ライフサイエンスコーパス: amino acid transporter

1 is imported by T cells via their ASC neutral amino acid transporter.

2 s and is a substrate of the system L neutral amino acid transporter.

3 l proximal tubule and functions as a neutral amino acid transporter.

4 into structural features of human excitatory amino acid transporters.

5 ported by cationic (CAT) and y(+)L (y(+)LAT) amino acid transporters.

6 changer, glutamate transporters, and neutral amino acid transporters.

7 signalling and decreased the activity of key amino acid transporters.

8 as the cell adhesion receptors integrins and amino acid transporters.

9 has been shown to function as a chaperone of amino acid transporters.

10 nalling pathways known to regulate placental amino acid transporters.

11 , which are positive regulators of placental amino acid transporters.

12 lysosomal membrane protein with homology to amino acid transporters.

13 ral l-amino acids are substrates of system L amino acid transporters.

14 hen compared with related mammalian cationic amino acid transporters.

15 f K(ATP) channels and activation of system-A amino acid transporters.

16 transferrin receptor and CD98 a subunit of L-amino acid transporters.

17 er of a large family of neurotransmitter and amino acid transporters.

18 intracellular amino acid levels mediated by amino acid transporters.

19 ologous to two sizable families of bacterial amino acid transporters.

20 vator" mechanism in the mammalian excitatory amino acid transporters.

21 riminate them from the termini of organellar amino acid transporters.

22 odel for the structure of the SLC1 family of amino acid transporters.

23 Cationic amino acid transporter 1 (CAT-1) is responsible for the

24 strocytic glutamate transport via excitatory amino acid transporter 1 (Eaat1), and blocking Eaat1 ext

25 expression of mRNA and protein of excitatory amino acid transporter 1 (GLAST), which is a major compo

26 e glutamate-aspartate transporter/excitatory amino acid transporter 1 (GLAST/EAAT1) in EAE cerebellum

27 The Large-neutral Amino Acid Transporter 1 (LAT-1)--a sodium-independent e

28 The l-type amino acid transporter 1 (LAT1) is a transmembrane prote

29 chanisms and pathogenesis, is mouse cationic amino acid transporter 1 (mCAT-1).

30 ] and SLC38 families [sodium-coupled neutral amino acid transporter 1 (SNAT1), SNAT2, and SNAT4].

31 Expression of the sodium-coupled neutral amino acid transporter 1 (SNAT1), which transports gluta

32 ons in the helical hairpin HP2 of excitatory amino acid transporter 1 form intersubunit disulfide cro

33 permeability-glycoprotein, and large neutral amino acid transporter 1 were significantly higher for 1

34 e-aspartate transporters (GLAST) (excitatory amino acid transporter 1) because they were weakly inhib

35 ate transporters, genderblind and excitatory amino acid transporter 1, in blood cells affects the fli

36 te in the cerebral cortex are the excitatory amino acid transporters 1-3 (EAAT1-3).

37 hieved by glutamate transporters (excitatory amino acid transporters 1-5, EAATs1-5) located on both t

38 taining for glutamine synthetase, excitatory amino-acid transporter 1 (EAAT1), and EAAT2.

39 ecotropic envelope receptor murine cationic amino acid transporter-1 (mCAT1) in the virus-producing

40 ammation and tumor sites upregulate cationic amino acid transporter 2 (Cat2), coordinately with Arg1

41 utamate transport and loss of the excitatory amino acid transporter 2 (EAAT2) .

42 sion of the glutamate transporter excitatory amino acid transporter 2 (EAAT2) in LPS-treated astrocyt

43 KEY POINTS: Excitatory amino acid transporter 2 (EAAT2) is present on astrocyte

44 caused a significant reduction in excitatory amino acid transporter 2 (EAAT2) protein levels in astro

45 aRs triggers coendocytosis of the excitatory amino acid transporter 2 (EAAT2).

