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1 ences for transmission caused by the loss of synaptogyrin.
2 mologue of a major synaptic vesicle protein, synaptogyrin.
3 rin that exhibits 47% sequence identity with synaptogyrin.
4                                              Synaptogyrin 1 is a synaptic vesicle protein; cellugyrin
5 erolateral thalamic nuclei, which all showed synaptogyrin 1 labeling, contained significantly less sy
6 3 compared to the ubiquitous distribution of synaptogyrin 1.
7 s associated with synaptic vesicles and that synaptogyrins 1 and 3 can reside on the same synaptic ve
8                   Synaptophysins 1 and 2 and synaptogyrins 1 and 3 constitute a major family of synap
9    Analysis of the relative distributions of synaptogyrins 1 and 3 in mouse brain revealed a more res
10 e-phosphorylated proteins with two neuronal (synaptogyrins 1 and 3) and one ubiquitous (cellugyrin) i
11  that control glutamate release (e.g., SV2A, synaptogyrin-1) and postsynaptic signaling (e.g., GluA1,
12 led a more restricted expression pattern for synaptogyrin 3 compared to the ubiquitous distribution o
13 naptic vesicles from mouse brain showed that synaptogyrin 3 is associated with synaptic vesicles and
14                                       Strong synaptogyrin 3 labeling was observed in the mossy fiber
15  situ hybridization experiments to correlate synaptogyrin 3 mRNA in cell bodies with synaptogyrin 3 p
16 late synaptogyrin 3 mRNA in cell bodies with synaptogyrin 3 protein at synapses.
17 n family, we studied the distribution of the synaptogyrin 3 protein in the nervous system.
18 rin 1 labeling, contained significantly less synaptogyrin 3.
19 urons confirmed the synaptic localization of synaptogyrin 3.
20 a was indispensable for the interaction with synaptogyrin-3 (Syngr3) and demonstrated that disrupting
21 identify a novel interaction between DAT and synaptogyrin-3 and suggest a physical and functional lin
22 at the cytoplasmic N termini of both DAT and synaptogyrin-3 are sufficient for this interaction.
23 , we identified the synaptic vesicle protein synaptogyrin-3 as a DAT interacting protein using the sp
24                                      DAT and synaptogyrin-3 colocalized at presynaptic terminals from
25                                 Instead, the synaptogyrin-3 effect on DAT activity was abolished in t
26              Functional assays revealed that synaptogyrin-3 expression correlated with DAT activity i
27        We show that heterozygous knockout of synaptogyrin-3 is benign in mice but strongly rescues mu
28                                 Tau binds to Synaptogyrin-3 on synaptic vesicles.
29 ceptor and of phospho-tau species with their synaptogyrin-3 synaptic vesicle receptor replace excessi
30 sults for novel PD targets, and one, SYNGR3 (Synaptogyrin-3), was manually investigated further as a
31 ase (3.6-fold increase in chronic mTBI); and synaptogyrin-3, 3.1-fold increase (1.3-fold increase in
32 nce for a biochemical complex involving DAT, synaptogyrin-3, and VMAT2.
33 rial creatine kinase U-type, beta-synuclein, synaptogyrin-3, synaptophysin, syntaxin 1B, synaptotagmi
34 en we remove the expression of one allele of synaptogyrin-3.
35 in(6) and its paralogues synaptoporin(7) and synaptogyrin(8) belong to a family of abundant synaptic
36                                              Synaptogyrin and synaptophysin are conserved MARVEL doma
37 aptic-like microvesicles (SLMVs), along with synaptogyrin and synaptophysin.
38  closely related to synaptic vesicle protein synaptogyrin and, more remotely, to synaptophysin.
