ライフサイエンスコーパス: glutamate transporter

1 ty that the parasite activates the host cell glutamate transporter.

2 amate and are not known to have a functional glutamate transporter.

3 by the gene expression for type 1 vesicular glutamate transporter.

4 a2b, which encodes Eaat2b, a plasma membrane glutamate transporter.

5 colabeled with antibodies against VGluT2, a glutamate transporter.

6 smission due to their abundant expression of glutamate transporters.

7 ly via expression and function of astroglial glutamate transporters.

8 eir highly branched morphologies and express glutamate transporters.

9 h necessitates the proper function of active glutamate transporters.

10 substance, cytochrome oxidase, and vesicular glutamate transporters.

11 domain movements in a bacterial homologue of glutamate transporters.

12 r glutamate, which is regulated primarily by glutamate transporters.

13 mino acids are kept low by the action of the glutamate transporters.

14 g also altered the expression of glucose and glutamate transporters.

15 l binding of two Na(+) ions in Na(+)-coupled glutamate transporters.

16 agnitude slower than those observed in other glutamate transporters.

17 ons contribute to the functional dynamics of glutamate transporters.

18 ls near astrocytes and tightly gated by Glt1 glutamate transporters.

19 1), voltage-gated sodium channels (Nav ) and glutamate transporters.

20 ine-induced suppression of the high-affinity glutamate transporter 1 (EAAT2/GLT-1) in the nucleus acc

21 e via specialized transporters such as glial glutamate transporter 1 (excitatory amino-acid transport

22 seeking while increasing the function of the glutamate transporter 1 (GLT-1) and system xC- (Sxc) in

23 his behavioral effect has been attributed to glutamate transporter 1 (GLT-1) and xCT (a catalytic sub

24 glutamate-aspartate transporter (GLAST) and glutamate transporter 1 (GLT-1) are reduced.

25 t TX enhanced the expression and function of glutamate transporter 1 (GLT-1) in rat astrocytes, an ef

26 ea, to promote the upregulation of the glial glutamate transporter 1 (GLT-1) on astrocytes and to red

27 hat astroglial glutamate transporter subtype glutamate transporter 1 (GLT1) and glutamate uptake is s

28 illary acidic protein, glutamine synthetase, glutamate transporter 1 (GLT1), aquaporin-4, aldehyde de

29 g the tibial nerve (TN), and using Vesicular GLUtamate Transporter 1 (VGLUT1) and the 65 kDa isoform

30 ectors to target expression of the vesicular glutamate transporter 1 (VGLUT1) following injection int

31 or NL2 after IUEP does not affect vesicular glutamate transporter 1 (vGlut1) in the glutamatergic co

32 for an increased expression of the vesicular glutamate transporter 1 (vGluT1) in the striatum of PD p

33 shown by using antibodies against vesicular glutamate transporter 1 [labeling all ON and OFF bipolar

34 tion with synaptic vesicle protein vesicular glutamate transporter 1 in stratum radiatum.

35 porter Sv2 (now known as SV2A) and Vesicular glutamate transporter 1 in the outer molecular layer of

36 ate transporter levels were higher and glial glutamate transporter 1 levels were lower in the DH of f

37 droxylase in periglomerular cells, vesicular glutamate transporter 1, a presynaptic protein, in mitra

38 microscopic level, the density of vesicular glutamate transporter 1-positive (i.e. cortico-subthalam

39 y synapses, defined by overlapping vesicular glutamate transporter 1-positive (VGlut1+) and postsynap

40 ory synapses (i.e., the overlap of vesicular glutamate transporter 1-positive [VGlut1+] puncta and po

41 studies showing that the number of vesicular glutamate transporter 1-positive terminals and of axon t

42 orm, neurofilament light chain and vesicular glutamate transporter 1.

