ライフサイエンスコーパス: transporter

1 a direct interaction of Gbetagamma with the transporter.

2 etion of Slc6a2 or inhibition of the encoded transporter.

3 ts an intracellular regulatory module of the transporter.

4 se are also accomplished by the deprotonated transporter.

5 One possibility invokes misexpression of a transporter.

6 This effect is mediated by the Glut4 glucose transporter.

7 using major structural rearrangements in the transporter.

8 nt of the initiation of apoptosis by the ion transporter.

9 B/CusC to form the CusCBA periplasm membrane transporter.

10 erol/CHS in Drosophila melanogaster dopamine transporter.

11 d the carbohydrate specificities of each PTS transporter.

12 on its function as a plasma membrane folate transporter.

13 thology due to loss of the Golgi GDP mannose transporter.

14 onstrated that SLC25A3 functions as a copper transporter.

15 r and might be overcome by inhibition of the transporter.

16 opment, as well as the transport of some ion transporters.

17 part mediated by ATP-binding cassette (ABC) transporters.

18 dynamically regulated by Cl(-) channels and transporters.

19 ithout modifying the expression of the other transporters.

20 1;7 and 1;8 to function as high affinity Pi transporters.

21 paradigm for this class of secondary active transporters.

22 n Vibrio cholerae, there are 13 distinct PTS transporters.

23 lular compartmentalization, specifically for transporters.

24 Erythrocyte equilibrative nucleoside transporter 1 (eENT1) levels are reduced in humans at hi

25 ile increasing the function of the glutamate transporter 1 (GLT-1) and system xC- (Sxc) in the nucleu

26 al nerve (TN), and using Vesicular GLUtamate Transporter 1 (VGLUT1) and the 65 kDa isoform of glutami

27 e by gamma-aminobutyric acid (GABA) membrane transporter 1 immunoreactivity is lower, whereas the den

28 orter levels were higher and glial glutamate transporter 1 levels were lower in the DH of female, but

29 ructural studies suggest that GLUT1 (glucose transporter 1)-mediated sugar transport is mediated by a

30 sion upregulates ferritin and divalent-metal-transporter-1 (DMT-1), indicating PrP(C)-mediated iron u

31 In mice, deleting monocarboxylate transporter-1 (MCT1) from tumor cells eliminated lactate

32 on of the HIF-1alpha targets VEGF-A, glucose transporter-1, and lactate dehydrogenase A.

33 The human peptide transporter 2 (PEPT2) expressed by proximal tubular cell

34 RP projections coexpress vesicular glutamate transporter 2 (VGLUT2), providing evidence that excitato

35 TH1-S31E associated with vesicular monoamine transporter 2 (VMAT2) and alpha-synuclein in neuroblasto

36 erotonin transporter and vesicular monoamine transporter 2 (VMAT2).

37 novel, highly selective vesicular monoamine transporter 2 inhibitor that demonstrated favorable effi

38 l cardiovascular effect of sodium glucose co-transporter 2 inhibitors in T2DM.

39 Sodium-glucose co-transporters 2 (SGLT-2) inhibitors have emerged as a nov

40 mal tubules express transmembrane fatty acid transporter-2 (FATP2), encoded by Slc27a2, but not the o

41 rt-term treatment with the sodium-glucose co-transporter-2 (SGLT2) inhibitor empagliflozin reduced al

42 icking of the neuronal excitatory amino acid transporter 3 (EAAT3) blocks potentiation, suggesting th

43 oid hormone (TH) transporter Monocarboxylate transporter 8 (MCT8) cause severe psychomotor retardatio

44 en proposed to function as a low-affinity Cu transporter, a lysosomal Cu exporter, or a regulator of

45 es have reported mutations in hepatocellular transporters (ABCB4, ABCB11).

46 with cis-expression of a reverse cholesterol transporter (ABCG1; P=7.2E-28) and incident cardiovascul

47 at alterations in the electrogenicity of the transporters accompanied changes in substrate specificit

48 On average, solute transporters accounted for 23% of identified protein seq

49 ortant switch loop of the trimeric multidrug transporter AcrB separates the access and deep drug bind

50 Our results suggest that the phospholipid transporter activity of ALA1/ALA2 may be necessary for t

51 Thus, we enhanced the neurotransmitter transporter activity of rigid nucleosides while reducing

52 Rather, a higher transporter activity was observed, which possibly acted

53 in RVH rats was not due to blunted glutamate transporter activity.

54 y cholesterol impacting on its stability and transporter activity.

