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1 and retromer and another possibly involving N-ethylmaleimide-sensitive factor.
2 ARE hybrid complex cannot be disassembled by N-ethylmaleimide-sensitive factor.
4 omotypic vesicle fusion by dephosphorylating N-ethylmaleimide-sensitive factor, a key regulator of ve
5 sively to the predicted syntaxin and soluble N-ethylmaleimide-sensitive factor accessory protein rece
7 lar C-terminus domain and the SNARE (soluble N-ethylmaleimide-sensitive factor activating protein rec
8 cer to prevent the completion of the soluble N-ethylmaleimide-sensitive factor activating protein rec
9 structures, and here we examine the role of N-ethylmaleimide-sensitive factor-activating protein rec
10 gral membrane transporters, ATPases, soluble N-ethylmaleimide-sensitive factor-activating protein rec
11 t significantly reduced formation of soluble n-ethylmaleimide sensitive factor adaptor protein recept
12 ction, enabling cooperation with the soluble N-ethylmaleimide sensitive factor adaptor protein recept
13 am of the Rab GTPase Sec4 to promote soluble N-ethylmaleimide-sensitive factor adaptor protein recept
14 or of the Sec4 Rab GTPase to promote soluble N-ethylmaleimide-sensitive factor adaptor protein recept
15 e presence of LPC as opposed to cholesterol, N-ethylmaleimide-sensitive factor + adenosine triphospha
16 trosylation, the specific S-nitrosylation of N-ethylmaleimide-sensitive factor and reduces the speed
18 amined whether genetic disruption of soluble N-ethylmaleimide-sensitive factor attached protein (SNAR
21 gmin, complexin, and neuronal SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec
22 tinct combinations of Munc18 and the soluble N-ethylmaleimide sensitive factor attachment protein rec
25 rt a role for tethering complexes in soluble N-ethylmaleimide sensitive factor attachment protein rec
26 domain, which likely participates in soluble N-ethylmaleimide sensitive factor attachment protein rec
27 ne protein) forms part of the SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec
28 constitution experiments have suggested that N-ethylmaleimide sensitive factor attachment protein rec
29 isiae, the developmentally regulated Soluble N-ethylmaleimide sensitive factor attachment protein rec
34 unc18-like) protein Munc18-1 and the soluble N-ethylmaleimide-sensitive factor attachment protein (SN
35 endritic surface occurs via a SNARE [soluble n-ethylmaleimide-sensitive factor attachment protein (SN
36 encoding SNAP-25, a component of the soluble N-ethylmaleimide-sensitive factor attachment protein (SN
37 SNARE) complexes in conjunction with soluble N-ethylmaleimide-sensitive factor attachment protein (SN
38 a (SNAP-25) is a key molecule in the soluble N-ethylmaleimide-sensitive factor attachment protein (SN
39 cognate acceptor compartments before soluble N-ethylmaleimide-sensitive factor attachment protein (SN
40 The assembly of the three neuronal soluble N-ethylmaleimide-sensitive factor attachment protein (SN
41 nd mutations of syntaxin and SNAP25 (soluble N-ethylmaleimide-sensitive factor attachment protein 25)
42 , which harbors a mutation in Napa [encoding N-ethylmaleimide-sensitive factor attachment protein alp
45 binds to and cleaves syntaxin 17, a soluble N-ethylmaleimide-sensitive factor attachment protein rec
47 organelles involves the formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec
48 ructural relationships among SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec
49 at Munc18c binds to the trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
50 n fusogens from vesicle trafficking (soluble N-ethylmaleimide-sensitive factor attachment protein rec
51 sis requires the concerted action of soluble N-ethylmaleimide-sensitive factor attachment protein rec
52 existence of the unproductive target soluble N-ethylmaleimide-sensitive factor attachment protein rec
53 proteins are important components of soluble N-ethylmaleimide-sensitive factor attachment protein rec
54 insulin granules, is carried out by soluble N-ethylmaleimide-sensitive factor attachment protein rec
57 Platelet exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec
58 of the fusion pore induced by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
60 ere is comparable fusion of 4-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
