ライフサイエンスコーパス: N-ethylmaleimide-sensitive factor

1 and retromer and another possibly involving N-ethylmaleimide-sensitive factor.

2 ARE hybrid complex cannot be disassembled by N-ethylmaleimide-sensitive factor.

3 We find that lotus encodes N-ethylmaleimide sensitive factor 2 (NSF2), whereas whee

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

6 lar C-terminus domain and the SNARE (soluble N-ethylmaleimide-sensitive factor activating protein rec

7 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 gral membrane transporters, ATPases, soluble N-ethylmaleimide-sensitive factor-activating protein rec

10 structures, and here we examine the role of N-ethylmaleimide-sensitive factor-activating protein rec

11 ction, enabling cooperation with the soluble N-ethylmaleimide sensitive factor adaptor protein recept

12 t significantly reduced formation of 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

17 NSF (N-ethylmaleimide sensitive factor) and its yeast counter

18 The ATPase NSF (N-ethylmaleimide-sensitive factor) and the adaptor prote

19 amined whether genetic disruption of soluble N-ethylmaleimide-sensitive factor attached protein (SNAR

20 Whereas SNARE (soluble N -ethylmaleimide-sensitive factor attachment protein re

21 We show that the gene for soluble N-ethylmaleimide sensitive factor attachment protein alp

22 Phosphorylation of this t-soluble N-ethylmaleimide sensitive factor attachment protein rec

23 tinct combinations of Munc18 and the soluble N-ethylmaleimide sensitive factor attachment protein rec

24 Sec1/Munc18 (SM) proteins and soluble N-ethylmaleimide sensitive factor attachment protein rec

25 Soluble N-ethylmaleimide sensitive factor attachment protein rec

26 rt a role for tethering complexes in soluble N-ethylmaleimide sensitive factor attachment protein rec

27 domain, which likely participates in soluble N-ethylmaleimide sensitive factor attachment protein rec

28 his study identifies the function of soluble N-ethylmaleimide sensitive factor attachment protein rec

29 study pinpoints the pivotal role of soluble N-ethylmaleimide sensitive factor attachment protein rec

30 ne protein) forms part of the SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec

31 constitution experiments have suggested that N-ethylmaleimide sensitive factor attachment protein rec

32 isiae, the developmentally regulated Soluble N-ethylmaleimide sensitive factor attachment protein rec

33 gmin, complexin, and neuronal SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec

34 SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec

35 Evolutionarily conserved SNARE (soluble N-ethylmaleimide sensitive factor attachment protein rec

36 Syntaxin (STX)-5 and alpha-soluble N-ethylmaleimide-sensitive factor attachment protein (al

37 The assembly of the three neuronal soluble N-ethylmaleimide-sensitive factor attachment protein (SN

38 Trans-soluble N-ethylmaleimide-sensitive factor attachment protein (SN

39 unc18-like) protein Munc18-1 and the soluble N-ethylmaleimide-sensitive factor attachment protein (SN

40 endritic surface occurs via a SNARE [soluble n-ethylmaleimide-sensitive factor attachment protein (SN

41 SNARE) complexes in conjunction with soluble N-ethylmaleimide-sensitive factor attachment protein (SN

42 a (SNAP-25) is a key molecule in the soluble N-ethylmaleimide-sensitive factor attachment protein (SN

43 cognate acceptor compartments before soluble N-ethylmaleimide-sensitive factor attachment protein (SN

44 nd mutations of syntaxin and SNAP25 (soluble N-ethylmaleimide-sensitive factor attachment protein 25)

45 , which harbors a mutation in Napa [encoding N-ethylmaleimide-sensitive factor attachment protein alp

46 his study, we identify the vesicular soluble N-ethylmaleimide-sensitive factor attachment protein rec

47 ular machines that are essential for soluble N-ethylmaleimide-sensitive factor attachment protein rec

48 thaliana, include complexes, such as soluble N-ethylmaleimide-sensitive factor attachment protein rec

49 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

50 erved increase in K(+) currents is a soluble N-ethylmaleimide-sensitive factor attachment protein rec

51 We identified a member of the soluble N-ethylmaleimide-sensitive factor attachment protein rec

52 tether at the plasma membrane before soluble N-ethylmaleimide-sensitive factor attachment protein rec