55 l and cell-surface expression of major Na(+) transporters all along the kidney tubule.

56 Aluminum-activated malate transporters (ALMTs) form a family of anion channels in

57 ance, lower brain glucose uptake and glucose transporters, alterations in glycolytic and acetate meta

58 the rhizosphere, the high-affinity ammonium transporters (AMTs) in Arabidopsis thaliana are efficien

59 In contrast to other bacterial sugar transporters analyzed so far, in GlcPSe sugar binding, t

60 se caused by mutation of glucose-6-phosphate transporter and characterized by altered glycogen/glucos

61 pression of the miR-183 cluster reduced zinc transporter and intracellular zinc levels in benign pros

62 complex (uniplex), an inner membrane Ca(2+) transporter and major pathway of mitochondrial Ca(2+) en

63 t systems, apical sodium-dependent bile acid transporter and Na(+) -taurocholate cotransporting polyp

64 n and connecting the external regions of the transporter and the central binding site.

65 evisiae are the Trk1 high affinity potassium transporter and the functionally redundant Hal4 (Sat4) a

66 were studied with tracers for the serotonin transporter and vesicular monoamine transporter 2 (VMAT2

67 restricted oxygen availability and specific transporters and catabolic pathways activated with incre

68 consistent with the known mechanisms of TRAP transporters and consider how the role of sugar oxidatio

69 expression of major hepatocellular bile salt transporters and cytochrome P450 7a1, the key regulator

70 cells resist, as they are well equipped with transporters and enzymes to regulate intracellular pH ho

71 by analyzing experimental structures of urea transporters and proteins crystallized in the presence o

72 ) gradient nor expression changes in key ion transporters and regulatory proteins.

73 thesis genes, known/predicted vitamin uptake transporters and the rbkR gene.

74 different databases; genes encoding membrane transporters and their regulators were enriched, highlig

75 athway, leading to reduced expression of MDR transporters and thereby an increased accumulation of so

76 g pathway, as well as transcription factors, transporters, antioxidant enzymes, and enzymes associate

77 Transporters are essential players in bacterial growth a

78 hanisms is puzzling because CLC channels and transporters are expected to share the same architecture

79 In land plants several transporters are involved in ion and metabolite flux acr

80 C were substrate-type releasers at monoamine transporters as determined in vitro, but only methylone

81 dels have been developed using bacterial ABC transporters as templates but these have low sequence si

82 cuses on some of these lysosomal enzymes and transporters, as well as current therapies that have eme

83 metabolites was then compared using in vitro transporter assays and in vivo microdialysis in rat nucl

84 proteasome and transported to the ER by the transporter associated with antigen processing (TAP).

85 al steps in the transport cycle by recording transporter-associated currents: the recovery rate of ca

86 We focused on copper and its transporter ATP7A because ATP7A null mutations cause neu

87 LptB2FG is unique among ATP-binding cassette transporters because it extracts lipopolysaccharide from

88 However, the function of this transporter besides its role in drug resistance is still

89 SLC39A8 encodes ZIP8, a divalent metal ion transporter best known for zinc transport.

90 icant group differences in striatal dopamine transporter binding (all age ranges in caudate and putam

91 2 binding, (18)F-FDOPA uptake, and serotonin transporter binding in multiple brain regions were compa

92 Parkinson's disease show increased serotonin transporter binding in the striatum, brainstem, and hypo

93 Striatal dopamine transporter binding, VMAT2 binding, (18)F-FDOPA uptake,

94 ression of regulation of Ca(2+) channels and transporters can cause acquired arrhythmias, and how the

95 rst experimental evidence that synthetic ion transporters can disrupt both autophagy and induce apopt

96 port-elicited ubiquitylation of the arginine transporter Can1 is promoted by transition to an inward-

97 Using the energy of ATP hydrolysis, ABC transporters catalyze the trans-membrane transport of mo

98 0, a cell-surface-localized manganese efflux transporter, cause a heritable manganese metabolism diso

99 ed increased translocation of the fatty acid transporter CD36 from its endosomal storage compartment

100 confirmed by differentially expressed lipid transporters CD36 and CPT1C.

101 oded by Slc27a2, but not the other candidate transporters CD36 and free fatty acid receptor 1.