43 oxide synthase, somatostatin, and vesicular glutamate transporters 1 and 2 accounted for a combined

44 imary afferents immunoreactive for vesicular glutamate transporters 1 and 2 and by intraspinal neuron

45 the entire macaque thalamus using vesicular glutamate transporters 1 and 2 to label cortical and sub

46 Glutamate/aspartate transporter (GLAST) and glutamate transporter-1 (GLT-1) are the most abundant su

47 Glutamate transporter-1 (GLT-1) is the main glutamate tr

48 glutamate-aspartate transporter (GLAST) and glutamate transporter-1 (GLT-1), which are essential for

49 n that E2 increases astrocytic expression of glutamate transporter-1 (GLT-1), which would prevent exc

50 B) receptor subunits, and a reduction in the glutamate transporter-1 (GLT-1).

51 Astrocytic glutamate transporter-1 (GLT-I) is critical to control t

52 aptic vesicle protein-2 (SV2), and vesicular glutamate transporter-1 (VGLUT1).

53 The glutamate transporter-1 [GLT-1 (excitatory amino acid tr

54 V1), neurofilament 200 (NF200), or vesicular glutamate transporter 2 (VGluT1).

55 Brains were then processed for vesicular glutamate transporter 2 (VGLUT2) and examined for AAS-in

56 by their immunoreactivity for the vesicular glutamate transporter 2 (VGluT2) and performed unbiased

57 Cre-expressing neurons or inducing vesicular glutamate transporter 2 (VGLUT2) deficiency in Trpv1-Cre

58 -Cre expressing neurons or induced vesicular glutamate transporter 2 (Vglut2) deficiency in Trpv1-Cre

59 ffect of deleting the gene for the vesicular glutamate transporter 2 (Vglut2) from neurons in the PB.

60 Based on PTH2R and vesicular glutamate transporter 2 (VGlut2) immunolabeling in anima

61 We have previously shown that vesicular glutamate transporter 2 (VGLUT2) is the predominant VGLU

62 s, including the expression of the vesicular glutamate transporter 2 (VGluT2) mRNA in Ipc neurons, ha

63 n the transcription factor Phox2b, vesicular glutamate transporter 2 (VGLUT2) mRNA, and a subset cont

64 r bouton size, and the presence of vesicular glutamate transporter 2 (Vglut2) or parvalbumin (PV).

65 he VTA has many neurons expressing vesicular glutamate transporter 2 (VGluT2) that also project to LH

66 onprimary boutons that express the vesicular glutamate transporter 2 (VGLUT2), and form asymmetrical

67 N-->CeA CGRP projections coexpress vesicular glutamate transporter 2 (VGLUT2), providing evidence tha

68 rojected to MDmc and expressed the vesicular glutamate transporter 2 (VGLUT2), which is found in high

69 atic rings of terminals expressing vesicular glutamate transporter 2 (VGLUT2)--to subdivide IC GABAer

70 H)-ir and the same proportion were vesicular glutamate transporter 2 (VGLUT2)-ir.

71 a, with or without the presence of vesicular glutamate transporter 2 (VGLUT2)-mediated glutamatergic

72 e, ionic zinc, neurofilaments, and vesicular glutamate transporter 2 (VGluT2).

73 utamatergic neurons expressing the vesicular glutamate transporter 2 (VGluT2).

74 tamate activity was examined using vesicular glutamate transporter 2 (VGLUT2).

75 rome oxidase, Nissl bodies, or the vesicular glutamate transporter 2 (vGluT2).

76 glutamatergic neurons that express vesicular glutamate transporter 2 (VgluT2).

77 markers [neurofilament, NeuN, and vesicular glutamate transporter 2 (VGlut2)], and cultures exhibite

78 (to visualize Purkinje cells) and vesicular glutamate transporter 2 (VGluT2, to visualize climbing f

79 lation of dopamine neurons express vesicular glutamate transporter 2 and make glutamatergic connectio

80 re GABAergic and were contacted by vesicular glutamate transporter 2-containing somatic terminals, as

81 cted in transgenic mice expressing vesicular glutamate transporter 2-enhanced green fluorescent prote

82 kers for both glutamate signaling (vesicular glutamate transporter 2; VGluT2) and GABA signaling (glu

83 with glutamate neurons (expressing vesicular glutamate transporter 2; VGluT2), which play roles in re

84 ricosities were immunoreactive for vesicular glutamate transporter-2 (78%).

