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2 Previous studies have demonstrated roles for vesicle-associated membrane protein 2 (VAMP 2) and VAMP
3 of multimeric protein complexes that include vesicle-associated membrane protein 2 (VAMP-2) and the p
4 tured neurotoxin with full-length substrates vesicle-associated membrane protein 2 (VAMP-2), synaptos
6 y bound to the SNARE-protein synaptobrevin-2/vesicle-associated membrane protein 2 (VAMP2) and promot
7 associates with synaptophysin in vivo after vesicle-associated membrane protein 2 (VAMP2) enters the
8 This requires nephrin, which interacts with vesicle-associated membrane protein 2 (VAMP2) on GLUT4 s
9 kDa (SNAP-25) interacts with syntaxin 1 and vesicle-associated membrane protein 2 (VAMP2) to form a
10 ntified SV2, synaptotagmin I, synaptophysin, vesicle-associated membrane protein 2 (VAMP2), and the v
11 function also blocked distal localization of vesicle-associated membrane protein 2 (VAMP2), which is
12 live hippocampal nerve terminals expressing vesicle-associated membrane protein 2 (VAMP2)-pHluorin w
17 rain extracts is promoted by dissociation of vesicle-associated membrane protein 2 from synaptophysin
18 docrine tissues, pantophysin associated with vesicle-associated membrane protein 2 in adipocytes.
19 t with the interaction of synaptophysin with vesicle-associated membrane protein 2 in neuroendocrine
20 replace the C-terminus of the SNARE motif of vesicle-associated membrane protein 2 in the four-helix
21 factor attachment receptor) proteins VAMP2 (vesicle-associated membrane protein 2) and syntaxin 4 (S
22 tein receptor) proteins: synaptobrevin 2 (or vesicle-associated membrane protein 2) on the synaptic v
23 tatory amino acid transporter 5), and VAMP2 (vesicle-associated membrane protein 2), are markedly red
24 onal interaction with synaptobrevin-2/VAMP2 (vesicle-associated membrane protein 2), leading to SNARE
25 some-associated protein of 25 kD) and VAMP2 (vesicle-associated membrane protein 2), precludes the in
26 eimide-sensitive fusion protein) and VAMP-2 (vesicle-associated membrane protein 2), stearoyl CoA des
27 f botulinum toxin in AgRP neurons to prevent vesicle-associated membrane protein 2-dependent vesicle
30 t protein receptors (SNAREs) cellubrevin and vesicle-associated membrane protein-2 (VAMP-2) and the t
31 ts spastic paralysis through the cleavage of vesicle-associated membrane protein-2 (VAMP-2) in neuron
32 ntaining diffuse staining for the prS marker Vesicle-Associated Membrane Protein-2 and (c) budding of
34 as the secretory organelle membrane proteins vesicle-associated membrane protein-2 and synaptotagmin
35 that TAT-SNAP-23 bound to the combination of vesicle-associated membrane protein-2 and syntaxin-4 but
36 tion by live-cell imaging of pHluorin-VAMP2 (vesicle-associated membrane protein-2), a pH-sensitive-G
37 either the 31-kDa subunit of H(+)-ATPase or vesicle-associated membrane protein-2, co-immunoprecipit
38 eaction we identified transcripts for rab3a, vesicle-associated membrane protein-2, synaptosome-assoc
39 parations contain rab3a and SNARE, including vesicle-associated membrane protein-2, syntaxin-4, synap
42 rotein receptor (v-SNARE) called cellubrevin/vesicle-associated membrane protein-3 (VAMP-3) in platel
43 TP vesicular transport and fusion, including vesicle-associated membrane protein-3 and vesicular nucl
44 estigate the role of the di-leucine motif of vesicle-associated membrane protein 4 (VAMP4) in adaptor
45 -Golgi SNARE and syntaxin 6-binding partner, vesicle-associated membrane protein 4 (VAMP4), at the ch
47 reased association of SNAP23, Syntaxin4, and vesicle-associated membrane protein 7 (VAMP7) is detecte
48 SNAREs Vps10p-tail-interactor-1a (vti1a) and vesicle-associated membrane protein 7 (VAMP7) to specifi
49 or budding from the ER membrane and contains vesicle-associated membrane protein 7, found in intestin
50 Previous work suggested that human VAMP-7 (vesicle-associated membrane protein-7) was a SNARE requi
52 cular mechanisms, we examined platelets from vesicle-associated membrane protein 8 (VAMP8) null mice.