46 lutamate transporters, especially excitatory amino acid transporter 2 (EAAT2, rodent analog GLT1) to

47 icle analysis of purified human 4F2hc/L-type amino acid transporter 2 (LAT2) heterodimers overexpress

48 ribed from the protein-coding mouse cationic amino acid transporter 2 (mCAT2) gene through alternativ

49 The sodium-coupled neutral amino acid transporter 2 (SNAT2) translocates small neut

50 nts from the cellular sodium-coupled neutral amino acid transporter 2 (SNAT2) versus the hepatitis C

51 The neutral amino acid transporter 2 (SNAT2), which belongs to the S

52 porter 2, increased expression of excitatory amino acid transporter 2 repressor ying yang 1, and redu

53 inducible nitric oxide synthase and cationic amino acid transporter 2 via gamma interferon.

54 onist of glutamate transporter-1 (excitatory amino acid transporter 2) and were absent from IPCs in G

55 EAAT2 (excitatory amino acid transporter 2) is a high affinity, Na+-depend

56 ne, SNAT2 (system A sodium-dependent neutral amino acid transporter 2), contains a C/EBP-ATF site tha

57 e glutamate transporter-1 [GLT-1 (excitatory amino acid transporter 2)] subtype of glutamate transpor

58 gnificantly lowered expression of excitatory amino acid transporter 2, increased expression of excita

59 transporter SLC7A2 (also known as "cationic amino acid transporter 2," or "CAT2") were decreased in

60 The glutamate (excitatory amino acid) transporter 2 (EAAT2; Slc1a2) has been hypot

61 as glial glutamate transporter 1 (excitatory amino-acid transporter 2).

62 roarray analyses showed decreased excitatory amino acid transporter-2 (EAAT-2) expression in high-gra

63 with L-arginine transport via mouse cationic amino acid transporter 2B (mCAT-2B).

64 xpression of the L-Arg transporter, cationic amino acid transporter 2B, and increased L-Arg uptake in

65 ndent trafficking of the neuronal excitatory amino acid transporter 3 (EAAT3) blocks potentiation, su

66 then taken up by neurons through excitatory amino acid transporter 3 [EAAT3; also termed Slc1a1 (sol

67 otropic glutamate receptor 1, and excitatory amino acid transporter 3) were validated by Western blot

68 ed by the PC-specific transporter excitatory amino acid transporter 4 (EAAT4).

69 and phosphofructokinase C and the excitatory amino acid transporter 4 (EAAT4).

70 SLC36A4, otherwise known as proton-assisted amino-acid transporter 4 (PAT4), in colorectal cancer.

71 glutamate transporter 1), EAAT5 (excitatory amino acid transporter 5), and VAMP2 (vesicle-associated

72 the identification of sodium-coupled neutral amino acid transporter 7 (SNAT7), encoded by the SLC38A7

73 We describe these amino acid transporters (AATs).

74 d trophoblast plasma membrane System A and L amino acid transporter activities and transporter isofor

75 TPM System A (-56%, P < 0.001) and System L amino acid transporter activity (-50%, P < 0.03).

76 ciency inhibits placental mTOR signaling and amino acid transporter activity and causes fetal growth

77 usly to transiently adapt placental System-A amino acid transporter activity relative to fetal growth

78 h wound closure, L-arginine uptake, cationic amino acid transporter activity, and activation of the m

79 d decreased proliferation, and had increased amino acid transporter activity.

80 The neutral amino acid transporter alanine-serine-cysteine transport

81 Asymmetric distribution of amino acid transporters, amino acid content, and activit

82 a 31-kilobase segment at rhg1-b, encoding an amino acid transporter, an alpha-SNAP protein, and a WI1

83 This program included expression of amino acid transporter and aminoacyl-tRNA synthetase gen

84 b region of DNA demonstrate expression of an amino acid transporter and an alpha soluble NSF attachme

85 ected, partially colocalizing with vesicular amino acid transporter and GABA(A)-receptor gamma2 subun

86 rogram through the up-regulation of selected amino acid transporters and aminoacyl-tRNA synthetases.

