ライフサイエンスコーパス: amino acid transporter

1 transporter, and alsT, encoding a predicted amino acid transporter.

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

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

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

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

6 into structural features of human excitatory amino acid transporters.

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

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

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

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

11 nalling pathways known to regulate placental amino acid transporters.

12 , which are positive regulators of placental 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 e solute carrier 36 family of proton-coupled amino acid transporters.

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

19 lysosomal membrane protein with homology to amino acid transporters.

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

21 nine metabolism, either by blocking cationic amino acid transporter 1 (CAT-1)-dependent arginine upta

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

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

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

25 ovascular-selective biomarkers large neutral amino acid transporter 1 (LAT-1), glucose transporter ty

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

27 The L-type amino acid transporter 1 (LAT1 or SLC7A5) transports lar

28 ilarly, pharmacological inhibition of l-type amino acid transporter 1 (LAT1) and GCN2 significantly i

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

30 L-type amino acid transporter 1 (LAT1) plays a role in transpor

31 L-type amino acid transporter 1 (LAT1), which is encoded by sol

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

33 nsated by increased levels of sodium neutral amino acid transporter 1 (SNAT1 or SLC38A1) and SNAT2 (S

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

35 amino groups that bind to the large neutral amino acid transporter 1 (which is expressed in most tum

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

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

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

39 icola The transporter, A. pisum nonessential amino acid transporter 1, or ApNEAAT1 (gene: ACYPI008971

40 transport protein, sodium-dependent neutral amino acid transporter 1, sodium-dependent glutamate/asp

41 uaporins and amino acid transporters (L-type amino acid transporter 1, sodium-independent amino acid

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

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

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

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

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

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

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

49 The excitatory amino acid transporter 2 (EAAT2) is the major glutamate

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 EAAC1; the rat homologue of human excitatory amino acid transporter 3 (EAAT3)).

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

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

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

71 Excitatory amino acid transporter 5 (EAAT5) is a protein that is kn

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

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

74 ilability, through endocytosis of sugar- and amino acid transporters (AATs) (Muller et al., 2015).

75 We describe these amino acid transporters (AATs).

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

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

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

79 nsporter-mediated histidine uptake, system L amino acid transporter activity and Na(+) K(+) -ATPase a

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

81 orter-mediated histidine uptake and system L amino acid transporter activity were similar in sarcolem

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

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

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

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

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

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

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

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

90 anges, we tested the hypothesis that ex vivo amino acid transporter and Na(+) K(+) -ATPase activity i

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

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

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

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

95 of Myc is to control expression of multiple amino acid transporters and that loss of a single Myc-co

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

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

98 how that TCR signaling induces expression of amino acid transporters, and renders amino acid-induced

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

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

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

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

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

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

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

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

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

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

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

110 amino acid transporter 1, sodium-independent amino acid transporter, B( degrees (,+))-type amino acid

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

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

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

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

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

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

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

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

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

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

125 y 7 member 5 (SLC7A5) gene, which encodes an amino acid transporter cause microcephaly and seizures,

126 Inhibition of the amino acid transporter CD98/LAT1 abrogated the leucine-d

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

146 Excitatory amino acid transporters (EAATs) are abundantly expressed

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

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

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

150 Excitatory amino acid transporters (EAATs) are important in many ph

151 Excitatory amino acid transporters (EAATs) are prototypical dual fu

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

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

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

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

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

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

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

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

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

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

162 Excitatory amino acid transporters (EAATs) represent a protein fami

163 Excitatory amino acid transporters (EAATs) terminate glutamatergic

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

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

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

167 brane transport proteins-known as excitatory amino acid transporters (EAATs).

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

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

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

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

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

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

174 ers and that loss of a single Myc-controlled amino acid transporter effectively phenocopies the impac

175 hough no structure of a human proton-coupled amino acid transporter exists, the crystal structure of

176 mour-autonomous Yorkie-mediated SLC36-family amino acid transporter expression as a proline-scavengin

177 Placental System A amino acid transporter expression correlated with protei

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

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

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

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

182 sodium gradient necessary for system A and N amino acid transporter function, was significantly reduc

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

184 Most significant amino acid transporter gene, AAP1 appeared associated wi

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

186 n muscle, TRF induces rhythmicity of several amino acid transporter genes and metabolites.

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

188 ferative skin disorder, the possible role of amino acid transporters has remained unexplored.

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

190 Heteromeric amino acid transporters (HATs) comprise a group of membr

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

192 Amino acid transporters have roles in amino acid uptake

193 To identify amino acid transporters impacting glutmatergic signal tr

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

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

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

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

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

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

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

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

202 ORC1, indicating that the high expression of amino acid transporters induces amino acid-driven mTORC1

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

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

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

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

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

208 2a (5HT2a), and the solute carrier 7-family amino acid transporter, JhI-21, as required for this pre

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

210 ght to investigate the role of the essential amino acid transporter L-type amino acid transporter (LA

211 d decreased the expression of aquaporins and amino acid transporters (L-type amino acid transporter 1

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

213 the essential amino acid transporter L-type amino acid transporter (LAT) 1 (SLC7A5) in psoriasis.

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 ne competes with leucine at the level of the amino acid transporter LAT1 for brain uptake.

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

220 The large, neutral L-type amino acid transporters (LAT1-LAT4) are sodium-independe

221 d by increased expression of the alternative amino acid transporters LAT2 and LAT3.

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

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

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

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

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

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

228 Amino acid transporter-mediated histidine uptake and sys

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

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

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

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

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

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

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

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

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

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

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

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

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

242 t an interaction with the lysosomal cationic amino acid transporter PQLC2 mediates C9orf72 complex re

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

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

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

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

247 Excitatory amino acid transporters remove synaptically released glu

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

249 the membrane carrier protein SCAMP3 and the amino acid transporters SLC1A5 and LAT1, directing them

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

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

252 ncluding transferrin receptor protein 1, the amino acid transporters SLC3A2 and SLC1A5, and the T-cel

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

254 ssion of HIE proinflammatory signals and the amino acid transporter SLC7A5.

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

256 dentified a differentially methylated CpG in amino acid transporter SLC7A8 that is highly reproducibl

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

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

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

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

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

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

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

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

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

266 Na(+) -coupled neutral amino acid transporters (SNATs) 2 and 4 are believed to

267 The neutral amino acid transporter solute carrier family 1 member 5

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 e smaller placentas with reduced activity of amino acid transporter systems A and L, thought to contr

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

293 at d3 revealed co-localization of the L-type amino acid transporter with GFAP-positive astrocytes but

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

295 day 3 revealed colocalization of the l-type amino acid transporter, with glial fibrillary acidic pro

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