53 aptic vesicles, including the SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

54 litate the formation of trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

55 etric levels with its cognate target-soluble N-ethylmaleimide-sensitive factor attachment protein rec

56 rs in membrane fusion events are the soluble N-ethylmaleimide-sensitive factor attachment protein rec

57 Membrane fusion is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

58 es depends on the disassembly of cis-soluble N-ethylmaleimide-sensitive factor attachment protein rec

59 ter release and vesicle recycling in soluble N-ethylmaleimide-sensitive factor attachment protein rec

60 UT4 vesicle fusion reaction requires soluble N-ethylmaleimide-sensitive factor attachment protein rec

61 organelles involves the formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec

62 ructural relationships among SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec

63 at Munc18c binds to the trans-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

64 n fusogens from vesicle trafficking (soluble N-ethylmaleimide-sensitive factor attachment protein rec

65 sis requires the concerted action of soluble N-ethylmaleimide-sensitive factor attachment protein rec

66 existence of the unproductive target soluble N-ethylmaleimide-sensitive factor attachment protein rec

67 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

68 proteins are important components of soluble N-ethylmaleimide-sensitive factor attachment protein rec

69 insulin granules, is carried out by soluble N-ethylmaleimide-sensitive factor attachment protein rec

70 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

71 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

72 Platelet exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

73 of the fusion pore induced by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

74 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

75 ere is comparable fusion of 4-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

76 he general membrane fusion machinery-soluble N-ethylmaleimide-sensitive factor attachment protein rec

77 f exocytosis by interacting with the soluble N-ethylmaleimide-sensitive factor attachment protein rec

78 ey synaptic proteins from the soluble SNARE (N-ethylmaleimide-sensitive factor attachment protein rec

79 v2.1 is postulated to be involved in soluble N-ethylmaleimide-sensitive factor attachment protein rec

80 icle marker proteins, glutamate, the soluble N-ethylmaleimide-sensitive factor attachment protein rec

81 labeled vesicle-associated v-SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

82 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

83 st that syt1 might facilitate SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

84 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

85 mediated by the formation of SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

86 between subsets of so-called SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

87 ric syntaxin 1A, and it can activate soluble N-ethylmaleimide-sensitive factor attachment protein rec

88 e Arabidopsis (Arabidopsis thaliana) soluble N-ethylmaleimide-sensitive factor attachment protein rec

89 Repeated release requires cycles of soluble N-ethylmaleimide-sensitive factor attachment protein rec

90 -overexpression of ER/Golgi arginine soluble N-ethylmaleimide-sensitive factor attachment protein rec

91 ed components: vacuolar lipids, four soluble N-ethylmaleimide-sensitive factor attachment protein rec

92 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

93 udies of membrane fusion mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

94 wo C2 domains, and the neuronal core soluble N-ethylmaleimide-sensitive factor attachment protein rec

95 oteins that regulate the activity of soluble N-ethylmaleimide-sensitive factor attachment protein rec

96 usion is mediated by the concerted action of N-ethylmaleimide-sensitive factor attachment protein rec

97 activity on one of the three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

98 ces derived from target- and vesicle-soluble N-ethylmaleimide-sensitive factor attachment protein rec

99 icularly involving small G proteins, soluble N-ethylmaleimide-sensitive factor attachment protein rec

100 ia a Gbetagamma interaction with the soluble N-ethylmaleimide-sensitive factor attachment protein rec

101 c1/Munc18 (SM) proteins bind cognate soluble N-ethylmaleimide-sensitive factor attachment protein rec

102 and botulinum neurotoxin C to cleave soluble N-ethylmaleimide-sensitive factor attachment protein rec

103 The role of soluble N-ethylmaleimide-sensitive factor attachment protein rec

104 with purified yeast vacuolar SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec

105 Yeast vacuole fusion requires soluble N-ethylmaleimide-sensitive factor attachment protein rec

106 mitter release requires three SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

107 ade transport of the plasma membrane soluble N-ethylmaleimide-sensitive factor attachment protein rec

108 otulinum neurotoxins cleave specific soluble N-ethylmaleimide-sensitive factor attachment protein rec

109 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

110 a do not contain the t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein rec

111 on and vacuole protein sorting), and soluble N-ethylmaleimide-sensitive factor attachment protein rec

