ライフサイエンスコーパス: symporter

1 of thyroglobulin (Tg) and the sodium/iodide symporter).

2 arK2 is proposed to be a Type I H(+)/nitrate symporter.

3 ortation of nitrate involved an H(+)/nitrate symporter.

4 We show that UCP1 is an LCFA anion/H(+) symporter.

5 oordinates of LacY and the oligopeptide/H(+) symporter.

6 pergillus nidulans purine-cytosine/H(+) FcyB symporter.

7 iver the cognate ligand to the transmembrane symporter.

8 g that PLUTO functions as a proton-substrate symporter.

9 as well as the X-ray structure of a related symporter.

10 ulaxalba, PtaSUT4, is a tonoplast (Group IV) symporter.

11 port in mammalian cells suggest Slc11a1 is a symporter.

12 ing hormone in stimulating the sodium-iodide symporter.

13 e, the channel functions as a proton/protein symporter.

14 s that express the endogenous or transfected symporter.

15 ing that it is likely to be a nitrate/proton symporter.

16 inase, HPr, enzyme I, and the galactose:H(+) symporter.

17 ssion of thyroglobulin and the sodium/iodide symporter.

18 in some experiments, encodes a Na(+)/malate symporter.

19 to decreased expression of the sodium-iodide symporter.

20 thymidine kinase and the human sodium-iodide symporter.

21 is based on the structure of a uracil-proton symporter.

22 and unbinding in the Na(+)-coupled substrate symporters.

23 d kinetic mechanism for the H(+)-coupled MFS symporters.

24 ovided from the environment via myo-inositol symporters.

25 ast, and bacteria as divalent metal ion/H(+) symporters.

26 that LmaNT3 and LmaNT4 are nucleobase/proton symporters.

27 ers, suggesting a distinctive fold for Na(+) symporters.

28 into the function of neurotransmitter:sodium symporters.

29 r phloem loading of sucrose via sucrose-H(+) symporters.

30 he enhanced accumulation of Suc via Suc/H(+) symporters.

31 In the LeuT family of sodium solute symporters, 13-17% of the residues in transmembrane doma

32 so indicated that LjSUT4 is a proton-coupled symporter: (14)C-sucrose uptake into LjSUT4-expressing o

33 volutionarily broad family nucleobase-cation symporter-2 (NCS2) encompasses transporters that are con

34 to investigate metabolic changes and iodide symporter activity in vitro.

35 e and H(+) ions and whether the lactate/H(+) symporter activity is sufficient to give rise to the obs

36 ires Na(+) influx, suggesting that Na(+) /Pi symporters also function in some streptophytes.

37 ansporter ProP of Escherichia coli, a proton symporter and a member of the major facilitator superfam

38 dosimetry in targeting of the sodium-iodine symporter and describe the clinical application of (124)

39 ssing cells also expressed the sodium iodide symporter and thyroglobulin genes.

40 sialic acid transporters: one sodium solute symporter and two ATP binding cassette (ABC) transporter

41 increase the expression of the sodium-iodide symporter and uptake of iodine.

42 residue conservation similar to that of the symporters and channels, and consistent with the crystal

43 ngs to the family of neurotransmitter:sodium symporters and controls dopamine (DA) homeostasis by med

44 nt action on sodium-coupled neurotransmitter symporters and elucidates critical elements of eukaryoti

45 for the mechanism of neurotransmitter sodium symporters and their modulation by therapeutic and illic

46 hyroglobulin, thyroperoxidase, sodium iodide symporter, and deiodinase type 2, and deiodinase type 2

47 ogen exchanger 3, aquaporin 7, sodium iodide symporter, and hydrogen potassium adenosine triphosphata

48 Git1p appears to act as a H(+)-symporter, and neither inositol nor phosphate effectivel

49 ression of thyroid peroxidase, sodium iodine symporter, and thyroglobulin.