87 chemia has been postulated to be mediated by amino acid transporters and can lead to excitotoxicity.

88 on in pregnant mice down-regulates placental amino acid transporters and decreases fetal growth.

89 a translational repressor of mRNAs encoding amino acid transporters and has been postulated to limit

90 eptor (TCR)-induced asymmetric expression of amino acid transporters and RagC-mediated translocation

91 RNA synthesis, but not for the expression of amino acid transporters and ribosomal protein genes.

92 milarity of SemiSWEETs and SWEETs to PQ-loop amino acid transporters and to mitochondrial pyruvate ca

93 how glutamate transporters function as both amino-acid transporters and Cl(-) channels.

94 Here we confirm that five putative amino acid transporters are highly expressed and/or high

95 Cationic amino acid transporters are highly selective for L-enant

96 System N (SNAT3 and SNAT5) amino acid transporters are key mediators of glutamine t

97 Long N-terminal tails of amino acid transporters are known to act as sensors of t

98 n of aspartate and expression of an aromatic amino acid transporter, as well as a tyrosine-specific t

99 cterized protein with sequence similarity to amino acid transporters, as a lysosomal transmembrane pr

100 f how substrate specificity is determined in amino acid transporters, as well as provide novel scaffo

101 ession of Glut1 (glucose) and ASCT2 (neutral amino acids) transporters, as well as that of PiT1 and P

102 For example, the neutral amino acid transporter ASCT1 is an effective transporter

103 apid glutamine uptake, which depended on the amino acid transporter ASCT2.

104 ological role in regulating the abundance of amino acid transporters at the cell surface.

105 apo-ApcT, a proton-coupled broad-specificity amino acid transporter, at 2.35 angstrom resolution.

106 We identified one amino acid transporter, AtCAT6, which is expressed in si

107 a19 gene as an example, encoding the neutral amino acid transporter B(0)AT1, we studied regulation of

108 omosome 13 that encodes the sodium-dependent amino acid transporter B(0)AT1.

109 inked membrane subunits: the carrier, b(0,+) amino acid transporter (b(0,+)AT), a polytopic protein,

110 ase after bath application of the excitatory amino acid transporter blocker DL-threo-beta-benzyloxyas

111 ssion of pathway inhibitors, upregulates key amino acid transporters, blocks translation initiation,

112 functional ammonium transporters and several amino acid transporters but found no evidence of a nitra

113 SSY1 is structurally similar to amino acid transporters but functions as a sensor of ami

114 o antigen by upregulating expression of many amino-acid transporters, but a single System L ('leucine

115 mTORC1 and mTORC2 regulate human trophoblast amino acid transporters by modulating the cell surface a

116 n complex 1 (mTORC1) and 2 (mTORC2) regulate amino acid transporters by post-translational mechanisms

117 In this study we establish that N-termini of amino acid transporters can also determine substrate spe

118 nslation of the mRNA for the arginine/lysine amino acid transporter Cat-1 increases during amino acid

119 hat the arginine transport protein, cationic amino acid transporter (CAT)2, has a critical role in re

120 Levels of the inducible cationic amino acid transporter (CAT)2, ODC, and iNOS were measur

121 ecreasing surface expression of the cationic amino acid transporters (CAT) 1 and 3.

122 The vacuolar amino acid transporter CAT2 from Solanum lycopersicum wa

123 in a region containing two genes: a cationic amino acid transporter (CAT4) and a polynucleotide phosp

124 This finding indicated that cationic amino acid transporters (CATs) act pathologically as vir

125 n assigned to the SLC7 subfamily of cationic amino acid transporters (CATs) due to sequence homology,

126 eurosecretion-it encodes a putative cationic amino acid transporter, closely related to the Slimfast

127 that differentially localised intracellular amino-acid transporters contribute to the activation of

128 uelae of growth factor deprivation including amino-acid transporter degradation, reduction of the gly

129 hat deletes the last 46 residues of the 2261 amino acid transporter (Delta46) and eliminates its lipi