112 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

113 -mediated selective concentration of soluble N-ethylmaleimide-sensitive factor attachment protein rec

114 2Delta) for the Tlg2 target membrane-soluble N-ethylmaleimide-sensitive factor attachment protein rec

115 mediated by syntaxin 4-based SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

116 Although concentrated soluble N-ethylmaleimide-sensitive factor attachment protein rec

117 e.g., microtubules, the exocyst, and soluble N-ethylmaleimide-sensitive factor attachment protein rec

118 g interaction of Gbetagamma with the soluble N-ethylmaleimide-sensitive factor attachment protein rec

119 out the regulatory roles of specific soluble N-ethylmaleimide-sensitive factor attachment protein rec

120 (GTX), a Drosophila t-SNARE (target-soluble N-ethylmaleimide-sensitive factor attachment protein rec

121 eurotransmitters are exocytosed in a soluble N-ethylmaleimide-sensitive factor attachment protein rec

122 otein linker between ZW10 and the ER soluble N-ethylmaleimide-sensitive factor attachment protein rec

123 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

124 f synaptotagmin to accelerate SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

125 he membrane-fusion proteins known as soluble N-ethylmaleimide-sensitive factor attachment protein rec

126 LC-mediated proteolysis of soluble N-ethylmaleimide-sensitive factor attachment protein rec

127 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

128 artment (ERGIC)-53 and the vesicular-soluble N-ethylmaleimide-sensitive factor attachment protein rec

129 The lysosomal vesicle-associated soluble N-ethylmaleimide-sensitive factor attachment protein rec

130 binds to and cleaves syntaxin 17, a soluble N-ethylmaleimide-sensitive factor attachment protein rec

131 hrough its effector RBF-1 to promote soluble N-ethylmaleimide-sensitive factor attachment protein rec

132 pid binding and/or by Ca2+-dependent soluble N-ethylmaleimide-sensitive factor attachment protein rec

133 how that fodrin interacts with the t-soluble N-ethylmaleimide-sensitive factor attachment protein rec

134 a (SNAP-25) is a component of neural soluble N-ethylmaleimide-sensitive factor attachment protein rec

135 protein, the major synaptic vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec

136 n of both the core fusion machinery [soluble N-ethylmaleimide-sensitive factor attachment protein rec

137 ing that RBO is required in the mechanism of N-ethylmaleimide-sensitive factor attachment protein rec

138 strating that latrunculin A supports soluble N-ethylmaleimide-sensitive factor attachment protein rec

139 by specific fusion proteins [such as soluble N-ethylmaleimide-sensitive factor attachment protein rec

140 To determine whether the soluble N-ethylmaleimide-sensitive factor attachment protein rec

141 e receptors codistribute with target soluble N-ethylmaleimide-sensitive factor attachment protein rec

142 soforms (I, VII, and IX) to regulate soluble N-ethylmaleimide-sensitive factor attachment protein rec

143 weakens Gbetagamma interactions with soluble N-ethylmaleimide-sensitive factor attachment protein rec

144 ood mechanism that probably involves soluble N-ethylmaleimide-sensitive factor attachment protein rec

145 related to the syntaxin subfamily of soluble N-ethylmaleimide-sensitive factor attachment protein rec

146 hagocytosis requires the ER resident soluble N-ethylmaleimide-sensitive factor attachment protein rec

147 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

148 Sec1/Mun18-like (SM) proteins and soluble N-ethylmaleimide-sensitive factor attachment protein rec

149 Gbetagamma bound soluble N-ethylmaleimide-sensitive factor attachment protein rec

150 many peptides, and VAMP2, a vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec

151 ic beta-cells, the syntaxin 6 (Syn6) soluble N-ethylmaleimide-sensitive factor attachment protein rec

152 le exocytosis is regulated by SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

153 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

154 Furthermore, syntaxin 1A, a soluble N-ethylmaleimide-sensitive factor attachment protein rec

155 The target-SNARE (N-ethylmaleimide-sensitive factor attachment protein rec

156 unc13-4 is a Ca(2+)-dependent SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

157 2+ dependently or independently with soluble N-ethylmaleimide-sensitive factor attachment protein rec

158 ciated protein A (hVAP-A), a cellular target N-ethylmaleimide-sensitive factor attachment protein rec

159 n proteoliposomes containing vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec

