ライフサイエンスコーパス: -transporting

1 ysical techniques to directly monitor Ca(2+)-transporting Abeta(25-35) pores in lipid membranes, to q

2 utant strain of CCC2, which encodes a Cu(2+)-transporting P-type ATPase, were investigated following

3 , direct evidence for its Ca(2+)- and Mn(2+)-transporting activities is still lacking.

4 ryotes and photosynthetic eukaryotes, Zn(2+)-transporting P-type ATPases of class IB (ZntA) are cruci

5 t CFTR and NBC3 reside in the same HCO(3)(-)-transporting complex with the aid of PDZ domain-containi

6 m for rat cholangiocytes and other bile acid-transporting epithelia to extrude bile acids.

7 and obligate efflux carriers in a bile acid-transporting epithelial cell.

8 In the bile acid-transporting McNtcp.24 rat hepatoma cell line, TCDC, but

9 the Escherichia coli xanthine- and uric acid-transporting homologs (XanQ and UacT, respectively) and

10 sine kinase pp60(c-src) coisolates with acid-transporting osteoclast membranes and hypothesized that

11 conclude that therapeutic DCs function as Ag-transporting cells rather than Ag-presenting cells to pr

12 Based on the migration of Ag-transporting cells (ATC) into lymphoid follicles and the

13 al cells of the caveolin-1-positive, albumin-transporting plasmalemma vesicles.

14 Solute levels are higher in sugar alcohol-transporting species, both herbs and trees, allowing the

15 in homologous to the mouse aminophospholipid-transporting ATPase Atp10c.

16 se (GS) were unaffected, whereas the ammonia-transporting RhBG protein was down-regulated by about 50

17 erentiation into bile acid-synthesizing and -transporting hepatocytes, suggesting that stellate cells

18 A subclass of bacterial CLC anion-transporting proteins, phylogenetically distant from lon

19 e salts, a process mediated by organic anion-transporting polypeptide (OATP) 1B2.

20 Human organic anion-transporting polypeptide (OATP) 2B1 (OATP-B; SLCO2B1) is

21 cellular entry of drugs is the organic anion-transporting polypeptide (OATP) 2B1.

22 l by showing that a Drosophila organic anion-transporting polypeptide (OATP), which we named Ecdysone

23 The organic anion-transporting polypeptide (OATP/Oatp) superfamily include

24 patic anion uptake transporter organic anion-transporting polypeptide 1A1 (Oatp1a1), the hepatobiliar

25 Organic anion-transporting polypeptide 1A2 (OATP1A2) (gene symbol, SLC

26 In this study, organic anion-transporting polypeptide 1A2 (OATP1A2) from chicken live

27 Organic anion-transporting polypeptide 1A2 (OATP1A2) is a drug uptake

28 The organic anion-transporting polypeptide 1b family (Oatp1b2 in rodents a

29 the hepatic transport proteins organic anion-transporting polypeptide 1B1 (OATP1B1) and 1B3 (OATP1B3)

30 transferase 2a1 (Sult2a1), and organic anion-transporting polypeptide 2 (Oatp2) in liver in mice.

31 st-stimulated platelets via an organic anion-transporting polypeptide and is retained in the cytosol

32 ce protein (ABCC/MRP), and the organic anion-transporting polypeptide protein (SLCO/OATP) families of

33 sm in the SLCO1B1 gene for the organic anion-transporting polypeptide that regulates statin uptake.

34 comparable MRP and OATP/SLCO (organic anion-transporting polypeptide) mRNA levels, and MRP1 protein

35 acid taurocholate (TC) by the organic anion-transporting polypeptide, (OATP)4A1, its effects on the

36 Organic anion-transporting polypeptides (OATP) 1B1 and 1B3 are widely

37 Organic anion-transporting polypeptides (OATPs) mediate the liver upta

38 ition are OATP1B1 and OATP1B3 (organic anion-transporting polypeptides 1B1 and 1B3, respectively).

