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1 eurotransmitter-containing vesicles with the presynaptic membrane.
2 drolysis before they could be fused with the presynaptic membrane.
3 nct functions after vesicle docking with the presynaptic membrane.
4 t did not label presynaptic terminals or the presynaptic membrane.
5 y" pathway, whereas others collapse into the presynaptic membrane.
6 cked vesicles are located within 8 nm of the presynaptic membrane.
7 ssion and Ca(V) 2.2 channel abundance at the presynaptic membrane.
8 vesicles of the synaptic vesicle pool to the presynaptic membrane.
9 usion event that joins synaptic vesicles and presynaptic membrane.
10 gulate or facilitate vesicle delivery to the presynaptic membrane.
11 edistributed synaptic vesicles closer to the presynaptic membrane.
12 oteins to anchor active-zone proteins to the presynaptic membrane.
13 density in mitochondrial membrane facing the presynaptic membrane.
14 lieved to drive fusion of the vesicle to the presynaptic membrane.
15 cted eight-pass transmembrane protein in the presynaptic membrane.
16 ts by fusing to other vesicles docked at the presynaptic membrane.
17 t by flattening out and becoming part of the presynaptic membrane.
18 ge-gated calcium channels (VGCCs) within the presynaptic membrane.
19 rs (SERT, NET, and DAT, respectively) in the presynaptic membrane.
20 s the collapse of synaptic vesicles into the presynaptic membrane.
21 ugh the fusion of synaptic vesicles with the presynaptic membrane.
22 n of neurotransmitter-filled vesicles at the presynaptic membrane.
23 fusion of neurotransmitter vesicles with the presynaptic membrane.
24 photoreceptors it attaches the ribbon to the presynaptic membrane.
25 whereas sGCbeta concentrates just inside the presynaptic membrane.
26 of proteins in the synaptic vesicles and the presynaptic membrane.
27 e machinery and morphological changes at the presynaptic membrane.
28 be explained solely by depolarization of the presynaptic membrane.
29 d ultrastructural analysis of the effects on presynaptic membranes.
30 termine the resting electrical properties of presynaptic membranes.
31 Mpp4, PMCAs were lost from rod photoreceptor presynaptic membranes.
32 his ready supply of synaptic vesicles at the presynaptic membranes.
33 t realized through lateral inhibition across presynaptic membrane, (2) the constraint of a single rel
34 Ultrafast endocytosis retrieves the expanded presynaptic membrane after 100 milliseconds.
35          Tightly docked vesicles contact the presynaptic membrane and are primed for release of neuro
36 eurotransmitter-laden vesicles fuse with the presynaptic membrane and discharge their contents into t
37       After fusion of synaptic vesicles with presynaptic membrane and secretion of the contents of th
38           Ribbons, typically anchored to the presynaptic membrane and surrounded by tethered synaptic
39  a dense body, or ribbon, is anchored to the presynaptic membrane and tethers synaptic vesicles; func
40 ate the fusion of synaptic vesicles with the presynaptic membrane and the ensuing transmitter release
41                             They bind to the presynaptic membrane and then translocate intracellularl
42 ity's base includes vesicles docked with the presynaptic membrane and thus presumably ready for relea
43 he regulation of synaptic vesicle docking to presynaptic membranes and dopamine transmission.
44 ld explain alpha-synuclein's localization to presynaptic membranes and raises the possibility that pe
45 enula of humans and rodents, is expressed at presynaptic membranes and synaptic vesicles and associat
46 defect is accompanied by an expansion of the presynaptic membrane, and a depletion of vesicles from t
47 es to each other, to calcium channels in the presynaptic membrane, and to synaptic vesicles docked on
48  which lose their tight association with the presynaptic membrane; and loss of the highly branched te
49  are transported and primed to fuse with the presynaptic membrane are important to all chemical synap
50 rotransmitter-containing vesicles and on the presynaptic membrane are thought to underlie docking and
51 ers of elements were in direct proportion to presynaptic membrane area.
