ライフサイエンスコーパス: water channel

1 s nor selected point mutations activated the water channel.

2 he methyl positioned to block formation of a water channel.

3 position, which forbids the formation of the water channel.

4 r switches for the formation of a continuous water channel.

5 aquaporin-5 mRNA and protein, a type I cell water channel.

6 es against aquaporin-4 (AQP4), an astrocytic water channel.

7 pairs of active sites controlled by a unique water channel.

8 g serine phosphorylation associated with the water channel.

9 to mediate opening and closing of the buried water channel.

10 the network of hydrogen bonds in the buried water channel.

11 ransmembrane helix is eliminated to open the water channel.

12 density of reconstituted aquaporin-0 (AQP0) water channels.

13 ciency of the major ocular surface aquaporin water channels.

14 ivated MAPKAP kinases, or ion, glycerol, and water channels.

15 tibody targets astrocytic aquaporin-4 (AQP4) water channels.

16 odium counterions that are arrayed along the water channels.

17 amorphous extracellular matrix with profound water channels.

18 ansferases is determined by the formation of water channels.

19 zed by pillars of bacteria interspersed with water channels.

20 acrocolonies and show a drastic reduction in water channels.

21 mbedded in matrix, which was interlaced with water channels.

22 large pillars of bacteria interspersed with water channels.

23 ad a diffuse matrix interlaced with multiple water channels.

24 Chemistry for his discovery of the aquaporin water channels.

25 belongs to the growing list of NH3-permeable water channels.

26 ions and small molecules, can also behave as water channels.

27 ps lining the water channels than within the water channels.

28 eled by downregulation of aquaporin-2 (AQP2) water channels.

29 ironmental regulation and involves aquaporin water channels.

30 NMO-IgG binds selectively to the aquaporin-4 water channel, a component of the dystroglycan protein c

31 ductance (IC50 of 14 muM), with no effect on water channel activity (at up to 200 muM).

32 demonstrated that SlPIP2s protein displayed water channel activity and facilitated water transport i

33 nd oocyte swelling assays showed that PIP2;5 water channel activity is negatively affected by SYP121-

34 d down-regulation of both the expression and water channel activity of AQP4 is likely to originate fr

35 e, we report that the post-Golgi traffic and water channel activity of PIP2;5 are regulated by the SN

36 We demonstrate that FaPIP1;1 has a high water channel activity when coexpressed as well as how P

37 In addition to a constitutive water channel activity, several studies suggest Aquapori

38 ctively inhibit the ion channel, but not the water channel, activity of AQP1.

39 n was held fixed, water molecules inside the water channel adopted the same positions as observed in

40 , we examined the role of aquaporin-4 (AQP4) water channels after experimental contusion injury in mi

41 Aquaporins (AQPs) are water channels allowing fast and passive diffusion of wa

42 The presence of a water channel allows dissociation of a proton to the sol

43 The water channel allows proton dissociation from both LSMT.

44 lts confirm that AQP1 can function as both a water channel and a gated ion channel.

45 est a novel interaction between an aquaporin water channel and intermediate filaments, an interaction

46 bonds, modifying the local architecture of a water channel and the interaction of second coordination

47 hioisatinate to a proton wire in an adjacent water channel and thus allows the proton released by the

48 f membrane transporters, including aquaporin water channels and sugar transporters, and mycorrhiza-in

49 minate in the phosphorylation of aquaporin-2 water channels and their redistribution from intracellul

50 aporins (AQPs), lens-specific AQP0 is a poor water channel, and its permeability was reported to be p

51 gulated-genes involved in energy metabolism, water channel, and muscle contraction.

52 crystal water that is part of a proton wire water channel, and this syn beta-elimination reaction is

53 AQP1 is a water channel, and under permissive conditions, a nonsel

54 omplex, lysine deprotonation through dynamic water channels, and a nucleophilic substitution (SN2) tr

55 ated with cell walls, nucleosome structures, water channels, and ion transporters and a significant u

56 The water channel appears in the presence of AdoMet (LSMT.Ly

57 The water channel appears in the presence of AdoMet, but is

58 wers the pK(a) of the Lys-NH(3)(+) entity, a water channel appears, and the proton escapes to the aqu

59 ing either the potassium channel KvAP or the water channel AQP0 to form membrane nanotubes with contr