130 such as induction of potassium channels and amino acid transporters, derepression of genes marked wi

131 A family of 17 putative preprotein and amino acid transporters designated PRAT has been identif

132 in Xenopus laevis oocytes, two bacteriocyte amino acid transporters displayed significant levels of

133 Astrocytic glutamate transporter excitatory amino acid transporter (EAAT) 1, also known as glutamate

134 rmational changes in the neuronal excitatory amino acid transporter (EAAT) 3 glutamate transporter co

135 n is terminated by members of the excitatory amino acid transporter (EAAT) family of proteins that re

136 f three identical subunits in the excitatory amino acid transporter (EAAT) family.

137 , we show that application of the excitatory amino acid transporter (EAAT) substrate d-aspartate stim

138 Excitatory amino acid transporter (EAAT)-2 is one of the major glut

139 haracteristics of members of the "excitatory amino acid transporter" (EAAT) family.

140 Glutamate transporters (excitatory amino acid transporters, EAAT) play an important role in

141 taxia (EA6) have mutations of the excitatory amino acid transporter EAAT1 (also known as GLAST), but

142 s glutamate transporter GLT-1 and excitatory amino acid transporter EAAT2.

143 reduced the expression of type 2 excitatory amino-acid transporter (EAAT2) and the astrocyte-specifi

144 , it stimulates endocytosis of an excitatory amino acid transporter, EAAT3, in dopamine neurons.

145 calized with the sodium-dependent excitatory amino acid transporter, EAAT3.

146 II spectrin binds directly to the excitatory amino acid transporter (EAAT4), the glutamate receptor d

147 Glutamate transporters (excitatory amino acid transporter (EAATs)) are critical for normal

148 (SLC1A), which also includes the excitatory amino acid transporters (EAATs) and the prokaryotic aspa

149 Excitatory amino acid transporters (EAATs) are a class of glutamate

150 Excitatory amino acid transporters (EAATs) are abundantly expressed

151 Excitatory amino acid transporters (EAATs) are crucial for glutamat

152 Excitatory amino acid transporters (EAATs) are crucial in maintaini

153 Excitatory amino acid transporters (EAATs) are essential for termin

154 Excitatory amino acid transporters (EAATs) are responsible for extr

155 mammalian central nervous system, excitatory amino acid transporters (EAATs) are responsible for the

156 Excitatory amino acid transporters (EAATs) are the primary regulato

157 Excitatory amino acid transporters (EAATs) control the glutamate co

158 ic transmission and activation of excitatory amino acid transporters (EAATs) for transmitter removal.

159 However, blocking excitatory amino acid transporters (EAATs) generates beam-like resp

160 s is sequestered by the action of excitatory amino acid transporters (EAATs) in glia and postsynaptic

161 +)/Ca(2+) exchanger (NCX) and the excitatory amino acid transporters (EAATs) in Glu uptake and recycl

162 In the CNS, excitatory amino acid transporters (EAATs) localized to neurons and

163 led a deeper understanding of how excitatory amino acid transporters (EAATs) mediate chloride permeat

164 The excitatory amino acid transporters (EAATs) play essential roles in

165 Excitatory amino acid transporters (EAATs) remove glutamate from sy

166 Excitatory amino acid transporters (EAATs) terminate glutamatergic

167 Excitatory amino acid transporters (EAATs) terminate signaling in t

168 Excitatory amino acid transporters (EAATs) use sodium and potassium

169 transporters, also referred to as excitatory amino acid transporters (EAATs), are membrane proteins t

170 tudies of mammalian and bacterial excitatory amino acid transporters (EAATs), as well as the crystal

171 ve synapses is carried out by the excitatory amino acid transporters (EAATs), involving the cotranspo

172 eviously reported for the related excitatory amino acid transporters (EAATs), suggesting that this le

173 uit of the transport proteins--or excitatory amino acid transporters (EAATs)--toward a similar end ha

174 occurs in part through astrocytic excitatory amino acid transporters (EAATs).

