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1 TPase that disassembles complexes of soluble NSF attachment protein receptors.
2  is mediated by assemblies of SNARE (soluble NSF-attachment protein receptor) and SM (Sec1/Munc18-lik
3 ke proteins) and SNARE proteins (for soluble NSF-attachment protein receptors) are essential for intr
4                              SNAREs (soluble NSF-attachment protein receptors) are generally acknowle
5 on is the pairing of SNARE proteins (soluble NSF attachment protein receptors) associated with the ve
6  (soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor)-catalyzed membrane fus
7 ptic membrane through formation of a soluble NSF attachment protein receptor complex (SNARE) with syn
8  triphosphate and to disassemble the soluble NSF attachment protein receptor complex.
9 hanism that requires a unique SNARE (soluble NSF-attachment protein receptor)-dependent fusion machin
10 nd that yeast vacuolar SNAREs (SNAP [Soluble NSF attachment protein] Receptors) increase the permeabi
11 ed coil domain-containing Q-SNARE (Q-soluble NSF attachment protein receptor) protein syntaxin 6 both
12 eraction of HOPS with certain SNARE (soluble NSF attachment protein receptor) proteins ensures the fu
13  NSF attachment proteins and SNAREs (soluble NSF attachment protein receptor), rab 5, dynamin, caveol
14 ellular trafficking by disassembling soluble NSF attachment protein receptor (SNARE ) complexes.
15 ogically, alpha-synuclein chaperones soluble NSF attachment protein receptor (SNARE) complex assembly
16        We show in human cells that a soluble NSF attachment protein receptor (SNARE) complex comprise
17       NO inhibits NSF disassembly of soluble NSF attachment protein receptor (SNARE) complexes by nit
18 nderstanding the fundamental role of soluble NSF attachment protein receptor (SNARE) complexes in mem
19 embrane trafficking by disassembling soluble NSF attachment protein receptor (SNARE) complexes that f
20  function of synaptotagmin-1 (syt-1):soluble NSF attachment protein receptor (SNARE) interactions dur
21 t Bet1p plays a role in potentiating soluble NSF attachment protein receptor (SNARE) interactions.
22 have not been shown to use canonical soluble NSF attachment protein receptor (SNARE) machinery for fu
23                         The ER/Golgi soluble NSF attachment protein receptor (SNARE) membrin, rsec22b
24 nteracting with a complex containing soluble NSF attachment protein receptor (SNARE) molecules, hydro
25                                      Soluble NSF attachment protein receptor (SNARE) proteins are ess
26 at platelet secretion is mediated by Soluble NSF Attachment Protein Receptor (SNARE) proteins from gr
27 functional trafficking steps used by soluble NSF attachment protein receptor (SNARE) proteins have be
28 petition indicated a requirement for soluble NSF attachment protein receptor (SNARE) proteins Tlg1p,
29 ) have linked genes encoding several soluble NSF attachment protein receptor (SNARE) regulators to ca
30 ions with lipid bilayers in Rab- and soluble NSF attachment protein receptor (SNARE)-dependent biolog
31 At this concentration of PI 4,5-P(2) soluble NSF attachment protein receptor (SNARE)-dependent liposo
32     Neurotransmission is achieved by soluble NSF attachment protein receptor (SNARE)-driven fusion of
33                           Defects in soluble NSF attachment protein receptor (SNARE)-mediated granule
34 t soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor (SNARE) complex plays a
35 e N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor (SNARE) complex that me
36 g soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor (SNARE) complexes and m
37 e N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor (SNARE) complexes betwe
38 e soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor (SNARE) proteins compri
39 f soluble N-ethylmaleimide-sensitive fusion (NSF) attachment protein receptor (SNARE) proteins, which
40 e N-ethylmaleimide-sensitive fusion protein (NSF)-attachment protein receptor (SNARE), is a membrane
41 is process involved formation of new soluble NSF-attachment protein receptor (SNARE) complexes as jud
42 he packaging of Yip1p, Yif1p, or the soluble NSF attachment protein receptor (SNAREs) into vesicles.
43                         Munc18-1 and soluble NSF attachment protein receptors (SNAREs) are critical f
44 ween synaptotagmin-1 (syt-1) and the soluble NSF attachment protein receptors (SNAREs) are required d
45                                      Soluble NSF attachment protein receptors (SNAREs) are the core p
46                                      Soluble NSF attachment protein receptors (SNAREs) are type II tr
47 ase of granular cargo is mediated by soluble NSF attachment protein receptors (SNAREs), but despite c
48 hylmaleimide (NEM)-sensitive fusion protein (NSF) attachment protein receptors (SNAREs) via two inter
49 s soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptors (SNAREs), have been im
50 r soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptors (SNAREs), phospholipid
51 f soluble N-ethylmaleimide sensitive factor (NSF) attachment protein receptors (SNAREs).
52 e soluble N-ethylmaleimide-sensitive factor (NSF)-attachment protein receptors (SNAREs) have been imp
53 s by cleaving their cytosolic SNARE (soluble NSF attachment protein receptor) substrates.
54  (soluble N-ethylmaleimide sensitive factor [NSF] attachment protein receptors) such as syntaxins 2,
55 tor protein Myosin Vb (Myo5B) or the soluble NSF attachment protein receptor Syntaxin 3 (Stx3) distur
56 , giving rise to two target-membrane soluble NSF attachment protein receptor (t-SNARE) isoforms.
57  interaction of a vesicle-associated soluble NSF attachment protein receptor (v-SNARE) on transport v

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