ライフサイエンスコーパス: aquaporin

1 e PM unless they are coexpressed with a PIP2 aquaporin.

2 w range of plants as a full clade within the aquaporins.

3 ling and osmolarity translated via different aquaporins.

4 or the involvement of water channels, called aquaporins.

5 cross the membranes of cells expressing both aquaporins.

6 the Tonoplast Intrinsic Protein subfamily of aquaporins.

7 Zea maize Plasma Membrane Intrinsic Protein aquaporins.

8 fferent transporters and channels, including aquaporins.

9 n of influx and efflux suggests mediation by aquaporins.

10 de metabolism, cuticle proteins, opsins, and aquaporins.

11 ility of the curvature-neutral water channel aquaporin 0 (AQP0) is insensitive to it.

12 Aquaporin 0 (AQP0), the major intrinsic protein of the e

13 esembling the phenotype reported for altered aquaporin-0 activity without detectable cytotoxic effect

14 reated lenses was preceded by an increase in aquaporin-0 serine-235 phosphorylation and levels of con

15 a tetrameric alpha-helical membrane channel (Aquaporin-0) solubilized by n-Dodecyl beta-D-Maltoside a

16 ion of expression, activity and stability of aquaporin-0, connexins, cytoskeletal proteins, and the m

17 However, abundantly expressed aquaporin 1 (AQP1) in erythrocytes is thought not to be

18 Aquaporin 1 (AQP1) is a plasma membrane water-transporti

19 the osmotic-permeability regulation of human aquaporin 1 (hAQP1) expressed in Xenopus oocyte membrane

20 , P-cadherin and beta-catenin) and function (aquaporin 1 and carbonic anhydrase IX).

21 with the overexpression of the water channel aquaporin 1, which was prevented by reactive oxygen spec

22 of Na(+)/Pi cotransporter 2, claudin-2, and aquaporin 1.

23 I reporters based on the human water channel aquaporin 1.

24 ility, sensitivity, and specificity of urine aquaporin-1 (AQP1) and perilipin-2 (PLIN2) concentration

25 Aquaporin-1 (AQP1) enables greatly enhanced water flux a

26 Aquaporin-1 (AQP1) is a major intrinsic protein that fac

27 Water channel aquaporin-1 (AQP1) is expressed at epithelial cell plasm

28 The aquaporin-1 (AQP1) water channel is a potentially import

29 sed a prototype adenoviral vector to express aquaporin-1 (AQP1), presumably in the ductal cell layer

30 proximal tubule is mediated predominantly by aquaporin-1 (AQP1).

31 The adenoviral gene transfer of human aquaporin-1 (hAQP1) water channels to the liver of 17alp

32 LIM-FRET) and identified interaction between aquaporin-1 and band 3 at a distance of 8 nm, within the

33 Adaptable interaction between aquaporin-1 and band 3 reveals a potential role of water

34 sporting capacity, which lags behind that of aquaporin-1 by 3 orders of magnitude.

35 onic anhydrase enzymes and the water channel Aquaporin-1 for targeting this subpopulation of platelet

36 imilarity between the pf values of SGLT1 and aquaporin-1 makes a transcellular pathway plausible, it

37 In particular, aquaporin-1 upregulation occurred in acquired resistance

38 synthase, but the expression of endothelial aquaporin-1 water channels was unaltered.

39 tissue in diseased rats was vascularized by aquaporin-1(+) high endothelial venules and vascular cel

40 Total aquaporin 2 (AQP2) and phospho-S256-AQP2 (pAQP2) protein

41 inase A (PKA) activation, phosphorylation of aquaporin 2 (AQP2) at serine 256, and translocation of A

42 Human aquaporin 2 (AQP2) is a water channel found in the kidne

43 ctive, alternative strategies for modulating aquaporin 2 (AQP2) trafficking have been sought.

