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1 integral membrane proteins known as SNAREs (SNAP receptors).
2 NSF attachment proteins (SNAPs), and SNAREs (SNAP receptors) are elements of a conserved molecular ma
3 Rab2, Rab7, and its effector, PLEKHM1; and a SNAP receptor complex consisting of Syntaxin 13, Snap29,
5 leimide-sensitive factor attachment protein (SNAP) receptor complex required for regulated neuroexocy
6 ew light on the mechanisms underlying SNARE (SNAP receptor) complex assembly and disassembly, and sug
7 a-SNAP.SNARE (soluble NSF attachment protein-SNAP receptor) complex, suggesting that only when the D1
8 leimide-sensitive factor attachment protein (SNAP) receptor]-dependent SNAP-23-mediated mechanism.
10 e-sensitive factor (NSF)-attachment protein (SNAP) receptor hypothesis (SNARE hypothesis), interactio
12 e-sensitive factor (NSF) attachment protein (SNAP) receptors in the target membrane], proteins that a
13 that alpha-SNAP, a soluble component of the SNAP receptor machinery, facilitates transport from endo
14 e-sensitive factor [NSF] attachment protein [SNAP] receptor) machinery in membrane traffic to the api
15 soluble NSF attachment proteins (SNAPs), and SNAP receptor (neuronal SNARE) complexes form 20 S parti
19 factor attachment protein receptor protein (SNAP) receptor) proteins, and this is coupled to cortica
21 can function as target membrane and vesicle SNAP receptors, respectively, for insulin-responsive GLU
22 maleimide fusion protein attachment protein (SNAP) receptor) SNAP-25 is not required for nerve growth
25 function by catalyzing the disassembly of a SNAP receptor (SNARE) complex consisting of membrane pro
28 -alpha soluble NSF attachment protein (SNAP)-SNAP receptor (SNARE) complexes, while delivery from the
30 nt negative Arf1, Rab1a/Rab2 GTPases, or the SNAp REceptor (SNARE) component syntaxin 5, all of which
35 rotein/synaptobrevin are collectively called SNAP receptor (SNARE) proteins, and they catalyze neuron
36 ipates with syntaxin and SNAP-25 in synaptic SNAP receptor (SNARE) ternary complex formation in Hirud
38 ment protein alpha (alpha Snap), involved in SNAP receptor (SNARE)-mediated vesicle fusion in many ce
40 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) complex formation between differe
41 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) complexes formed between the SNAR
43 t rearranges soluble NSF attachment protein (SNAP) receptor (SNARE) protein complexes was proposed to
44 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) proteins synaptobrevin 2, syntaxi
45 leimide-sensitive factor attachment protein (SNAP) receptor (SNARE) proteins syntaxin-1, SNAP-25, and
46 ne fusion is mediated by complexes formed by SNAP-receptor (SNARE) and Secretory 1 (Sec1)/mammalian u
47 pete with alpha-SNAP for binding to synaptic SNAP receptors (SNAREs) and consequently inhibit disasse
49 NSF), soluble NSF attachment protein (SNAP), SNAP receptors (SNAREs), rab-type GTPases, and Sec1p hom
52 leimide-sensitive factor-attachment protein (SNAP) receptors (SNAREs) on the fusion of egg L-alpha-ph
54 s, together with the general target membrane SNAP receptor (t-SNARE) protein SNAP-23 appear to make u
56 lpha-granule release is dependent on vesicle SNAP receptor-target SNAP receptor (vSNARE-tSNARE) inter
57 ein syntaxin 1a (where SNARE is derived from SNAP receptor (the soluble N-ethylmaleimide-sensitive fu
58 y of target (t-SNARE) and vesicle-associated SNAP receptor (v-SNARE) proteins is a critical step for
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