50 mologue of mammalian neurotransmitter sodium symporters, and show that the tricyclic antidepressant (

51 homolog of mammalian neurotransmitter sodium symporters; and 2), rhodopsin and the beta1- and beta2-a

52 ligand-binding protein, and a transmembrane symporter apparatus comprising the M and Q components (M

53 the amphotropic receptor Pit-2, a phosphate symporter, appears to be low in human and murine hematop

54 Neurotransmitter sodium symporters are integral membrane proteins that remove ch

55 olecular events driving transport by Pi:H(+) symporters are unclear.

56 pallidum, tp0957 (the SBP), and tp0958 (the symporter), are in an operon with an uncharacterized thi

57 levels of BvSUT1, a sugar beet leaf sucrose symporter, are negatively regulated specifically by sucr

58 and binding sites in neurotransmitter/sodium symporters arose from conflicting data in crystal struct

59 transporters able to function as Na(+)-K(+) symporters, at least when expressed in yeast (Saccharomy

60 n of the high-affinity monosaccharide/proton symporter AtSTP1 of Arabidopsis.

61 g a T-DNA disruption of the bile acid sodium symporter BASS6 show decreased photosynthesis and slower

62 the corresponding structures of the related symporter BetP reveals alternating orientations of the b

63 The Na(+)-coupled betaine symporter BetP senses changes in the membrane state and

64 -binding sites in the sodium-coupled betaine symporter BetP.

65 sporters, the ABC transporter CbcXWV and two symporters, BetT1 and BetT3, in P. aeruginosa growth on

66 downstream of the neurotransmitter reuptake symporter bloated tubules (blot), whose Drosophila ortho

67 was required for expression of sodium-iodide symporter but was not required for thyroglobulin express

68 tic understanding of neurotransmitter sodium symporters but have left fundamental questions unanswere

69 roteins are hypothesized to be the Na(+) /Pi symporters catalysing Pi uptake in chlorophytes, whereas

70 Among the proton-sucrose symporters cloned to date, only the histidine residue at

71 alyzed by immunohistochemistry expressed the symporter, compared with none of the normal (nonlactatin

72 olarization similar to the non-GLR, putative symporter component and in most cases evoked little or n

73 hat under aerobic conditions the lactate-/H+ symporter could be the most active exchanger in the regu

74 The putative H+/Cl- symporter cycloprodigiosin-HCl (cPrG-HCl) was used to in

75 tein is a member of the divalent anion/Na(+) symporter (DASS) family and shares significant sequence

76 cS, is a member of the divalent anion sodium symporter (DASS) family that also includes the mammalian

77 embrane proteins of the divalent anion/Na(+) symporter (DASS) family translocate dicarboxylate, trica

78 porter is a member of the divalent-anion/Na+ symporter (DASS) family, a group that includes the mamma

79 -mediated reduction of PttSUT3 (for Suc/H(+) symporter) during secondary cell wall formation in devel

80 We tested the hypothesis that Na(+) /Pi symporters exist in streptophytes.

81 dium-dependent lysophosphatidylcholine (LPC) symporter expressed at the blood-brain barrier that tran

82 Sodium iodide symporter expression in patient tumors after treatment w

83 ion was the lack of detectable sodium-iodide symporter expression in TSHR-KO thyroid glands.

84 We show that, whereas thyroidal Na(+)/I(-) symporter expression is thyroid-stimulating hormone (TSH

85 member from each of the three more distinct symporter families, i.e., a TrkH protein from Escherichi

86 litator superfamily (MFS), the sodium solute symporter family (SSF; only in the animal kingdom), and

87 aemolyticus is a member of the sodium:solute symporter family (SSS).

88 rs (NATs) within the sodium-neurotransmitter symporter family and have characterized a member of the

89 the only member of the oligosaccharide:H(+) symporter family in the Major Facilitator Superfamily th

90 permease belongs to the oligosaccharide:H(+) symporter family of the Major Facilitator Superfamily an

91 caK and is conserved in the aromatic acid/H+ symporter family of the major facilitator superfamily of

92 rved among members of the aromatic acid/H(+) symporter family of the MFS, was found to be critical fo

93 arding glycoside-pentoside-hexuronide:cation symporter family transporters and other Na(+)-coupled pe

94 to the glycoside-pentoside-hexuronide:cation symporter family, a part of the major facilitator superf

95 ymporter PutP, a member of the solute/sodium symporter family, was investigated.