160 evidence of four tonoplast-localized soluble N-ethylmaleimide-sensitive factor attachment protein rec

161 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

162 Syntaxin1A, a neural-specific N-ethylmaleimide-sensitive factor attachment protein rec

163 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

164 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

165 The SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

166 ily GTPases, their effector tethers, soluble N-ethylmaleimide-sensitive factor attachment protein rec

167 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

168 y and activation of (phago)lysosomal soluble N-ethylmaleimide-sensitive factor attachment protein rec

169 brane protein 4 (VAMP4), a vesicular soluble N-ethylmaleimide-sensitive factor attachment protein rec

170 which, in turn, interacts with the lysosomal N-ethylmaleimide-sensitive factor attachment protein rec

171 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

172 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

173 n vitro and to separate the roles of soluble N-ethylmaleimide-sensitive factor attachment protein rec

174 Synaptic soluble N-ethylmaleimide-sensitive factor attachment protein rec

175 nal by cooperating with the neuronal soluble N-ethylmaleimide-sensitive factor attachment protein rec

176 er release requires the formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec

177 11 interact with the vacuolar SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

178 NSF disassembles soluble N-ethylmaleimide-sensitive factor attachment protein rec

179 nner with syntaxin-3 and syntaxin-1A soluble N-ethylmaleimide-sensitive factor attachment protein rec

180 a component of the synaptic vesicle soluble N-ethylmaleimide-sensitive factor attachment protein rec

181 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

182 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

183 stituted with the target (t)-SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec

184 loit a polarized distribution of the soluble N-ethylmaleimide-sensitive factor attachment protein rec

185 gue Dawley rats, 4 dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein rec

186 iated by the formation of functional soluble N-ethylmaleimide-sensitive factor attachment protein rec

187 s the Rab GTPase Ypt7p, four SNAREs (soluble N-ethylmaleimide-sensitive factor attachment protein rec

188 cellular transport vesicles requires soluble N-ethylmaleimide-sensitive factor attachment protein rec

189 h abnormal expression or function of soluble N-ethylmaleimide-sensitive factor attachment protein rec

190 Although epsinR is known to be an N-ethylmaleimide-sensitive factor attachment protein rec

191 se from beta-cells, specifically the soluble N-ethylmaleimide-sensitive factor attachment protein rec

192 vitro by arresting the late steps of soluble N-ethylmaleimide-sensitive factor attachment protein rec

193 o an open conformation to accelerate soluble N-ethylmaleimide-sensitive factor attachment protein rec

194 transmitters and hormones depends on soluble N-ethylmaleimide-sensitive factor attachment protein rec

195 mice expressing a dominant-negative soluble N-ethylmaleimide-sensitive factor attachment protein rec

196 Neuronal exocytosis is mediated by soluble N-ethylmaleimide-sensitive factor attachment protein rec

197 SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein rec

198 Soluble N-ethylmaleimide-sensitive factor attachment protein rec

199 The soluble N-ethylmaleimide-sensitive factor attachment protein rec

200 ent work suggested that ER-localized soluble N-ethylmaleimide-sensitive factor attachment protein rec

201 is depends on efficient formation of soluble N-ethylmaleimide-sensitive factor attachment protein rec

202 Mast cell degranulation requires N-ethylmaleimide-sensitive factor attachment protein rec

203 guanosine 5'-3-O-(thio)triphosphate, soluble N-ethylmaleimide-sensitive factor attachment protein, an

204 nt protein receptor (SNARE) proteins soluble N-ethylmaleimide-sensitive factor attachment protein-25

205 02590 (a predicted alpha-SNAP [alpha-soluble N-ethylmaleimide-sensitive factor attachment protein]).

