ライフサイエンスコーパス: glutamate transporter

1 colabeled with antibodies against VGluT2, a glutamate transporter.

2 otential rather than acting as a presynaptic glutamate transporter.

3 by rodents but was shown to be a functional glutamate transporter.

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

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

6 majority of GLT-1, the brain's most abundant glutamate transporter.

7 In addition, GltS was identified as a glutamate transporter.

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

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

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

11 ly via expression and function of astroglial glutamate transporters.

12 proteins, synapsin 1, unique microRNAs, and glutamate transporters.

13 eir highly branched morphologies and express glutamate transporters.

14 h necessitates the proper function of active glutamate transporters.

15 domain movements in a bacterial homologue of glutamate transporters.

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

17 into mechanisms of allosteric modulation for glutamate transporters.

18 smission due to their abundant expression of glutamate transporters.

19 substance, cytochrome oxidase, and vesicular 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 t TX enhanced the expression and function of glutamate transporter 1 (GLT-1) in rat astrocytes, an ef

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

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

27 The glutamate transporter 1 (GLT1) is upregulated during ast

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 hR2) is conditionally expressed in vesicular glutamate transporter 1 (Vglut1) sensory neurons (Vglut1

33 optogenetically activate cutaneous vesicular glutamate transporter 1 (Vglut1)-positive LTMRs.

34 ere identified in both nuclei: (a) vesicular glutamate transporter 1 (vGluT1)-positive terminals form

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

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

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

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

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

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

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

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

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

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

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

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

47 utamatergic terminals express both vesicular glutamate transporters 1 and 2 denoting a specific sourc

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

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

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

51 and (1)H-MRS methods, lower levels of glial glutamate transporter-1 and ATP-alpha, but increased lev

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

53 glutamatergic neurons that express vesicular glutamate transporter 2 (VGlut2) and are located in subc

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

55 ea dopamine (DA) neurons expresses vesicular glutamate transporter 2 (VGluT2) and releases glutamate

56 the adult, healthy brain expresses vesicular glutamate transporter 2 (VGluT2) and thus releases gluta

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 rminals, which are associated with vesicular glutamate transporter 2 (Vglut2) expression, in the dors

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

61 tive to previous expression of the vesicular glutamate transporter 2 (Vglut2) gene, coupled with immu

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

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

64 xpressing GFP under control of the vesicular glutamate transporter 2 (vGluT2) promoter.

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

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

75 the VP [VP neurons expressing the vesicular glutamate transporter 2 (VP(VGluT2))], whose activation

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

77 ar layer, while immunostaining for vesicular glutamate transporter 2 and neurofilament H indicate tha

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

79 s in the PVH co-localized with the vesicular glutamate transporter 2.

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

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

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

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

84 2 signals alongside an increase in vesicular glutamate transporter-2 signals on PV+ cells in MeCP2-de

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

86 K neurons is composed of transient vesicular glutamate transporter 3 (tVGLUT3) neurons, which convey

87 Vesicular glutamate transporter 3 (VGluT3) amacrine cells are a re

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

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

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

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

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

96 Small-diameter vesicular glutamate transporter 3-lineage (Vglut3(lineage)) dorsal

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

98 ner hair cells in mice lacking the vesicular glutamate transporter-3 (Vglut3(KO) ), at 9-11 weeks, ap

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

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

101 Glutamate transporters actively take up glutamate into t

102 ociated with reduced placental glutamine and glutamate transporter activity and expression, and propo

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

104 esis and suggest that abnormal glutamine and glutamate transporter activity is part of the spectrum o

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

106 EAAT5 acts as a slow glutamate transporter and also as glutamate-gated chlori

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

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

109 symporter, Glt(Ph) is an archaeal homolog of glutamate transporters and has been extensively used to

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

111 Although mitochondrial glutamate transporters and transporters for neutral amin

112 vesicle transport at neuronal synapses), the glutamate transporter, and a voltage-gated calcium chann

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

114 GLT-1 is the major glutamate transporter, and most GLT-1 is expressed in as

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

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

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

118 By limiting spillover, glutamate transporters are believed to prevent excessive

119 Mammalian glutamate transporters are crucial players in neuronal c

120 Glutamate transporters are essential for recovery of the

121 Glutamate transporters are essential players in glutamat

122 Glutamate transporters are integral membrane proteins th

123 A glutamate transporter-associated chloride channel blocke

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

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

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

127 ons and following selective and nonselective glutamate transporter blockade.

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

129 n thus prompts spatial retreat of astroglial glutamate transporters, boosting glutamate spillover and

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

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

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

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

134 Whereas mammalian glutamate transporters can translocate both glutamate an

135 Glutamate transporters clear up excess extracellular glu

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

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

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

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

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 show reduced levels of one such client, the glutamate transporter EAAT1.