96 old with LeuT of the neurotransmitter-sodium symporter family.

97 The symporters for the biogenic amines serotonin (SERT), dop

98 ional mechanism of the Na(+)-sugar melibiose symporter from Escherichia coli.

99 The Na(+)/dicarboxylate symporter from Staphylococcus aureus, named SdcS, is a m

100 endent, whereas many neurotransmitter:sodium symporters from higher organisms depend on Cl(-) ions.

101 s suggests that the vacuolar sodium/inositol symporters function to reduce sodium amounts in cells of

102 In vitro iodide transport shows that the symporter functions similarly in rNIS-transduced tumor c

103 pared with all other neurotransmitter:sodium:symporters, GAT-1 and other members of the GABA transpor

104 MV engineered to express the sodium iodide symporter gene (MV-NIS) facilitates localization of vira

105 The rat sodium/iodide symporter gene (rNIS) was cloned into a retroviral vecto

106 ber of the sodium-dependent neurotransmitter symporter gene family in C. elegans.

107 n transcription of a phloem-specific sucrose symporter gene in a regulatory system that may play a pi

108 NA levels of a stress-related monosaccharide symporter gene, STP4.

109 ition of the expression of the sodium iodide symporter gene.

110 rium Pyrococcus horikoshii, sodium/aspartate symporter GltPh, suggested the molecular basis of the tr

111 cinia virus carrying the human sodium iodide symporter GLV-1h153.

112 ve results indicate that the KtrAB family of symporters has remained closest to the single-MPM ancest

113 cDNAs encoding three such symporters have very recently been cloned and sequenced.

114 folate transporter (PCFT) is a folate-proton symporter highly expressed in solid tumors that can sele

115 ssp. indica) homologous to the wheat K+/Na+-symporter HKT1.

116 We incorporated the human sodium iodide symporter (hNIS) and the human somatostatin receptor 2 (

117 n, including the loss of human sodium iodide symporter (hNIS) expression, radioactive iodide (RAI) th

118 nic antigen (CEA) or the human sodium iodide symporter (hNIS) for oncolytic potential in hepatocellul

119 mulation mediated by the human sodium iodide symporter (hNIS) gene in conjunction with various imagin

120 cardiac gene expression after sodium iodide symporter (hNIS) gene transfer in cardiac transplantatio

121 Anion transport by the human sodium-iodide symporter (hNIS) is an established target for molecular

122 ted vector coding for the human sodiumiodide symporter (hNIS) led to hNIS expression by these cells a

123 rine transporter (hNET), human sodium-iodide symporter (hNIS), a human deoxycytidine kinase double mu

124 rus, GLV-1h153, carrying human sodium iodide symporter (hNIS), in combination with radioiodine in an

125 ioligand for imaging the human sodium/iodide symporter (hNIS).

126 tal structure of the neurotransmitter/sodium symporter homolog LeuT revealed an occluded binding pock

127 to LeuT, a bacterial neurotransmitter:sodium symporter homolog.

128 BLI and sodium-iodide symporter imaging may be useful for in vivo optimization

129 vidence that cPrG acts as a potential H+/Cl- symporter in aleurone is presented.

130 the Staphylococcus epidermidis glucose/H(+) symporter in an inward-facing conformation at 3.2-A reso

131 e molecular dynamics simulations of the UraA symporter in phospholipid bilayers consisting of: 1) 1-p

132 own expression domain of the AtSUC2 Suc-H(+) symporter in the epidermis of the cell division zone of

133 that a specialized form of the sodium/iodide symporter in the mammary gland mediates active iodide tr

134 ine isotopes for targeting the sodium-iodine symporter in thyroid cancer and nonthyroidal neoplasms a

135 resses hNIS, increases the expression of the symporter in TNBC cells, and serves both as a gene marke

136 oncogenes actively accumulate iodide by this symporter in vivo.