60 responding residues in the high-permeability water channel AQP1 have additive effects and together in

61 of vesicles contain three proteins (ie, the water channel AQP1, the chloride channel CFTR, and the a

62 rotein abundance of the collecting duct (CD) water channel AQP2 decreased by 52 % (P < 0.0003) and 73

63 and Hsc70; and can directly ubiquitylate the water channel AQP2 in vitro shRNA knockdown of CHIP in C

64 In summary, these data suggest that the water channel AQP2 interacts with integrins to promote r

65 A total of 131 proteins, including the water channel AQP2, exhibited significant changes in abu

66 resulted from a mutation in the aquaporin-2 water channel (AQP2) was characterized, and the source o

67 We conclude that the water channel AQP4 confers partial protection against ce

68 , we show that GABA(A)Rs colocalize with the water channel aquaporin (AQP) 4 in prominin-1 immunoposi

69 Water channel aquaporin (AQP)-4 is expressed in Muller c

70 hereas the mobility of the curvature-neutral water channel aquaporin 0 (AQP0) is insensitive to it.

71 The water channel aquaporin 1 (AQP1) and certain Rh-family m

72 colocalization studies that OEG express the water channel aquaporin 1 (AQP1), both in vivo and in vi

73 re associated with the overexpression of the water channel aquaporin 1, which was prevented by reacti

74 ew class of MRI reporters based on the human water channel aquaporin 1.

75 e localization of the vasopressin-responsive water channel aquaporin 2 compared with wild-type mice.

76 it Barttin, the urea transporter-A1, and the water channel aquaporin 2, all of which are regulated by

77 calcium-activated potassium channel and the water channel aquaporin 2, and improved polyuria and hyp

78 odies targeting the collecting duct-specific water channel aquaporin 2, whereas autoantibodies of the

79 ve synergistic cooperation between the glial water channel aquaporin 4 (AQP4) and the transient recep

80 Water channel aquaporin 4 (AQP4) plays a key role in the

81 in water homeostasis.SIGNIFICANCE STATEMENT Water channel aquaporin 4 (AQP4) plays a key role in the

82 d by removal of the perivascular pool of the water channel aquaporin 4 (AQP4), suggesting that an eff

83 berrant antibody responses to the astrocytic water channel aquaporin 4 have been described.

84 including mislocalization of the astrocytic water channel aquaporin 4 persisted long after injury, r

85 NMO-IgG reacts with the water channel aquaporin 4.

86 The membrane water channel aquaporin 5 (AQP5) plays an important role

87 By contrast, expression of TMEM16A, the water channel aquaporin 5 (AQP5), and other regulators o

88 nducting subfamily into the Escherichia coli water channel aquaporin Z (AqpZ).

89 hannel-forming proteins in the eye lens, the water channel aquaporin-0 (AQP-0) and the connexins Cx46

90 rystallographic studies of the lens-specific water channel aquaporin-0 (AQP0) revealed atomistic view

91 Water channel aquaporin-1 (AQP1) is expressed at epithel

92 bitors of carbonic anhydrase enzymes and the water channel Aquaporin-1 for targeting this subpopulati

93 Regulation in the exosomal sorting of the water channel aquaporin-1 represents a newly described m

94 apping manner with the vasopressin-sensitive water channel aquaporin-2 (AQP-2).

95 ns interact with phosphorylated forms of the water channel aquaporin-2 (AQP2) and modulate its functi

96 The interaction between the renal water channel aquaporin-2 (AQP2) and the lysosomal traff

97 the basis of cell-specific expression of the water channel aquaporin-2 (AQP2) in the renal collecting

98 n part, by controlling the abundances of the water channel aquaporin-2 (AQP2) protein and regulatory

99 tion largely through actions to regulate the water channel aquaporin-2 in collecting duct principal c

100 Here we report that the water channel Aquaporin-3 (AQP3) can facilitate the upta

101 changes in the expression of the astrocytic water channel aquaporin-4 (AQP4) and changes in glymphat

102 Autoantibodies against astrocyte water channel aquaporin-4 (AQP4) are highly specific for

103 Autoantibodies against astrocyte water channel aquaporin-4 (AQP4) are thought to be patho

104 The shorter "M23" isoform of the glial cell water channel aquaporin-4 (AQP4) assembles into orthogon

105 (NMO-immunoglobulin [Ig]G) against astrocyte water channel aquaporin-4 (AQP4) cause complement- and c