148 ncluding AMPA and kainate receptor subunits, glutamate transporters EAAT1 and EAAT2, and the GABA(A)

149 correlated with expression of the astrocytic glutamate transporters EAAT1 and EAAT2.

150 Glial glutamate transporter EAAT2 plays a major role in glutam

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

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

153 els are tightly controlled by the astrocytic glutamate transporter EAAT2, influencing synaptic functi

154 The glutamate transporter EAAT2, which is primarily localize

155 extracellular glutamate through reducing the glutamate transporter EAAT2.

156 -181A > C) SNP in the promoter of astroglial glutamate transporter (EAAT2) and the same approach was

157 The SLC1A1 gene encoding the neuronal glutamate transporter EAAT3 has been proposed as a candi

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

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

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

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

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

163 st the effects of K(+) and Na(+) on neuronal glutamate transporter excitatory amino acid carrier 1 (E

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

165 Astrocytic glutamate transporter excitatory amino acid transporter

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

167 an excitatory neuronal marker, the vesicular glutamate transporter, expanding the possible roles of S

168 EAAT1 is a glutamate transporter expressed by astrocytes and other

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

170 gnaling is a positive regulator of astrocyte glutamate transporter expression and function, an essent

171 a brain tumor stem cells with low astrocytic glutamate transporter expression are dependent on GLS to

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

173 While glutamate transporter expression is reduced in numerous

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

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

176 y-dependent increase in Drosophila vesicular glutamate transporter expression.

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

178 te earlier developmental roles in regulating glutamate transporter function.SIGNIFICANCE STATEMENT In

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

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

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

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

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

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

185 ibution of the mitochondrial markers and the glutamate transporter, GLAST.

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

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

188 ining, we assessed surface expression of the glutamate transporter GLT-1 and glutamate efflux in the

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

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

191 The glutamate transporter GLT-1 is highly expressed in astro

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

193 elegans by inactivating the conserved glial glutamate transporter GLT-1.

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

195 Loss of one glutamate transporter (GLT-1) from VTA astrocytes select

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

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

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

199 eurotrophic factors, BDNF and IGF-1, and the glutamate transporter, GLT-1 after ischemic brain damage

200 s, BDNF and IGF-1, as well as the astrocytic glutamate transporter, GLT-1.

201 Mn dysregulates astrocytic glutamate transporters, GLT-1 and GLAST, and dopaminergi

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

203 -124-3p further up-regulates the predominant glutamate transporter GLT1 by suppressing GLT1-inhibitin

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

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

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

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

208 Glutamate transporters harness the ionic gradients acros

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

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

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

212 e fluorescence imaging of the archaeal model glutamate transporter homologue Glt(Ph) from Pyrococcus

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

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

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

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

217 mino acid transporter 2 (EAAT2) is the major glutamate transporter in the brain expressed predominant

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

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

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

221 gulates the trafficking of both dopamine and glutamate transporters in dopamine neurons by increasing

222 Glutamate transporters in the brain remove the neurotran

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

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

225 ed with LTP magnitude following nonselective glutamate transporter inhibition but not following selec

226 Although glutamate transporter inhibition reduced the postsynapti

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

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

229 Labeling for vesicular glutamate transporter is evident at the motor endplate.

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

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

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

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

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

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

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

237 Glutamate transporters maintain synaptic concentration o

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

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

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

241 relapse to opioid use, and downregulation of glutamate transporters on astroglial processes adjacent

242 Plasma membrane-associated glutamate transporters play a key role in signaling by t

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

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

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

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

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

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

249 Glutamate transporters terminate neurotransmission by cl

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

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

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

253 Molecular identification of vesicular glutamate transporter three and cholecystokinin expressi

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

255 Using vesicular glutamate transporter type 2 immunohistochemistry, we la

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

257 Glutamate homeostasis is maintained by glutamate transporter type-1 (GLT-1), which plays a vita

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

259 ate of glutamate clearance through astrocyte glutamate transporters under high-frequency stimulation

260 ed the accumulation of presynaptic vesicular glutamate transporter (VGlut) and increased spontaneous

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

262 Vesicular glutamate transporter (VGLUT) proteins regulate the stor

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

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

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

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

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

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

269 Vesicular Glutamate Transporters (VGLUT) accumulate glutamate into

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

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

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

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

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

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

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

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

278 We demonstrate that the vesicular glutamate transporter VGLUT2 may be exploited to drive r

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

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

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

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

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

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

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

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

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

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

289 The vesicular glutamate transporters (VGLUTs) concentrate the principa

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

291 release machinery mediated through vesicular glutamate transporters (VGLUTs) that ultimately dictate

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

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

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

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

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

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

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

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

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