ライフサイエンスコーパス: solute carrier

1 transporter belonging to the SLC1 family of solute carriers.

2 tural determination of many other small size solute carriers.

3 the respiratory supercomplex (RSC) and other solute carriers.

4 structurally and functionally related human solute carriers.

5 glutamate transporter subtypes belong to the solute carrier 1 (SLC1) family and a second family, SLC6

6 ysteine transporter 2 (ASCT2) belongs to the solute carrier 1 (SLC1) family of solute transporters an

7 y the neutral amino acid transporters of the solute carrier 1 [SLC1, alanine serine cysteine transpor

8 ine cysteine transporter 2), a member of the solute carrier 1 family, mediates Na(+)-dependent exchan

9 conserved properties predicted for the Nramp/Solute carrier 11 (Slc11) family, such as 12-transmembra

10 etal transporter/divalent cation transporter/solute carrier 11 group A member 2 or 3 (DMT1/DCT1/SLC11

11 Solute carrier 11A1 (SLC11A1) is a divalent ion transpor

12 -, alanine-rich kinase directly regulate the solute carrier 12 family of cation-chloride cotransporte

13 icarboxylate cotransporters (NaDC1) from the solute carrier 13 (SLC13) family.

14 peptidyl-prolyl cis-trans isomerase (PPIF), solute carrier 15 (SLC15), solute carrier family 43 memb

15 Members of the solute carrier 15 family (SLC15) transport di- and tripe

16 The solute carrier 16 (SLC16) family represents a diverse gr

17 Members of the solute carrier 17 (SLC17) family use divergent mechanism

18 Sialin, a member of the solute carrier 17 (SLC17) transporter family, is unique

19 Other solute carrier 17 members including the lysosomal sialic

20 g the complete transport cycle shared by the solute carrier 1A transporter family.

21 gens (DDX3Y; ribosomal protein S4, Y linked; solute carrier 1A5; and signal sequence receptor 1) were

22 To date, mutations in five genes including solute carrier 20 member 2 (SLC20A2), xenotropic and pol

23 ation transporters (OCTs) are members of the solute carrier 22 family of transporter proteins that ar

24 r-3), a polyspecific drug transporter in the solute carrier 22 family.

25 The human solute carrier 22A (SLC22A) family consists of 23 member

26 endent Na(+)/Ca(2+) exchangers belong to the solute carrier 24 (SLC24A1-5) gene family of membrane tr

27 Solute carriers--solute carrier 25A23 (SLC25A23), SLC25A24, and SLC25A25-

28 ere, we reveal that the orphan mitochondrial solute carrier 25A45 (SLC25A45) is required for the mito

29 Here we identify a solute carrier 26 (Slc26) family protein as an essential

30 The solute carrier 26 (SLC26) transporters are anion transpo

31 Mutations in SLC26A3 (solute carrier 26 family member 3), which functions as a

32 lyspecific organic cation transporter in the solute carrier 29 (SLC29) family.

33 racellular nucleoside transporter within the solute carrier 29 (SLC29) gene family, cause an expandin

34 Some candidate genes include solute carrier 35A1 (SLC35A1), retinoic acid-inducible g

35 on electrochemical gradient, as found in the solute carrier 36 family of proton-coupled amino acid tr

36 ZIP14 (encoded by the solute carrier 39 family member 14 (SLC39A14) gene) is a

37 and 3; SLC4A1) is the founding member of the solute carrier 4 (SLC4) family of bicarbonate transporte

38 y associated with homozygous mutation of the solute carrier 4 family gene SLC4A4.

39 The choline transporter-like protein 1/solute carrier 44A1 (CTL1/SLC44A1) and mRNA expression w

40 Point mutations in solute carrier 6 (SLC6) family members cause folding dis

41 Folding-deficient mutants of solute carrier 6 (SLC6) family members have been linked

42 The folding trajectory of solute carrier 6 (SLC6) family members is of interest be

43 Many solute carrier 6 (SLC6) family transporters require anci

44 The solute carrier 6 (SLC6) is a family of ion-dependent tra

45 Here, we report the identification of the solute carrier 6 (SLC6) transporter protein SNF-10 as a

46 This analysis was extended to other SLC6 (solute carrier 6) transporter family members: siRNA-depe

47 Trh), serotonin receptor 2a (5HT2a), and the solute carrier 7-family amino acid transporter, JhI-21,

48 r expression [notably a leucine transporter, solute carrier 7A5 (SLC7A5)] is required to initiate AA-