39 The organic anion-transporting polypeptides represent an important family

40 Neutrophils are antigen-transporting cells that generate vaccinia virus (VACV)-s

41 a, termed lymphoepithelium, contains antigen-transporting M cells that lie above regions where S100+

42 -P motif that seems to be specific for auxin-transporting ABCBs, which we now refer to as ATAs.

43 Thus, auxin-transporting tissues can sustain relatively high auxin e

44 e physiological functions of individual Ca2+-transporting ATPases in vivo.

45 ns of intracellular and plasma membrane Ca2+-transporting ATPases in the control of cytosolic and org

46 hibition of sarco-endoplasmic reticulum Ca2+-transporting ATPase (SERCA; 10 microM cyclopiazonic acid

47 on and then the inactivation of the two Ca2+-transporting proteins.

48 (-7) at rs6564903) and that encoding calcium-transporting ATPase, type2C, member2 (ATP2C2, minP = 2.0

49 omologous to a human plasma membrane calcium-transporting ATPase (PMCA).

50 The calcium-transporting ATPase ATP2A2, also known as SERCA2a, is a

51 Outside the calcium-transporting epithelia, CaT1 is highly expressed in exoc

52 vered that the bacterium produces a 2-carbon-transporting folate in the form of 5,10-ethenyl-tetrahyd

53 nknown, of activating myosin VIIA as a cargo-transporting motor.

54 on of myosin VIIA is important for its cargo-transporting activity.

55 depends on the binding selectivity of cargo-transporting colloidal particles.

56 e MyRip/Rab27a complex facilitates the cargo-transporting activity of myosin VIIA, which is achieved

57 en the perovskite absorber layer and carrier-transporting materials on the performance of the solar c

58 ATP4 is thought to be a cation-transporting ATPase responsible for maintaining low intr

59 ding cassette (ABC) transporter and a cation-transporting ATPase were upregulated in GECs.

60 These results suggest that PepO, a cation-transporting ATPase, and an ABC transporter are required

61 s 2 main secretory cell types: active cation-transporting principal cells, wherein the aquaglyceropor

62 embles that of the well-characterized cation-transporting P-type ATPases, and it is unknown whether t

63 protein, which are integral membrane cation-transporting P-type ATPases involved in copper trafficki

64 which belongs to the P-type family of cation-transporting ATPases, is activated up to 10-fold by grow

65 , which belongs to the P2 subgroup of cation-transporting ATPases, is encoded by the PMA1 gene and fu

66 (WNDP) belongs to the large family of cation-transporting P-type ATPases, however, the detailed chara

67 ic compartments, but their kinship to cation-transporting P-type transporters raised doubts about whe

68 Within the large family of P-type cation-transporting ATPases, members differ in the number of C-

69 molecular strings of ions built along charge-transporting channels are shown to dramatically increase

70 exciton generation, dissociation, and charge-transporting properties of blend films are improved by u

71 mixtures to create amorphous organic charge-transporting glasses.

72 The charge-transporting activity of the Na(+),K(+)-ATPase depends o

73 To these charge-transporting channels, coaxial strings of anions or cati

74 gradient after incorporation of these charge-transporting units into the dendrons is supported by cyc

75 combining these building blocks with charge-transporting materials to give organic nanofibers with o

76 Chloride-transporting membrane proteins of the CLC family appear

77 E4 allele, a locus coding for a cholesterol-transporting lipoprotein, have a modified risk for both

78 Thus, in addition to its cholesterol-transporting properties, HDL favorably regulates endothe

79 d citrate, which predict how a human citrate-transporting DASS may interact with its bound substrate.

80 lizes with NKCC1 and KCC1/2 in diverse Cl(-)-transporting epithelia and in neurons expressing ionotro

81 The CLC family of Cl(-)-transporting proteins includes both Cl(-) channels and C

82 olate (TC) uptake and sodium taurocholate co-transporting polypeptide (Ntcp) translocation in hepatoc

83 ile acid importer, the Na(+)/taurocholate co-transporting polypeptide (Ntcp, Slc10a1).

