ライフサイエンスコーパス: symporter

1 thymidine kinase and the human sodium-iodide symporter.

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

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

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

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

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

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

8 iver the cognate ligand to the transmembrane symporter.

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

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

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

12 h a second protein, PitA, a cation-phosphate symporter.

13 port in mammalian cells suggest Slc11a1 is a symporter.

14 ing hormone in stimulating the sodium-iodide symporter.

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

16 s that express the endogenous or transfected symporter.

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

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

19 ssion of thyroglobulin and the sodium/iodide symporter.

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

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

22 insights into substrate selectivity in AgcS symporters.

23 ovided from the environment via myo-inositol symporters.

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

25 that LmaNT3 and LmaNT4 are nucleobase/proton symporters.

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

27 into the function of neurotransmitter:sodium symporters.

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

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

30 e coupled to protons via the monocarboxylate 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 s maripaludis, the alanine or glycine:cation symporter (AgcS), with l- or d-alanine bound.

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

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

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

40 demonstrate that it functions as a K(+)/H(+) symporter and report a 3.7 angstrom cryo-EM structure of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 Neurotransmitter sodium symporters are integral membrane proteins that remove ch

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

73 ructure of Escherichia coli D-galactonate/H+ symporter D-galactonate transporter (DgoT) in 2 states:

74 The divalent anion sodium symporter (DASS) family (SLC13) plays critical roles in

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

76 d into the cell by the divalent anion sodium symporter (DASS) family of plasma membrane transporters,

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

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

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

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

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

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

83 Sodium iodide symporter expression in patient tumors after treatment w

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

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

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 epresentative of the neurotransmitter:sodium symporter family of secondary transporters(3), by imagin

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

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

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 y or the Na(+) coupled divalent anion-sodium symporter family.

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

98 e eukaryotic SLC6 family of Na(+) -dependent symporters for amino acids, neurotransmitters, osmolytes

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

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

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

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

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

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

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

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

109 The Staphylococcus epidermidis glucose/H(+) symporter (GlcP(Se)) is a membrane transporter highly sp

110 We consider the trimeric Na(+)-aspartate symporter Glt(Ph), a homolog of an important class of ne

111 odel archaeal homolog, sodium, and aspartate symporter Glt(Ph).

112 The sodium-coupled Asp symporter, Glt(Ph) is an archaeal homolog of glutamate t

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

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

115 late transporter 4 (MCT4) is an H(+)-coupled symporter highly expressed in metastatic tumors and at i

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

138 oncogenes actively accumulate iodide by this symporter in vivo.

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

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

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

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

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

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

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

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 F1 increased thyroglobulin and sodium/iodide symporter mRNA levels, cell migration, and proliferation

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

170 e chain reaction for gal-3 and sodium-iodide symporter (NIS) expression.

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 required for iodide uptake, which fac

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

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

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

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

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

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

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

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

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

194 The Na(+)/I(-) symporter (NIS), the plasma membrane protein that active

195 pothyroidism: mice lacking the sodium/iodide symporter (NIS), the plasma membrane protein that mediat

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

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

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

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

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

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

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

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

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

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

210 , are members of the neurotransmitter sodium symporter (NSS) family.

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

212 Neurotransmitter:sodium symporters (NSS) are conserved from bacteria to man and

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

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

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

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

217 Neurotransmitter:sodium symporters (NSSs) in the SLC6 family terminate neurotran

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

243 ium that expresses a neurotransmitter sodium symporter-related protein with sequence and structural h

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

259 exported transporters and the proton/sucrose symporter Sucrose Transporter1 To accumulate plant sugar

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

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

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

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

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

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

266 ons of the CTNS gene, encoding cystinosin, a symporter that mediates cystine efflux from lysosomes.

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

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

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

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

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

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

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

274 also inhibited the activities of two proton symporters, the osmosensing transporter ProP and the lac

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

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

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

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

279 46 [HPr(Ser-P)], binds to the galactose:H(+) symporter to uncouple sugar transport from proton sympor

280 phy imaging of the hNIS (human sodium/iodide symporter) to noninvasively quantify adeno-associated vi

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

282 ll lines showed an increase in sodium-iodine symporter transcription when treated with a MEK or BRAF(

283 r PI3'K inhibition upregulated sodium-iodine symporter transcription.

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

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

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

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

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

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

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

291 1 is a member of the neurotransmitter:sodium:symporters, which are crucial for synaptic transmission.

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

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

294 8 is a member of the family of sodium solute symporters, which are now added as a class of candidate

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

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

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

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

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

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