44 ency led to a reduction in the percentage of aquaporin 2 (Aqp2)(+) principal cells (PCs) in the colle

45 KCC2), sodium chloride co-transporter (NCC), aquaporin 2 (AQP2), and EGFR abundances using western bl

46 odies against the exosomal proteins CD24 and aquaporin 2 (AQP2), conjugated to a fluorophore, we coul

47 Taking advantage of the distribution of aquaporin 2 (Aqp2), which localizes to principal cells o

48 This effect decreased the abundance of aquaporin 2 and enhanced its intracellular retention, su

49 tubular cells with ET but not PA, and urine aquaporin 2 levels were higher with ET (5.52 +/- 1.06 ng

50 T5 transcription factors, which regulate the aquaporin 2 promoter.

51 Upon immunohistochemistry, aquaporin 2 was concentrated along the apical membrane o

52 ated potassium channel and the water channel aquaporin 2, and improved polyuria and hypokalemia in mu

53 s and prevented AVP-induced translocation of aquaporin 2, further suggesting the effects in SHR-A3 re

54 g the collecting duct-specific water channel aquaporin 2, whereas autoantibodies of the two other pat

55 C-like cells selectively integrated into the aquaporin 2-positive medullary collecting duct when micr

56 d mCCDcl1 cells, and DHHC 3 was expressed in aquaporin 2-positive principal cells of mouse aldosteron

57 We observed PON-2 expression in aquaporin 2-positive principal cells of the distal nephr

58 , including the AVP-regulated water channel, aquaporin 2.

59 odium potassium chloride cotransporter 2 and aquaporin 2.

60 th phosphorylated forms of the water channel aquaporin-2 (AQP2) and modulate its function.

61 interaction between the renal water channel aquaporin-2 (AQP2) and the lysosomal trafficking regulat

62 kidney, and immunolocalized its protein and aquaporin-2 (AQP2) in CD principal cells.

63 Aquaporin-2 (AQP2) is the vasopressin-regulated water ch

64 sed diuresis paralleled by downregulation of aquaporin-2 (AQP2) water channels.

65 luminal fluid of the nephron occurs through aquaporin-2 (AQP2) water pores in principal cells that l

66 in abundance by vasopressin; interacts with aquaporin-2 (AQP2), Hsp70, and Hsc70; and can directly u

67 idiuresis and increased urine osmolality and aquaporin-2 abundance.

68 binds to the cytoplasmic PDZ-ligand motif of aquaporin-2 and accelerates its endocytosis in the absen

69 d dedifferentiation of CD cells with loss of aquaporin-2 and epithelial-mesenchymal transition-like p

70 ressin-regulated expression and insertion of aquaporin-2 channels in the luminal membrane of renal pr

71 Lithium-induced NDI is caused by aquaporin-2 downregulation and a reduced ratio of princi

72 the interaction, in association with reduced aquaporin-2 endocytosis and prolonged plasma membrane aq

73 ase in water retention, urine osmolality and aquaporin-2 expression and phosphorylation.

74 cellular vesicles and causes accumulation of aquaporin-2 in the Golgi compartment.

75 utant kidneys showed increased expression of aquaporin-2 mRNA but mislocalized expression of aquapori

76 ith type I PDZ sequences from the C-tails of aquaporin-2 or GluR1 recycled in a SAP97- and PKA-depend

77 Vasopressin-induced aquaporin-2 phosphorylation within the type I PDZ-ligand

78 aporin-2 mRNA but mislocalized expression of aquaporin-2 protein in the cytoplasm of CD cells.

79 nary concentrating ability, with a preserved aquaporin-2 response to desmopressin and an intact respo

80 -2 endocytosis and prolonged plasma membrane aquaporin-2 retention.

81 attenuated lithium-induced downregulation of aquaporin-2 through a mechanism different from that of a

82 l step in vasopressin-induced trafficking of aquaporin-2 to the apical plasma membrane.

83 The molecular mechanisms that control aquaporin-2 trafficking and the consequent water reabsor

84 ation of 4-acetyldiphyllin as a modulator of aquaporin-2 trafficking.