84 tic recirculation, the Na(+)-taurocholate co-transporting polypeptide (NTCP; also known as SLC10A1) e

85 Copper-transporting ATPase ATP7A is essential for mammalian cop

86 Copper-transporting ATPase ATP7B is essential for human copper

87 Copper-transporting ATPase ATP7B is essential for normal distri

88 Copper-transporting ATPases differ from other P-type ATPases in

89 r of infancy caused by mutations in a copper-transporting adenosine triphosphatase gene, ATP7A.

90 y mutations in ATP7B, which encodes a copper-transporting adenosine triphosphatase.

91 tion mutations in the gene encoding a copper-transporting ATPase (Atp7a) on the X chromosome.

92 sed by mutations in a gene encoding a copper-transporting ATPase (Wilson's disease protein, WNDP).

93 Wilson's disease protein (WNDP) is a copper-transporting ATPase essential for normal distribution of

94 The Atp7b protein is a copper-transporting ATPase expressed predominantly in the liver

95 Human Wilson protein is a copper-transporting ATPase located in the secretory pathway pos

96 Wilson's disease protein (WNDP) is a copper-transporting ATPase regulating distribution of copper in

97 The ATP7A gene encodes a copper-transporting ATPase.

98 Wilson disease protein (ATP7B) is a copper-transporting P(1B)-type ATPase that regulates copper hom

99 The Menkes protein (MNK; ATP7A) is a copper-transporting P-type ATPase that is defective in the copp

100 PAA2 encodes a copper-transporting P-type ATPase with sequence similarity to P

101 a role in the trafficking of Atp7a, a copper-transporting P-type ATPase, and peptidylglycine alpha-am

102 The disease-associated gene encodes a copper-transporting P-type ATPase, the WND protein, the subcell

103 utations in the ATP7A gene encoding a copper-transporting P-type Atpase.

104 from the absence or dysfunction of a copper-transporting P-type ATPase.

105 sed by mutations in a gene encoding a copper-transporting P-type ATPase.

106 PAA2/HMA8 is a copper-transporting P1B -type ATPase in the thylakoid membrane,

107 ATP7B is a copper-transporting P1B-type ATPase (Cu-ATPase) with an essenti

108 dentifies an equivalent mutation in a copper-transporting P1B-type ATPase of a Wilson disease patient

109 omain of WNDP and is conserved in all copper-transporting ATPases from bacteria to mammals; however,

110 ATP7A and ATP7B are copper-transporting P(1B)-type ATPases (Cu-ATPases) that are cr

111 key catalytic properties of the ATP7B copper-transporting ATPase and provide a foundation for quantit

112 sease (WD), functional loss of ATPase copper-transporting beta (ATP7B) impairs biliary copper excreti

113 serotype 8 encoding the human ATPase copper-transporting beta polypeptide (ATP7B) complementary DNA

114 Reports of membrane-bound, copper-transporting adenosine triphosphatases (Cu-ATPases) sele

115 , alpha-catenin, tubulin alpha-chain, copper-transporting ATPase, salivary gland protein SGS-3 precur

116 of Escherichia coli lacking the CopA copper-transporting ATPase was hypersensitive to killing by RAW

117 by knockdown of ATP7A, a trans-Golgi, copper-transporting ATPase that traffics to the plasma membrane

118 erevisiae deficient in the homologous copper-transporting ATPase CCC2, suggesting that this protein m

119 n copper-dependent functions of human copper-transporting adenosine triphosphatases (Wilson's and Men

120 in the Wilson (WND) and Menkes (MNK) copper-transporting P1B-type ATPases.

121 clooctene, have mutations in the RAN1 copper-transporting P-type ATPase, once again linking copper io

122 used by mutations in a liver-specific copper-transporting ATPase, ATP7B.

