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1 elinated primary afferents) or the vesicular glutamate transporter 1.
2 orm, neurofilament light chain and vesicular glutamate transporter 1.
3 Kir4.1, and to take up excess glutamate via glutamate transporter 1, a glial-specific glutamate tran
4 droxylase in periglomerular cells, vesicular glutamate transporter 1, a presynaptic protein, in mitra
5 tamatergic innervation using pre- (vesicular glutamate transporter 1 and 2) and postsynaptic (postsyn
6 oxide synthase, somatostatin, and vesicular glutamate transporters 1 and 2 accounted for a combined
7 imary afferents immunoreactive for vesicular glutamate transporters 1 and 2 and by intraspinal neuron
8 the entire macaque thalamus using vesicular glutamate transporters 1 and 2 to label cortical and sub
9 urochemical phenotypes such as the vesicular glutamate transporters-1 and 2 (VGLUT-1, VGLUT-2), or th
11 ker proteins synaptophysin and the vesicular glutamate transporter 1, but not with the postsynaptic d
12 ine-induced suppression of the high-affinity glutamate transporter 1 (EAAT2/GLT-1) in the nucleus acc
13 ched components, including vGLUT1 (vesicular glutamate transporter 1), EAAT5 (excitatory amino acid t
14 e via specialized transporters such as glial glutamate transporter 1 (excitatory amino-acid transport
15 nhibited by dihydrokainate, an antagonist of glutamate transporter-1 (excitatory amino acid transport
16 y may be in part due to increased Kir4.1 and glutamate transporter 1 expression in astrocytes leading
18 ouble hybridization of mRNA encoding NBC and glutamate transporter 1 (glial marker) confirmed that bo
19 seeking while increasing the function of the glutamate transporter 1 (GLT-1) and system xC- (Sxc) in
20 his behavioral effect has been attributed to glutamate transporter 1 (GLT-1) and xCT (a catalytic sub
22 t TX enhanced the expression and function of glutamate transporter 1 (GLT-1) in rat astrocytes, an ef
23 well as the stress-induced increase in glial glutamate transporter 1 (GLT-1) mRNA expression and the
24 ea, to promote the upregulation of the glial glutamate transporter 1 (GLT-1) on astrocytes and to red
25 h that correlates with reduced expression of glutamate transporter-1 (GLT-1) and occurs concurrent wi
26 Glutamate/aspartate transporter (GLAST) and glutamate transporter-1 (GLT-1) are the most abundant su
29 glutamate-aspartate transporter (GLAST) and glutamate transporter-1 (GLT-1), which are essential for
30 n that E2 increases astrocytic expression of glutamate transporter-1 (GLT-1), which would prevent exc
32 rter (GLAST)] and green fluorescent protein [glutamate transporter-1 (GLT-1)] reporter transgenic mic
35 hat astroglial glutamate transporter subtype glutamate transporter 1 (GLT1) and glutamate uptake is s
36 e, since others have purified the astrocytic glutamate transporter 1 (GLT1) from crude synaptosomal f
38 illary acidic protein, glutamine synthetase, glutamate transporter 1 (GLT1), aquaporin-4, aldehyde de
40 porter Sv2 (now known as SV2A) and Vesicular glutamate transporter 1 in the outer molecular layer of
41 shown by using antibodies against vesicular glutamate transporter 1 [labeling all ON and OFF bipolar
42 ate transporter levels were higher and glial glutamate transporter 1 levels were lower in the DH of f
43 microscopic level, the density of vesicular glutamate transporter 1-positive (i.e. cortico-subthalam
44 y synapses, defined by overlapping vesicular glutamate transporter 1-positive (VGlut1+) and postsynap
45 ory synapses (i.e., the overlap of vesicular glutamate transporter 1-positive [VGlut1+] puncta and po
46 studies showing that the number of vesicular glutamate transporter 1-positive terminals and of axon t
47 in response to Kal7 are apposed to vesicular glutamate transporter 1-positive, bassoon-positive presy
48 treatment (50 nM) is sufficient to increase glutamate transporter 1 protein expression in spinal cor
50 e to dihydrokainate suggests that the GLT-1 (glutamate transporter-1) subtype primarily mediates the
51 n inversely correlated increase in vesicular glutamate transporter-1 (VGluT-1) occurred in DGiml of t
52 g the tibial nerve (TN), and using Vesicular GLUtamate Transporter 1 (VGLUT1) and the 65 kDa isoform
53 ectors to target expression of the vesicular glutamate transporter 1 (VGLUT1) following injection int
54 or NL2 after IUEP does not affect vesicular glutamate transporter 1 (vGlut1) in the glutamatergic co
55 for an increased expression of the vesicular glutamate transporter 1 (vGluT1) in the striatum of PD p
57 o immunolabeled with antibodies to vesicular glutamate transporter 1 (VGLUT1), vesicular gamma-aminob
59 gated expression of glutamatergic [vesicular glutamate transporter 1 (VGLUT1)] and GABA/glycinergic [
60 ochemical markers [parvalbumin and vesicular glutamate transporter 1 (VGLUT1)] showed that most embry
61 ransporter 2 (EAAT2) and increased vesicular glutamate transporter-1 (VGLUT1) immunoreactivity in a v
62 ses of neurons; in particular, the vesicular glutamate transporter-1 (VGLUT1) promoter supports expre
64 minals [i.e., terminals containing vesicular glutamate transporter-1 (VGLUT1)] on SOL motoneurons wer
65 irect translational regulation of Kir4.1 and glutamate transporter 1 via genomic oestrogen receptors.
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