ライフサイエンスコーパス: exporter

1 ere it functions as a metabolite and protein exporter.

2 of ferroportin, the only known cellular iron exporter.

3 y characterized, mammalian, basolateral iron exporter.

4 n detail or investigated in the MsbA lipid A exporter.

5 luding ndvA, which encodes the cyclic glucan exporter.

6 of ferroportin, the sole known cellular iron exporter.

7 nd independent of fpn1's function as an iron exporter.

8 resulting in a permanently "turned on" iron exporter.

9 ed to allow the production of this potential exporter.

10 o that caused by overproduction of the AcrEF exporter.

11 hat conferred by overproduction of the MdtEF exporter.

12 oportin (FPN), the only known mammalian iron exporter.

13 ables substrate transfer in a eukaryotic ABC exporter.

14 (WWTP) from an energy consumer to an energy exporter.

15 p PCC 6803 and named this protein Mnx for Mn exporter.

16 n a refined model of solute transport by ABC exporters.

17 d extended the X loop, which is found in ABC exporters.

18 s that Mmt1/2 function as mitochondrial iron exporters.

19 ard-open and inward-open conformation of ABC exporters.

20 for directional transport, namely PIN auxin exporters.

21 e flexible than other structurally known ABC exporters.

22 ains in the conformational transition of ABC exporters.

23 on in the same epithelium of other bile acid exporters.

24 er folds, namely large ABC importers and ABC exporters.

25 erent substrate recognition profile from the exporters.

26 h current structural models of bacterial ABC exporters.

27 rs with a high degree of similarity to lipid exporters.

28 hormone by inhibiting membrane-based steroid exporters.

29 ight on a role for broad-spectrum amino acid exporters.

30 aryotic ABC transporters, focusing on type I exporters.

31 tors, activating expression of multiple drug exporters.

32 es as previously proposed for multi-drug ABC exporters.

33 entiating heterodimeric from homodimeric ABC exporters.

34 drolysis and defined the architecture of ABC exporters, a detailed structural dynamic understanding o

35 cription studies indicate that the alcaligin exporter activity of AlcS is required to maintain approp

36 ating access models for ATP-binding cassette exporter activity suggest that ATP binding at the two cy

37 Down-regulation of either exporter affected the subcellular distribution of tRNAs.

38 FLVCR expression in cell lines suggest this exporter also impacts heme trafficking in intestine and

39 of sialin (SLC17A5), a lysosomal sialic acid exporter also recently implicated in exocytotic release

40 P1B4-type ATPase that functions as an Fe(II) exporter and aids GAS defenses against iron intoxication

41 (Arabidopsis thaliana) PHOSPHATE1 (PHO1) Pi exporter and defined the functions of its different doma

42 s reports, we show that ABCB10 is not a heme exporter and instead is required for the early mitochond

43 FrvA is a high affinity Fe(II) exporter and its induction imposes severe iron limitatio

44 paratus functions as a proton-driven protein exporter and that ATP hydrolysis is not essential for ty

45 ablish that CUA-1 is a key intestinal copper exporter and that its trafficking is regulated to mainta

46 rence in the transport mechanism between ABC exporters and ABC importers.

47 We identified key exporters and importers from the number of shipments a c

48 orters, suggesting that ATP-binding cassette exporters and importers may use similar mechanisms to ac

49 Cs), KCC2 and NKCC1, which serve as chloride exporters and importers, respectively.

50 eported high NBD fluctuations in several ABC exporters and possibly represents a fundamental differen

51 The miR122 efficiently silenced the drug exporters and the oncogenic proteins.

52 e-bound, outward-facing conformations of ABC exporters and which binds ATP.

53 tion-chloride cotransporter KCC2 (K(+)/Cl(-) exporter) and a reduced KCC2/NKCC1 (Na(+)/K(+)/Cl(-) imp

54 SR-B1 (a CE influx protein), ABCA1 (a FC exporter), and HMG CoA reductase protein/mRNA levels wer

55 porter), a short yeast MRP (Yor1p oligomycin exporter), and human CFTR channels.