54 18 not only interacted with Syntaxin (Syn)7, vesicle-associated membrane protein 8, and Vti1-b but al
55 med complexes with syntaxin-11, SNAP-23, and vesicle-associated membrane protein-8 in human platelets
56 P-25) family helices, and an arginine (R) in vesicle-associated membrane protein (a 3Q:1R ratio).
59 econdensation, with the unusual retention of vesicle-associated membrane protein and the perinuclear
60 s was dependent on tetanus toxin-insensitive vesicle-associated membrane proteins and calcium mobiliz
61 nd tensin homolog (PTEN) and its ceRNA VAMP (vesicle-associated membrane protein)-associated protein
62 vity and was constitutively colocalized with vesicle-associated membrane protein-associated protein A
63 1 (Bin1, also known as amphiphysin II), and vesicle-associated membrane protein-associated protein A
64 found the interaction between NS5A and human vesicle-associated membrane protein-associated protein A
65 hybrid screen identified the SNARE regulator vesicle-associated membrane protein-associated protein A
66 binding partner for the resident ER protein vesicle-associated membrane protein-associated protein B
67 gh transgenic mice overexpressing the mutant vesicle-associated membrane protein-associated protein B
68 Proline with Serine at residue 56 (P56S) of vesicle-associated membrane protein-associated protein B
69 titution at position 56 in the gene encoding vesicle-associated membrane protein-associated protein B
70 titution at position 56 in the gene encoding vesicle-associated membrane protein-associated protein B
71 gue of the integral ER membrane protein VAP (vesicle-associated membrane protein-associated protein)
72 d hVAP-33 (the human homologue of the 33-kDa vesicle-associated membrane protein-associated protein),
73 increasing NS5A interaction with the 33-kDa vesicle-associated membrane protein-associated protein.
74 ction with the human homologue of the 33-kDa vesicle-associated membrane protein-associated protein.
75 otein, NET3C, and phylogenetically conserved vesicle-associated membrane protein-associated proteins
76 d together by a tethering complex of VAPA/B (vesicle-associated membrane protein-associated proteins
77 xtended synaptotagmins), and Scs2 and Scs22 (vesicle-associated membrane protein-associated proteins)
79 platelets with an antibody directed against vesicle-associated membrane protein completely inhibited
80 syntaxin-1, SNAP-25, and synaptobrevin/VAMP (vesicle-associated membrane protein) constitute the core
81 iated through NSF/GluR2 interactions but not vesicle-associated membrane protein-dependent exocytosis
82 isassemble the 20S complex and did not allow vesicle-associated membrane protein dissociation to any
84 ogen granules (ZG) express 2 isoforms of the vesicle-associated membrane protein family (VAMP2 and -8
85 cle protein synaptobrevin (also called VAMP, vesicle-associated membrane protein) forms part of the S
87 oluble form of the green fluorescent protein/vesicle-associated membrane protein (GFP-VAMP) was bound
89 RE proteins, secretory protein (MoSec22) and vesicle-associated membrane protein (MoVam7), as being i
91 otagmin binding overlap with the domains for vesicle-associated membrane protein (or VAMP) and alpha-
92 icles are capable of docking even when VAMP (vesicle-associated membrane protein) or syntaxin is clea
93 SNAP-25, and synaptobrevin-2 (also known as vesicle-associated membrane protein, or VAMP-2) bind to
95 ease from platelets, we examined the role of vesicle-associated membrane protein, SNAP-23, and syntax
98 me-associated protein of 25 kD (SNAP25), and vesicle-associated membrane protein/synaptobrevin are co
101 y oriented plasma membrane protein and VAMP (vesicle-associated membrane protein; synaptobrevin) is a
102 n three different PC12 cell lines expressing vesicle-associated membrane protein-T Antigen derivative
103 regulated, in part, by the interaction of a vesicle-associated membrane protein termed synaptobrevin
105 totagmin 1 and 2 (syt 1, syt 2) are synaptic vesicle-associated membrane proteins that act as calcium
107 e of FM1-43, or abolish immunoreactivity for vesicle-associated membrane protein, the toxin substrate
108 tein receptor tetanus neurotoxin insensitive vesicle-associated membrane protein (TI-VAMP)/VAMP7 was