123 Collectively, these data suggest that copper-transporting ATPases, CopA and ATP7A, in both bacteria a

124 The copper-transporting ATPase ATP7A has an essential role in human

125 The copper-transporting ATPase ATP7B has a dual intracellular local

126 The copper-transporting ATPase ATP7B is essential for normal distri

127 y sequence analysis suggests that the copper-transporting ATPase ATP7B or the Wilson's disease protei

128 one Atox1 directly interacts with the copper-transporting ATPases and plays a critical role in perina

129 The copper-transporting ATPases ATP7A and ATP7B play a central role

130 the function and localization of the copper-transporting ATPases in mammalian cells and provide comp

131 for copper-dependent movement of the copper-transporting ATPases within the secretory compartment an

132 of mutations in the gene encoding the copper-transporting P-type ATPase (ATP7B).

133 homeostasis in mammalian cells is the copper-transporting P-type ATPase ATP7A, which mediates copper

134 c disorder caused by mutations in the copper-transporting P-type ATPase ATP7B.

135 o encode a protein with similarity to copper-transporting P-type ATPases, including the human Menkes/

136 ed family of metallochaperones and to copper-transporting P-type ATPases.

137 olecular understanding of ion entry in Cu(+)-transporting P-type ATPases.

138 Two membrane-bound Cu-transporting ATPase enzymes, ATP7A and ATP7B, the produc

139 g heavy metal-associated (HMA) domains of Cu-transporting ATPases (Cu-ATPases), and the genes for cop

140 which the gene expressing the major digoxin-transporting P-glycoprotein has been disrupted.

141 ly confirmed the profound effect of the drug-transporting ABCB1 P-glycoprotein on the pharmacokinetic

142 Electron-transporting multi-heme cytochromes are essential to the

143 us titanium dioxide (mp-TiO2) as an electron-transporting layer.

144 bis(triphenylsilyl)dibenzofuran, an electron-transporting material synthesized to serve as a host in

145 support for dye molecules and as an electron-transporting medium.

146 (hole-transporting) and n-channel (electron-transporting) semiconductors with a single combination o

147 ully shown to function as efficient electron-transporting materials (ETMs) for perovskite solar cells

148 Pyr-hPDI3 (2) are used as efficient electron-transporting materials (ETMs) in inverted planar perovsk

149 Conductive fullerene electron-transporting layers (ETLs) are developed to facilitate t

150 and nanostructured films of a model electron-transporting polymer.

151 brication by solution processing of electron-transporting (n-channel) blend-based organic thin-film t

152 ature, solution-processable organic electron-transporting material (ETM) is successfully developed fo

153 0-60 ns makes this dyad a potential electron-transporting catalyst to carry out energy-demanding phot

154 tely 120 nm) provides a respectable electron-transporting property to yield a promising power convers

155 ted to serve as a stable and robust electron-transporting layer for high-performance perovskite solar

156 sporting P3HT, (ii) semicrystalline electron-transporting N2200, (iii) low-crystallinity hole-transpo

157 allinity, the relatively thick SnO2 electron-transporting layer ( approximately 120 nm) provides a re

158 This enhancement of the electron-transporting properties in comparison with DTP derivativ

159 unit of the phagocyte oxidase), the electron-transporting subunit of phagocytic NADPH oxidase, and co

160 ter understanding and tuning of the electron-transporting/accepting ability of the indenofluorene cor

161 ne-8-olate) (Alq(3)), a widely used electron-transporting and light-emitting material in the field of

162 (CFTR)-mediated Cl(-) secretion across fluid-transporting epithelia is regulated, in part, by modulat

163 essed in the apical plasma membrane in fluid-transporting epithelia.

164 (-)-selective ion channel expressed in fluid-transporting epithelia.

165 Thus, capaR acts in the key fluid-transporting tissue to regulate responses to desiccation

166 Many fluid-transporting epithelia possess dead-end, long, and narro

167 or decades that the tight junctions of fluid-transporting epithelia are leaky to ions, it has not bee

168 essed in the apical plasma membrane of fluid-transporting epithelia, where the plasma membrane abunda

169 el expressed in the apical membrane of fluid-transporting epithelia.

170 uid transport across the epithelium of fluid-transporting organs.