49 Membrane solute carriers are key proteins involved in drug transp

50 In eukaryotes the SLC35 family of solute carriers are responsible for their selective upta

51 kidney-restricted plasma membrane-localized solute carriers, as physiologic urine Lac-Phe transporte

52 esults reveal the principles of glycoprotein-solute carrier assembly and provide templates for improv

53 reabsorbed through the concerted actions of solute carrier channels and aquaporins at various positi

54 Another solute carrier (Cl(-)/HCO3- exchanger) gene, Ae3, is in

55 f a newly discovered memory suppressor gene, Solute Carrier DmSLC22A, a member of the organic cation

56 n of a multigene transport system, involving solute carriers (encoded by Slc26a4, Slc4a8, and Slc4a9)

57 ar matrix protein-expressing M-pericytes and solute carrier-expressing T-pericytes.

58 cassette (ABC) transporters and the organic solute carrier family (SLC) proteins.

59 organic cation and anion transporters of the solute carrier family (SLC22), which are implicated in c

60 is a member of the vertebrate mitochondrial solute carrier family (SLC25) that we call mitoferrin (m

61 ne, and cysteine transporters) belong to the solute carrier family 1 (SLC1), which also includes the

62 hannel, subfamily J, member 13 (KCNJ13), and solute carrier family 1 member 1 (SLC1A1) in the jejunum

63 id transporter 3 [EAAT3; also termed Slc1a1 (solute carrier family 1 member 1)] to support de novo gl

64 -364, of human glutamate transporter SLC1A2 (solute carrier family 1 member 2), also known as glutama

65 A/glutamate receptor subunit 2C, calmodulin, solute carrier family 1 member 2, and glutamine syntheta

66 The neutral amino acid transporter solute carrier family 1 member 5 (SLC1A5 or ASCT2) is ov

67 , FTO demethylates the glutamine transporter solute carrier family 1 member 5 (SLC1A5) messenger RNA

68 s away from the SLC1A5 gene, a member of the solute carrier family 1, had a genome-wide significant a

69 The glutamate transporter gene solute carrier family 1, member 1 (SLC1A1) is a promisin

70 In contrast, the expression of solute carrier family 10 member 1 (Slc10a1) and solute c

71 umonji domain containing 1C, AC074212.3, and solute carrier family 10A member 2 [SLC10A2]) and six kn

72 Solute carrier family 11 member 1 (SLC11A1) is critical

73 screening and subsequent analysis identified solute carrier family 11 member 1 (SLC11A1; formerly NRA

74 Solute carrier family 11, member 2 (SLC11A2) is the only

75 Solute carrier family 12 member 2 and cystic fibrosis tr

76 iptional repression of ecto-5'-nucleotidase, solute carrier family 12 member 8, and nicotinamide ribo

77 otinamide adenine mononucleotide transporter solute carrier family 12 member 8, and the nicotinamide

78 his gene SLC12A8, coding for a member of the solute carrier family 12 proteins.

79 The solute carrier family 13 (slc13) transporters mediate tr

80 The solute carrier family 13 member 5 (SLC13A5) is a sodium-

81 The solute carrier family 13 member 5 (SLC13A5), a sodium-co

82 A new study reports that loss of solute carrier family 13 member 5, which transports citr

83 The signal localizes to the solute carrier family 14 member 1 gene, SLC14A1, a urea

84 at impairs the peptide/histidine transporter solute carrier family 15, member 4 (SLC15A4).

85 NC93B1 and the endosomal proton transporter, solute carrier family 15, member 4.

86 by increased expression of hexokinase 2 and solute carrier family 16 member 1 in stenotic fibroblast

87 n 1 protein (EPAS1, also called HIF2A), CA9, solute carrier family 16 member 4 (SLC16A4, also called

88 als a loss-of-function mutation in slc16a6a (solute carrier family 16a, member 6a), a gene that we sh

89 ets of a glutamatergic population expressing Solute carrier family 17 (Slc17a6) (VGLUT2).