102 e basal forebrain increased cortical choline transporter (CHT)-mediated choline transport in GTs, par

103 ction due to loss of the endolysosomal Cl(-) transporter ClC-b/CLCN7 delayed degradation of internali

104 LR4-NF-kappaB signaling or the SPAK-NKCC1 co-transporter complex.

105 d in axon initial segments, and form channel-transporter complexes in vitro and in vivo KCNQ2/3 coexp

106 Although the copper ion transporter CopA has been known in Escherichia coli, no

107 s of astaxanthin biosynthesis, including ABC transporters, cytochrome P450 enzymes, and an acyltransf

108 The dopamine transporter (DAT) belongs to the neurotransmitter:sodium

109 uman alpha-synuclein A53T mutant or dopamine transporter (DAT) blockers also differentially affects t

110 To determine the usefulness of dopamine transporter (DAT) imaging to identify idiopathic rapid e

111 We report here an atypical dopamine (DA) transporter (DAT) inhibitor, CTDP-32476, that may have t

112 As the dopamine transporter (DAT) plays a prominent role in the reinforc

113 tolerance to cocaine effects at the dopamine transporter (DAT) with aberrant cocaine-taking behaviors

114 duction of potassium channels and amino acid transporters, derepression of genes marked with histone

115 The loss of a single transporter did not affect S. aureus However, disruption

116 bidopsis (Arabidopsis thaliana) boron efflux transporter displayed boron deficiency phenotypes.

117 system that utilizes both activity-dependent transporter downregulation and regulation of transporter

118 ism of dietary salt excretion relies on urea transporter-driven urea recycling by the kidneys and on

119 MalE, and maltose on the conformation of the transporter during the transport cycle, we have reconsti

120 n the contribution of the neuronal glutamate transporter EAAC1 to the onset of compulsive behaviors.

121 machinery, including the vesicular glutamate transporter eat-4/VGLUT, induction of neuropeptide expre

122 bstituent of 4-MA reduces potency to inhibit transporters, eliminates substrate activity at DAT and N

123 ished models and that acquisition of a third transporter enhances the ability of the bacterium to cau

124 Equilibrative nucleoside transporters (ENTs) translocate hydrophilic nucleosides

125 econstituted in proteoliposomes by measuring transporter equilibrium potentials.

126 P6 also interacts with ZIP10 and the two ZIP transporters exhibit interdependency during their expres

127 ne triphosphate (ATP)-binding cassette (ABC) transporter expressed at the canalicular membrane of hep

128 ABCA7 is an ABC transporter expressed on the plasma membrane, and active

129 is tissue, and coincided with enhanced lipid transporter expression in the fetoplacental unit.

130 e and leukocyte zinc concentrations and zinc transporter expressions were not altered.

131 ton binding to the extracellular side of the transporter facilitates a reorientation from an inward-

132 fructose-specific transporter in the glucose transporter family (GLUT, SLC2 gene family).

133 The multidrug and toxin extrusion (MATE) transporter family comprises 70 members in the Medicago

134 Members of the molybdate transporter family Molybdate Transporter type 1 (MOT1) w

135 Lotus japonicus nitrate transporter1/peptide transporter family, LjNPF8.6 The phenotypic characteriza

136 ochromatosis caused by mutations in the iron transporter ferroportin (Fpn), resulting in parenchymal

137 explaining how substrate binding primes the transporter for ATP hydrolysis.

138 Although mammalian Ctr1 functions as a Cu(+) transporter for Cu acquisition and is essential for embr

139 ly 2 member 14 (SLC2A14) gene, is a putative transporter for dehydroascorbic acid and glucose.

140 accharomyces cerevisiae and C. albicans have transporters for farnesylated peptides, like the a-facto

141 ABC transporters form one of the largest protein superfamili

142 Although other CLC channels and transporters form stable dimers, ClC-4 was mostly observ

143 -facing states of a concentrative nucleoside transporter from Neisseria wadsworthii.

144 ructural insight into the functional amyloid transporter from Pseudomonas, FapF.

145 that transfers Cu(I) and Ag(I) to the CusCBA transporter from the periplasm.

146 n is the SBP of VcSiaPQM, a sialic acid TRAP transporter from Vibrio cholerae.

147 why NasA, NarK1 and NarK2, as well as other transporters from this protein family, have such differe

148 n of proteins between synapses, and chloride transporter function at excitatory and inhibitory synaps

149 hat individual protomers within the trimeric transporter function fully independently.

150 ires adjustment of ion channel, receptor, or transporter function in response to changes in membrane

151 directs reduced expression of the serotonin transporter gene (5-HTT).