171 airways, pancreas, intestine and other fluid-transporting tissues.

172 These results suggest that the MTT formazan-transporting vesicles may be involved in cellular choles

173 GLUT5, a fructose-transporting member of the facilitative glucose transpor

174 d-fructose, demonstrating that the fructose-transporting GLUT2, GLUT5, GLUT8, and GLUT12 do not medi

175 shing water-selective homologs from glycerol-transporting homologs were not conserved in AqpM.

176 and encodes a 292-amino acid water/glycerol-transporting glycoprotein expressed in kidney, large air

177 Aquaporin-3 (AQP3) is a water/glycerol-transporting protein expressed strongly at the plasma me

178 H(+)-transporting F1F0 ATP synthase catalyzes the synthesis o

179 ATPase H(+)-transporting lysosomal accessory protein 2 (Atp6ap2), al

180 Among these, ATP6ap2 (ATPase H(+)-transporting lysosomal accessory protein 2) was identifi

181 sified into two homologous subfamilies: H(+)-transporting (found in prokaryotes, protists, and plants

182 The stoichiometry of c subunits in the H(+)-transporting F(o) rotary motor of ATP synthase is uncert

183 The multicopy subunit c of the H(+)-transporting F1Fo ATP synthase of Escherichia coli folds

184 cles to cellular membranes and with the H(+)-transporting lysosomal ATPase macrocomplex but uncovered

185 Additionally, H+-transporting two-sector ATPase, syntaxin binding protein

186 The essential H+-transporting Asp61 residue is located at a slight break

187 The multicopy c subunit of the H+-transporting ATP synthase of Escherichia coli folds thro

188 tructure of the subunit c oligomer of the H+-transporting ATP synthase of Escherichia coli has been m

189 The multicopy subunit c of the H+-transporting F1F0 ATP synthase of Escherichia coli is th

190 The H+-transporting ionophores nigericin/K+ and carbonyl cyanid

191 Asp-61, the H+-transporting residue, packs toward the center of the fou

192 The vacuolar-type H+-transporting ATPase (V-ATPase), rather than other Ca2+ t

193 A hole-transporting large-bandgap polymer (poly[bis(4-phenyl)(2

194 ype inorganic semiconductor CuGaO2 as a hole-transporting layer (HTL) in perovskite solar cells (PSCs

195 olar-cell devices without an additional hole-transporting material.

196 ave been shown to be promising host and hole-transporting materials in organic electroluminescence du

197 e relying on junctions of electron- and hole-transporting materials.

198 us TiO2 layer but in the absence of any hole-transporting material with an unprecedented photocurrent

199 ounds can be potentially of interest as hole-transporting compounds.

200 ased semiconductors work efficiently as hole-transporting materials (HTMs) for n-i-p structured PVSCs

201 ings, are benchtop stable and behave as hole-transporting or ambipolar semiconductors in organic fiel

202 reatment of the substrates, a planar Au/hole-transporting material/CH(3)NH(3)PbI(3)-xClx/substrate ce

203 PSCs) composed of organic polymer-based hole-transporting materials (HTMs) are considered to be an im

204 rmore, compatibility of both p-channel (hole-transporting) and n-channel (electron-transporting) semi

205 sporting N2200, (iii) low-crystallinity hole-transporting PBDTT-FTTE, and (iv) low-crystallinity cond

206 processed, reliable, and cost-efficient hole-transporting materials without compromising efficiency,

207 been further converted to blue-emissive hole-transporting material via a simple chemical transformati

208 mistry, is demonstrated as an excellent hole-transporting layer (HTL) for thin-film perovskite solar

209 ich likely contributes to the excellent hole-transporting properties.

210 ed to serve as an efficient dopant-free hole-transporting material (HTM) for perovskite solar cells (

211 ew class of electrochemically generated hole-transporting (p-type) polymeric semiconductors (HTPS), w

212 The concept of a neutral hole-transporting polymer is realized for the first time, by

213 e the electrical conductivity of a NiOx hole-transporting layer (HTL) to achieve high-efficiency plan

214 ementary materials such as electron- or hole-transporting molecules via self-assembly.