85 echanisms that regulate the abundance of the aquaporin-2 water channel in renal collecting duct cells

86 nts that culminate in the phosphorylation of aquaporin-2 water channels and their redistribution from

87 A-dependent phosphorylation at serine 256 of aquaporin-2, which triggers the redistribution to the pl

88 xP-flanked PKD1 gene and heterozygous for an aquaporin-2-Cre recombinase transgene to achieve collect

89 despite normal effects on the transcellular aquaporin-2-dependent pathway.

90 eraction involving the water channel protein aquaporin-2.

91 Aquaporin 3 (AQP3), a water/glycerol channel protein, ha

92 and ERKs 1/2, and decreased Src kinases and aquaporins 3 and 4.

93 Aquaporin-3 (AQP3) is a small transmembrane water/glycer

94 Aquaporin-3 (AQP3) is a water and glycerol channel expre

95 ds on entry into the cell by transit through aquaporin-3 (AQP3), a plasma membrane H2O2-conducting ch

96 Aquaporin 4 (AQ4) is not expressed in the choroid plexus

97 cooperation between the glial water channel aquaporin 4 (AQP4) and the transient receptor potential

98 Aquaporin 4 (AQP4) appeared distributed all over the cel

99 neuritis (ON), the presence of antibodies to aquaporin 4 (AQP4) has diagnostic and prognostic value.

100 d protein) and supramolecular aggregation of aquaporin 4 (AQP4) in mouse, rat, and human tissues.

101 staining showed aberrant co-localization of aquaporin 4 (AQP4) in retracted GFAP+ astrocytes with di

102 Aquaporin 4 (AQP4) is highly expressed at perivascular g

103 Aquaporin 4 (AQP4) is highly expressed in the glial cell

104 ostasis.SIGNIFICANCE STATEMENT Water channel aquaporin 4 (AQP4) plays a key role in the regulation of

105 Water channel aquaporin 4 (AQP4) plays a key role in the regulation of

106 Moreover, mRNA expression of water channel, aquaporin 4 (AQP4) was increased after Dp71 deletion.

107 receptor potential isoform 4 (TRPV4) and the aquaporin 4 (AQP4) water channel in retinal Muller cells

108 tion of an astrocytic water channel protein, Aquaporin 4 (AQP4), is known to predominantly contribute

109 2) and the astrocyte-specific water channel, aquaporin 4 (AQP4).

110 ic neuritis and myelitis and the presence of aquaporin 4 antibodies (AQP4-abs).

111 Testing for aquaporin 4 antibodies was undertaken in all suspected c

112 Aquaporin 4 antibodies were tested using 2 sensitive ass

113 Aquaporin 4 antibody (AQP4-Ab)-negative patients with lo

114 sability Status Scale score), change in anti-aquaporin 4 antibody, and safety of rituximab treatment.

115 Aquaporin 4 antibody-negative neuromyelitis optica (NMO)

116 s, an IgG autoantibody binding to astrocytic aquaporin 4, the principal water channel of the central

117 arget antigens included CASPR2, LGI1, NMDAR, aquaporin 4, Tr (DNER [delta/notch-like epidermal growth

118 METHOD: (1) Retrospective cohort of 76 aquaporin 4-antibody (AQP4-Ab)-positive patients from Ox

119 (1) Retrospective cohort of 76 aquaporin 4-antibody (AQP4-Ab)-positive patients from Ox

120 icrocystic changes in terms of age, sex, and aquaporin 4-IgG antibody status.

121 ange, 13-81 years); 84% were women; 80% were aquaporin 4-IgG seropositive; and the median Expanded Di

122 ian age of 39 years (range, 26-40 years) and aquaporin 4-positive NMO.