61 he general membrane fusion machinery-soluble N-ethylmaleimide-sensitive factor attachment protein rec
62 f exocytosis by interacting with the soluble N-ethylmaleimide-sensitive factor attachment protein rec
63 y and activation of (phago)lysosomal soluble N-ethylmaleimide-sensitive factor attachment protein rec
64 ey synaptic proteins from the soluble SNARE (N-ethylmaleimide-sensitive factor attachment protein rec
65 v2.1 is postulated to be involved in soluble N-ethylmaleimide-sensitive factor attachment protein rec
66 icle marker proteins, glutamate, the soluble N-ethylmaleimide-sensitive factor attachment protein rec
67 labeled vesicle-associated v-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
69 st that syt1 might facilitate SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
71 mediated by the formation of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
72 ric syntaxin 1A, and it can activate soluble N-ethylmaleimide-sensitive factor attachment protein rec
73 e Arabidopsis (Arabidopsis thaliana) soluble N-ethylmaleimide-sensitive factor attachment protein rec
74 Repeated release requires cycles of soluble N-ethylmaleimide-sensitive factor attachment protein rec
75 -overexpression of ER/Golgi arginine soluble N-ethylmaleimide-sensitive factor attachment protein rec
76 ed components: vacuolar lipids, four soluble N-ethylmaleimide-sensitive factor attachment protein rec
77 udies of membrane fusion mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec
78 wo C2 domains, and the neuronal core soluble N-ethylmaleimide-sensitive factor attachment protein rec
79 oteins that regulate the activity of soluble N-ethylmaleimide-sensitive factor attachment protein rec
80 usion is mediated by the concerted action of N-ethylmaleimide-sensitive factor attachment protein rec
81 activity on one of the three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
82 ces derived from target- and vesicle-soluble N-ethylmaleimide-sensitive factor attachment protein rec
83 icularly involving small G proteins, soluble N-ethylmaleimide-sensitive factor attachment protein rec
84 ia a Gbetagamma interaction with the soluble N-ethylmaleimide-sensitive factor attachment protein rec
85 c1/Munc18 (SM) proteins bind cognate soluble N-ethylmaleimide-sensitive factor attachment protein rec
86 and botulinum neurotoxin C to cleave soluble N-ethylmaleimide-sensitive factor attachment protein rec
87 with purified yeast vacuolar SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec
89 which, in turn, interacts with the lysosomal N-ethylmaleimide-sensitive factor attachment protein rec
90 mitter release requires three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
91 ade transport of the plasma membrane soluble N-ethylmaleimide-sensitive factor attachment protein rec
92 otulinum neurotoxins cleave specific soluble N-ethylmaleimide-sensitive factor attachment protein rec
93 a do not contain the t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein rec
94 on and vacuole protein sorting), and soluble N-ethylmaleimide-sensitive factor attachment protein rec
97 -mediated selective concentration of soluble N-ethylmaleimide-sensitive factor attachment protein rec
98 2Delta) for the Tlg2 target membrane-soluble N-ethylmaleimide-sensitive factor attachment protein rec
99 mediated by syntaxin 4-based SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
102 e.g., microtubules, the exocyst, and soluble N-ethylmaleimide-sensitive factor attachment protein rec
103 g interaction of Gbetagamma with the soluble N-ethylmaleimide-sensitive factor attachment protein rec
104 out the regulatory roles of specific soluble N-ethylmaleimide-sensitive factor attachment protein rec
105 (GTX), a Drosophila t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein rec
106 eurotransmitters are exocytosed in a soluble N-ethylmaleimide-sensitive factor attachment protein rec
107 by specific fusion proteins [such as soluble N-ethylmaleimide-sensitive factor attachment protein rec
108 otein linker between ZW10 and the ER soluble N-ethylmaleimide-sensitive factor attachment protein rec
109 f synaptotagmin to accelerate SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
110 he membrane-fusion proteins known as soluble N-ethylmaleimide-sensitive factor attachment protein rec
113 artment (ERGIC)-53 and the vesicular-soluble N-ethylmaleimide-sensitive factor attachment protein rec