152 re- recombinase expression is under dopamine transporter gene (DAT) promoter control to ablate Cnr2 g

153 Analysis of shikimic acid accumulation, ABC-transporter gene expression, and cell death were used to

154 Functional validation of this transporter gene revealed that in vitro SLC16A5-silencin

155 Here, we reported that a choline transporter gene, CTL1, controls ionome homeostasis by r

156 d at least one short allele of the serotonin transporter gene.

157 eceptors, tyrosine hydroxylase, and dopamine transporter genes in the zebrafish brain.

158 of cell cycle, meiosis-related and nutrient transporter genes, suggesting a fine control of nutrient

159 nregulation of the glial glutamate-aspartate transporter (GLAST), which causes an enhancement of the

160 nt expression levels of facilitative glucose transporter (GLUT)1 in up to 50% of all patients.

161 ion, reduces sulfenylation of SIRT6, glucose transporter Glut1 expression, glucose uptake, and glycol

162 Indeed, the glucose transporter GLUT2 is located at the basolateral, vascula

163 ed on addiction to the high-affinity glucose transporter, Glut3.

164 firing, nerve terminals rely on the glucose transporter GLUT4 as a glycolytic regulatory system to m

165 aracterisation of high affinity and specific transporters has implications for the marine phosphorus

166 Forty-eight human ABC transporters have been identified in the genome, and the

167 Amino acid transporters have roles in amino acid uptake from soil,

168 but have a two-protein system comprised of a transporter (i.e., CblT) and a kinase (i.e., CblS) that

169 dly elevated expression of the GLUT1 glucose transporter in lung SqCC, which augments glucose uptake

170 MacB represents an ABC transporter in pathogenic microorganisms with unique str

171 Human GLUT5 is a fructose-specific transporter in the glucose transporter family (GLUT, SLC

172 This process requires an ABC transporter in the inner envelope membrane with three su

173 lex, and decreases the expression of several transporters in ambient CO2 growth conditions.

174 and supports the centrality of these "drug" transporters in independently and synergistically regula

175 Essential functions of nitrogen transporters in source and sink organs and their importa

176 role in regulating the function of dopamine transporters in the striatum.SIGNIFICANCE STATEMENT Deli

177 le for reduced Slc6a15, a neutral amino acid transporter, in nucleus accumbens (NAc) in depression an

178 dynamics trajectories of the human dopamine transporter, in which multiple spontaneous Na(+) release

179 by the protein siderocalin-a mammalian metal transporter-in contrast to the negatively charged specie

180 The in situ expression of solute transporters indicates that the heterotrophic prokaryoti

181 1, Slco1b2, Slco1a4) and hepatocyte-to-blood transporter induction (Abcc4, Abcc3).

182 n, a rho-kinase inhibitor and norepinephrine transporter inhibitor, in patients with open-angle glauc

183 These are the first ABC transporter inhibitors shown to block ATPase activity by

184 lular defense protein P-glycoprotein, termed transporter interfering compounds (TICs), ranged from 0.

185 conditions stimulates the ferroportin (FPN) transporter internalization, impairing the iron absorpti

186 tes affect the function of a monocarboxylate transporter involved in nutrient flux and hepatic lipid

187 change the expression of the following liver transporters involved in drug clearance: SLC10A1, SLC22A

188 Long-sought transporters involved in mitochondrial calcium influx an

189 The presynaptic, high-affinity choline transporter is a critical determinant of signalling by t

190 he carbohydrate specificity of each of these transporters is not currently defined.

191 ana auxin efflux transporter pin1 and influx transporter lax2 mutants showed reduced vein numbers.

192 Glutamate aspartate transporter levels were higher and glial glutamate trans

193 sion imaging studies show increased dopamine transporter levels, but changes in other aspects of dopa

194 otein (P-gp) is a polyspecific ATP-dependent transporter linked to multidrug resistance in cancer; it

195 domain protein as a regulator of plant metal transporter localization, providing evidence that PH dom

196 her, or both, the glial and neuronal glycine transporters markedly decreased PV+ IN excitability, as

197 hagosomal transport systems and the pathogen transporter may serve as therapeutic targets for infecti

198 +)-coupled lactate efflux on monocarboxylate transporters (MCTs).

199 The subfamily C ATP-binding cassette (ABCC) transporters mediate multidrug resistance and ion conduc

200 handle iron, highlighting how iron and heme transporters mediate the exchange and distribution of bo

201 dependent on vesicular inhibitory amino acid transporter-mediated signaling.