215 Four spirobisacridine (SBA) hole-transporting materials were synthesized and employed in

216 he entire class of organics as scalable hole-transporting materials for perovskite solar cells.

217 his series includes (i) semicrystalline hole-transporting P3HT, (ii) semicrystalline electron-transpo

218 that are used in sDSCs as a solid-state hole-transporting material.

219 t the C(8) -BTBT-rich phase acts as the hole-transporting channel, while the quantum wells in (PEA)(2

220 biphenyl (TPDSi(2)), which combines the hole-transporting efficiency of N,N-diphenyl-N,N-bis(3-methyl

221 T:PSS) has been extensively used as the hole-transporting layer (HTL) in bulk heterojunction (BHJ) so

222 uced charge transport resistance in the hole-transporting layer, as potentiated by PIL-doping.

223 ates voids or pinholes generated in the hole-transporting layer.

224 inserted between the perovskite and the hole-transporting layers to enhance the build-in field (BIF),

225 only in the visible region, keeping the hole-transporting pathways as well as the optimized film morp

226 to) conductivity and finally limits the hole-transporting property of the rear subcell.

227 Three hole-transporting materials (HTMs) were prepared following a

228 rein, a unique strategy of "transparent hole-transporting frameworks" is proposed.

229 erichia coli, a Pb(II)-, Zn(II)-, and Cd(II)-transporting ATPase, has an approximately 120 residue am

230 it assembly, it is only functional as an ion-transporting ATPase in the presence of the beta-subunit.

231 Several bacterial ion-transporting proteins or their auxiliary subunits posses

232 cause of the favourable electron- and Li-ion-transporting capacity provided by the ordered rylene dii

233 ted with HVT by promoting recruitment of ion-transporting proteins from intracellular pools to the pl

234 gain insight into the properties of the ion-transporting pathways in acinar cells that might account

235 the safety of batteries by piercing the ion-transporting separators between the cathode and anode.

236 defense mechanism mediated by conserved iron-transporting proteins transferrins.

237 receptor for transferrin, the mammalian iron-transporting glycoprotein.

238 a hereditary or acquired deficiency of iron-transporting protein function that diminishes transmembr

239 the case of a missense mutation in the iron-transporting protein divalent metal transporter 1.

240 hows higher similarity to the bacterial K(+)-transporting ATPase KdpB than to the mammalian Ca(2+)-AT

241 MP-PMP-bound form of the Escherichia coli K+-transporting Kdp-ATPase and to the Wilson disease protei

242 L-Lactate-transporting SLC16 family members play essential roles i

243 To explore the function of the lactate-transporting monocarboxylate transporters (MCTs), we use

244 s, which, in turn, control the fusion of LAT-transporting Rab27 and Rab37 vesicles and the formation

245 uble lipid carriers and membrane-bound lipid-transporting complexes, as well as the mechanisms for re

246 was added exogenously to SMG via a membrane-transporting carrier in the presence of PI 3-kinase inhi

247 ith the 4-phosphatase or disrupting membrane-transporting motors induces a decline in PM PI(4,5)P2.

248 ssesses signatures of a P1B-type heavy metal-transporting ATPase that is widely distributed from bact

249 eraction with the Cu transporter Heavy metal-transporting P-type ATPase5.

250 Transition metal-transporting P1B-type CPx ATPases play crucial roles in

251 We have identified the P-type metal-transporting ATPase ZosA (formerly YkvW) as an additiona

252 Microsphere-transporting cells were distinct from resident skin DCs,

253 that OsMTP11 predominantly functions as a Mn-transporting CDF with lower affinity for Zn.

254 The Golgi-localized Ca2+- and Mn2+-transporting ATPase Pmr1 is important for secretory path

255 prokaryotes, protists, and plants) and Na(+)-transporting (found in prokaryotes).

