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1 epend on the presence of alpha-SNAP (soluble NSF-attachment protein).
2 actor), working together with SNAPs (soluble NSF attachment proteins).
3 an effect that was rescued by alpha-soluble NSF attachment protein.
6 g soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein alpha (alpha Snap), involved in
7 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein alpha (alphaSNAP) is a well know
8 A soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein alpha (alphaSNAP) is an essentia
9 kDa protein (SNAP-25), n-sec1, alpha soluble NSF attachment protein (alpha SNAP), and synaptotagmin.
10 (NSF) and its adaptor protein alpha-soluble NSF attachment protein (alpha-SNAP) sustain membrane tra
11 transport machinery component, alpha soluble NSF attachment protein (alpha-SNAP), occurring during de
12 hylmaleimide-sensitive factor, alpha-soluble NSF attachment protein (alpha-SNAP), synaptosome-associa
15 Soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (alpha-SNAP) is a multifunctiona
16 e N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein (alpha-SNAP) is a soluble protei
17 d soluble N-ethylmaleimide sensitive factor (NSF) attachment protein (alpha-SNAP), are essential for
18 itive fusion protein [NSF]), Sec17p (soluble NSF attachment protein [alpha-SNAP]), and typical vesicl
19 [soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein; alpha-SNAP] and Sec18 (NSF) per
21 ntain complexes that comprise beside soluble NSF attachment proteins and SNAREs (soluble NSF attachme
22 le trafficking (e.g., two alpha-type soluble NSF attachment proteins), and other, unknown conserved c
23 tor (SNARE, where SNAP is defined as soluble NSF attachment protein, and NSF is defined as N-ethylmal
25 and the adaptor protein alpha-SNAP (soluble NSF attachment protein) disassemble all SNARE complexes
26 sitive factor), together with SNAPs (soluble NSF attachment protein), disassembles the SNARE complex
27 , soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (gamma-SNAP), and the transmembr
28 amino acid transporter and an alpha soluble NSF attachment protein gene specifically in syncytia und
29 n analyses that identified the alpha soluble NSF attachment protein (Gm-alpha-SNAP) resistance gene b
32 ogically, alpha-synuclein chaperones soluble NSF attachment protein receptor (SNARE) complex assembly
34 memory enhancement and requires the soluble NSF attachment protein receptor (SNARE) complex, a GBy e
36 nderstanding the fundamental role of soluble NSF attachment protein receptor (SNARE) complexes in mem
37 embrane trafficking by disassembling soluble NSF attachment protein receptor (SNARE) complexes that f
38 function of synaptotagmin-1 (syt-1):soluble NSF attachment protein receptor (SNARE) interactions dur
39 t Bet1p plays a role in potentiating soluble NSF attachment protein receptor (SNARE) interactions.
40 have not been shown to use canonical soluble NSF attachment protein receptor (SNARE) machinery for fu
42 nteracting with a complex containing soluble NSF attachment protein receptor (SNARE) molecules, hydro
43 entified a novel druggable target, a soluble NSF attachment protein receptor (SNARE) protein called y
44 blocking ykt6, a farnesyl-regulated soluble NSF attachment protein receptor (SNARE) protein that is
46 at platelet secretion is mediated by Soluble NSF Attachment Protein Receptor (SNARE) proteins from gr
47 yst and fusion driven by assembly of soluble NSF attachment protein receptor (SNARE) proteins from th
48 functional trafficking steps used by soluble NSF attachment protein receptor (SNARE) proteins have be
49 petition indicated a requirement for soluble NSF attachment protein receptor (SNARE) proteins Tlg1p,
50 ) have linked genes encoding several soluble NSF attachment protein receptor (SNARE) regulators to ca
51 ions with lipid bilayers in Rab- and soluble NSF attachment protein receptor (SNARE)-dependent biolog
52 At this concentration of PI 4,5-P(2) soluble NSF attachment protein receptor (SNARE)-dependent liposo
53 Neurotransmission is achieved by soluble NSF attachment protein receptor (SNARE)-driven fusion of
55 he packaging of Yip1p, Yif1p, or the soluble NSF attachment protein receptor (SNAREs) into vesicles.