114 The lysosomal vesicle-associated soluble N-ethylmaleimide-sensitive factor attachment protein rec
115 hrough its effector RBF-1 to promote soluble N-ethylmaleimide-sensitive factor attachment protein rec
116 pid binding and/or by Ca2+-dependent soluble N-ethylmaleimide-sensitive factor attachment protein rec
117 n vitro and to separate the roles of soluble N-ethylmaleimide-sensitive factor attachment protein rec
118 how that fodrin interacts with the t-soluble N-ethylmaleimide-sensitive factor attachment protein rec
119 a (SNAP-25) is a component of neural soluble N-ethylmaleimide-sensitive factor attachment protein rec
120 protein, the major synaptic vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec
121 n of both the core fusion machinery [soluble N-ethylmaleimide-sensitive factor attachment protein rec
122 ing that RBO is required in the mechanism of N-ethylmaleimide-sensitive factor attachment protein rec
123 strating that latrunculin A supports soluble N-ethylmaleimide-sensitive factor attachment protein rec
125 e receptors codistribute with target soluble N-ethylmaleimide-sensitive factor attachment protein rec
126 soforms (I, VII, and IX) to regulate soluble N-ethylmaleimide-sensitive factor attachment protein rec
127 weakens Gbetagamma interactions with soluble N-ethylmaleimide-sensitive factor attachment protein rec
128 ood mechanism that probably involves soluble N-ethylmaleimide-sensitive factor attachment protein rec
129 related to the syntaxin subfamily of soluble N-ethylmaleimide-sensitive factor attachment protein rec
131 hagocytosis requires the ER resident soluble N-ethylmaleimide-sensitive factor attachment protein rec
133 Sec1/Mun18-like (SM) proteins and soluble N-ethylmaleimide-sensitive factor attachment protein rec
135 many peptides, and VAMP2, a vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec
136 ic beta-cells, the syntaxin 6 (Syn6) soluble N-ethylmaleimide-sensitive factor attachment protein rec
137 le exocytosis is regulated by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
141 2+ dependently or independently with soluble N-ethylmaleimide-sensitive factor attachment protein rec
142 ciated protein A (hVAP-A), a cellular target N-ethylmaleimide-sensitive factor attachment protein rec
143 nal by cooperating with the neuronal soluble N-ethylmaleimide-sensitive factor attachment protein rec
144 n proteoliposomes containing vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec
145 evidence of four tonoplast-localized soluble N-ethylmaleimide-sensitive factor attachment protein rec
148 er release requires the formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec
151 presence of a conserved R-SNARE (for soluble N-ethylmaleimide-sensitive factor attachment protein rec
152 vacuole/prevacuole-associated target soluble N-ethylmaleimide-sensitive factor attachment protein rec
153 ps proteins function during multiple soluble N-ethylmaleimide-sensitive factor attachment protein rec
156 fusion requires that membrane-bound soluble N-ethylmaleimide-sensitive factor attachment protein rec
157 Moreover, we show that blocking soluble N-ethylmaleimide-sensitive factor attachment protein rec
158 , form a complex that interacts with soluble N-ethylmaleimide-sensitive factor attachment protein rec
160 conserved family of proteins termed soluble N-ethylmaleimide-sensitive factor attachment protein rec
162 11 interact with the vacuolar SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
164 nner with syntaxin-3 and syntaxin-1A soluble N-ethylmaleimide-sensitive factor attachment protein rec
165 a component of the synaptic vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec
168 stituted with the target (t)-SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec
169 loit a polarized distribution of the soluble N-ethylmaleimide-sensitive factor attachment protein rec
170 gue Dawley rats, 4 dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein rec
171 iated by the formation of functional soluble N-ethylmaleimide-sensitive factor attachment protein rec
172 s the Rab GTPase Ypt7p, four SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec
173 unc13-4 is a Ca(2+)-dependent SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
174 cellular transport vesicles requires soluble N-ethylmaleimide-sensitive factor attachment protein rec