109 rol fusion of tetanus neurotoxin insensitive vesicle-associated membrane protein (TiVAMP)/VAMP-7 vesi
111 yers bound soluble green fluorescent protein/vesicle-associated membrane protein (v-SNARE), and the S
112 asma membrane require the interaction of the vesicle-associated membrane protein VAMP with the plasma
113 xperiments using antibodies to synaptobrevin/vesicle associated membrane protein (VAMP) 1, 2, or rat
114 of the SNARE complex, SNAP-25, Syntaxin, and vesicle associated membrane protein (VAMP/also Synaptobr
118 ngly, complexin 2 was found to interact with vesicle-associated membrane protein (VAMP) 2, syntaxins
119 romiscuous Qb,c-SNARE SNAP33 and the R-SNARE vesicle-associated membrane protein (VAMP) 721,722, also
121 ent protein receptor (SNARE) proteins of the vesicle-associated membrane protein (VAMP) and syntaxin
122 This protein forms a ternary complex with vesicle-associated membrane protein (VAMP) and syntaxin,
123 5 kDa (SNAP25) and the vesicle SNARE protein vesicle-associated membrane protein (VAMP) are essential
124 SNAP-25, syntaxin 1A, and synaptobrevin/vesicle-associated membrane protein (VAMP) are SNARE pro
125 pression of a syntaxin 4 mutant in which the vesicle-associated membrane protein (VAMP) binding site
128 ctionally identify the site of action of the vesicle-associated membrane protein (VAMP) family of R-S
129 VAMP4, a recently discovered member of the vesicle-associated membrane protein (VAMP) family of tra
130 SNARE complexes between five proteins of the vesicle-associated membrane protein (VAMP) family, three
131 ferent members of the syntaxin, SNAP-25, and vesicle-associated membrane protein (VAMP) gene families
132 red a second pathway that sorts the synaptic vesicle-associated membrane protein (VAMP) into similarl
134 ertion sequence of the v-SNARE synaptobrevin/vesicle-associated membrane protein (VAMP) phenocopied t
135 at hippocampal synapses, using synaptobrevin/vesicle-associated membrane protein (VAMP) tagged with v
139 es comprised of the SNARE proteins syntaxin, vesicle-associated membrane protein (VAMP), and the syna
140 tion was inhibited by antibodies directed at vesicle-associated membrane protein (VAMP), demonstratin
142 1A, N-ethylmaleimide-sensitive factor (NSF), vesicle-associated membrane protein (VAMP), synaptosome-
144 ein receptor (SNARE) proteins syntaxin 4 and vesicle-associated membrane protein (VAMP)-2 were also o
146 actin cytoskeleton and track the movement of vesicle-associated membrane protein (VAMP)-8-containing
149 SNARE and SNARE-associated proteins such as vesicle-associated membrane protein (VAMP)/synaptobrevin
150 synaptosome-associated protein (SNAP25), and vesicle-associated membrane protein (VAMP)/synaptobrevin
151 e used pharmacologic inhibitors of Snap25 or vesicle-associated membrane protein (VAMP)/synaptobrevin
153 Syntaxin 4 activation and docking/fusion of vesicle-associated membrane protein (VAMP)2-containing i
154 In both cell types, TNF colocalized with vesicle-associated membrane protein (VAMP)3-positive com
155 ral SNARE proteins were found in adipocytes: vesicle-associated membrane protein (VAMP-2), its relate
156 s of synaptophysin as well as synaptobrevin [vesicle-associated membrane protein (VAMP-2)], a protein
158 nules in pancreatic acinar cells express two vesicle-associated membrane proteins (VAMP), VAMP2 and -
159 synaptosomal-associated protein 25 [SNAP25], vesicle-associated membrane protein [VAMP]) forming the
161 actions involving components of the vesicle (vesicle-associated membrane protein; VAMP) and plasma me
162 d that the v-SNARE tetanus toxin-insensitive vesicle-associated membrane protein (VAMP7) differs from
163 of a fusogenic trans-SNARE complex involving vesicle-associated membrane protein (VAMP8), but not VAM
164 ensus on t-SNAREs usage, it is unclear which Vesicle Associated Membrane Protein (VAMPs: synaptobrevi
165 e show that two highly homologous exocytotic vesicle-associated membrane proteins (VAMPs) are require
166 s question, we evaluated the localization of vesicle-associated membrane proteins (VAMPs) in spread p
167 the role of vesicular SNARE proteins, i.e., vesicle-associated membrane proteins (VAMPs), remains en
168 f 25-kDa synaptosome-associated protein, and vesicle-associated membrane protein] were found to be ex
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