90 injection of adeno-associated virus carrying solute carrier family 17, member 8 (Slc17A8), which enco

91 present evidence that the gene SLC19A2 (for solute carrier family 19 (thiamine transporter), member

92 Solute Carrier Family 19 Member 2 (SLC19A2) encodes thia

93 regulation of metallothioneine-2A (MT2A) and solute carrier family 19 member 2 (SLC19A2), two GR targ

94 cysteine transporters (ASCTs) belong to the solute carrier family 1A (SLC1A), which also includes th

95 etin), SLC2A1 (also known as GLUT1, encoding solute carrier family 2 (facilitated glucose transporter

96 Several SNPs of SLC2A1 (solute carrier family 2 [facilitated glucose transporter

97 sms in genes involved in fructose transport (solute carrier family 2 facilitated glucose transporter,

98 d glucose transporter, member 2 (SLC2A2) and solute carrier family 2 facilitated glucose/fructose tra

99 ansporter member 14 (GLUT14), encoded by the solute carrier family 2 member 14 (SLC2A14) gene, is a p

100 ICI and the neighboring protein-coding gene, solute carrier family 2 member 3 (SLC2A3) which encodes

101 ontan failure predicted cell death pathways (Solute carrier family 2, Angiotensinogen, CD14) and mito

102 glucose transporter 1 (Glut1), also known as solute carrier family 2, facilitated glucose transporter

103 We demonstrate that solute carrier family 2, member 2 (also known as GLUT2),

104 requency (MAF) = 25-44%; P < 3 x 10(-14)) of solute carrier family 2, member 9 (SLC2A9) and rs4148145

105 have consistently identified associations of solute carrier family 2, member 9 (SLC2A9), polymorphism

106 that extracellular phosphate uptake through solute carrier family 20 (phosphate transporter), member

107 Solute carrier family 20 member 2 (SLC20A2) and xenotrop

108 ysophosphatidylcholine acetyl-transferase 3, solute carrier family 22 member 16, glucose 6-phosphate

109 C, we studied LCN2 and its specific receptor solute carrier family 22 member 17 (SLC22A17) in human p

110 sing a single nucleotide polymorphism in the solute carrier family 23 member 1 (SLC23A1) gene (rs3397

111 reated mice deficient in the mouse ortholog (solute carrier family 23 member 1 or Slc23a1) of a rat a

112 Solute carrier family 24, member 4 (SLC24A4), is a Na(+)

113 The human genome encodes 53 members of the solute carrier family 25 (SLC25), also called the mitoch

114 The human genome encodes 53 members of the solute carrier family 25 (SLC25), also called the mitoch

115 Members of the mitochondrial carrier family [solute carrier family 25 (SLC25)] transport nucleotides,

116 purinergic receptor, P2RX4, to initiate the solute carrier family 25 member 11 (SLC25A11)-dependent

117 mitochondrial pyruvate carrier 1 (Mpc1), and solute carrier family 25 member 19 (Slc25a19)] involved

118 In mice, the gene encoding Mfrn1, solute carrier family 25 member 37 (Slc25a37), is highly

119 GSH is transported into mitochondria via the solute carrier family 25 member 39 (SLC25A39) transporte

120 he mitochondrial fusion-fission-related gene solute carrier family 25 member 46 (Slc25a46) and treate

121 In particular, our analysis identified solute carrier family 25 member 48 (SLC25A48) as a genet

122 nemia (CSA) is due to mutations in SLC25A38 (solute carrier family 25 member A38), which supplies mit

123 growth factor receptor (EGFR), mitochondrial solute carrier family 25A37 (SLC25A37), and import inner

124 ic stress or coinjection of oocytes with the solute carrier family 26 (anion exchanger)-member 9 (SLC

125 ansmembrane conductance regulator (CFTR) and solute carrier family 26 (SLC26) Cl(-)/HCO3(-) exchanger

126 We detected biallelic mutations in SLC26A1 (solute carrier family 26 member 1) in two unrelated indi

127 ory bowel diseases has reduced expression of solute carrier family 26 member 3 (SLC26A3, also called