85 , acetylcholinesterase (AChE), and vesicular glutamate transporter-2 (VGluT2) preparations, received

86 glutamatergic neurons--expressing vesicular glutamate transporter-2 (VGluT2)--project to limbic and

87 rformed antibody stainings against vesicular glutamate transporter-2, which suggested that cytochrome

88 -originating pathway consisting of vesicular glutamate transporter 3 (VGluT3) containing neurons that

89 The vesicular glutamate transporter 3 (VGLUT3) is expressed by striata

90 Vesicular glutamate transporter 3 (VGLUT3) loads glutamate into se

91 sent in mutants that lacked either Vesicular glutamate transporter 3 (Vglut3) or Ca(V)1.3.

92 dings to characterize responses of vesicular glutamate transporter 3 (VGluT3)-expressing amacrine cel

93 ch depend on the expression of the vesicular glutamate transporter 3 (VGLUT3).

94 of basket cells expressing CCK and vesicular glutamate transporter 3 (VGlut3).

95 transporter 1(+), somatostatin(+), vesicular glutamate transporter 3 (VGLUT3)/cholecystokinin/CB(1) c

96 Moreover, there is no vesicular glutamate transporter 3-immunoreactive bouton, specific

97 Vesicular glutamate transporter 3-positive (VGluT3(+)) primary aff

98 Mice lacking the vesicular glutamate transporter-3 (VGLUT3) are congenitally deaf d

99 The EAAT2 glutamate transporter, accounts for >90% of hippocampal

100 cise, controlled manner in response to glial glutamate transporter activation.

101 Glutamate transporters actively take up glutamate into t

102 suggest that the Kir4.1 conductance affects glutamate transporter activity in a dual manner: (1) by

103 t mutants to explore the effects of impaired glutamate transporter activity on locomotor network func

104 mate tone in RVH rats was not due to blunted glutamate transporter activity.

105 Glutamate transporters also display an anion conductance

106 nd glutamate transporter expression (glial L-glutamate transporter and L-glutamate/L-aspartate transp

107 EAATs are glutamate transporters and anion-selective ion channels,

108 y (MNTB) are stimulated by the activation of glutamate transporters and consequently release glutamin

109 rgic neurotransmission (astrocyte-restricted glutamate transporters and glutamine synthetase).

110 toward the majority of previously identified glutamate transporters and permeability pathways.

111 Although mitochondrial glutamate transporters and transporters for neutral amin

112 none oxidoreductase 1 (NQO1), Bach1, cystine/glutamate transporter, and glutamate cysteine ligase.

113 pic and metabotropic glutamate receptors and glutamate transporters, and altered neuronal excitabilit

114 /H(+) exchanger, ClC-7 H(+)/Cl(-) exchanger, glutamate transporters, and neutral amino acid transport

115 ound in episodic ataxia of the dual-function glutamate transporter/anion channel EAAT1, and discovere

116 Glutamate transporters are essential for recovery of the

117 Glutamate transporters are integral membrane proteins th

118 intained in physiological solutions and that glutamate transporters are ready to quickly bind glutama

119 nal-glial microenvironment, as well as glial glutamate transporters, are expected to affect eNMDAR-me

120 ique piston-like quaternary rearrangement in glutamate transporters, as evidenced by the difference b

121 Pharmacological blockade of GLT1 astrocyte glutamate transporters, as well as the gliotoxin alpha-a

122 A glutamate transporter-associated chloride channel blocke

123 By expressing vesicular glutamate transporters at high levels in plasma membrane

124 tamate binding can be isolated in the mutant glutamate transporter because reactions, such as glutama

125 d EPSCs in afferent fibers are unaffected by glutamate transporter blockade, suggesting that transmit

126 ncreased (or decreased) in the presence of a glutamate transporter blocker (or a competitive glutamat

127 DVGLUT functions not only as a vesicular glutamate transporter but also serves as an acid-extrudi

128 They are not only secondary active glutamate transporters but also function as anion channe

129 EAATs are not only secondary active glutamate transporters but also function as anion channe

130 n synaptic vesicles is mediated by vesicular glutamate transporters called VGLUTs.