56 plasmic cystine, as opposed to an l-cysteine exporter, and further elucidate a link between oxidative

57 of ferroportin, the presumed intestinal iron exporter, and have evaluated its potential role in regul

58 e, that we name aerE, encodes the aerobactin exporter, and LuxT is a transcriptional activator of aer

59 ore synthetase subunits, a integral membrane exporter, and three genes with no obvious role in sidero

60 pH, (2) adequate expression of the key HCO3- exporter, anion exchanger 2 (AE2), and (3) an intact cho

61 Moreover, the discovery that potassium exporters are c-di-AMP targets indicates that this secon

62 ABC exporters are present both in prokaryotes and eukaryotes

63 Main virtual water exporters are the South and Central agrarian regions: An

64 Multidrug ATP binding cassette (ABC) exporters are ubiquitous ABC transporters that extrude c

65 e regulator (CFTR) (ABCC7), unique among ABC exporters as an ion channel, regulates ion and fluid tra

66 and express lower levels of the cholesterol exporter ATP-binding cassette transporter A1 (ABCA1) in

67 dium-dependent bile acid transporter) and an exporter (ATP-binding cassette subfamily C member 3) wer

68 copper transporter 1) but also by the copper exporter ATP7A (Menkes ATPase), whose function is achiev

69 BC transporter, get translocated through the exporter by following its large-scale alternating access

70 on and appear to downregulate the K(+)-Cl(-) exporter channel KCC2 following peripheral nerve damage,

71 BMY, which is mediated by binding to nuclear exporter chromosome region maintenance 1 and further enr

72 P binding cassette (ABC) transporters of the exporter class harness the energy of ATP hydrolysis in t

73 Deletion of the S Typhimurium copper exporters, CopA and GolT, was found to decrease infectio

74 centrated orange juice and, unlike the other exporter countries, the domestic consumption is mainly b

75 the K(+)/H(+) antiporter KhtT, the potassium exporter CpaA (YjbQ), the osmoprotectant transporter sub

76 Inhibition of the nuclear exporter CRM1 by leptomycin B did not interfere with NEM

77 ally similar to the Escherichia coli amyloid exporter CsgG; however, unlike CsgG, PelC does not posse

78 is via characterization of a putative copper exporter, CtpV.

79 in the margin that utilize a PIN-based auxin exporter/CUC2 transcription factor system to define regi

80 sed by inactivation of the lysosomal cystine exporter cystinosin(7-9).

81 d in S. pneumoniae by expression of the zinc exporter CzcD, whose expression is activated by the nove

82 Cystinosin, the lysosomal cystine exporter defective in cystinosis, is the founding member

83 The existence of multiple tRNA exporters, each with different tRNA preferences, may ind

84 ype, unlike that of the bona fide l-cysteine exporter eamA, parallels that of the l-cystine importer

85 further demonstrated that loss of the copper exporter encoded by copA led to decreased virulence in p

86 Deletion of either the exporter, encoded by copA, or the chaperone, encoded by

87 Ferroportin is an iron exporter essential for releasing cellular iron into circ

88 In particular, heterodimeric ABC exporters exhibit pronounced allosteric coupling between

89 ous manner compared with the mammalian eIF5A-exporter Exportin 4.

90 Brazil is the world's largest beef exporter, exporting approximately one-fifth of its produ

91 MacB is a founding member of the Macrolide Exporter family of transporters belonging to the ATP-Bin

92 encodes a member of the ATP-binding cassette exporter family.

93 also related to mRNA expression of the heme exporter feline leukemia virus subgroup C receptor 1 (be

94 on between the hormone hepcidin and the iron exporter ferroportin (Fpn) regulates plasma iron concent

95 Mutations in the iron exporter ferroportin (Fpn) result in iron overload in ma

96 The macrophage iron exporter ferroportin (FPN) was up-regulated in the Hfe(-

97 mporter DMT1 (Ireg1, MTP, DCT1) and the iron exporter ferroportin (SLC11A3, Ireg, MTP1) have been clo

98 s exhibited increased expression of the iron exporter ferroportin and decreased expression of the iro

99 tigated the influence of the macrophage iron exporter ferroportin and its ligand hepcidin on intracel

100 is is tightly regulated by the membrane iron exporter ferroportin and its regulatory peptide hormone

101 such stimuli causing degradation of the iron exporter ferroportin and reduced iron release from macro

102 fen-inducible deletion of the mammalian iron exporter ferroportin exclusively in intestinal epithelia

103 imarily from the liver, it inhibits the iron exporter ferroportin in the gut and spleen, the sites of

104 Adipocyte-specific loss of the iron exporter ferroportin resulted in iron loading and decrea

105 les, we show that low expression of the iron exporter ferroportin results in a susceptibility of thes

106 ne, hepcidin induces degradation of the iron exporter ferroportin to control iron entry into the bloo

107 tide hormone that binds to the cellular iron exporter ferroportin, causing its internalization and de

108 creasing cell surface expression of the iron exporter ferroportin, hepcidin decreases iron absorption

109 Hepcidin binds to the iron exporter ferroportin, inducing its degradation and thus

110 ates iron homeostasis by binding to the iron exporter ferroportin, inducing its internalization and d

111 It acts by binding to the iron exporter ferroportin, inducing its internalization and d

112 copper status affects expression of the iron exporter ferroportin-1 (FPN1), J774 macrophage cells wer

113 ve increased duodenal expression of the iron exporter ferroportin-1, consistent with increased uptake

114 levels by promoting degradation of the iron exporter ferroportin.