128 The anion-conducting transporter solute carrier family 26 member 9 (SLC26A9) is a promisi

129 ductance regulator (CFTR) anion channels and solute carrier family 26 member A6 (SLC26A6) anion excha

130 ger], mainly AE1, AE2, and AE3) and Slc26a6 (solute carrier family 26 member A6), which, in the heart

131 (NBC1) and apical Cl(-) /HCO3(-) exchanger (solute carrier family 26 member A6; SLC26A6), increasing

132 Prestin, a member of the solute carrier family 26, is expressed in the basolatera

133 mice with disruptions in genes encoding the solute carrier family 26, member 6 (Slc26a6(-/-) mice) a

134 Cl(-)/HCO(3)(-) exchange mediated by luminal solute carrier family 26, member 6 (Slc26a6) and CFTR.

135 To determine the role of the solute carrier family 26, member 9 (SLC26A9) Cl- channel

136 eceptor-gamma-DBD-interacting protein 1; and solute carrier family 27 (fatty acid transporter), membe

137 in A1, apolipoprotein A4, apolipoprotein C2, solute carrier family 27 member 2, solute carrier family

138 otein C2, solute carrier family 27 member 2, solute carrier family 27 member 4, fatty acid synthase,

139 nd the intronic variant rs885004 in SLC28A3 (solute carrier family 28 member 3) as statistically asso

140 Here we show that zebrafish solute carrier family 3 member 2 (Slc3a2) is expressed s

141 Solute carrier family 30 (SLC30A) proteins maintain cyto

142 nymous single nucleotide polymorphism in the solute carrier family 30 (zinc transporter) member eight

143 studies demonstrated that common variants of solute carrier family 30 member 8 gene (SLC30A8) increas

144 We showed that SLC30A9 (solute carrier family 30 member 9; also known as ZnT-9)

145 n-American populations, risk variants at the solute carrier family 30, member 8 (SLC30A8) locus were

146 s well as in sodium-dependent Pi transporter solute carrier family 34, member 1 (NaPi2a)-knockout (Na

147 ygous and homozygous (comp/hom) mutations in solute carrier family 34, member 3 (SLC34A3), the gene e

148 Pathogenic variants in solute carrier family 34, member 3 (SLC34A3), the gene e

149 -acetylneuraminic acid synthetase (Cmas) and solute carrier family 35 member A1 (Slc35a1), promote si

150 ty of a mouse UDP-GlcNAc transporter, murine solute carrier family 35 member A3 (mSlc35a3).

151 yrosylprotein sulfotransferase 2 (TPST2) and solute carrier family 35 member B2 (SLC35B2) function in

152 ulfate proteoglycan synthesis encoded by the solute carrier family 35 member B2 gene (SLC35B2).

153 Solute Carrier Family 35 Member C1 (SLC35C1) can transpo

154 = 1.33 x 10-9 for the meta-analysis) in the solute carrier family 35 member G1 gene (SLC35G1); and r

155 gf2 (insulin-like growth factor 2), Slc38a4 (solute carrier family 38 member 4), and Peg1 (paternally

156 SLC38A5 (solute carrier family 38 member 5), an AA transporter, s

157 4 (LPPR4) (OR, 2.30; P = 4.82 x 10(-6)) and solute carrier family 38 member 8 (SLC38A8) (OR, 3.14; P

158 the cytoplasmic tail of the human lysosomal solute carrier family 38 member 9 (SLC38A9) destabilizes

159 We studied the functions of the solute carrier family 39 member 4 (SLC39A4, also called

160 f this is a single-nucleotide variant in the Solute Carrier Family 39 Member 8 (SLC39A8) gene encodin

161 Genetic variants at the solute carrier family 39 member 8 (SLC39A8) gene locus a

162 work in our laboratory has revealed that the solute carrier family 39 member A2 (SLC39A2/ZIP2) increa

163 nine at position 391 in the zinc transporter solute carrier family 39, member 8 protein (SLC39A8 alan

164 Solute carrier family 4 (SLC4) transporters mediate the

165 that osteoclast-targeted deletion in mice of solute carrier family 4 anion exchanger member 2 (Slc4a2