131 Whereas mammalian glutamate transporters can translocate both glutamate an

132 cone during electrical stimulation activates glutamate transporter Cl(-) conductances on neighboring

133 Glutamate transporters clear synaptically released gluta

134 Astrocytes also show diminished glutamate transporter current, are significantly depolar

135 or voltage-clamped astrocytes and respective glutamate transporter currents (GTCs) were induced by ph

136 examined intracellular Na(+) transients and glutamate transporter currents as the most telling indic

137 rescued by increasing the expression of the glutamate transporter dEaat1.

138 elates with the upregulation of an astrocyte glutamate transporter, delayed and reduced glutamate acc

139 ate the dynamic regulation and importance of glutamate transporters during development.

140 /Na(+) exchange via the Drosophila vesicular glutamate transporter (DVGLUT).

141 These findings indicate that astrocytic glutamate transporter dysfunction may play an important

142 oduced two cysteine residues in the neuronal glutamate transporter EAAC1 at positions predicted to be

143 g debate on the contribution of the neuronal glutamate transporter EAAC1 to the onset of compulsive b

144 plicate Slc1a1, a gene encoding the neuronal glutamate transporter EAAC1, with obsessive-compulsive d

145 increase the expression and activity of the glutamate transporter (EAAT(2)) on glial cells, blocks m

146 e up-regulated proteins (GFAP, high affinity glutamate transporter (EAAT-2), apo-J (Clusterin), and p

147 Glial glutamate transporter EAAT2 plays a major role in glutam

148 Previous literature has indicated that glial glutamate transporter EAAT2 plays an essential role in c

149 Riluzole is known to increase the glutamate transporter EAAT2's ability to scavenge excess

150 lies, the DA transporter (DAT) and the glial glutamate transporter EAAT2, and we identified a conserv

151 s internalization of AQP4 and the associated glutamate transporter EAAT2, leading to glutamate excito

152 The glutamate transporter EAAT2, which is primarily localize

153 -181A > C) SNP in the promoter of astroglial glutamate transporter (EAAT2) and the same approach was

154 stabilization of the Purkinje cell-specific glutamate transporter EAAT4 at the plasma membrane.

155 c vesicle machinery, including the vesicular glutamate transporter eat-4/VGLUT, induction of neuropep

156 ture of glutamatergic neurons, the vesicular glutamate transporter EAT-4/VGLUT, is expressed in 38 of

157 tumor mediated by the system x(c)(-) cystine-glutamate transporter (encoded by Slc7a11).

158 tatory amino acid transporter 2)] subtype of glutamate transporter ensures crisp excitatory signaling

159 Perisynaptic astrocytes express important glutamate transporters, especially excitatory amino acid

160 Moreover, we show that neuronal glutamate transporters, especially those localized at th

161 ous glutamate levels controlled by astrocyte glutamate transporters, evokes a transient and reversibl

162 uated glutamate uptake and expression of the glutamate transporter excitatory amino acid transporter

163 Astrocytic glutamate transporter excitatory amino acid transporter

164 mily 1 (SLC1), which also includes the human glutamate transporters (excitatory amino acid transporte

165 Spinal expression of a glutamate transporter, excitatory amino acid carrier 1 (

166 EAAT1 is a glutamate transporter expressed by astrocytes and other

167 ted with increases in Cx43, Cx30, Panx1, and glutamate transporter expression (glial L-glutamate tran

168 ssociated membrane protein 1), and astrocyte glutamate transporter expression (glutamate/aspartate tr

169 duced conflicting results and the changes in glutamate transporter expression have not yet been exami

170 Hypoxia and JAK/STAT inhibition reduce glutamate transporter expression in astrocytes, but unli

171 dition, ENT1 inhibition or knockdown reduces glutamate transporter expression in cultured astrocytes.