175 glutamate transporters known as "excitatory amino acid transporters (EAATs)." Here we cloned and fun

176 Excitatory amino-acid transporters (EAATs) bind and transport gluta

177 napse is tightly regulated by the excitatory amino-acid transporters (EAATs).

178 the human glutamate transporters (excitatory amino acid transporters, EAATs) and the prokaryotic aspa

179 utamate transporters (also called excitatory amino acid transporters, EAATs) bind extracellular gluta

180 pendent glutamate cotransporters (excitatory amino acid transporters; EAATs) exist exclusively in abl

181 Placental System A amino acid transporter expression correlated with protei

182 othelial, and less astroglial LAT1/LAT2/CD98 amino acid transporter expression.

183 Secondary transporters in the excitatory amino acid transporter family terminate glutamatergic sy

184 of structure-function of the members in this amino acid transporter family.

185 , as well as other members of the excitatory amino acid transporter family.

186 c acid, a specific inhibitor of the system L amino acid transporter family.

187 Here, we show that the glial amino-acid transporter genderblind controls whether Dros

188 lc38a4, the imprinted member of the System A amino acid transporter gene family.

189 n proximal tubular cells, mRNA levels of the amino acid transporter gene SLC38A2 were diminished and

190 transcription was demonstrated for the cat-1 amino acid transporter gene.

191 Deletion of two amino acid transporters (GlnHPQ and MetNIQ) in a Deltamd

192 Heteromeric amino acid transporters (HATs) are the unique example, k

193 To date, four amino acid transporters have been found to be expressed

194 Amino acid transporters have roles in amino acid uptake

195 To identify amino acid transporters impacting glutmatergic signal tr

196 products of which heterodimerize to form an amino acid transporter in HT-29 cells after bacterial in

197 rotyrosine is transported via the l-aromatic amino acid transporter in nondopaminergic NT2 cells, whe

198 plasma membrane levels of CAT1 and y(+)LAT1 amino acid transporters in endothelial cells.

199 There are approximately two-dozen amino acid transporters in humans, and tumor cells must

200 ies suggest that the increased expression of amino acid transporters in islets can serve as early dia

201 The main apical membrane neutral amino acid transporters in mouse intestine and kidney, B

202 Amino acid transporters in plants often show tissue-spec

203 trates a role for reduced Slc6a15, a neutral amino acid transporter, in nucleus accumbens (NAc) in de

204 ed in ATF4-dependent upregulation of several amino acid transporters, including SLC1A5 and its trunca

205 in ceramide, VPA decreased the expression of amino acid transporters, increased the expression of ER

206 and activity of the System A/SNAT2 (SLC38A2) amino acid transporter is up-regulated by amino acid sta

207 esearch demonstrates that Slc6a15, a neutral amino acid transporter, is associated with depression su

208 otein expression of SNAT1, 2 and 4 (System A amino acid transporter isoforms) and LAT1 and LAT2, but

209 ) and LAT1 and LAT2, but not CD98, (System L amino acid transporter isoforms) was down-regulated by f

210 h that of BATs, and as LeuT is a promiscuous amino acid transporter, it does not recapitulate the pha

211 2a (5HT2a), and the solute carrier 7-family amino acid transporter, JhI-21, as required for this pre

212 SLC7A10 (Asc-1) is a sodium-independent amino acid transporter known to facilitate transport of

213 o assess skeletal muscle anabolic signaling, amino acid transporters [large neutral and small neutral

214 o acid transporter (SNAT), and large neutral amino acid transporter (LAT) isoforms in syncytiotrophob

215 Both L-type amino acid transporter (LAT)1 and LAT2 subtypes of syste

216 sine derivative rapidly transported by the l-amino acid transporter (LAT-1), with a faster blood pool

217 tein CD98, which comprises the large neutral amino acid transporter LAT1 (SLC7A5) in cells.