115 gered a TLR4-dependent reduction in the iron exporter ferroportin.

116 nduces the degradation of the exclusive iron exporter ferroportin.

117 on of the only known mammalian cellular iron exporter ferroportin.

118 the FPN1 gene, encoding a cell surface iron exporter [ferroportin (Fpn)], are responsible for hemoch

119 Loss of the cellular iron exporter, ferroportin, had no apparent consequences.

120 ession of iron importers as well as the iron exporter, ferroportin, suggesting an impaired ability to

121 Mice lacking the heme exporter FLVCR1 have a severe macrocytic anemia; however

122 stal structure of apo-ABCB10 shows a classic exporter fold ABC transporter structure, in an open-inwa

123 However, the predicted ABC exporter fold of IrtAB is seemingly contradictory to its

124 c has a bacterial ATP-binding cassette (ABC)-exporter fold(1).

125 eal that the protein indeed contains the ABC-exporter fold, as well as a large water-filled cavity of

126 copy not only confirms that IrtAB has an ABC exporter fold, but also reveals structural peculiarities

127 sults demonstrate that RanBP3L, as a nuclear exporter for BMP-specific Smads, plays a critical role i

128 Ts function both as maturation proteases and exporters for quorum-sensing or antimicrobial polypeptid

129 amino acids, carbohydrates, and vitamins and exporters for toxins, quorum-sensing peptides, and uncha

130 Transforming P-gp or an ABC drug exporter from an efflux transporter into a drug uptake p

131 r-stimulated trafficking of the ATP7A copper exporter from the Golgi to vesicles that partially overl

132 TmrAB is a heterodimeric ABC exporter from the thermophilic Gram-negative eubacterium

133 he resistance nodulation cell division (RND) exporters from Gram-negative bacteria.

134 been achieved in the structural analysis of exporters from the superfamily of adenosine triphosphate

135 t eukaryotic homologs [renamed FEX (fluoride exporter)] function in fluoride export.

136 a dimer in solution, implying that the MbfA exporter functions as a dimer.

137 gnition leads to specific activation of drug exporter genes and to drug resistance.

138 to derepression of the acrEF and mdtEF drug exporter genes.

139 ce by regulating the expression of multidrug exporter genes.

140 ion in the membrane component of an ABC drug exporter have been biochemically characterized.

141 ms likely that the TMDs of ABC importers and exporters have evolved different mechanisms to couple to

142 n1 (fpn1), an intestinal and macrophage iron exporter, have been identified between transmembrane hel

143 ferroportin 1 (Fpn1), the sole cellular iron exporter identified to date.

144 st molecular characterization of a polyamine exporter in animal cells and indicate that the diamine p

145 ggesting that this protein serves as an iron exporter in cells that recycle iron from senescent red b

146 tightly to TmrAB, and imply a role for this exporter in glycolipid translocation.

147 17) has been characterized as a vacuolar Fru exporter in leaves, its expression in leaves is low.

148 Ferroportin (FPN1) is the sole iron exporter in mammals, but its cell-specific function and

149 ion by ferroportin, the unique cellular iron exporter in mammals, leading to organ iron overload and

150 pass membrane protein that serves as an iron exporter in many vertebrate cell types.

151 nt genetic model to explore the role of this exporter in Mn homeostasis.

152 )/Ca(2+) exchanger 1 (NCX1), a major calcium exporter in renal epithelial cells, regulates epithelial

153 otransporter 2 (KCC2), the predominant Cl(-) exporter in the adult brain.

154 Ferroportin (Fpn) is the only known iron exporter in vertebrate cells and plays a critical role i

155 Ferroportin (Fpn) is the only known iron exporter in vertebrates.

156 We also analyzed the levels of Zn-exporters in a panel of PCa cells derived from EA and AA

157 ted the role of potential SWEET family sugar exporters in AM symbiosis in Medicago truncatula.