172 vation and lysosomal pathology, and restored glutamate transporter expression to levels observed in W

173 trocytes, as well as compromise in astrocyte glutamate transporter expression.

174 GLUT3 is an atypical member of the vesicular glutamate transporter family.

175 s study enhances our understanding as to how glutamate transporters function as both amino-acid trans

176 Additionally, the expression of two known glutamate transporters, genderblind and excitatory amino

177 dates include non-recurrent deletions at the glutamate transporter gene SLC1A1, a CNV locus recently

178 The gene for EAAT2, the major astrocytic glutamate transporter, generates two carrier isoforms (E

179 ontrast levels of the predominant cerebellar glutamate transporter GLAST, expressed in Bergmann glia,

180 The compound did not affect the astrocytic glutamate transporter GLAST, nor did it block glutamate

181 s that increase expression of the astroglial glutamate transporter GLT-1 (N-acetylcysteine and ceftri

182 te carrier family 1 member 2), also known as glutamate transporter GLT-1 and excitatory amino acid tr

183 ed to increased expression of the astrocytic glutamate transporter GLT-1 and to attenuated changes in

184 in hemichannels and glutamate uptake via the glutamate transporter GLT-1 in rat glial cells.

185 e; then, using an antisense strategy against glutamate transporter GLT-1, we found that restored tran

186 ed a progressive depletion of the astroglial glutamate transporters GLT-1 and GLAST.

187 efrontal cortical blockade of the astrocytic glutamate transporter (GLT-1) induces anhedonia and c-Fo

188 removing glutamate from the synapse via the glutamate transporter (GLT-1).

189 Impairment of astrocytic glutamate transporter (GLT-1; EAAT2) function is associa

190 g glutamate spillover by blocking astroglial glutamate transporters (GLT-1) had no effect on reinstat

191 ease in expression and function of the major glutamate transporter, GLT-1.

192 , presumably through dysregulated astroglial glutamate transporter GLT1 and impaired glutamate uptake

193 , likely through the dysregulated astroglial glutamate transporter GLT1 expression and impaired gluta

194 We found that functional expression of glutamate transporter GLT1 is 40% decreased in i-astro-F

195 on of important functional proteins, such as glutamate transporter GLT1.

196 ficantly reduced expression of the major CNS glutamate transporter, GLT1, in superficial dorsal horn

197 ransiently increased, and the glial-specific glutamate transporters glutamate-aspartate transporter (

198 Dysfunction of glutamate transporters has been proposed to promote neur

199 SLC1A3 encodes the glial glutamate transporter hEAAT1, which removes glutamate fr

200 utward- and inward-facing conformations of a glutamate transporter homolog from archaebacterium Pyroc

201 based on crystal structures of the bacterial glutamate transporter homolog Glt(Ph).

202 Crystallographic studies of a glutamate transporter homologue from the archaeon Pyroco

203 y proteins defining glutamatergic signaling (glutamate transporter-I [GLT-I], N-methyl-D-aspartate re

204 Ceftriaxone modulated the expression of the glutamate transporter in a critical region of the cortic

205 We find that a putative glutamate transporter in Drosophila melanogaster, polyph

206 for early expression of the type 2 vesicular glutamate transporter in mesencephalic DA neurons, we hy

207 GLT-1, the major glutamate transporter in the adult brain, is abundantly

208 GLT-1 (EAAT2; slc1a2) is the major glutamate transporter in the brain, and is predominantly

209 Glutamate transporter-1 (GLT-1) is the main glutamate transporter in the central nervous system, and

210 AT5 may not act as a classical high-capacity glutamate transporter in the retina; rather, it may func

211 results indicate a role for neuron-specific glutamate transporters in AMPAR synaptic localization an

212 Here we elucidated the roles of these two glutamate transporters in cerebellar pathogenesis mediat

213 Glutamate transporters in the brain remove the neurotran

214 ssion for the typically astroglial-localized glutamate transporters in the mediodorsal and ventral ti