166 CO(3)(-) cotransport mediated by basolateral solute carrier family 4 member 4 (NBCe1-B) and by Cl(-)/

167 ort that the bicarbonate/chloride exchanger, solute carrier family 4, anion exchanger, member 2 (SLC4

168 osis gene (Hfe)] and ferroportin [encoded by solute carrier family 40 (iron-regulated transporter), m

169 Significant downregulation of solute carrier family 43 A3 (SLC43A3), an equilibrative

170 isomerase (PPIF), solute carrier 15 (SLC15), solute carrier family 43 member 1 (SLC43A1), and solute

171 ene fusions and identified the SLC45A3-BRAF (solute carrier family 45, member 3-v-raf murine sarcoma

172 sly unrecognized role for the lipid flippase solute carrier family 47 member 1 (SLC47A1) as a regulat

173 the main proximal tubule glucose transporter solute carrier family 5 member 2 (Sglt2) in mice.

174 ed that riboflavin absorption occurs through solute carrier family 52 members (SLC52) A1, A2 and A3.

175 lymorphism of the serotonin transporter gene solute carrier family 6 (neurotransmitter transporter, s

176 rs 1 and 2 (GlyT1 and GlyT2)--members of the solute carrier family 6 (SLC6).

177 n receptor 1a) gene and STin2 in the SLC6A4 (solute carrier family 6 [neurotransmitter transporter, s

178 Solute carrier family 6 member 1 (SLC6A1) is abundantly

179 an SNP in the 3'-untranslated region of the solute carrier family 6 member 14 (SLC6A14) gene (P = 0.

180 As encoding tryptophan 2,3-dioxygenase-2 and solute carrier family 6 member 19 (also called B0AT1) we

181 the angiotensin I-converting enzyme 2 (ACE2)-solute carrier family 6 member 19 (SLC6A19) dimer.

182 ly has been believed to occur solely through solute carrier family 6 member 2 (SLC6A2) expressed on s

183 at mediate clearance of NE via expression of solute carrier family 6 member 2 (SLC6A2), an NE transpo

184 ed the functions of the creatine transporter solute carrier family 6 member 8 (SLC6A8, also called CR

185 f the human norepinephrine transporter gene [solute carrier family 6, member 2 (SLC6A2)].

186 nes (plasmacytoma expressed transcript 1 and solute carrier family 6, member 4) in the zebrafish.

187 Variations in solute carrier family 6A, member 3 (SLC6A3/DAT1), the hu

188 cysteine ligase catalytic subunit (GCLC) and solute carrier family 7 member 11 (SLC7A11).

189 te carrier family 43 member 1 (SLC43A1), and solute carrier family 7 member 11 (SLC7A11).

190 The glutamate/cystine antiporter solute carrier family 7 member 11 (SLC7A11, also called

191 In this study, solute carrier family 7 member 11 and glutathione peroxi

192 urthermore, LCN2 regulated the expression of solute carrier family 7 member 11 by interacting with th

193 AD(P)H quinone dehydrogenase 1) and SLC7A11 (solute carrier family 7 member 11), decreased the GSH/GS

194 e demonstrate that mediators of ferroptosis, solute carrier family 7 member 11, SLC3A2, and glutathio

195 Solute carrier family 7 member 2 (SLC7A2, also known as

196 Pathogenic mutations in the solute carrier family 7 member 5 (SLC7A5) gene, which en

197 We asked if SLC7A14 (solute carrier family 7 member A14), an orphan protein a

198 Solute carrier family 7, member 11 (Slc7a11) is a plasma

199 n channel subfamily M, member 4 (TRPM4), and solute carrier family 8 member B1 (SLC24A6) or mitochond

200 Three single nucleotide polymorphisms in solute carrier family 8, member 1 (SLC8A1), a sodium/cal

201 found increased expression of proximal colon solute carrier family 9 (sodium/hydrogen exchanger), mem

202 Mutations in solute carrier family 9 isoform 6 on chromosome Xq26.3 e

203 x/WD repeat-containing protein 7 (Fbxw7) and solute carrier family 9 member 3 (Slc9a3).