158 egarded as a model system for asymmetric ABC exporters in general, and for TAP in particular.

159 ains (CLD) in substrate recruitment in toxin exporters in Gram-negative bacteria.

160 urther explored the expression profile of Zn-exporters in PCa using Oncomine database.

161 Our study provides an insight regarding Zn-exporters in PCa, which may open new avenues for future

162 highlight the unexpected flexibility of ABC exporters in the resting state and underline the power o

163 United States is one of the largest soybean exporters in the world.

164 xpression is in contrast to many other toxin exporters in yeast, and this, along with the fact that t

165 erroportin-1 (Fpn1), the major cellular iron exporter, in mouse and human cells.

166 In addition to known exporters, in BGCs we found many importer-specific trans

167 Current alternating access models for ABC exporters including the multidrug and Lipid A transporte

168 tructures of three full-length ABC multidrug exporters (including MsbA) have been published recently

169 n by sequence analysis to be also present in exporters, including MDR1.

170 We find that all of the newly identified exporters indeed fall into one of the two above-mentione

171 They have developed a large subfamily of ABC exporters involved in pleiotropic drug resistance (PDR)

172 It is concluded that the cGMP exporter is distinct from MRP1 and has properties simila

173 of ZntR rises, and transcription of the zntA exporter is increased.

174 Elevated expression of the ATP7A Cu exporter is known to confer copper tolerance, however, t

175 ose that the motif present in DrrB and other exporters is actually a modified version of the EAA moti

176 P1, the duodenal enterocyte basolateral iron exporter, is also expressed in the cells of the reticulo

177 transport mechanism, especially of human ABC exporters, is scarce.

178 y member Los1 (Exportin-t) has been the only exporter known to execute nuclear export of newly transc

179 g the Mn importer, and mntE, encoding the Mn exporter, lead to Mn sensitivity during aerobiosis.

180 In addition to auxin exporters, leaves also express auxin importers, notably

181 ce ferroportin, the only known cellular iron exporter, limit the intracellular growth of these bacter

182 rm1 and Mex67, but not by the canonical tRNA exporters Los1 or Msn5.

183 because it is essential, but the known tRNA exporters (Los1 [exportin-t] and Msn5 [exportin-5]) are

184 nction, yet the one known yeast tRNA nuclear exporter, Los1, is nonessential.

185 Transnational exporters market fruit of the Cavendish cultivars, which

186 s secreted by the ATP-binding cassette (ABC) exporter McjD, which ensures self-immunity of the produc

187 antially increased abundance) or the maltose exporter MEX1 (substantially decreased abundance).

188 bundle interactions in ATP-binding cassette exporters might offer a potent strategy to alter their t

189 pneumoniae, the Mn-specific importer PsaBCA, exporter MntE, and transcriptional regulator PsaR establ

190 ies on the homodimeric multidrug/lipid A ABC exporter MsbA from Escherichia coli, we performed cystei

191 study the prototypical ATP-binding cassette exporter MsbA reconstituted in nanodiscs at 37 degrees C

192 on bacterial K+ channels, while the lipid-A exporter, MsbA, provides a template for the MDR-like cor

193 a previously unrecognized class of fluoride exporter necessary for survival in standard environmenta

194 Inhibition of the endosomal cholesterol exporter NPC1 greatly reduced sphingosine phosphorylatio

195 n-Pick type C (NPC), loss of the cholesterol exporter, NPC1, causes cholesterol accumulation within l

196 duit for surfactant export and the other the exporter of a molecule that is required for induction or

197 ese results define the function of Fpn as an exporter of both iron and Mn and highlight the potential

198 The Na(+)/Ca(2+) exchanger is the major exporter of Ca(2+) across the cell membrane of cardiomyo

199 Brazil is currently the largest exporter of concentrated orange juice and, unlike the ot

200 cluding ndvA, which encodes an ATP-dependent exporter of cyclic beta glucans.

201 rter ABCC4 is recognized as an ATP-dependent exporter of endogenous substances as well as an increasi

202 cilitator Superfamily pump EntS is the major exporter of enterobactin and the ABC transporter IroC ex

203 protein-1 (MRP1) and use this as their major exporter of GSSG.