137 ke of the resultant free radioiodine by Na/I symporters in the gastric mucosa.

138 of PM proteins like Pma1p and nutrient H(+)-symporters inducing their ubiquitination and internaliza

139 lactoside, probably by converting the proton symporter into a uniporter.

140 ns identified in this and other Na(+)/solute symporters introduce premature termination codons or imp

141 indicate that TcPho91 is a phosphate sodium symporter involved in Pi homeostasis in T. cruzi.

142 trate transport in sodium-coupled amino acid symporters involves a large-scale conformational change

143 The Escherichia coli UraA H+-uracil symporter is a member of the nucleobase/ascorbate transp

144 The Staphylococcus epidermidis glucose/H(+) symporter is homologous to human glucose transporters, i

145 K(+) channels and the four families of K(+) symporters is further supported by the accompanying manu

146 ium-selective uniporters or sodium-potassium symporters is widely held.

147 Na(+) and sugar transport by cotransporters (symporters) is thought to occur as a series of ordered l

148 genes homologous to H+[or Na+]/myo-inositol symporters (ITRs), not previously studied in plants.

149 y firefly luciferase and human sodium-iodide symporter labeling of cardiosphere-derived cells were in

150 Few side chains in the galactoside/H(+) symporter LacY (lactose permease of Escherichia coli) ar

151 peat similar to that in the amino acid/Na(+) symporter LeuT.

152 ndicate that the mammary gland sodium/iodide symporter may be an essential breast cancer marker and t

153 The sodium/iodide symporter mediates active iodide transport in both healt

154 A proton-sucrose symporter mediates the key step in carbon export from le

155 r was determined to be homologous to that of symporters mediating the transport of the same or relate

156 ia coli HS4006 containing the melibiose-H(+) symporter (MelY) from Enterobacter cloacae that had enha

157 ational cycle of the Na(+)-coupled hydantoin symporter Mhp1 from Microbacterium liquefaciens.

158 eishmania donovani has a myo-inositol/proton symporter (MIT) that is a member of a large sugar transp

159 the observed ability of the portions of the symporter models derived from the KcsA crystal structure

160 s, using a mutant lacking the nitrate/proton symporter NasA from the assimilatory nitrate reductase p

161 ncodes a phloem-localized sucrose (Suc)/H(+) symporter necessary for efficient Suc transport from sou

162 rine interferon beta (IFNbeta)-sodium iodide symporter (NIS) (VSV-mIFNbeta-NIS) oncolytic virus has s

163 ome breast cancers express the sodium/iodide symporter (NIS) and concentrate iodide.

164 y involves transduction of the sodium iodide symporter (NIS) and free radionuclide therapy.

165 roviral vectors containing the sodium iodide symporter (NIS) and thyroperoxidase (TPO) genes.

166 cer model expressing the human sodium iodide symporter (NIS) as a reporter.

167 The application of sodium iodide symporter (NIS) as a theranostic gene allows noninvasive

168 the current study, we used the sodium iodide symporter (NIS) as a theranostic gene to investigate whe

169 to express functionally active sodium iodide symporter (NIS) by targeted NIS gene transfer might offe

170 The sodium/iodide symporter (NIS) concentrates iodide in the thyroid and l

171 ls stably expressing the human sodium iodide symporter (NIS) fused to a red fluorescent protein, ther

172 rotein and expresses the human sodium iodide symporter (NIS) gene.

173 The sodium/iodide symporter (NIS) has been identified as an attractive tar

174 The Na(+)/I(-) symporter (NIS) has been proposed as an imaging reporter

175 chemistry confirmed expression of Na(+)-I(-) symporter (NIS) in the airways.