106 The astroglial water channel aquaporin-4 (AQP4) facilitates water movem

107 The water channel aquaporin-4 (AQP4) forms supramolecular cl

108 The astrocyte water channel aquaporin-4 (AQP4) is expressed as heterot

109 evidence suggests that the Muller/glial cell water channel aquaporin-4 (AQP4) modulates K(+) channel

110 ssion and cellular localization of the brain water channel aquaporin-4 (AQP4) was investigated during

111 ic IgG autoantibodies (NMO-IgG) to astrocyte water channel aquaporin-4 (AQP4).

112 MO-immunoglobulin G [IgG]) against astrocyte water channel aquaporin-4 (AQP4).

113 nock-out of the gene encoding the astroglial water channel aquaporin-4, which is importantly involved

114 This biomarker targets the water channel aquaporin-4, which is lost in neuromyeliti

115 pathogenic autoantibodies against astrocyte water channel aquaporin-4.

116 o)/D of 2.9+/-0.3) in mice lacking the glial water channel aquaporin-4.

117 mbrane proteins, including the AVP-regulated water channel, aquaporin 2.

118 Moreover, mRNA expression of water channel, aquaporin 4 (AQP4) was increased after Dp

119 ansporter (EAAT2) and the astrocyte-specific water channel, aquaporin 4 (AQP4).

120 s, we studied the extent of a brain-specific water channel, aquaporin-4 (AQP4), using confocal and el

121 e versus transgenic mice lacking each of the water channels, aquaporin (AQP)-1, -3, and -5, normally

122 s in guard cell volume, the role of membrane water channels (aquaporins) has remained hypothetical.

123 is evidence from other species that cellular water channels, aquaporins (AQP), are central to both pr

124 re, we show that increased expression of the water channel Aquoporin-1 is responsible for the deleter

125 ilic peptide loops of the aquaporin-4 (AQP4) water channel are delivered to cytosolic and lumenal com

126 Aquaporin (AQP) water channels are expressed in high-grade tumor cells o

127 Aquaporin-1 (AQP1) water channels are expressed in the plasma membrane of d

128 Aquaporin-4 (AQP4) water channels are expressed strongly in glial cells, wh

129 Aquaporin-1 (AQP1) water channels are expressed widely in organ and tumor m

130 Aquaporin (AQP) water channels are found throughout nature and confer hi

131 g structures in a lipid bilayer, we mapped a water channel as one of the half-channels.

132 quaporins, MIP is suggested to function as a water channel, as an adhesion molecule, and is required

133 The effective size of the Nafion water channels at various hydration levels are estimated

134 orter 1 (SGLT1) and of aquaporin 1 (Aqp1), a water channel, at the attachment site.

135 A water channel between the active site and bulk water all

136 in the M state results in the formation of a water channel between the Schiff base and asp96.

137 Here, we show that AQP2 is not only a water channel but also an integrin-binding membrane prot

138 ke other aquaporins, AQP6 functions not as a water channel but as an anion-selective channel.

139 They proved that aquaporin-1 is a specific water channel by cRNA expression studies in Xenopus oocy

140 quential sites within TM2 of the aquaporin-1 water channel by in vitro translation of truncated mRNAs

141 actant mesophase which forms 2.3 nm diameter water channels by lyotropic self-assembly.

142 ave provided evidence for the involvement of water channels, called aquaporins.

143 opy (FFEM) indicates that aquaporin-4 (AQP4) water channels can assemble in cell plasma membranes in

144 and permeability changes indicate that hAQP1 water channels can transit from a high-water-permeabilit

145 The structure shows a buried water channel capable of facilitating peroxide access to

146 proton collection and timely closure of the water channel, conformational dynamics after photolysis

147 ary or inflammation-related abnormalities in water channels contribute to the exocrinopathy.

148 ed the expression of aquaporin 4, astrocytic water channels coupled to K(+) channels.

149 work revealed that aquaporin 5 expression, a water channel critical for salivary gland fluid secretio

150 l phase, in which hexagonal arrays of 3.4-nm water channels defined by lipid tubes are formed.