202 We observed transporter-mediated uptake of fluorescently labeled NEF

203 Facilitated glucose transporter member 14 (GLUT14), encoded by the solute ca

204 aused by a combination of PD defects and ion transporter misregulation.

205 d with an A309P mutation in the mycolic acid transporter MmpL3.

206 gy modeling supported the alternating access transporter model for sugar transport by confirming at l

207 gradient copolymer, resulting in two protein transporter molecules more efficacious than currently co

208 vating mutations in the thyroid hormone (TH) transporter Monocarboxylate transporter 8 (MCT8) cause s

209 transport activity of two other major efflux transporters, multidrug resistance protein 2 and breast

210 TaVIT2 also complemented a manganese transporter mutant but not a vacuolar zinc transporter m

211 e transporter mutant but not a vacuolar zinc transporter mutant.

212 ion of the apical sodium-dependent phosphate transporters, NaPi-IIa/NaPi-IIc/Pit2.

213 C4A7 encodes the electroneutral Na+/HCO3- co-transporter NBCn1 which regulates intracellular pH (pHi)

214 nsmembrane protein that regulates the sterol transporter NPC1.

215 two "drug" transporters of the organic anion transporter (OAT) family: OAT1 (SLC22A6, originally NKT)

216 ned that low expression of the ergothioneine transporter OCTN1 (SLC22A4; ETT) strongly predicts poor

217 tions, we suggest that CENP-F might act as a transporter of mitochondria and other cellular cargoes b

218 have characterized a nodule-specific citrate transporter of the multidrug and toxic compound extrusio

219 pressed in the CNS and the major anterograde transporters of cargos, such as mitochondria, synaptic v

220 vering that their association with magnesium transporters of the cyclin M (CNNM) family causes a rise

221 eal unique and opposing functions for copper transporters of the host and pathogen during infection.

222 enine, creatinine, urate) include two "drug" transporters of the organic anion transporter (OAT) fami

223 dicates that the kidney proximal tubule (PT) transporters of uremic toxins and solutes (e.g., indoxyl

224 T10-1 and TbAAT2-4 as the parasite ornithine transporters, one of which can be modulated by histidine

225 es the expression and activity of the efflux transporter P-glycoprotein (P-gp) encoded by ABCB1 in hu

226 and gate ring of helices, distinct from the transporter pathway.

227 and 2 and requires the proton-coupled folate transporter (PCFT, SLC46A1).

228 Arabidopsis (Arabidopsis thaliana) phosphate transporter PHO1;H3 comprising MYB15, MYB84, bHLH35, and

229 ally, both Arabidopsis thaliana auxin efflux transporter pin1 and influx transporter lax2 mutants sho

230 f the cell, suggesting that the two types of transporters play different roles in glucose sensing.

231 ETRATION 3 (PEN3) ATP binding cassette (ABC) transporter plays a role in defense against numerous pat

232 member 5 (SLC13A5), a sodium-coupled citrate transporter, plays a key role in importing citrate from

233 ABCC6 is an efflux transporter primarily expressed in liver facilitating th

234 synaptic termination, and the glutamatergic transporter profiles of DCN A and C fibers and their rel

235 rphology of the fusion product and regulates transporter protein degradation.

236 Meldonium reduced carnitine transporter protein expression across muscles of differe

237 oprotein transport activity without changing transporter protein expression.

238 es in P-glycoprotein activity independent of transporter protein expression.

239 ng glucose reabsorption by sodium glucose co-transporter proteins (SGLTs) in the kidneys is a relativ

240 These transporter proteins are targetable by dietary intervent

241 ins necessary for PT function, including ion transporters, receptors, and membrane-trafficking machin

242 chiometries of electrogenic secondary active transporters reconstituted in proteoliposomes by measuri

243 enolic inhibitors of SGLT1 and GLUT2 glucose transporters, reduced the glucose transport of almost 10

244 confirmed that the plasma membrane-localized transporter (renamed CDR6/ROA1 for consistency with C. a

245 .4-fold, consistent with blood-to-hepatocyte transporter repression (Slco1a1, Slc10a1, Slco2b1, Slco1

246 bly expressing specific uptake and/or efflux transporters revealed that OATP1B1, OATP1B3, and OATP1A2

247 ication is not compromised by the absence of transporter SbnD.

248 sized that biosynthesis of the selenium (Se) transporter selenoprotein P (SELENOP) is particularly se

249 otentially attributed to a reduced serotonin transporter (SERT) function.