176 , thiocyanate, and nitrate are sodium/iodide symporter (NIS) inhibitors that block iodide uptake into

177 The Na+/I- symporter (NIS) is a key plasma membrane glycoprotein th

178 The Na(+)/I(-) symporter (NIS) is a key plasma membrane glycoprotein th

179 The Na(+)/I(-) symporter (NIS) is a key plasma membrane protein that me

180 The Na(+)/I(-) symporter (NIS) is a plasma membrane glycoprotein that m

181 The sodium/iodide symporter (NIS) is under investigation as a reporter for

182 The sodium/iodide symporter (NIS) mediates active I(-) transport in the th

183 The Na(+)/I(-) symporter (NIS) mediates active I(-) transport--the firs

184 The sodium/iodide symporter (NIS) mediates active iodide (I(-)) accumulati

185 ctor PBF repress expression of sodium iodide symporter (NIS) messenger RNA (mRNA), and inhibit iodide

186 The sodium/iodide symporter (NIS) stimulates iodide uptake in normal lacta

187 In this study, sodium iodide symporter (NIS) transgene imaging was evaluated as an ap

188 Established cell lines expressing the Na/I symporter (NIS) were used to quantify the effect of ICM

189 biosynthesis, is mediated by the Na(+)/I(-) symporter (NIS) with an electrogenic 2Na(+):1I(-) stoich

190 to express functionally active sodium iodide symporter (NIS) would enable those cells to concentrate

191 uptake, which is mediated by the Na(+)/I(-) symporter (NIS), in vivo (dSUV/dt: vehicle, 0.028 +/- 0.

192 ntranslated region of PAX8 and sodium/iodide symporter (NIS), leading to impaired protein translation

193 ne kidney cells expressing the sodium iodide symporter (NIS), pendrin, or NIS and pendrin using a bic

194 C1 decreases expression of the sodium/iodide symporter (NIS), the molecule that mediates radioiodide

195 We examined the sodium-iodide symporter (NIS), which promotes in vivo cellular uptake

196 most promising candidates for sodium iodide symporter (NIS)-mediated gene therapy.

197 The Na+/I- symporter (NIS)-mediated iodide uptake activity is the b

198 roidal tissues is mediated by the Na(+)/I(-) symporter (NIS).

199 in the thyroid is mediated by the Na(+)/I(-) symporter (NIS).

200 and breast is mediated by the sodium/iodide symporter (NIS).

201 thyroid tissue mediated by the sodium-iodide symporter (NIS).

202 t MV-Edm encoding the human thyroidal iodide symporter (NIS).

203 le in tumor progression of the sodium/iodide symporter (NIS; aka SLC5A5), which is upregulated and mi

204 ial homologue of the neurotransmitter:sodium symporter (NSS) family and, being the only NSS member to

205 member (Tyt1) of the neurotransmitter:sodium symporter (NSS) family has been cloned from Fusobacteriu

206 ryotic member of the neurotransmitter/sodium symporter (NSS) family is a major advance toward underst

207 (DAT) belongs to the neurotransmitter:sodium symporter (NSS) family of membrane proteins that are res

208 rs in characterizing neurotransmitter:sodium symporter (NSS) family structure and function.

209 Neurotransmitter:sodium symporter (NSS) proteins are secondary Na(+)-driven acti

210 Neurotransmitter:Na(+) symporters (NSS) remove neurotransmitters from the synap

211 Neurotransmitter:sodium symporters (NSSs) are integral membrane proteins respons

212 Neurotransmitter/sodium symporters (NSSs) are responsible for Na(+)-dependent re

213 Neurotransmitter/sodium symporters (NSSs) couple the uptake of neurotransmitter

214 Neurotransmitter:sodium symporters (NSSs) mediate reuptake of neurotransmitters

215 Neurotransmitter:sodium symporters (NSSs) play a critical role in signaling by r

216 Neurotransmitter: sodium symporters (NSSs) regulate neuronal signal transmission

217 The Neurotransmitter:Sodium Symporters (NSSs) represent an important class of protei

218 Neurotransmitter/Na(+) symporters (NSSs) terminate neuronal signalling by recap

219 Neurotransmitter:sodium symporters (NSSs) terminate neurotransmission by Na(+)-d

220 Neurotransmitter:sodium symporters (NSSs) terminate neurotransmission by the reu

221 Eukaryotic neurotransmitter:sodium symporters (NSSs), targets for antidepressants and psych

222 gue of the mammalian neurotransmitter/sodium symporters (NSSs), we studied the properties of proteomi

223 e gating dynamics of neurotransmitter:sodium symporters (NSSs).

