ライフサイエンスコーパス: -transporting

1 ity to activate the human erythrocyte Ca(2+)-transporting ATPase (Ca(2+)-ATPase) was evaluated.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

32 The organic anion-transporting polypeptides represent an important family

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

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

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

36 ide biochemical evidence that PMR1 is a Ca2+-transporting ATPase in the Golgi, a hitherto unusual loc

37 e released by 1 micromol/l ionomycin, a Ca2+-transporting ionophore.

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

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

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

41 Ca2+ channel are two major sarcolemmal Ca2+-transporting proteins of cardiac myocytes.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

63 mixtures to create amorphous organic charge-transporting glasses.

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

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

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

67 Chloride-transporting membrane proteins of the CLC family appear

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

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

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

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

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

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

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

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

76 Copper-transporting ATPase ATP7A is essential for mammalian cop

77 Copper-transporting ATPase ATP7B is essential for human copper

78 Copper-transporting ATPase ATP7B is essential for normal distri

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

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

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

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

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

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

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

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

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

88 The ATP7A gene encodes a copper-transporting ATPase.

89 s disease gene (MNK), which encodes a copper-transporting ATPase.

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

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

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

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

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

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

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

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

98 , the WD gene (ATP7B) appears to be a copper-transporting P-type ATPase.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

113 absence or dysfunction of a putative copper-transporting P-type ATPase encoded on the X chromosome.

114 tations in a gene encoding a putative copper-transporting P-type ATPase.

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

116 ns in distinct genes encoding similar copper-transporting P-type ATPases.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

148 0-60 ns makes this dyad a potential electron-transporting catalyst to carry out energy-demanding phot

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

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

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

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

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

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

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

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

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

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

159 l membrane protein expressed widely in fluid-transporting epithelia.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

215 To our knowledge, this is the first iodide-transporting molecule to have its cDNA cloned, providing

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

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

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

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

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

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

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

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

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

225 Release of iron from transferrin, the iron-transporting protein of the circulation, is a concerted

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

241 distant similarity to a subunit of the Na(+)-transporting ATPase of Enterococcus hirae.

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

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

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

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

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

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

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

249 at higher pH, it converts to a purple proton-transporting form similar to bacteriorhodopsin (lambda m

250 nd Schiff base proton acceptor in the proton-transporting high-pH form of sensory rhodopsin I similar

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

273 I of the phosphoenolpyruvate-dependent sugar-transporting phosphotransferase system (PTS) have previo

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

275 ges in cell volume were measured under sugar-transporting and nontransporting conditions.

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

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

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

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

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

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

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

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

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

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

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