215 of glial (GLT-1, GLAST) and neuronal (EAAC1) glutamate transporters in these brain areas were assesse

216 se was tightly controlled by plasma membrane glutamate transporters, indicating that clearance of syn

217 orters, the reverse dialysis of ammonia, the glutamate transporter inhibitor, DL-threo-beta-benzyloxy

218 nion conducting conformation of the neuronal glutamate transporter is associated with an early step o

219 Specifically, the vesicular glutamate transporter is upregulated, leading to over-ac

220 opose that the switch to the dynamic mode in glutamate transporters is due to separation of the trans

221 ific subtypes of receptors, ion channels and glutamate transporters is revealed at peripheral and cen

222 The dominant glutamate transporter isoform in the mammalian brain, GL

223 y studying the expression of EAAT1 and EAAT2 glutamate transporters, it was possible to document the

224 uptake is mediated by members of a family of glutamate transporters known as "excitatory amino acid t

225 elated enzymes (glutamine synthetase and the glutamate transporter) known to play critical roles in g

226 ical rat neurons, we show that inhibition of glutamate transporters leads to rapid reduction in AMPAR

227 ate signaling dynamics, increased astrocytic glutamate transporter levels and alleviated multiple sig

228 uggests that abnormalities in the astroglial glutamate transporter localization and function may unde

229 the peptide transporter CstA, PEB1 aspartate/glutamate transporter, LutABC lactate dehydrogenase and

230 Glutamate transporters maintain synaptic concentration o

231 Finally, to model dysfunction of glutamate transporters, manganese was used, and G1 was f

232 itochondria and suggest a mechanism by which glutamate transporters might retain mitochondria at site

233 ription polymerase chain reaction to examine glutamate transporter mRNA expression in the hippocampus

234 erlie their capacity to upregulate the glial glutamate transporter on astrocytes through the vascular

235 Glutamate transporters play a crucial role in this respe

236 lar glutamate levels influenced by astrocyte glutamate transporters resulted in a significant inhibit

237 calcium pump SERCA, leucine transporter and glutamate transporter shows that ANMPathway yields resul

238 responding serine residue, Ser-364, of human glutamate transporter SLC1A2 (solute carrier family 1 me

239 id application of glutamate to the wild-type glutamate transporter subtype EAAC1 (excitatory amino ac

240 We found that astroglial glutamate transporter subtype glutamate transporter 1 (G

241 Other studies report that ceftriaxone, a glutamate transporter subtype-1 activator, is neuroprote

242 Of the five known glutamate transporter subtypes, the retina-specific subt

243 ate in glutathione biosynthesis, the cystine/glutamate transporter (system xc(-)) represents a potent

244 Glutamate transporters terminate neurotransmission by cl

245 rter (GLAST) in rodents, is one of two glial glutamate transporters that are responsible for removing

246 mate receptors, GABA receptors (GABARs), and glutamate transporters that have been implicated in pain

247 ino acid transporters (EAATs) are a class of glutamate transporters that terminate glutamatergic syna

248 sociated protein 25, syntaxin, and vesicular glutamate transporter type 1), together with an increase

249 Immunostaining of vesicular glutamate transporter type 2 demonstrated a decrement in

250 Using vesicular glutamate transporter type 2 immunohistochemistry, we la

251 napses and were immunoreactive for vesicular glutamate transporter type 2.

252 The atypical vesicular glutamate transporter type 3 (VGLUT3) is expressed by su

253 inals that lack VMAT2, but contain vesicular glutamate transporters type 2 (VGluT2).

254 The vesicular glutamate transporter (VGLUT) plays an essential role in

255 Vesicular glutamate transporter (VGLUT) proteins regulate the stor

256 study with probes for the lamprey vesicular glutamate transporter (VGLUT) provides an anatomical bas

257 ded into synaptic vesicles via the vesicular glutamate transporter (VGLUT), a mechanism conserved acr

258 eracidification is mediated by the vesicular glutamate transporter (VGLUT).