52 ors, even while moving en masse again to the presynaptic membrane as a prelude for another round of e
53 onnected to synaptic vesicles contacting the presynaptic membrane at sites where fusion does not occu
54                   Synucleins are a family of presynaptic membrane binding proteins.
55 ble vesicles were not clustered close to the presynaptic membrane but instead were dispersed almost r
56 at high concentrations to large areas of the presynaptic membrane, but actin assembly and productive
57 e vesicles are only briefly connected to the presynaptic membrane by a transient fusion pore.
58  associated (docked) at release sites of the presynaptic membrane, called active-zones.
59 crine cells, we have simultaneously measured presynaptic membrane capacitance changes and EPSCs.
60                                              Presynaptic membrane capacitance measurements directly d
61    Here, we address this issue by performing presynaptic membrane capacitance measurements together w
62 ly 60% of VDCCs are mobile while confined to presynaptic membrane compartments.
63 eatment parallels the rapid expansion of the presynaptic membrane consequent to the massive vesicle f
64 icles may help account for a greater vesicle-presynaptic membrane contact area during docking and a g
65 erlying AZ abnormalities including pervasive presynaptic membrane detachments and reduced synaptic ve
66 via the fusion of synaptic vesicles with the presynaptic membrane, driven by the formation of SNARE c
67 , positioning alpha-synuclein to function on presynaptic membranes during or after stimulation.
68             We combine optical recordings of presynaptic membrane dynamics and ultrastructural analys
69  of voltage-activated Ca(2+) channels in the presynaptic membrane for neurotransmitter release, some
70 on puncta within an NMJ were attached to the presynaptic membrane from postnatal day 0 to adulthood,
71 havbeta3 receptors and SERTs are enriched in presynaptic membranes from several brain regions and tha
72 ch encodes Munc18-1, a core component of the presynaptic membrane-fusion machinery, cause infantile e
73                                              Presynaptic membranes have been marked by FM dyes in stu
74          Tightly docked vesicles contact the presynaptic membrane, have partially formed SNARE comple
75 sis and endocytosis are balanced to maintain presynaptic membrane homeostasis and, thereby, sustain b
76 tagmin 1-induced lipid signaling to maintain presynaptic membrane homeostasis in central nervous syst
77 s vesicles were found within 150 nm from the presynaptic membrane; however, no vesicles were at 450-6
78 munoreactivity was not found associated with presynaptic membranes in the inner plexiform layer and w
79 r Maxi-K) channels have been investigated in presynaptic membranes in Xenopus motoneurone-muscle cell
80 tion with CSPalpha and SNARE proteins on the presynaptic membrane interface.
81 the extruded hair cells, indicating that the presynaptic membrane is still attached to the postsynapt
82 assembly's shape relative to the AZM and the presynaptic membrane is the same vesicle to vesicle, whe
83 e postulate that tension on integrins in the presynaptic membrane is transduced mechanically into cha
84  Ca2+ metabolism and occurs via pores in the presynaptic membrane, large enough to allow efflux of ne
85 machinery that drives fusion of SVs with the presynaptic membrane, little progress has been made in u
86 he ribbon tethers numerous vesicles near the presynaptic membrane, most of the tethered vesicles are
87 mber of vesicles immediately adjacent to the presynaptic membrane near active zones was still reduced
88 at connected a subset of mitochondria to the presynaptic membrane near active zones.
89 rat GABA transporter GAT-1 is located in the presynaptic membrane of axons where it plays a role in t
90 ly at punctate sites located just inside the presynaptic membrane of each terminal bouton.
91 inhibition of synaptic vesicle fusion to the presynaptic membrane of human motor neurons are responsi
92  number of synaptic vesicles adjacent to the presynaptic membrane of inhibitory synapses without affe
93 type-1 receptors (Cb1R) are expressed in the presynaptic membrane of many synapses, including paralle
94 hat chemical LTP increased the length of the presynaptic membrane of mossy fiber boutons, associated
95               Synaptic ribbons, found at the presynaptic membrane of sensory cells in both ear and ey
96 owed the protein in the cytoplasm and on the presynaptic membranes of the photoreceptor synapses.