123 e expression of the astrocytic water channel aquaporin-4 (AQP4) and changes in glymphatic pathway fun

124 onally, loss of astrocytic laminin decreases aquaporin-4 (AQP4) and tight junction protein expression

125 However, since the discovery of NMO-IgG or aquaporin-4 (AQP4) antibody (AQP4-antibody), an NMO-spec

126 ogy compatible with targeting of sarcolemmal aquaporin-4 (AQP4) by complement-activating IgG implies

127 Perivascular localization of aquaporin-4 (AQP4) facilitates the clearance of intersti

128 The water channel aquaporin-4 (AQP4) forms supramolecular clusters whose s

129 Two major isoforms of aquaporin-4 (AQP4) have been described in human tissue.

130 The organization of aquaporin-4 (AQP4) into large plasma membrane assemblies

131 The astrocyte water channel aquaporin-4 (AQP4) is expressed as heterotetramers of M1

132 Aquaporin-4 (AQP4) is found on the basolateral plasma me

133 Using an aquaporin-4 (AQP4) M1-isoform-specific enzyme-linked imm

134 toantibodies (NMO-immunoglobulin G [IgG]) to aquaporin-4 (AQP4) on astrocytes, which initiates comple

135 ular localization of the brain water channel aquaporin-4 (AQP4) was investigated during the neurologi

136 biogenesis, hydrophilic peptide loops of the aquaporin-4 (AQP4) water channel are delivered to cytoso

137 Aquaporin-4 (AQP4) water channel-specific IgG distinguis

138 earance mechanism additionally suggests that aquaporin-4 (AQP4) water channels facilitate convective

139 s optica-immunoglobulin G (NMO-IgG) binds to aquaporin-4 (AQP4) water channels in the central nervous

140 ous studies have reported an upregulation of aquaporin-4 (AQP4), a water channel protein, following b

141 MO patients carry IgG autoantibodies against aquaporin-4 (AQP4), an astrocytic water channel.

142 Determination of antibodies to NMDAR, aquaporin-4 (AQP4), and myelin oligodendrocyte glycoprot

143 e-specific major water channel in the brain, aquaporin-4 (AQP4), in brain plasticity and learning.

144 -IgGs) against supra-molecular assemblies of aquaporin-4 (AQP4), known as orthogonal array of particl

145 Aquaporin-4 (AQP4), the primary water channel in glial c

146 Aquaporin-4 (AQP4), the principal water channel in astro

147 e discovery of serum antibodies (Ab) against aquaporin-4 (AQP4), which unequivocally differentiate NM

148 ord MRIs for ring-enhancing lesions from 284 aquaporin-4 (AQP4)-IgG seropositive patients at Mayo Cli

149 ptic neuritis, multiple sclerosis (MS), anti-aquaporin-4 (AQP4)-negative neuromyelitis optica (NMO),

150 Aquaporin-4 (AQP4)-specific T cells are expanded in neur

151 er fluxes augmented by vasopressin-regulated aquaporin-4 (AQP4).

152 pectrum disorder have autoantibodies against aquaporin-4 (AQP4-Abs), but recently, myelin-oligodendro

153 known to modulate edema formation, including aquaporin-4 and AMP-activated protein kinase and its dow

154 Patients with neuromyelitis optica who have aquaporin-4 antibodies are being identified and receivin

155 rtunistic retinal infection in patients with aquaporin-4 antibodies who are receiving immunosuppressa

156 nistic infections can occur in patients with aquaporin-4 antibodies who are receiving relatively low

157 We describe 2 patients with aquaporin-4 antibodies who were receiving conventional d

158 come, and prognostic features in relation to Aquaporin-4 antibody (AQP4-Ab) status, and compared to a

159 O according to Wingerchuk's 2006 criteria or aquaporin-4 antibody-positive NMO spectrum disorder (NMO

160 ing in the setting of neoplasia suggest that aquaporin-4 autoimmunity may in some cases have a parane

161 athogenic IgG that competes with NMO-IgG for aquaporin-4 binding, significantly reduced NMO-IgG and h

162 At a molecular level, aquaporin-4 expression decreased and the expression and

163 Placental aquaporin-4 expression is high during mid-gestation and

164 OSD whose test results were seropositive for aquaporin-4 IgG and who had a hepatic metastasis from a

165 ysed using cell-based assays for MOG-IgG and aquaporin-4 immunoglobulin G (AQP4-IgG).