218 ransporters [large neutral and small neutral amino acid transporters (LAT1, SNAT2) and CD98], and myo

219 -[(18)F]15 but not (S)-[(18)F]14 by system L amino acid transporters led to approximately 8-10-fold h

220 he past decade, the structure of a bacterial amino acid transporter, leucine transporter (LeuT), has

221 zed sodium-coupled symporters: the bacterial amino acid transporter LeuT, which is the prototype for

222 ered monoamine-like version of the bacterial amino acid transporter LeuT.

223 ed an NFAT-dependent reduction in excitatory amino acid transporter levels, indicating a possible mec

224 e gene respectively in Citrus instead of the amino acid transporter like gene upstream and a sugar tr

225 ich microdomains is important for excitatory amino acid transporter localization and function.

226 er transporter 7a5 (SLC7A5), a large neutral amino acid transporter localized at the blood brain barr

227 aracter is dependent on vesicular inhibitory amino acid transporter-mediated signaling.

228 rized the gene encoding the porcine cationic amino acid transporter, member 1 (CAT-1) (HGMW-approved

229 rokaryotic NSS homolog, the multihydrophobic amino acid transporter (MhsT) from Bacillus halodurans,

230 CD98hc (SLC3A2), a heterodimeric amino acid transporter, modulates integrin signaling in

231 We identify a unique population of nutrient amino acid transporters (NATs) within the sodium-neurotr

232 rystal structure of ApcT, a proton-dependent amino acid transporter of the APC superfamily, a homolog

233 e, is mediated, among others, by the neutral amino acid transporters of the solute carrier 1 [SLC1, a

234 Lat1 (SLC7A5) is an amino acid transporter often required for tumor cell imp

235 ptake of glutamate by the type 2A excitatory amino acid transporter on photoreceptors.

236 Blockade of excitatory amino acid transporters or vesicular glutamate release d

237 onjugate (LPS) to interact with ATB(0,+), an amino acid transporter overexpressed in hepatocarcinoma

238 Unexpectedly, members of the proton-assisted amino-acid transporter (PAT or SLC36) family emerged fro

239 This mutant disrupts a putative amino acid transporter, Pathetic (Path), that localizes

240 s related to mammalian proton-assisted SLC36 amino acid transporters (PATs), CG3424 and CG1139, are p

241 osine is a known substrate of proton-coupled amino acid transporters (PATs), which are overexpressed

242 We have identified a vacuolar cationic amino acid transporter (PhCAT2) that contributes to sequ

243 coding a Petunia hybrida plastidial cationic amino-acid transporter (PhpCAT) functioning in plastidia

244 Folate, nucleoside, and amino acid transporters positively correlated with chemo

245 d-based radiotracers predominantly visualize amino acid transporter processes, and in many cases they

246 A3, two key members of the glutamate/neutral amino acid transporter protein family, SLC1.

247 nit and the presynaptic vesicular inhibitory amino acid transporter protein showed similar expression

248 KSHV also utilizes the amino acid transporter protein xCT for infection of adhe

249 c protein, and the helper, related to b(0,+) amino acid transporter (rBAT), a type II glycoprotein.

250 Excitatory amino acid transporters remove synaptically released glu

251 asm and nucleus, including the expression of amino acid transporters, ribosomal RNAs and ribosomal pr

252 One amino acid transporter, Schistosome Permease 1 light cha

253 ound that IL-2 upregulates expression of the amino acid transporters SLC1A5 and CD98.

254 placental expression of glucose and system A amino acid transporters Slc2a1 and Slc38a2, respectively

255 GLUT1 and one isoform the System A family of amino acid transporters, Slc38a2/SNAT2.

256 leukin 4-dependent induction of the cationic amino acid transporter SLC7A2 (also known as "cationic a

257 regulates transcription of genes that encode amino acid transporters (SLC7A5 and SLC3A2) to promote b

258 no acid uptake by reducing the levels of the amino acid transporter Slimfast caused clones of PTEN mu

259 Here we report the characterization of the amino-acid transporter Slimfast (Slif) from the yellow-f

260 protein expression of sodium-coupled neutral amino acid transporter (SNAT) 2 was elevated 9-fold.