151 The water channel does not appear for proton dissociation fr

152 ever, this reaction does not occur because a water channel does not form to allow the proton dissocia

153 The formation of a water channel does not occur on formation of the SET7/9.

154 Teashirt controls the expression of the water channel Drip, the chloride conductance channel CLC

155 eu(25), Tyr(108), and Phe(253) The resulting water channel enables the binding/dissociation of the Na

156 Aquaporin-4 (AQP4) is the major water channel expressed at fluid-tissue barriers through

157 Aquaporin-4 (AQP4), a water channel expressed in astrocytes, plays a key role

158 Aquaporin-1 (AQP1) is a water channel expressed strongly at the ventricular-faci

159 The aquaporin 2 (AQP2) water channel, expressed in kidney collecting ducts, con

160 dditionally suggests that aquaporin-4 (AQP4) water channels facilitate convective transport through b

161 ytes, overexpression of ion transporters and water channels facilitates fluid secretion into the cyst

162 yceroporins form the subset of the aquaporin water channel family that is permeable to glycerol and c

163 facilitator GlpF, a member of the aquaporin water channel family, by molecular dynamics simulations.

164 Aquaporin (AQP) 6 belongs to the aquaporin water channel family.

165 Tetramers of aquaporin-4 (AQP4) water channels form supramolecular assemblies in cell me

166 ed for three-dimensional tower structure and water channel formation.

167 Human aquaporin 2 (AQP2) is a water channel found in the kidney collecting duct, where

168 Aquaporin-4 water channel gene deletion caused significant extracell

169 evealed a complete loss of expression of the water-channel gene Aqp2 in PKA knockout cells.

170 Agre's discovery of the first water channel has spurred a revolution in animal and pla

171 itis optica) a serum antibody to aquaporin-4 water channels has been detected.

172 e spatially heterogeneous diffusivity across water channels has never been shown to directly influenc

173 and that Aqp0b, though possibly a secondary water channel, has an unidentified function in the lens.

174 At 20 vol% water, the water channels have diameters of between 1.8 and 3.5 nm,

175 Aquaporins are known as water channels; however, an additional ion channel funct

176 ter region of the channel approaches that of water, channel hydrophilicity dominated water conduction

177 s bacopaside II selectively blocked the AQP1 water channel (IC50 18 muM) without impairing the ionic

178 lowing events occur: (i) the appearance of a water channel, (ii) a depronation of p53-Lys4-NH 3 (+) v

179 Aquaporin-4 (AQP4), the principal water channel in astrocytes, is involved in brain water

180 lon, our results uncover a potential role of water channel in blood CO2 transport and respiration.

181 rin-1 and band 3 reveals a potential role of water channel in blood CO2 transport.

182 Aquaporin-4 (AQP4), the primary water channel in glial cells of the mammalian brain, pla

183 In addition to its function as a water channel in maintaining fluid homeostasis, AQP1 als

184 at regulate the abundance of the aquaporin-2 water channel in renal collecting duct cells.

185 isoform 4 (TRPV4) and the aquaporin 4 (AQP4) water channel in retinal Muller cells.

186 There is no water channel in the absence of AdoMet.

187 on by up-regulation of aquaporin 4 (AQP4), a water channel in the brain that has been shown to positi

188 lore the role of an astrocyte-specific major water channel in the brain, aquaporin-4 (AQP4), in brain

189 Aquaporin-4 (AQP4) is the major water channel in the brain, expressed predominantly in a

190 -specific autoantibody to AQP4, the dominant water channel in the central nervous system densely expr

191 Aquaporin-4 (AQP4) is the major water channel in the CNS and is primarily expressed in a

192 ently, aquaporin-4 (AQP4), the most abundant water channel in the CNS, was identified as its target a

193 Aquaporin (AQP) 4 is the predominant water channel in the mammalian brain, abundantly express

194 Aquaporin-4 (AQP4) is the primary water channel in the mammalian brain, particularly abund

195 the enzyme, followed by attack by H2O via a water channel in the protein.

196 fiber cells, not only serves as the primary water channel in this tissue but also appears to mediate

197 A-tag at its N terminus converted Aqp0b to a water channel in Xenopus oocytes.

198 d that amiloride-inhibitable aquaporin (AQP) water channels in airway epithelia modulate airway surfa

199 Our findings support a fundamental role of water channels in cell migration, which is central to di

200 erize macrophage activation, but the role of water channels in inflammation remains unclear.