57 interaction of a vesicle-associated soluble NSF attachment protein receptor (v-SNARE) on transport v
58 ptic membrane through formation of a soluble NSF attachment protein receptor complex (SNARE) with syn
60 tor protein Myosin Vb (Myo5B) or the soluble NSF attachment protein receptor Syntaxin 3 (Stx3) distur
61 ed coil domain-containing Q-SNARE (Q-soluble NSF attachment protein receptor) protein syntaxin 6 both
62 eraction of HOPS with certain SNARE (soluble NSF attachment protein receptor) proteins ensures the fu
64 NSF attachment proteins and SNAREs (soluble NSF attachment protein receptor), rab 5, dynamin, caveol
65 t soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor (SNARE) complex plays a
66 e N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor (SNARE) complex that me
67 g soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor (SNARE) complexes and m
68 e N-ethylmaleimide-sensitive fusion protein (NSF) attachment protein receptor (SNARE) complexes betwe
69 e soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor (SNARE) proteins compri
70 f soluble N-ethylmaleimide-sensitive fusion (NSF) attachment protein receptor (SNARE) proteins, which
71 (soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptor)-catalyzed membrane fus
72 e N-ethylmaleimide-sensitive fusion protein (NSF)-attachment protein receptor (SNARE), is a membrane
73 idic fusion pore flanked by putative soluble NSF-attachment protein receptor (SNARE) complexes and th
74 is process involved formation of new soluble NSF-attachment protein receptor (SNARE) complexes as jud
75 is mediated by assemblies of SNARE (soluble NSF-attachment protein receptor) and SM (Sec1/Munc18-lik
76 hanism that requires a unique SNARE (soluble NSF-attachment protein receptor)-dependent fusion machin
78 (soluble N-ethylmaleimide-sensitive factor [NSF]-attachment protein receptor) synaptobrevin (also ca
80 ween synaptotagmin-1 (syt-1) and the soluble NSF attachment protein receptors (SNAREs) are required d
83 ase of granular cargo is mediated by soluble NSF attachment protein receptors (SNAREs), but despite c
84 on is the pairing of SNARE proteins (soluble NSF attachment protein receptors) associated with the ve
86 hylmaleimide (NEM)-sensitive fusion protein (NSF) attachment protein receptors (SNAREs) via two inter
87 s soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptors (SNAREs), have been im
88 r soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein receptors (SNAREs), phospholipid
91 e soluble N-ethylmaleimide-sensitive factor (NSF)-attachment protein receptors (SNAREs) have been imp
92 ke proteins) and SNARE proteins (for soluble NSF-attachment protein receptors) are essential for intr
94 (soluble N-ethylmaleimide sensitive factor [NSF] attachment protein receptors) such as syntaxins 2,
95 nd that yeast vacuolar SNAREs (SNAP [Soluble NSF attachment protein] Receptors) increase the permeabi
96 ssembly with dominant-negative alpha-soluble NSF attachment protein (SNAP) also inhibited tethering,
97 maleimide-sensitive factor (NSF) and soluble NSF attachment protein (SNAP) are cytosolic factors that
98 nsitive fusion protein 2 (dNSF2) and soluble NSF attachment protein (Snap) as strong genetic modifier
99 gh its binding to and disassembly of soluble NSF attachment protein (SNAP) receptor (SNARE) complexes
100 de-sensitive factor) that rearranges soluble NSF attachment protein (SNAP) receptor (SNARE) protein c
101 hylmaleimide-sensitive factor (NSF), soluble NSF attachment protein (SNAP), SNAP receptors (SNAREs),
104 ith syntaxin-1A as bait, we isolated soluble NSF attachment protein (SNAP)-29 from a human brain cDNA
105 leimide-sensitive factor (NSF)-alpha soluble NSF attachment protein (SNAP)-SNAP receptor (SNARE) comp
106 A and R388A) did not effect basal or soluble NSF attachment protein (SNAP)-stimulated ATPase activity
108 d soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptors (SNAREs) on thi
109 [soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP) receptors in the target m
110 , soluble N-ethylmaleimide-sensitive factor (NSF) attachment protein (SNAP), and NSF, that play a rol
111 e soluble N-ethylmaleimide-sensitive factor (NSF)-attachment protein (SNAP) receptor hypothesis (SNAR
113 (soluble N-ethyl maleimide-sensitive factor [NSF] attachment protein [SNAP] receptor) machinery in me
114 e N-ethylmaleimide-sensitive fusion protein [NSF] attachment protein [SNAP] receptor) with covalently
115 (soluble N-ethylmaleimide-sensitive factor [NSF] attachment protein [SNAP] receptors) of the syntaxi
116 F to interact with alpha-SNAP.SNARE (soluble NSF attachment protein-SNAP receptor) complex, suggestin
117 hylmaleimide-sensitive factor (NSF), soluble NSF attachment proteins (SNAPs), and SNAP receptor (neur
118 studies have demonstrated that NSF, soluble NSF attachment proteins (SNAPs), and SNAP receptors from
119 mide-sensitive fusion protein (NSF), soluble NSF attachment proteins (SNAPs), and SNAREs (SNAP recept
120 hylmaleimide-sensitive factor (NSF), soluble NSF attachment proteins (SNAPs), and SNAREs in synaptic
121 on protein (NSF) and alpha- and beta-soluble NSF attachment proteins (SNAPs), as well as dendritic co
122 nsitive fusion protein (NSF/Sec18p), soluble NSF attachment proteins (SNAPs/Sec17p) and SNAP receptor