166 The tumor cells expressed aquaporin-4 immunoreactivity.

167 In this study, we show that aquaporin-4 is expressed in the syncytiotrophoblast of h

168 t of cerebral edema; 2) perivascular pool of aquaporin-4 plays a critical role in water egress from b

169 yn) that demonstrate diminished perivascular aquaporin-4 pool but retain the non-endfoot and ependyma

170 od-brain barrier disruption via perivascular aquaporin-4 pool.

171 Total aquaporin-4 protein expression was not different between

172 content, blood-brain barrier disruption, and aquaporin-4 protein expression were determined at 24 hou

173 etiformis and antibody test findings against aquaporin-4 were positive, leading to a diagnosis of neu

174 totic, express glutamate receptors, and form aquaporin-4(+) perivascular endfeet.

175 tic and expressed increased levels of water (aquaporin-4) and ion (Kir4.1) channels.

176 eally injected NMO-IgG binds mouse placental aquaporin-4, activates coinjected human complement, and

177 synthetase, glutamate transporter 1 (GLT1), aquaporin-4, aldehyde dehydrogenase 1 family member L1,

178 hich recognize the immunodominant epitope of aquaporin-4, exhibit Th17 polarization and cross-react w

179 as no damage to maternal organs that express aquaporin-4, including the brain, spinal cord, kidneys,

180 Less frequent were aquaporin-4, voltage-gated Kv1 potassium channel-complex

181 e gene encoding the astroglial water channel aquaporin-4, which is importantly involved in paravascul

182 n both N-methyl-D-aspartate receptor-IgG and aquaporin-4-IgG coexisted (71%).

183 ence (on December 31, 2011) of NMO/NMOSD and aquaporin-4-IgG seroincidence and seroprevalence (sera c

184 idemiological studies are limited by lack of aquaporin-4-IgG seroprevalence assessment, absence of po

185 Aquaporin-4-IgG was measured by M1-isoform-fluorescent-a

186 ng diseases (IDD) with a specific biomarker, aquaporin-4-IgG.

187 All NMOSD patients were positive for aquaporin-4-immunoglobulin G, and all sarcoidosis cases

188 ting its effect via the perivascular pool of aquaporin-4.

189 as LGI1, N-methyl-D-aspartate receptor, and aquaporin-4.

190 against the astrocytic water channel protein aquaporin-4.

191 st, expression of TMEM16A, the water channel aquaporin 5 (AQP5), and other regulators of sweat gland

192 secretion accompanied by down-regulation of aquaporin 5 and an increase in anti-M3R autoantibodies.

193 mma markedly improved salivary secretion and aquaporin 5 expression in anti-PD-L1-treated NOD/ShiLtJ

194 The present work revealed that aquaporin 5 expression, a water channel critical for sal

195 carinic Acetylcholine receptor M3) and AQP5 (Aquaporin 5) protein expression, b) decreased saliva sec

196 fied in AQP5, encoding water-channel protein aquaporin-5 (AQP5).

197 r epithelial type I (AT1) cell-specific gene aquaporin-5 (Aqp5).

198 Aquaporin-8 (AQP8) channels facilitate the membrane tran

199 7 induces expression of the glycerol channel aquaporin 9 (AQP9) in virus-specific memory CD8+ T cells

200 aCl) triggered a rapid repression of overall aquaporin activity in both genotypes.

201 rt during salt stress conditions to modulate aquaporin activity, thereby significantly altering the p

202 The small intestine is void of aquaporins adept at facilitating vectorial water transpo

203 Here, we describe AqF026, an aquaporin agonist that is a chemical derivative of the a

204 pmental mechanisms such as stomata aperture, aquaporin and lateral root positioning.

205 bility, indicating the functional absence of aquaporins and gas channels.

206 rable with channel-forming proteins, such as aquaporins and gramicidin-A.