250 number of PET studies imaging the serotonin transporter (SERT) have been used and provided evidence

251 FP-CIT has modest affinity for the serotonin transporter (SERT), predominantly represented in extrast

252 The serotonin transporter (SERT/SLC6A4) has a rich pharmacology includ

253 Using immunostaining for the serotonin transporter, SERT, we describe the complete pattern of d

254 Transporters shuttle molecules across cell membranes by

255 and expression of both major classes of drug transporters, SLC and ABC, in resting human blood neutro

256 tinal reabsorption due to induction of ileal transporters (Slc10a2, Slc51a) and increases in whole gu

257 d significantly increased levels of the urea transporter SLC14A1 in the OVT73 striatum, along with ot

258 based on structural data from related anion transporters (SLC26Dg and UraA), to have a 7 + 7 inverte

259 rnal polymorphism, 5HTTLPR, in the serotonin transporter, SLC6A4, coupled with prenatal stress is rep

260 r DAT and SERT N and C termini contribute to transporter substrate and inhibitor affinities.

261 However, mutations made within the predicted transporter substrate channel differentially altered the

262 of the biosynthetic pathways, exemplify how transporter substrate specificities originate and evolve

263 Linking the evolutionary path of transporter substrate specificities to that of the biosy

264 Transporters such as ABCB1 and ABCG2 limit the exposure

265 gic layer, substrate affinities of expressed transporters suggest that, in addition to amino acids, p

266 the structure and mechanism of an entire ABC transporter superfamily and the many diverse functions i

267 ment of short-chain lipids in activating the transporter supports a model for regulation within the h

268 How sucrose transporters (SUTs) regulate phloem unloading in monocot

269 transporter downregulation and regulation of transporter synthesis by internal nutrient levels can cr

270 From differential expression of bacterial transporter systems, we hypothesize that nine diatom met

271 water column, with yet higher abundances of transporters targeting aromatic compounds in the bathype

272 entified nuclear export factor 3 (NXF3) as a transporter that alters the nucleocytoplasmic distributi

273 rotein MRP1 is an ATP-binding cassette (ABC) transporter that confers resistance to many anticancer d

274 racts with the conserved regions in the LAT1 transporter that have been shown to bind to cholesterol/

275 e nematode C. elegans, sid-1 encodes a dsRNA transporter that is highly conserved throughout animal e

276 P14 (SLC39A14) is viewed primarily as a zinc transporter that is inducible via proinflammatory stimul

277 FATP2 is a major apical proximal tubule NEFA transporter that regulates lipoapoptosis and may be an a

278 ansport is mediated by an alternating access transporter that successively presents exofacial (e2) an

279 The Mce systems are complex ABC transporters that are encoded by different numbers of ho

280 in large (MmpL) proteins are cell wall lipid transporters that are important for basic mycobacterial

281 purified P-gp and other ATP-binding cassette transporters that transport amphipathic or hydrophobic s

282 ds and organic cations may interact with the transporter through different functional groups some of

283 In this study, we engineered the transporter to dissect interdomain communication paths.

284 encoding drug-metabolizing enzymes and drug transporters to essentially detoxify and eliminate xenob

285 rganic anion transporting polypeptide (OATP) transporters to the disposition of doxorubicin.

286 f the molybdate transporter family Molybdate Transporter type 1 (MOT1) were identified in the model l

287 Vesicular monoamine transporter type 2 (VMAT2) imaging with PET allows asses

288 T-type calcium channel variants and 1 ABCB1 transporter variant were associated with differential dr

289 by expression of mRNA for the vesicular GLU transporter (vGluT).

290 u hybridization to label vesicular glutamate transporters (vglut1, vglut2.1, vglut3), glutamate decar

291 characterized homologs of the VACUOLAR IRON TRANSPORTER (VIT).

292 Vacuolar iron transporters (VITs) are a poorly understood family of in

293 crystal structure of an NST, the GDP-mannose transporter Vrg4, in both the substrate-free and the bou

294 One ion transporter was also shown to cause additional changes i

295 s cytoplasmic chaperones and plasma membrane transporters, whereas CopR/S responds to periplasmic Cu(

296 ma membranes occurs via the large amino acid transporter, which is overexpressed in malignant cells,

297 omain of the Escherichia coli polysaccharide transporter Wza.

298 The metal transporter ZIP14 (SLC39A14) is viewed primarily as a zi

299 We have explored a role for the metal transporter ZIP14 during pharmacologically and high-fat

300 266634 in the SLC30A8 gene encoding the zinc transporter ZnT8, is associated with an increased risk f