204 dentified numerous variants of the endosomal solute carrier family 9 member A6 (SLC9A6)/(Na(+),K(+))/

205 ntain the psoriasis candidate genes SLC9A3R (solute carrier family 9, isoform 3 regulatory factor), N

206 fied an in-frame 9 base pair deletion in the solute carrier family 9, isoform A6 (SLC9A6 gene), which

207 tathione S-transferase, Indian hedgehog, and solute carrier family genes.

208 oferrin-1 (Mfrn1; Slc25a37), a member of the solute carrier family localized in the mitochondrial inn

209 d genetic validation, we have identified the solute carrier family member SLC35F2 as a unique transpo

210 ity, which was possibly modulated by various solute carrier family members present in the entire hepa

211 Amino acid uptake by the solute carrier family of transporter proteins is critica

212 SLC3A2, a member of the solute carrier family, was identified by proteomics meth

213 are homologous members of the mitochondrial solute carrier family.

214 iled-coil-domain-containing 57 (CCDC57), and solute-carrier family 16, member 3 (SLC16A3).

215 The solute carrier gene family 26 (SLC26) encodes membrane p

216 SLC39A8 is a member of the solute carrier gene family known to import Mn, Zn, and o

217 cima-1 encodes a solute carrier in the SLC17 family of transporters that

218 ining computational modeling and cryo-EM for solute carrier ligand discovery.

219 Here we report the study of 13 human solute carrier membrane transporters using the highly ac

220 Two solute carrier (Na(+)/H(+) exchanger) genes, Nhe2 and Nh

221 ute carrier family 10 member 1 (Slc10a1) and solute carrier organic anion transporter family member (

222 cgammaRIIIA, ferritin light chain (FTL), and solute carrier organic anion transporter family member 2

223 The SLC15 family of proton-coupled solute carriers PepT1 and PepT2 play a central role in h

224 The A. stephensi solute carriers prestinA and NDAE1 were up-regulated in

225 s inducible nitric oxide synthase (iNOS) and solute carrier protein 11A1 (SLC11A1).

226 o a distinct anion transporter family called solute carrier protein 26A, or SLC26A.

227 c properties acquired the ability to use the solute carrier protein family 35 member F2 (SLC35F2) as

228 ne bound molecular motors, identified as the solute carrier protein SLC26a5, that drive somatic motil

229 MFSD1 is a lysosomal membrane-bound solute carrier protein with no previously described func

230 Solute carrier proteins (SLCs) are pivotal for maintaini

231 is a member of a very interesting family of solute carrier proteins (SLCs), some of which have been

232 bal sialome and proximal proteins, including solute carrier proteins that regulate metabolite and ion

233 Increased expression of additional solute carrier proteins, including Slc5a12 (>10-fold) we

234 tokines, and several proteasome subunits and solute carrier proteins, whereas it downregulated antiap

235 SLC44A2, a member of the solute carrier series 44 (SLC44) family, remains underch

236 In general, SLC26 solute carriers serve to transport a variety of anions a

237 ate efflux transporter Bor1, a member of the solute carrier (SLC) 4 transporter family with homology

238 disease, and transport studies suggest that solute carrier (SLC) and ATP binding cassette (ABC) mult

239 are affected, including those controlled by solute carrier (SLC) and ATP-binding cassette (ABC) tran

240 ingly, prestin is a member of a gene family, solute carrier (SLC) family 26, that encodes anion trans

241 Solute carrier (Slc) family 26A encodes different anion

242 ing neuro-glial communication, including the solute carrier (Slc) gene family.

243 Solute carrier (SLC) genes encode the largest membrane t

244 cy, <5%) and by variants in the proximity of solute carrier (SLC) genes.

245 A plasma membrane transporter, the solute carrier (SLC) human multidrug and toxin extrusion

246 multiple amino acids and their transporters, solute carrier (SLC) members.

247 With more than 400 members, the solute carrier (SLC) membrane transport proteins are the

248 Solute carrier (SLC) membrane transport proteins control

249 A number of solute carrier (SLC) proteins are subject to changes in

250 Solute carrier (SLC) proteins play critical roles in mai

251 iptionally altered the genes that encode the solute carrier (SLC) proteins SLC12A2 and SLC12A4.