207 aperone-like genes or the down-regulation of aquaporins and metal transmembrane transporters that was

208 Diffusivity was unaffected by blockers of aquaporins and Rh complex (Hg(2+), p-chloromercuribenzoi

209 Proteins, such as aquaporins and Rh complex, have been proposed to facilit

210 Pyramidal neurons do not express aquaporins and thus display low inherent water permeabil

211 report the results of a multicentre study of aquaporin (AQP) 4 antibody (AQP4-Ab) assays in neuromyel

212 GABA(A)Rs colocalize with the water channel aquaporin (AQP) 4 in prominin-1 immunopositive (P(+)) pr

213 We show here that, in vitro, aquaporin (AQP) blockade or deficiency results in reduce

214 The aquaporin (AQP) family of integral membrane protein chan

215 The function of aquaporin (AQP) protein in transporting water is crucial

216 tatic field emanating from the center of the aquaporin (AQP) water and solute channel is responsible

217 e regulation might include interactions with aquaporin (AQP) water channel isoforms, although the pro

218 Aquaporin- (AQP) 3, a water and glycerol channel, plays

219 Aquaporins (AQPs) are biological water channels known fo

220 Aquaporins (AQPs) are integral membrane proteins whose f

221 Aquaporins (AQPs) are water channel proteins that are es

222 Aquaporins (AQPs) are water channels allowing fast and p

223 Aquaporins (AQPs) in the major intrinsic family of prote

224 Our understanding of the cellular role of aquaporins (AQPs) in the regulation of whole-plant hydra

225 Compared to other aquaporins (AQPs), lens-specific AQP0 is a poor water ch

226 Aquaporins are water channel proteins that mediate the f

227 milarity of water and NH3 has pointed to the aquaporins as putative NH3-permeable pores.

228 ipts associated with stress avoidance (e.g., aquaporins), as well as those involved in the prevention

229 we present the crystal structure of a yeast aquaporin at 0.88 angstrom resolution.

230 draulic conductivity can be accounted for by aquaporins but this must be integrated with anatomical c

231 The ubiquitous aquaporin channels are able to conduct water across cell

232 This suggests that the hourglass shape of aquaporins could be the result of a natural selection pr

233 transport across membranes is facilitated by aquaporins, denoted as peroxiporins.

234 f needles, where we also observed increasing aquaporin densities in the phloem and endodermis.

235 This is done by changing aquaporin density and activity in the membrane, includin

236 The regulation of aquaporin density in cell membranes is essential to cont

237 ROS-scavenging system, Heat Shock Proteins, aquaporins, expansins, and desiccation related proteins

238 r mixed populations comprising as few as 10% aquaporin-expressing cells are sufficient to produce MRI

239 ), comparable to that of other cells lacking aquaporin expression.

240 water permeability) and NHDF-Ad fibroblasts (aquaporin-facilitated water permeability).

241 revealed that tls1 encodes a protein in the aquaporin family co-orthologous to known B channel prote

242 The aquaporin family of integral membrane proteins is compos

243 unravel how FaPIP1;1, a fruit-specific PIP1 aquaporin from Fragaria x ananassa, contributes to the m

244 Accordingly, a range of aquaporins from mammals, plants, fungi, and protozoans d

245 n of plasma membrane intrinsic protein (PIP) aquaporins from the plasma membrane (PM) to intracellula

246 the identification and characterization of a aquaporin gene, MusaPIP2;6 which is involved in salt str

247 egulation of plasma membrane protein1 (PIP1) aquaporin genes.

248 7 and SlPIP2;5, were identified as candidate aquaporins genes because of highly expressed in tomato r

249 volume, the role of membrane water channels (aquaporins) has remained hypothetical.

250 asma membrane Intrinsic Protein 2;1 (PIP2;1) aquaporin have a defect in stomatal closure, specificall

251 y expressed, the role and properties of PIP1 aquaporins have therefore remained masked.

252 ta and emphasizes the central role played by aquaporins in regulating plant water relations.

253 effect on intercellular water trafficking by aquaporins in stem xylem during soil drying and recovery

254 a polarized distribution of Na+/H+ pumps and aquaporins in the cell membrane, which creates a net inf

255 OsPIP1;3 and OsPIP2;6 lines was inhibited by aquaporin inhibitors, silver nitrate and sodium azide.

256 simultaneous transcriptional repression and aquaporin internalization to modify root cell water cond

257 lipid composition we are able to direct the aquaporin into specific immiscible liquid domains in gia

258 t the individual and integrated functions of aquaporins involved in drought response remains unclear.