175 h abnormal expression or function of soluble N-ethylmaleimide-sensitive factor attachment protein rec
177 vitro by arresting the late steps of soluble N-ethylmaleimide-sensitive factor attachment protein rec
178 o an open conformation to accelerate soluble N-ethylmaleimide-sensitive factor attachment protein rec
179 transmitters and hormones depends on soluble N-ethylmaleimide-sensitive factor attachment protein rec
181 mice expressing a dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein rec
182 Neuronal exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec
186 ent work suggested that ER-localized soluble N-ethylmaleimide-sensitive factor attachment protein rec
187 is depends on efficient formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec
190 erved increase in K(+) currents is a soluble N-ethylmaleimide-sensitive factor attachment protein rec
192 tether at the plasma membrane before soluble N-ethylmaleimide-sensitive factor attachment protein rec
193 aptic vesicles, including the SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
194 litate the formation of trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec
195 etric levels with its cognate target-soluble N-ethylmaleimide-sensitive factor attachment protein rec
196 rs in membrane fusion events are the soluble N-ethylmaleimide-sensitive factor attachment protein rec
198 es depends on the disassembly of cis-soluble N-ethylmaleimide-sensitive factor attachment protein rec
199 ter release and vesicle recycling in soluble N-ethylmaleimide-sensitive factor attachment protein rec
200 UT4 vesicle fusion reaction requires soluble N-ethylmaleimide-sensitive factor attachment protein rec
201 guanosine 5'-3-O-(thio)triphosphate, soluble N-ethylmaleimide-sensitive factor attachment protein, an
202 nt protein receptor (SNARE) proteins soluble N-ethylmaleimide-sensitive factor attachment protein-25
203 02590 (a predicted alpha-SNAP [alpha-soluble N-ethylmaleimide-sensitive factor attachment protein]).
204 role of the fusion proteins, SNAREs (soluble N-ethylmaleimide-sensitive factor attachment proteins),
205 osine triphosphate-binding proteins, soluble N-ethylmaleimide-sensitive factor attachment proteins, a
206 , but not with other plasma membrane soluble N-ethylmaleimide-sensitive factor attachment receptor (S
207 ocytosis relies on assembly of three soluble N-ethylmaleimide-sensitive factor attachment receptor (S
209 Syntaxin 1a is a plasma membrane soluble N-ethylmaleimide-sensitive factor attachment receptor pr
210 ions homologous to eukaryotic SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor) d
211 Syt 1 using a reconstituted, SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor)-m
212 of tail-anchored proteins, including soluble N-ethylmaleimide-sensitive factor attachment receptors (
213 vesicles in the brain harbor several soluble N-ethylmaleimide-sensitive-factor attachment protein rec
214 ific proteolysis of one of the three soluble N-ethylmaleimide-sensitive-factor attachment protein rec
215 suggest an association of vesicular soluble N-ethylmaleimide-sensitive-factor attachment protein rec
216 ing one of the three proteins of the soluble N-ethylmaleimide-sensitive-factor attachment protein rec
217 Syntaxin-1, a core protein of the soluble N-ethylmaleimide-sensitive-factor attachment protein rec
218 of one of the three proteins of the soluble N-ethylmaleimide-sensitive-factor attachment protein rec
219 ly of proteins known as SNAREs [soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein re
220 , an essential component of the soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein re
222 his study investigated the effect of soluble N-ethylmaleimide-sensitive factor-attachment protein (SN
223 with fMLF induced phosphorylation of soluble N-ethylmaleimide-sensitive factor-attachment protein (SN
224 During synaptic vesicle fusion, the soluble N-ethylmaleimide-sensitive factor-attachment protein rec
225 n 18 is a target membrane-associated soluble N-ethylmaleimide-sensitive factor-attachment protein rec
226 ogenetic approach to identify target soluble N-ethylmaleimide-sensitive factor-attachment protein rec
228 SF attachment protein, and NSF is defined as N-ethylmaleimide-sensitive factor) complexes catalyze sy
229 of early endosomes in an ATP-, cytosol-, and N-ethylmaleimide sensitive factor-dependent manner.