252 Orphan solute carrier (SLC) represents a group of membrane tran

253 The Solute Carrier (SLC) superfamily of integral membrane pr

254 showed that hOAT2 (SLC22A7), a member of the solute carrier (SLC) superfamily, was a facilitative tra

255 roup of membrane proteins that belong to the solute carrier (SLC) superfamily.

256 between CFTR, epithelium sodium channel, and solute carrier (SLC) transporter family membrane protein

257 OATP2B1, a member of the solute carrier (SLC) transporter family, is an important

258 tinosin is a member of the PQ-loop family of solute carrier (SLC) transporters and uses the proton gr

259 Solute carrier (SLC) transporters are promising drug tar

260 n to develop prodrug molecules, which hijack solute carrier (SLC) transporters for active transport i

261 There are over 420 human solute carrier (SLC) transporters from 65 families that

262 of this locus, the role of SLC28A3 and other solute carrier (SLC) transporters in anthracycline-induc

263 MCT8 and OATP1C1, two solute carrier (SLC) transporters, mediate the passage o

264 Solute carriers (SLC) and ABC transporters represented a

265 Solute carriers (SLC) are membrane proteins that facilit

266 Nearly half of these belong to the solute carriers (SLC) supergroup, the largest class of m

267 TASL is an immune adaptor that binds to the solute carrier SLC15A4 and facilitates activation of the

268 Two proteins from the solute carrier SLC19A gene family have been identified a

269 ous studies identified several isoforms of a solute carrier Slc26a6 to be highly expressed in cardiom

270 stolic BP and the previously uncharacterized solute carrier SLC35F3.

271 proton-coupled amino acid transporter 1), or solute carrier SLC36A1, represents the imino acid carrie

272 High affinity transporters in the solute carrier SLC6A family function in removing monoami

273 periments were designed to determine whether solute carrier SLC6A14 is the molecular correlate of the

274 ction variants associating with SCr in three solute carriers (SLC6A19, SLC25A45 and SLC47A1) and two

275 owing association with SNP rs13120371 in the solute carrier SLC7A11, previously implicated in chemore

276 Solute carrier (SLCs) transporters mediate the transport

277 ATP-binding cassette (ABC) transporters and solute carriers (SLCs), have been identified in platelet

278 Solute carriers--solute carrier 25A23 (SLC25A23), SLC25A

279 Solute carrier spinster homolog 2 (SPNS2), one of only f

280 These proteins comprise several solute carriers, such as the ATP/ADP antiporter nucleoti

281 to significant changes in the expression of solute carriers, such as the urea transporters encoded b

282 The SLC26/SulP (solute carrier/sulphate transporter) proteins are a ubiq

283 10 human integral membrane proteins from the solute carrier superfamily.

284 is the Slc39a8 gene encoding a member of the solute-carrier superfamily.

285 By structural homology to other solute carriers, TMD2 may form part of the PCFT substrat

286 ce has highlighted the importance of various solute carriers to the toxicity of anticancer drugs, the

287 unique patterns along the renal tubule were solute carriers, transcription factors, or G protein-cou

288 The solute carrier transmembrane protein prestin (SLC26A5) d

289 ke function has not been demonstrated by any solute carrier transport system identified at the molecu

290 Here, we show that the solute carrier transporter 7a5 (SLC7A5), a large neutral

291 id transporter 1 (LAT1), which is encoded by solute carrier transporter 7a5 (Slc7a5), plays a crucial

292 ycin complex 1 gene signature, modifying the solute carrier transporter repertoire, and improving bot

293 tive nucleoside transporters, members of the solute carrier transporter superfamily SLC28, use an ion

294 dies suggested that MTCH2 has evolved from a solute carrier transporter.

295 elected one candidate transporter, the SLC7 (Solute Carrier) transporter family member JhI-21 (Juveni

296 Solute carrier transporters are integral membrane protei

297 nism by the human SLC13 family and other key solute carrier transporters.

298 ated associations of the amine compound SLC (solute-carrier) transporters gene set with the learning

299 s: cell adhesion molecules, ion channels and solute carriers/transporters, ATP-binding proteins, syna

300 the evolutionarily conserved exchangers and solute carriers, which are also involved in ion transpor