204 largest swine population but is not a major exporter of live swine, and is not an important source o

205 and protein levels of RSB1, which encodes an exporter of long chain bases dihydrosphingosine (DHS) an

206 SUR4 were decreased, and expression of YOR1 (exporter of PHS-1P) and DPL1 (lyase that degrades DHS-1P

207 s) mobilized the exocyst complex, a powerful exporter of subcellular vesicles, to rapidly expel intra

208 drug resistance B (EmrB) family is a primary exporter of trimethoprim in Burkholderia thailandensis,

209 2 and Ypq1-3 proteins are lysosomal/vacuolar exporters of CAAs and suggest that small-molecule transp

210 ant displacer overall, while the largest net exporters of embodied environmental pressures were Polan

211 .5) health consequences; some states are net exporters of health impacts, other are net importers.

212 ntinental margins and North Atlantic are key exporters of organic carbon.

213 philic molecules, analogous to the multidrug exporters of the ABC transporter family, which pump out

214 In addition to these exporters, one importer, Pseudomonas aeruginosa Q9I147,

215 chanistic insight into how heterodimeric ABC exporters operate.

216 ng the potential for Cca1p to function as an exporter or an adapter in this tRNA nuclear export pathw

217 and can be adapted to specific cases of data exporters or data converters that need to be implemented

218 ctions can be established between countries (exporters or importers) and industries.

219 range conformational couplings, e.g., in ABC exporters or other ATP-driven molecular machines.

220 (orfs 13, 19, 32 and 33) and three putative exporters or self-resistance genes (orfs 14, 20 and 30).

221 out of the lysosome via specific catabolite exporters or via vesicular membrane trafficking.

222 low-affinity Cu transporter, a lysosomal Cu exporter, or a regulator of Ctr1 activity, but its funct

223 the body may be influenced by the multi-drug exporter P-glycoprotein.

224 t of rapamycin activity and net hydrogen ion exporters, particularly sodium bicarbonate co-transporte

225 eraction partners and identified the calcium exporter plasma membrane calcium ATPase isoform 4 (PMCA4

226 Ferroportin is an iron exporter present on the surface of absorptive enterocyte

227 rst time that targeted inhibition of nuclear exporter protein exportin 1 (XPO1) also known as chromos

228 hepatic HAX-1 deficiency increases bile salt exporter protein levels, thereby promoting enterohepatic

229 oteins by interacting with the major nuclear exporter protein, CRM1.

230 response to SL is the removal of PIN1 auxin exporter proteins from the plasma membrane in vascular-a

231 nts use a recently discovered family of F(-) exporter proteins to lower cytoplasmic F(-) levels to co

232 pport the structural homology of MurJ to MOP exporter proteins, suggesting that MurJ might function a

233 ABC exporters pump substrates across the membrane by couplin

234 s the transcription of the Co(II) and Ni(II) exporter, RcnAB, by binding to DNA as an apoprotein and

235 s the transcription of the Co(II) and Ni(II) exporter, RcnAB.

236 ough ABCC4 is an important cyclic nucleotide exporter, red blood cells from ABCC4null/PEL-negative in

237 Others were exotic and/or invasive in exporters' regions.

238 val in vivo depended on CaxP, the first Ca2+ exporter reported in bacteria.

239 deletion in mneA, which encodes a manganese exporter, restored ROS resistance of the toxR mutant.

240 stent with a role for Abc3 as vacuolar hemin exporter, results with hemin-agarose pulldown assays sho

241 esting the increased expression of some drug exporter(s) in this mutant.

242 s as an adaptor or coactivator of amino acid exporter(s).

243 ported structures of the bacterial multidrug exporter Sav1866 suggest a domain architecture in which

244 istent with the hypothesis that these copper exporters sequester the platinum drugs into subcellular

245 Only two, ZnT1 and ZnT2 (both cellular Zn exporters), show a progressive down-regulation under Zn-

246 in and the exporting activity of the nuclear exporter signal (NES) near the N terminus.

247 s study, we determined the involvement of Zn-exporters, SLC30A 1-10 in PCa, in the context of racial

248 in 2012, is caused by mutations in the metal exporter SLC30A10 and is characterized by Mn excess, dys

249 GM-CSF upregulated expression of Zn exporters, Slc30a4 and Slc30a7; the metal was shuttled a

250 ery of a selective nuclear androgen receptor exporter (SNARE) that functions to exclude AR from the n

251 In contrast to other ABC exporter structures, the nucleotide binding domains (NBD

252 In a homodimeric ABC exporter such as MsbA responsible for lipid A transport

253 al structures of bacterial and mammalian ABC exporters suggest a common alternating access mechanism

254 Similarities to ABC exporters suggest that ATG9A could be a transporter that

255 ily members Tbx3 and Brachyury with the CRM1 exporter, suggesting general significance.