259 Regulation of aquaporins is a key process of living organisms to count

260 expression of the main root plasma membrane aquaporins is associated with the increase of root hydra

261 indings establish how regulation of a single aquaporin isoform in leaf veins critically determines le

262 Low aquaporin levels or mixed populations comprising as few

263 The aquaporin ligand bumetanide derivative AqB011 was the mo

264 hether the characteristic hourglass shape of aquaporins may arise from a geometrical optimum for such

265 the narrowest opening in naturally occurring aquaporins measuring approximately 3 A across, and hence

266 ansport in such cells to be dominated by the aquaporin-mediated cell-to-cell path.

267 At the whole organ level aquaporins modify water conductance and gradients at key

268 ions between specific SNARE proteins and PIP aquaporins modulate their post-Golgi trafficking and thu

269 ds for pharmaceutic development of selective aquaporin modulators.

270 , boric acid, and H2O2 Thus, we propose that aquaporins NIP4;1 and NIP4;2 are exclusive components of

271 Aqy1, which is a water transporting aquaporin of the yeast Pichia pastoris, is suggested to

272 rized NIP4;1 and NIP4;2, two pollen-specific aquaporins of Arabidopsis thaliana.

273 otrimeric G protein subunit interactions and aquaporin oligomerization, >99% of the interactions were

274 We show that aquaporin overexpression produces contrast in diffusion-

275 racting partners uncovered a plasma membrane aquaporin, PIP2;7.

276 the particular case of plant plasma membrane aquaporins (PIPs), PIP1 and PIP2 monomers interact to fo

277 tal complexes and showed that members of the aquaporin plasma membrane intrinsic protein (PIP) subfam

278 The plant aquaporin plasma membrane intrinsic proteins (PIP) subfa

279 This suggests that aquaporins play a limited role in controlling water upta

280 Aquaporins play important roles in maintaining plant wat

281 High Lpr and aquaporin protein activity were associated with peak VvP

282 ntact xylem, phloem, and parenchyma, whereby aquaporins reduce resistances along the symplastic pathw

283 n of membrane water permeability (Pf) and pH aquaporin regulation.

284 otein-protein interaction and demonstrate an aquaporin regulatory mechanism involving TSPO.

285 n: the dual asparagine-proline-alanine (NPA) aquaporin signature motif and the aromatic and arginine

286 Taken together, this study concludes that aquaporins (SlPIP2;1, SlPIP2;7 and SlPIP2;5) contribute

287 cle film swelled with membrane protein using aquaporin SoPIP2;1 as an illustration.

288 s) plasma membrane intrinsic protein (ZmPIP) aquaporin subfamily, which is divided into two sequence-

289 lasma membrane intrinsic proteins (PIPs) are aquaporins that facilitate the passive movement of water

290 sion across cell membranes is facilitated by aquaporins that provide plants with the means to rapidly

291 ion to information on cellular regulation of aquaporins, this study provides novel and complementary

292 membrane channels called tonoplast-intrinsic aquaporins (TIP-AQPs).

293 also altered, as shown by retargeting of the aquaporin TIP1g from the tonoplast membrane to the symbi

294 gulation of membrane transporters, including aquaporin water channels and sugar transporters, and myc

295 al and environmental regulation and involves aquaporin water channels.

296 elated dynamics of molecules passing through Aquaporin water transport complexes located within the i

297 HpUreI conducts water at rates equivalent to aquaporins, which might be essential for efficient trans

298 ervous system (CNS) and on the regulation of aquaporins while LXRalpha has its most marked effects on

299 hanism for intracellular sequestration of PM aquaporins without further degradation.

300 e (MscL) from Mycobacterium tuberculosis and aquaporin Z (AqpZ) and the ammonia channel (AmtB) from E