97 rminals, with the mature process targeted to presynaptic membrane opposed to muscle, and an abnormall
98  release site or whether it remains bound to presynaptic membranes or proteins after its release.
99           However, translocation occurs from presynaptic membranes other than synaptic vesicles and i
100 ell membrane fusion thereby further augments presynaptic membrane packing, enhancing membrane protect
101 ediated interaction between microtubules and presynaptic membrane plays a pivotal role during bouton
102        Synaptic vesicles (SVs) fuse with the presynaptic membrane (PM) at specialized regions called
103 ability of its membrane (VM) fusing with the presynaptic membrane (PM) when a nerve impulse arrives.
104 ating range, which means it is unlikely that presynaptic membrane potential controls transmitter rele
105 smitter typically graded with respect to the presynaptic membrane potential, but release can be maint
106 usion pumps, interact with an Mpp4-dependent presynaptic membrane protein complex that includes Veli3
107                                          The presynaptic membrane protein SNAP-25 colocalized with DA
108                                     When the presynaptic membrane protein syntaxin is coexpressed in
109 -associated protein of 25 kDa (SNAP-25) is a presynaptic membrane protein that has been clearly impli
110          The dopamine transporter (DAT) is a presynaptic membrane protein that regulates dopaminergic
111 nic lines overexpressing ROP and syntaxin, a presynaptic membrane protein, indicate that ROP interact
112     In the present study we investigated the presynaptic membrane protein, syntaxin-1, in circumvalla
113 hat is believed to play a critical role with presynaptic membrane proteins (SNAP-25 and syntaxin) dur
114 A subunit of P/Q-type Ca2+ channels with the presynaptic membrane proteins syntaxin and SNAP-25 in vi
115 in, and synaptotagmin, without affecting the presynaptic membrane proteins syntaxin and SNAP-25, or t
116  immobilized recombinant proteins and native presynaptic membrane proteins, we found that the synprin
117 is known about the molecular organization of presynaptic membrane proteins.
118 cate, vesicles from one neuron fuse with the presynaptic membrane releasing chemicals that signal to
119 , while the number of vesicles docked to the presynaptic membrane remained unchanged.
120 A, an SV GTPase involved in SV targeting and presynaptic membrane tethering.
121 ynaptic vesicles immediately adjacent to the presynaptic membrane, the pool that includes the docked
122 ilitate fusion of synaptic vesicles with the presynaptic membrane through formation of a soluble NSF
123  alpha-synuclein relocalizes from SVs to the presynaptic membrane upon stimulation, positioning alpha
124  PPK16-containing DEG/ENaC channel modulates presynaptic membrane voltage and, thereby, controls calc
125  and modulates exocytosis through control of presynaptic membrane voltage.
126                      WT alpha-syn binding to presynaptic membranes was not affected by phosphorylatio
127 arify whether it is also associated with the presynaptic membrane, we employed immunogold electron mi
128 d certain other proteins associated with the presynaptic membrane were absent from DA-IPC varicositie
129 cked vesicles are located within 8 nm of the presynaptic membrane where SNARE complexes begin to form
130 m channels are known to form clusters at the presynaptic membrane where they mediate calcium influx,
131 e interactions between synaptotagmin and the presynaptic membrane, which are mediated by the basic re
132 s trigger very rapid endocytosis, retrieving presynaptic membrane with a time constant of 470 ms.
133 ) sensor protein that binds to and bends the presynaptic membrane with its C2B domain, and thereby in
134 disrupts a Ca(2+) extrusion mechanism at the presynaptic membranes, with ensuing adaptive responses b
135 ld that enhances delivery of vesicles to the presynaptic membrane without requiring an active transpo

 
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