206 role of the fusion proteins, SNAREs (soluble N-ethylmaleimide-sensitive factor attachment proteins),

207 osine triphosphate-binding proteins, soluble N-ethylmaleimide-sensitive factor attachment proteins, a

208 In neurons, soluble N-ethylmaleimide-sensitive factor attachment receptor (S

209 ocytosis relies on assembly of three soluble N-ethylmaleimide-sensitive factor attachment receptor (S

210 lysosomes for degradation following soluble N-ethylmaleimide-sensitive factor attachment receptor (S

211 We discovered soluble N-ethylmaleimide-sensitive factor attachment receptor (S

212 Syntaxin 1a is a plasma membrane soluble N-ethylmaleimide-sensitive factor attachment receptor pr

213 ions homologous to eukaryotic SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor) d

214 Syt 1 using a reconstituted, SNARE (soluble N-ethylmaleimide-sensitive factor attachment receptor)-m

215 of tail-anchored proteins, including soluble N-ethylmaleimide-sensitive factor attachment receptors (

216 vesicles in the brain harbor several soluble N-ethylmaleimide-sensitive-factor attachment protein rec

217 ific proteolysis of one of the three soluble N-ethylmaleimide-sensitive-factor attachment protein rec

218 suggest an association of vesicular soluble N-ethylmaleimide-sensitive-factor attachment protein rec

219 ing one of the three proteins of the soluble N-ethylmaleimide-sensitive-factor attachment protein rec

220 Syntaxin-1, a core protein of the soluble N-ethylmaleimide-sensitive-factor attachment protein rec

221 of one of the three proteins of the soluble N-ethylmaleimide-sensitive-factor attachment protein rec

222 , an essential component of the soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein re

223 ly of proteins known as SNAREs [soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein re

224 alpha-SNAP [soluble NSF (N-ethylmaleimide-sensitive factor) attachment protein] a

225 his study investigated the effect of soluble N-ethylmaleimide-sensitive factor-attachment protein (SN

226 with fMLF induced phosphorylation of soluble N-ethylmaleimide-sensitive factor-attachment protein (SN

227 During synaptic vesicle fusion, the soluble N-ethylmaleimide-sensitive factor-attachment protein rec

228 n 18 is a target membrane-associated soluble N-ethylmaleimide-sensitive factor-attachment protein rec

229 The soluble N-ethylmaleimide-sensitive factor-attachment protein rec

230 ogenetic approach to identify target soluble N-ethylmaleimide-sensitive factor-attachment protein rec

231 SF attachment protein, and NSF is defined as N-ethylmaleimide-sensitive factor) complexes catalyze sy

232 ndence in the NSF gene, encoding the protein N-Ethylmaleimide-Sensitive Factor essential for synaptic

233 ndent kinase II and the trafficking proteins N-ethylmaleimide-sensitive factor, GABA receptor-associa

234 hibiting the binding of SNAREs to Sec18p, an N-ethylmaleimide-sensitive factor homologue responsible

235 Using the trimerized alphaSNAP, we find that N-ethylmaleimide-sensitive factor hydrolyzes 10 ATP mole

236 identified an essential requirement for nsf (N-ethylmaleimide sensitive factor) in the organization o

237 19712) or by inhibiting exocytosis (TAT-NSF, N-ethylmaleimide-sensitive factor inhibitor).

238 requires membrane fusion mediated by soluble N -ethylmaleimide-sensitive factor (NSF) attachment prot

239 e release machinery, this assay incorporates N-ethylmaleimide sensitive factor (NSF) and alpha-SNAP,

240 ion of nitric oxide (NO), which nitrosylates N-ethylmaleimide sensitive factor (NSF) and inhibits exo

241 olecule binds our two model His(6) proteins, N-ethylmaleimide sensitive factor (NSF) and O(6)-alklygu

242 nillin, citron-kinase (CG10522), and soluble N-ethylmaleimide sensitive factor (NSF) attachment prote

243 Moreover, we provided evidence for a role of N-ethylmaleimide sensitive factor (NSF) in regulating Mu

244 s of nitric oxide (NO), which S-nitrosylated N-ethylmaleimide sensitive factor (NSF), a critical regu

245 H(2)O(2) regulates exocytosis by inhibiting N-ethylmaleimide sensitive factor (NSF), a protein that

246 ated by NMDA receptor (NMDAR) activation and N-ethylmaleimide sensitive factor (NSF).

247 aptor-binding site for the p97/VCP homologue N-ethylmaleimide sensitive factor (NSF).