224 ters of fungal and animal origin and H(+)/Pi symporters of bacterial origin.

225 transporter family, which includes Na(+)/Pi symporters of fungal and animal origin and H(+)/Pi sympo

226 roposed to function as either nitrate/proton symporters or nitrate/nitrite antiporters based on seque

227 either "apoplastically" (by using H+/sucrose symporters) or "symplastically" (through plasmodesmata).

228 ermease; PA2042 for a putative sodium:serine symporter; PA3934, which belongs to the family of small

229 ese viruses use the related sodium-phosphate symporters Pit1 and Pit2, respectively, as receptors in

230 ns and use related Na(+)-dependent phosphate symporters, Pit1 and Pit2, respectively, as their recept

231 H(+) symporter ProP serves as a paradigm for the study of osm

232 ne protein (specifically H(+)-osmoprotectant symporter ProP) to the Escherichia coli cell poles.

233 Further analysis showed that symporter protein and message are both degraded rapidly.

234 time that the involvement of a sodium solute symporter protein as a Bt functional receptor has been d

235 as caused by a reduction in the abundance of symporter protein.

236 subunit and the transmembrane subunit of the symporter proteins are postulated to have four correspon

237 rily conserved among neurotransmitter:sodium symporter proteins as a binding pocket for small molecul

238 the criteria and principles suggest that the symporter proteins from fungi and plants (i.e., Trk1,2 a

239 that at least four families of putative K(+) symporter proteins, Trk and KtrAB from prokaryotes, Trk1

240 TM10' are explored using the sodium/proline symporter PutP as a model.

241 , the function of TM6' in the sodium/proline symporter PutP, a member of the solute/sodium symporter

242 on of the eukaryotic neurotransmitter:sodium:symporters remains unknown.

243 the first exon of SLC13A1, a sodium/sulfate symporter responsible for regulating serum levels of ino

244 RNA gel blot analysis of the leaf symporter revealed that message levels also declined, an

245 The Na(+)/dicarboxylate symporter (SdcS) from Staphylococcus aureus is a homolog

246 akes up citrate as a nutrient via the sodium symporter SeCitS.

247 The symporter sequences appear to contain four sequential M1

248 glucose transporters (GLUTs), sodium-glucose symporters (SGLTs), and SWEETs.

249 plying that SSSs and neurotransmitter-sodium symporters share common mechanistic elements in substrat

250 f a homologous archaeal sodium and aspartate symporter showed that a dedicated transport domain carri

251 on decreased expression of the sodium iodide symporter SLC5A5 (NIS), diminished membrane targeting of

252 NCS1 proteins are H(+)/Na(+) symporters specific for the uptake of purines, pyrimidin

253 lactose transporter (vSGLT), a solute-sodium symporter (SSS) from Vibrio parahaemolyticus, shares a c

254 l structure of a member of the solute sodium symporters (SSS), the Vibrio parahaemolyticus sodium/gal

255 Solute:sodium symporters (SSSs) transport vital molecules across the p

256 fied mutants of the plasma membrane Suc/H(+) symporter SUC1, indicating that the accumulation of Suc

257 in the mechanism of neurotransmitter-sodium symporters, such as the human dopamine transporter.

