaptic membrane contact area during docking and a g
52 erlying AZ abnormalities including pervasive presynaptic membrane detachments and reduced synaptic ve
53 of voltage-activated Ca(2+) channels in the presynaptic membrane for neurotransmitter release, some
54 on puncta within an NMJ were attached to the presynaptic membrane from postnatal day 0 to adulthood,
55 havbeta3 receptors and SERTs are enriched in presynaptic membranes from several brain regions and tha
56 ch encodes Munc18-1, a core component of the presynaptic membrane-fusion machinery, cause infantile e
58 munoreactivity was not found associated with presynaptic membranes in the inner plexiform layer and w
59 r Maxi-K) channels have been investigated in presynaptic membranes in Xenopus motoneurone-muscle cell
61 the extruded hair cells, indicating that the presynaptic membrane is still attached to the postsynapt
62 assembly's shape relative to the AZM and the presynaptic membrane is the same vesicle to vesicle, whe
63 e postulate that tension on integrins in the presynaptic membrane is transduced mechanically into cha
64 Ca2+ metabolism and occurs via pores in the presynaptic membrane, large enough to allow efflux of ne
65 machinery that drives fusion of SVs with the presynaptic membrane, little progress has been made in u
66 he ribbon tethers numerous vesicles near the presynaptic membrane, most of the tethered vesicles are
67 mber of vesicles immediately adjacent to the presynaptic membrane near active zones was still reduced
69 rat GABA transporter GAT-1 is located in the presynaptic membrane of axons where it plays a role in t
71 inhibition of synaptic vesicle fusion to the presynaptic membrane of human motor neurons are responsi
72 number of synaptic vesicles adjacent to the presynaptic membrane of inhibitory synapses without affe
73 hat chemical LTP increased the length of the presynaptic membrane of mossy fiber boutons, associated
75 owed the protein in the cytoplasm and on the presynaptic membranes of the photoreceptor synapses.
76 rminals, with the mature process targeted to presynaptic membrane opposed to muscle, and an abnormall
79 ediated interaction between microtubules and presynaptic membrane plays a pivotal role during bouton
81 ability of its membrane (VM) fusing with the presynaptic membrane (PM) when a nerve impulse arrives.
82 ating range, which means it is unlikely that presynaptic membrane potential controls transmitter rele
83 smitter typically graded with respect to the presynaptic membrane potential, but release can be maint
84 usion pumps, interact with an Mpp4-dependent presynaptic membrane protein complex that includes Veli3
87 -associated protein of 25 kDa (SNAP-25) is a presynaptic membrane protein that has been clearly impli
89 nic lines overexpressing ROP and syntaxin, a presynaptic membrane protein, indicate that ROP interact
90 In the present study we investigated the presynaptic membrane protein, syntaxin-1, in circumvalla
91 hat is believed to play a critical role with presynaptic membrane proteins (SNAP-25 and syntaxin) dur
92 A subunit of P/Q-type Ca2+ channels with the presynaptic membrane proteins syntaxin and SNAP-25 in vi
93 in, and synaptotagmin, without affecting the presynaptic membrane proteins syntaxin and SNAP-25, or t
94 immobilized recombinant proteins and native presynaptic membrane proteins, we found that the synprin
96 cate, vesicles from one neuron fuse with the presynaptic membrane releasing chemicals that signal to
99 ynaptic vesicles immediately adjacent to the presynaptic membrane, the pool that includes the docked
100 ilitate fusion of synaptic vesicles with the presynaptic membrane through formation of a soluble NSF
101 PPK16-containing DEG/ENaC channel modulates presynaptic membrane voltage and, thereby, controls calc
104 arify whether it is also associated with the presynaptic membrane, we employed immunogold electron mi
105 d certain other proteins associated with the presynaptic membrane were absent from DA-IPC varicositie
106 m channels are known to form clusters at the presynaptic membrane where they mediate calcium influx,
107 e interactions between synaptotagmin and the presynaptic membrane, which are mediated by the basic re
108 s trigger very rapid endocytosis, retrieving presynaptic membrane with a time constant of 470 ms.
109 ) sensor protein that binds to and bends the presynaptic membrane with its C2B domain, and thereby in
110 disrupts a Ca(2+) extrusion mechanism at the presynaptic membranes, with ensuing adaptive responses b
111 ld that enhances delivery of vesicles to the presynaptic membrane without requiring an active transpo
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