248 y related to the single N domains in p97 and N-ethylmaleimide sensitive factor (NSF); N1 of Pex1 is m

249 18-1 (stabilizes assembled SNARE complexes), N-ethylmaleimide-sensitive factor (NSF) (disassembles SN

250 The time at which the N-ethylmaleimide-sensitive factor (NSF) acts during syna

251 The N-ethylmaleimide-sensitive factor (NSF) and soluble NSF

252 For example, Mg2+ is a cofactor for the N-ethylmaleimide-sensitive factor (NSF) ATPase, and the

253 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

254 t is directly involved in regulating soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

255 domain and modulate the affinity for soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

256 isoforms to directly regulate SNARE (soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

257 of Golgi matrix proteins, Rab1, and soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

258 In eukaryotic cells, the soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

259 e mutation in the gene Napa encoding soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

260 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

261 Sec17 [soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

262 A soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

263 ly AAA domain-containing protein 1), soluble N-ethylmaleimide-sensitive factor (NSF) attachment prote

264 GEC1 interacted with N-ethylmaleimide-sensitive factor (NSF) in pull-down ass

265 N-Ethylmaleimide-sensitive factor (NSF) is a homo-hexame

266 daptor molecule for the SNARE-priming enzyme N-ethylmaleimide-sensitive factor (NSF) is known to be c

267 novel synaptic interaction between Arr1 and N-ethylmaleimide-sensitive factor (NSF) that is enhanced

268 Co-expression of N-ethylmaleimide-sensitive factor (NSF) with the CRLR-RA

269 ATPase activity and disassembly activity of N-ethylmaleimide-sensitive factor (NSF), a critical comp

270 inhibits exocytosis by chemically modifying N-ethylmaleimide-sensitive factor (NSF), a key component

271 n kinase Cepsilon (PKCepsilon) regulates the N-ethylmaleimide-sensitive factor (NSF), an ATPase criti

272 The human beta2AR carboxyl end binds to the N-ethylmaleimide-sensitive factor (NSF), an ATPase integ

273 Exocytosis is mediated in part by N-ethylmaleimide-sensitive factor (NSF), an ATPase that

274 se mutation in the nsf-1 gene, which encodes N-ethylmaleimide-sensitive factor (NSF), an intracellula

275 s hepatic secretion of VLDL-TAG by targeting N-ethylmaleimide-sensitive factor (NSF), both in vivo an

276 N-ethylmaleimide-sensitive factor (NSF), first discovere

277 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

279 lex is disassembled by an AAA+ ATPase called N-ethylmaleimide-sensitive factor (NSF).

280 ) family proteins and non-PDZ binding to the N-ethylmaleimide-sensitive factor (NSF).

281 d iPSC-derived human neurons, among them the N-ethylmaleimide-sensitive factor (NSF).

282 KMzeta maintains late-LTP through persistent N-ethylmaleimide-sensitive factor (NSF)/glutamate recept

283 enishment and release did not require ATP or N-ethylmaleimide-sensitive factor (NSF); however, this p

284 diverse cellular activities (AAA+) protein, N-ethylmaleimide-sensitive factor (NSF/Sec18), and its c

285 rate that interaction of AMPA receptors with N-ethylmaleimide-sensitive factor plays a critical role

286 ane-resident syntaxin-like glutamine-soluble N-ethylmaleimide-sensitive factor protein attachment pro

287 P2;5 are regulated by the SNARE (for soluble N-ethylmaleimide-sensitive factor protein attachment pro

288 SNARE (soluble N-ethylmaleimide-sensitive factor protein attachment pro

289 ve interaction of the GluR2 subunit with the N-ethylmaleimide-sensitive factor protein is required fo

290 ated with Plasmodium homologues of COPII and N-ethylmaleimide-sensitive factor, proteins involved in

291 R-SNAREs (soluble N-ethylmaleimide-sensitive factor receptor), Q-SNAREs, a

292 taining lipid bilayers as well as to soluble N-ethylmaleimide sensitive factor receptors (SNAREs) and

293 N-Ethylmaleimide sensitive factor recycles SNAREs after

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

296 The ATPase NSF (N-ethylmaleimide sensitive factor), together with SNAPs

297 ents, whereas further incubation with p97 or N-ethylmaleimide-sensitive factor (two AAA ATPases invol

298 e SNARE bundles are reactivated by hexameric N-ethylmaleimide-sensitive factor, vesicle-fusing ATPase

299 In addition, the distribution of NSF (N-ethylmaleimide-sensitive factor) was affected in GABAR

300 SNX27-independent recycling may involve N-ethylmaleimide-sensitive factor, which binds both PDZ