261 Members of system N/A amino acid transporter (SNAT) family mediate transport o

262 transporter (TAUT), sodium-dependent neutral amino acid transporter (SNAT), and large neutral amino a

263 l accessory proteins Vpu or Nef included the amino acid transporter SNAT1 and the serine carriers SER

264 Impairment of 80S complex assembly on the amino acid transporter SNAT2 IRES was rescued by purifie

265 The sodium-coupled neutral amino acid transporter SNAT2 mediates cellular uptake of

266 s the induction of expression of the neutral amino acid transporter SNAT2.

267 R stress, including sodium-dependent neutral amino acid transporter, SNAT2.

268 We also found that GAP1, a general amino acid transporter, strongly contributes to the indu

269 (18)F-fluoro-phenylalanine ((18)F-FDOPA), an amino acid transporter substrate, as an independent mark

270 selective inhibitors of the human excitatory amino acid transporter subtype 1 (EAAT1) and its rodent

271 all compound library at the three excitatory amino acid transporter subtypes 1-3 (EAAT1-3) resulted i

272 pharmacological properties at the excitatory amino acid transporter subtypes EAAT1, EAAT2, and EAAT3.

273 hypothesis that facilitated diffusion by the amino acid transporters TAT1, LAT3 and LAT4 plays an imp

274 analysed two mutants of AAP1 (At1g58360), an amino acid transporter that was localized to Arabidopsis

275 ndidate binding lipoproteins associated with amino acid transporters that may function in indirect se

276 which also includes the mammalian excitatory amino acid transporters that take up the neurotransmitte

277 llular glutamate were mediated by excitatory amino-acid transporters, the reverse dialysis of ammonia

278 ining with gephyrin and vesicular inhibitory amino acid transporter to label GABAergic postsynaptic d

279 ginine-deprived T cells upregulated system L amino acid transporters to increase uptake of essential

280 hc mediates integrin signaling and localizes amino acid transporters to the plasma membrane.

281 xtracellular glutamate through an excitatory amino-acid transporter to cause excitotoxicity.

282 , and they direct downregulation of distinct amino acid transporters triggered by specific stimuli.

283 EAAT3 (excitatory amino acid transporter type 3, the neuron-specific gluta

284 ioid receptors, morphine inhibits excitatory amino acid transporter type 3-mediated cysteine uptake v

285 VGLUT2) and inhibitory (vesicular inhibitory amino acid transporter VIAAT) transporter mRNA and synap

286 genetically target the vesicular inhibitory amino acid transporter (VIAAT) in Renshaw cells.

287 trong expression of the vesicular inhibitory amino acid transporter (VIAAT) mRNA, suggesting a GABAer

288 The vesicular inhibitory amino acid transporter, VIAAT (also known as vesicular G

289 nohistochemical assessment of LAT1/LAT2/CD98 amino acid transporters was performed in seizure-affecte

290 across plasma membranes occurs via the large amino acid transporter, which is overexpressed in malign

291 regions in neuropil, and express excitatory amino acid transporters, which are presumably required f

292 roliferating tumor cells upregulate specific amino acid transporters, which hold great potential for

293 fetal growth by down-regulation of placental amino acid transporters, which limits fetal nutrient ava

294 operon, urea transport genes (urtBCDE), and amino acid transporters while significant decreases in t

295 SLC6A14, also known as ATB(0,+), is an amino acid transporter with unique characteristics.

296 hat it acts as a sodium-independent cationic amino acid transporter, with unique selectivity to L-his

297 te endosomes and lysosomes is facilitated by amino-acid transporters within the solute-linked carrier

298 beta1, alphaVbeta3, and alphaVbeta5, and the amino acid transporter x-CT protein and enters via c-Cbl

299 general and specialized members of the yeast amino acid transporter (YAT) family, a branch of the ami

300 We identified a yeast vacuolar amino acid transporter, Ypq1, that is selectively sorted