256 /oligosaccharidyl-lipid/polysaccharide (MOP) exporter superfamily (TC #2.A.66) consists of four previ

257 /oligosaccharidyl-lipid/polysaccharide (MOP) exporter superfamily member MurJ.

258 Escherichia coli, MurJ, a member of the MOP exporter superfamily, has been recently shown to have li

259 drug/oligo-saccharidyl-lipid/polysaccharide) exporter superfamily, which includes flippases that tran

260 Our data also show that tRNA exporters surprisingly exhibit differential tRNA substra

261 At least eight drug exporter systems require TolC for their functions.

262 Using silencing RNAs to the bulk mRNA exporter Tap/NXF1, we observed a significantly increased

263 study provides insights into an unusual ABC exporter that evolved as highly specialized siderophore-

264 tidrug resistance protein 1 (MRP1) is an ABC exporter that extrudes a variety of chemotherapeutic age

265 eceptor 1a (FLVCR1a) is plasma membrane heme exporter that is ubiquitously expressed and controls int

266 receptor 1 (FLVCR1) is a cell membrane heme exporter that maintains the balance between heme levels

267 e establish ATP13A2 as a lysosomal polyamine exporter that shows the highest affinity for spermine am

268 resentative of the heterodimer family of ABC exporters that have an intrinsically impaired nucleotide

269 rexpression of mutant derivatives of the ABC exporters that lacked the peptides also resulted in impa

270 pose a novel mechanism for toxic peptide ABC exporters that only requires the transient opening of th

271 of the ABC transporters includes active drug exporters (the multidrug resistance proteins (MRPs)) and

272 ructure determination of substrate-bound ABC exporters, the inherently dynamic mechanism of substrate

273 nificant economic loss to both producers and exporters, the seed export industry urgently requires ra

274 t the apo structure of the heterodimeric ABC exporter TM287/288 and compare it to the previously solv

275 trate translocation in the heterodimeric ABC exporter TM287/288 from the hyperthermophilic bacterium

276 DEER measurements on the heterodimeric ABC exporter TM287/288 from Thermotoga maritima, which conta

277 hina, have shifted from being a net emission exporter to being a net emission importer.

278 al pathogens use the ESAT-6 system 1 (Esx-1) exporter to promote virulence.

279 ptogenetic tool, the light-inducible nuclear exporter, to control the subcellular location of the H2B

280 ing of ferroportin, the major mammalian iron exporter, to the surface of iron-recycling macrophages.

281 s transition, the vacuolar Suc importers and exporters TONOPLAST SUGAR TRANSPORTER2;1 and SUCROSE TRA

282 meostasis is maintained by intestinal copper exporter trafficking that is coordinated with extraintes

283 The mycobacterial Esx-1 (ESAT-6 system 1) exporter translocates virulence factors across the cytop

284 n) is the only known mammalian cellular iron exporter, understanding its localization and regulation

285 function screens reveal that ATP7A, a copper-exporter upregulated by mutant KRAS, is essential for ne

286 ATP-binding cassette exporters use the energy of ATP hydrolysis to transport

287 whereas MCT4 is a well-characterized lactate exporter, we found that both intracellular and extracell

288 Zn-exporters were found to be differentially expressed at t

289 Amino acid exporters were identified in MAGs identified as importan

290 nes were lower and levels of major bile acid exporters were similar, which therefore could not explai

291 , we demonstrated that SpoIIIE acts as a DNA exporter: When SpoIIIE was synthesized in the larger of

292 the liver cancer cells overexpress the drug exporters which cause high drug effluxion from liver can

293 both the degradation pathway and a chloride exporter, which preempted the adaptive process and direc

294 redicted that SMu0836 and SMu0837 encode ABC exporters, which we designated rcrPQ (rel competence-rel

295 mational transition of MsbA, a bacterial ABC exporter whose structure has been solved in multiple fun

296 analysis revealed several interactions of Zn-exporters with certain tumor suppressor and promoter pro

297 ite highlights the articulated design of ABC exporters, with ligands and nucleotides spanning structu

298 urreducens GSU1501, part of an ATP-dependent exporter within an operon of polysaccharide biosynthesis

299 Functional analysis of the phosphate exporter xenotropic and polytropic retrovirus receptor 1

300 nvolving both zinc importers (Zip3) and zinc exporters (ZnT-1, ZnT-2, and ZnT-4).