256 the membrane impedances under control Na(+)-transporting and amiloride-inhibited conditions.

257 tracellular Cl(-) also inhibited ENaC in Na+-transporting epithelia.

258 ducting pathways are general features of Na+-transporting systems.

259 Nitrophorins (NPs) are a class of NO-transporting and histamine-sequestering heme b proteins

260 istry, we identified two populations of NRTN-transporting DRG neurons: a major population of small, R

261 Nutrient-transporting enterocytes interact with their luminal env

262 surface-exposed, host-interactive, nutrient-transporting proteins like the SPRM1 heterodimer are pro

263 Within the intestine, the nutrient-transporting enterocytes utilize the intermicrovillar ad

264 esentative example of the MFS, is an oxalate-transporting membrane protein in Oxalobacter formigenes.

265 By coupling single-component proton-transporting optogenetic tools to ASICs to create two-co

266 This is particularly true for proton-transporting materials essential for applications in sen

267 Asp-97 is relatively high (7.1), the proton-transporting photocycle is produced only at alkaline pH.

268 The discovery of the receptor-transporting protein family has facilitated the effectiv

269 d accessory proteins, including the receptor-transporting proteins (RTPs) and Ric8b.

270 ly and composition of ribonucleic acid (RNA)-transporting particles for asymmetric messenger RNA (mRN

271 ith MS, we identified Staufen-containing RNA-transporting granules and Ro ribonucleoprotein complexes

272 As are recruited into Staufen-containing RNA-transporting granules in the presence of A3G.

273 A-protein complexes that include Staufen RNA-transporting granules.

274 nding motif of HDAg are required for the RNA-transporting activity of HDAg.

275 ding motifs was sufficient to confer the RNA-transporting activity.

276 not essential and is likely missing from RNP-transporting kinesin-1.

277 oma cells differentiate into water- and salt-transporting columnar enterocytes and therefore model no

278 tures of mouse hepatocytes and the bile-salt-transporting McNtcp.24 rat hepatoma cell line.

279 ansporter family, conserved in metazoan salt-transporting tissues, is required to control ion and flu

280 tion of dune orientation with effective sand-transporting winds suggests that large dunes may not be

281 ignificant changes in other water- or sodium-transporting proteins in the gene-modified mice.

282 In other sodium-transporting proteins, the structures that carry out the

283 ce and phosphorylation of other renal sodium-transporting proteins, including NaPi-IIa, NKCC2, and EN

284 precipitation of syntaxin 1A from the sodium-transporting epithelial cell line, A6, co-precipitates E

285 The water/small solute-transporting protein aquaporin-3 (AQP3) was found by imm

286 Furthermore, under substrate-transporting conditions, the same cotransporters serve a

287 Maize ZmSWEET4c, as opposed to its sucrose-transporting homologs, mediates transepithelial hexose t

288 Several sucrose-transporting plants have been shown to be apoplastic loa

289 (HPr) is an essential component of the sugar-transporting phosphotransferase system (PTS) in many bac

290 of apoB-100 may impair its triglyceride (TG)-transporting capability and alter its catabolism.

291 s isolated and encodes a 384-amino acid urea-transporting glycoprotein expressed in kidney, spleen, b

292 gly apparent in crops, especially for ureide-transporting woody perennials, but its physiological rol

293 reteric branch tips (UBTs) creates the urine-transporting collecting system.

294 quaporin 1 (AQP1) is a plasma membrane water-transporting protein expressed strongly in tumor microva

295 The aquaporins (AQPs) are a family of water-transporting proteins that facilitate osmotically driven

296 Aquaporin-1 (AQP1) is the principal water-transporting protein in cell plasma membranes in kidney

297 h is predicted to cause closure of the water-transporting aquaporin gate, consistent with ABA's role

298 results define for the first time the water-transporting properties of the two principal ocular surf

299 The loss of xylem water-transporting function, assessed by MRI, has been also co

300 minal domain (ZiaA(N)) of the P(1)-type zinc-transporting ATPase is especially similar to the copper