230 ndence in the NSF gene, encoding the protein N-Ethylmaleimide-Sensitive Factor essential for synaptic
231 ndent kinase II and the trafficking proteins N-ethylmaleimide-sensitive factor, GABA receptor-associa
232 hibiting the binding of SNAREs to Sec18p, an N-ethylmaleimide-sensitive factor homologue responsible
233 Using the trimerized alphaSNAP, we find that N-ethylmaleimide-sensitive factor hydrolyzes 10 ATP mole
234 identified an essential requirement for nsf (N-ethylmaleimide sensitive factor) in the organization o
236 e release machinery, this assay incorporates N-ethylmaleimide sensitive factor (NSF) and alpha-SNAP,
237 ion of nitric oxide (NO), which nitrosylates N-ethylmaleimide sensitive factor (NSF) and inhibits exo
238 olecule binds our two model His(6) proteins, N-ethylmaleimide sensitive factor (NSF) and O(6)-alklygu
239 nillin, citron-kinase (CG10522), and soluble N-ethylmaleimide sensitive factor (NSF) attachment prote
240 Moreover, we provided evidence for a role of N-ethylmaleimide sensitive factor (NSF) in regulating Mu
241 s of nitric oxide (NO), which S-nitrosylated N-ethylmaleimide sensitive factor (NSF), a critical regu
242 H(2)O(2) regulates exocytosis by inhibiting N-ethylmaleimide sensitive factor (NSF), a protein that
245 y related to the single N domains in p97 and N-ethylmaleimide sensitive factor (NSF); N1 of Pex1 is m
246 18-1 (stabilizes assembled SNARE complexes), N-ethylmaleimide-sensitive factor (NSF) (disassembles SN
252 t is directly involved in regulating soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote
253 domain and modulate the affinity for soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote
254 isoforms to directly regulate SNARE (soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote
255 of Golgi matrix proteins, Rab1, and soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote
256 e mutation in the gene Napa encoding soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote
260 ly AAA domain-containing protein 1), soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote
264 daptor molecule for the SNARE-priming enzyme N-ethylmaleimide-sensitive factor (NSF) is known to be c
265 novel synaptic interaction between Arr1 and N-ethylmaleimide-sensitive factor (NSF) that is enhanced
267 ATPase activity and disassembly activity of N-ethylmaleimide-sensitive factor (NSF), a critical comp
268 inhibits exocytosis by chemically modifying N-ethylmaleimide-sensitive factor (NSF), a key component
269 is likely that the SNARE accessory protein, N-ethylmaleimide-sensitive factor (NSF), affects the com
270 n kinase Cepsilon (PKCepsilon) regulates the N-ethylmaleimide-sensitive factor (NSF), an ATPase criti
271 The human beta2AR carboxyl end binds to the N-ethylmaleimide-sensitive factor (NSF), an ATPase integ
273 se mutation in the nsf-1 gene, which encodes N-ethylmaleimide-sensitive factor (NSF), an intracellula
274 s hepatic secretion of VLDL-TAG by targeting N-ethylmaleimide-sensitive factor (NSF), both in vivo an
276 cate a core complex of proteins comprised of N-ethylmaleimide-sensitive factor (NSF), soluble NSF att
278 the polar residues of the zero layer enable N-ethylmaleimide-sensitive factor (NSF)-mediated SNARE c
283 KMzeta maintains late-LTP through persistent N-ethylmaleimide-sensitive factor (NSF)/glutamate recept
284 enishment and release did not require ATP or N-ethylmaleimide-sensitive factor (NSF); however, this p
285 sodium-hydrogen exchanger regulatory factor, N-ethylmaleimide-sensitive factor, or some related prote
286 sts a regulatory role of chaperones, such as N-ethylmaleimide-sensitive factor, or the membrane envir
287 rate that interaction of AMPA receptors with N-ethylmaleimide-sensitive factor plays a critical role
288 P2;5 are regulated by the SNARE (for soluble N-ethylmaleimide-sensitive factor protein attachment pro
290 ve interaction of the GluR2 subunit with the N-ethylmaleimide-sensitive factor protein is required fo
291 ated with Plasmodium homologues of COPII and N-ethylmaleimide-sensitive factor, proteins involved in
292 taining lipid bilayers as well as to soluble N-ethylmaleimide sensitive factor receptors (SNAREs) and
294 utely disrupts the interaction of GluR2 with N-ethylmaleimide-sensitive factor selectively depletes G
295 RE complex is disassembled by the AAA-ATPase N-ethylmaleimide-sensitive factor that requires the cofa
297 ents, whereas further incubation with p97 or N-ethylmaleimide-sensitive factor (two AAA ATPases invol
300 uman beta2AR carboxyl terminus also binds to N-ethylmaleimide-sensitive factor, which does not contai
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