259 press three different types of the vesicular glutamate transporter (VGLUT).

260 Among these SV cargos is the vesicular glutamate transporter (vGlut).

261 e by controlling expression of the vesicular glutamate transporter (VGlut).

262 xide synthase as well as the three vesicular glutamate transporters (VGLUT 1-3) in the locus coeruleu

263 transporter [vGAT]) or glutamate (vesicular glutamate transporter [vGLUT]) into vesicles, as well as

264 logy and increasing levels of the excitatory glutamate transporter VGLUT1.

265 fore mapped boutons expressing the vesicular glutamate transporters VGluT1 and VGluT2, together with

266 aptic vesicles for release via the vesicular glutamate transporters VGLUT1 and VGLUT2.

267 rents and of central neurons (with vesicular glutamate transporters VGLUT1 or VGLUT2, respectively),

268 he two predominant isoforms of the vesicular glutamate transporter (VGLUT1 and VGLUT2) participate in

269 utamate decarboxylase (GAD67), and vesicular glutamate transporters (vGLUT1 and vGLUT2) in postmortem

270 ing in situ hybridization to label vesicular glutamate transporters (vglut1, vglut2.1, vglut3), gluta

271 e reported expression of all three vesicular glutamate transporters (VGLUT1-3) by astrocytes suggests

272 Vesicular glutamate transporters (VGLUT1-3) carry glutamate into s

273 res, which can be identified using vesicular glutamate transporters, VGLUT1 and VGLUT2.

274 specific genetic disruption of the vesicular glutamate transporter VGLUT2 or the obligatory NMDA rece

275 unopositive for met-enkephalin and vesicular glutamate transporter VGLUT2, but not for GABAergic mark

276 resynaptic machinery including the vesicular glutamate transporter VGLUT2, several synaptic vesicle m

277 e terminals were demonstrated to express the glutamate transporter VGlut2, the projections are presum

278 fied through the expression of the vesicular glutamate transporter VGLUT2.

279 ed on coexpression of mRNA for the vesicular glutamate transporter (vGlut2) and the GABA synthetic en

280 most neurons in the GT express the vesicular glutamate transporter (VGluT2) mRNA, indicating a glutam

281 ecarboxylase 65 (GAD65) and type 2 vesicular glutamate transporter (VGLUT2) mRNAs, respectively.

282 r the glutamatergic marker, type 2 vesicular glutamate transporter (VGLUT2), and the GABA synthetic e

283 ially labeled by an isoform of the vesicular glutamate transporter, VGluT2.

284 them with staining patterns of the vesicular glutamate transporter, VGLUT2.

285 Interestingly, the third vesicular glutamate transporter (VGLUT3) is primarily found in neu

286 Vesicular glutamate transporters (VGLUTs) are essential for fillin

287 Vesicular glutamate transporters (VGLUTs) have been extensively st

288 The vesicular glutamate transporters (VGLUTs) package glutamate into s

289 apse in NTS, we determined whether vesicular glutamate transporters (VGLUTs) were differentially dist

290 ecord currents associated with the vesicular glutamate transporters (VGLUTs), we characterize a chlor

291 Previous work showed that vesicular glutamate transporters (VGluTs; specific markers for glu

292 ecently, a new model for glutamate uptake by glutamate transporters was proposed based on crystal str

293 T), which is a major component of astrocytic glutamate transporters, was reduced by TNR knockdown.

294 for Nissl, cytochrome oxidase, and vesicular glutamate transporters, we investigated the primary soma

295 This effect was enhanced when glutamate transporters were inhibited, and reduced when

296 It belongs to the widespread family of glutamate transporters, which also includes the mammalia

297 hrin-A2 in the cortex colocalized with glial glutamate transporters, which were significantly downreg

298 We found GLT-1c to be an effective glutamate transporter with high affinity for Na(+) and g

299 SLC25A22 encodes a glutamate transporter with strong expression in the deve

300 First, block of glutamate transporters with a nonsubstrate antagonist ex