258 els to the KtrAB, Trk, Trk1,2, and HKT1 K(+) symporter superfamily of both prokaryotes and eukaryotes

259 ma membrane, proton-coupled Group II sucrose symporters (SUT) mediate apoplastic phloem loading and s

260 N-I), E-cadherin (TcCad1), and sodium solute symporter (TcSSS) have been identified by ligand blot as

261 the suc2 mutation disables a sucrose/proton symporter that facilitates sucrose loading from leaves i

262 ansporter (PCFT; SLC46A1) is a proton-folate symporter that is abundantly expressed in solid tumors a

263 accumulation of HAK5, a putative (H(+))/K(+) symporter that mediates a high-affinity uptake during K(

264 The proton-sucrose symporter that mediates phloem loading is a key componen

265 f the four consecutive M1-P-M2 motifs in the symporters that can be aligned with K(+) channel sequenc

266 ANSPORTER 1 (PHT1) proteins are the H(+) /Pi symporters that carry out Pi uptake in angiosperms.

267 eurotransmitter transporters are ion-coupled symporters that drive the uptake of neurotransmitters fr

268 as a homolog of Pho4, a family of phosphate symporters that includes the bacterial PitA proteins.

269 Substrate and H(+)-binding sites in symporters that transport substrates, ranging from simpl

270 It is likely that ZIP8 is a Mn2+/HCO3- symporter, that a HCO3- gradient across the plasma membr

271 essenger), which binds to the galactose:H(+) symporter (the target), resulting in uncoupling of sugar

272 LC5A8 gene, is 70% similar to the Na(+)/I(-) symporter, the protein that mediates active I(-) uptake

273 cus on two well-characterized sodium-coupled symporters: the bacterial amino acid transporter LeuT, w

274 In SLC5 symporters, three aromatic residues in TM6 (SGLT1 W289,

275 suppressing expression of the sodium iodide symporter, thyroid peroxidase, TG, and thyrotropin recep

276 ic target genes thyroglobulin, sodium iodide symporter, thyroperoxidase, and thyroid-stimulating horm

277 crease in the rate of return of the unloaded symporter to the outer face of the membrane.

278 46 [HPr(Ser-P)], binds to the galactose:H(+) symporter to uncouple sugar transport from proton sympor

279 (LeuT), a model for neurotransmitter sodium symporters, to show that various amino acid substrates i

280 n of Na+/H+-antiporters and Na+/myo-inositol symporters transfers sodium from vacuoles in root cells

281 The uric acid/xanthine H(+) symporter, UapA, is a high-affinity purine transporter f

282 the Vibrio parahaemolyticus sodium/galactose symporter (vSGLT).

283 e deduced amino acid sequence of each insect symporter was determined to be homologous to that of sym

284 t encoding a putative plasma membrane proton symporter was isolated, because it was coordinately regu

285 egulation of the mammary gland sodium/iodide symporter, we demonstrate by scintigraphy that mammary a

286 xpression in frog oocytes shows Slc11a2 is a symporter, whereas Slc11a1 is an antiporter fluxing diva

287 GAT-1 belongs to the neurotransmitter:sodium:symporters which are crucial for synaptic transmission.

288 t is a member of the neurotransmitter:sodium:symporters, which are crucial for synaptic transmission.

289 and a member of the neurotransmitter:sodium:symporters, which are crucial for synaptic transmission.

290 1 is a member of the neurotransmitter:sodium:symporters, which are crucial for synaptic transmission.

291 8 is a member of the family of sodium solute symporters, which are now added as a class of candidate

292 TrkA and KtrA subunits of the Trk and KtrAB symporters, which in turn are homologous to known dinucl

293 ort that NarK1 functions as a nitrate/proton symporter while NarK2 is a nitrate/nitrite antiporter.

294 folate transporter (PCFT) is a folate-proton symporter with an acidic pH optimum, approximating the m

295 folate transporter (PCFT) is a proton-folate symporter with an acidic pH optimum.

296 NarK1 appears to be a nitrate/proton symporter with high affinity for nitrate and NarK2 a nit

297 that recombinant SITs are Na(+)/silicic acid symporters with a 1:1 protein: substrate stoichiometry a

298 Symporters with mutations at His-65 exhibited a range of

299 Significantly, those symporters with substitutions of His-65 that remained tr

300 radioiodine in tissues that express the Na/I symporter without affecting the ability to image the tum