39 totagmin I, synapsin, bassoon, syntaxin, and synaptogyrin, appeared not to be associated with DA neur
40  cells demonstrated that both cellugyrin and synaptogyrin are tyrosine phosphorylated in vivo by pp60
41                           Drosophila lacking synaptogyrin are viable and fertile and have no overt de
42                                 All of these synaptogyrins are composed of a short conserved N-termin
43                     Our results suggest that synaptogyrins are conserved components of the exocytotic
44  Altogether, our data indicate that neuronal synaptogyrins are differentially expressed protein isofo
45               In rat tissues, cellugyrin and synaptogyrins are expressed in mirror image patterns.
46         Previous studies have indicated that synaptogyrins are involved in the regulation of neurotra
47    We have now identified a novel isoform of synaptogyrin called cellugyrin that exhibits 47% sequenc
48                               Cellugyrin and synaptogyrin co-localize when transfected into COS cells
49                                              Synaptogyrins comprise a family of tyrosine-phosphorylat
50                                              Synaptogyrins constitute a family of synaptic vesicle pr
51 of VAMP2/synaptobrevin 2, synaptophysin, and synaptogyrin demonstrated significant intervesicle varia
52 y were severely reduced in the synaptophysin/synaptogyrin double knockout mice.
53 n synaptogyrin isoform, we now show that the synaptogyrin family in vertebrates includes two neuronal
54          We have studied the localization of synaptogyrin family members in vivo.
55     In an effort to further characterize the synaptogyrin family, we studied the distribution of the
56  represent components of signals that target synaptogyrin for endocytosis from the plasma membrane an
57 relocalize cellugyrin, a nonneuronal form of synaptogyrin, from nonsynaptic regions such as the senso
58 e proteins, we generated and characterized a synaptogyrin (gyr)-null mutant in Drosophila, whose geno
59                           Our data show that synaptogyrin I and synaptophysin I perform redundant and
60               We have generated mice lacking synaptogyrin I and synaptophysin I to explore the functi
61       Moreover, expression of cellugyrin (or synaptogyrin) in PC12 cells dramatically and specificall
62 ta suggest that the synaptic vesicle protein synaptogyrin is a specialized version of a ubiquitous pr
63                                              Synaptogyrin is an abundant membrane protein of synaptic
64 aled that the conserved N-terminal domain of synaptogyrin is essential for inhibition, whereas the lo
65 ting of exogenously expressed cellugyrin and synaptogyrin is high.
66      Similarly, the C-terminal domain of rat synaptogyrin is necessary for localization in hippocampa
67                  Furthermore, GFP-tagged rat synaptogyrin is synaptically localized in neurons of C.
68 in Drosophila, whose genome encodes a single synaptogyrin isoform and lacks a synaptophysin homolog.
69 ith the full-length structure of a new brain synaptogyrin isoform, we now show that the synaptogyrin
70   Our study suggests that the mechanisms for synaptogyrin localization are likely to be conserved fro
71                   These results suggest that synaptogyrin modulates the synaptic vesicle exo-endocyti
72 ious studies in PC12 cells demonstrated that synaptogyrin or its nonneuronal paralog cellugyrin targe
73               We demonstrate that Drosophila synaptogyrin plays a modulatory role in synaptic vesicle
74 h the lowest levels in brain tissue, whereas synaptogyrin protein is only detectable in brain.
75 nsmembrane domain proteins synaptophysin and synaptogyrin represent the major constituents of synapti
76                   Analysis of the regions of synaptogyrin required for inhibition revealed that the c
77  protein (GFP)-tagged Caenorhabditis elegans synaptogyrin (SNG-1) are expressed in neurons and synapt
78 localization, abundance, and conservation of synaptogyrins suggest a function in exocytosis.
79 d tyrosine phosphorylation of cellugyrin and synaptogyrins suggests a link between tyrosine phosphory
80  of syp and the related tetraspanner protein synaptogyrin (syg).
81 ocytosis from the plasma membrane and direct synaptogyrin to synaptic vesicles, respectively.
82  expressed but correlated with the amount of synaptogyrin transfected.
83 naptophysin I, which is distantly related to synaptogyrins, was also inhibitory but less active.
84  or alpha-latrotoxin, co-transfection of all synaptogyrins with hGH inhibited hGH exocytosis as stron