201 ggest the expression of aquaporin (AQP)-type water channels in mitochondria from liver (AQP8) and bra

202 tional studies that have identified putative water channels in Photosystem II.

203 regulated trafficking of aquaporin-2 (AQP2) water channels in renal collecting duct epithelial cells

204 ulin G (NMO-IgG) binds to aquaporin-4 (AQP4) water channels in the central nervous system leading to

205 ese residues may be in contact with putative water channels in the photosystem.

206 Our model also includes water-channel interactions that preferentially align the

207 a depronation of p53-Lys4-NH 3 (+) via this water channel into the aqueous solvent, and (iii) AdoMet

208 f the mitochondrial inner membrane through a water channel into the hydrogen bond network.

209 asma membrane assembly of aquaporin-4 (AQP4) water channels into orthogonal arrays of particles (OAPs

210 The aquaporin-1 (AQP1) water channel is a potentially important drug target, as

211 We suggest that the geometry of the water channel is an important feature for the molecular

212 lockage of spontaneous proton back-leak, the water channel is closed upon O2 binding to the second he

213 That the formation of a water channel is combined with AdoMet binding was first

214 , in Xenopus oocytes, the aquaporin-1 (AQP1) water channel is cotranslationally directed into a four

215 The lack of formation of a water channel is due to the positioning of the methyl su

216 We find that a water channel is formed to allow escape of the proton to

217 A water channel is not formed in the ground state of SET7/

218 It was found that the appearance of a water channel is required for the stepwise methylation b

219 A central water channel is separated from two outer channels beari

220 The data suggest that a water molecule in a water channel is the direct proton donor to enolpyruvate

221 The astrocytic aquaporin-4 (AQP4) water channel is the target of pathogenic antibodies in

222 estimated antimicrobial occupation in these water channels is nonlinear and jumps from approximately

223 Aquaporin-1 (AQP-1), the universal water channel, is responsible for rapid response of cell

224 nal H(II) phase, which consists of arrays of water channels, is induced by a small number of antimicr

225 ht include interactions with aquaporin (AQP) water channel isoforms, although the proposed requiremen

226 Aquaporins (AQPs) are biological water channels known for fast water transport ( approxim

227 including those induced by pathogens and the water-channel LeAqp2 gene.

228 rom approximately 1 to 3 per 4 nm of induced water channel length as the global antimicrobial concent

229 gGs) directed against the aquaporin-4 (AQP4) water channel located on astrocyte foot processes in the

230 kcal/mol) corresponded to that reported for water-channel-mediated water transport in lipid membrane

231 The detected pores had a water channel of radius 23-33 A.

232 ing to astrocytic aquaporin 4, the principal water channel of the central nervous system, is detected

233 se results suggest that Aqp0a is the primary water channel of the lens and that Aqp0b, though possibl

234 e proton-transfer kinetics in the nanoscopic water channels of Nafion fuel cell membranes at various

235 es having three-dimensionally interconnected water channels of uniform diameter, with reproducible gl

236 forms a gate that opens to form a continuous water channel only upon receptor activation.

237 probably either the open probability of the water channel, or open-channel permeability.

238 Aquaporin-1 (AQP1) is a water channel, overexpressed in cirrhosis, that promotes

239 Calculation of the unitary water channel permeability, pf, yielded similar values f

240 d environment provides a means of regulating water channel permeability.

241 horylation and activation of the aquaporin-2 water channel present in the principal cells of the coll

242 a coniferous tree which displays remarkable water channelling properties.

243 lating IgG1 antibodies against the astrocyte water channel protein aquaporin 4 (AQP4) and the evidenc

244 PDZ domain-ligand interaction involving the water channel protein aquaporin-2.

245 hogenic autoantibodies against the astrocyte water channel protein aquaporin-4 (AQP4).

246 Abs, termed NMO-IgG, against the astrocytic water channel protein aquaporin-4.

247 ciated with autoantibodies against the glial water channel protein aquaporin-4.

248 Aquaporin-4 (AQP4) is a water channel protein expressed in astrocytes throughout

249 Aquaporin-1 (AQP1) is a water channel protein expressed widely in vascular endot

250 argets aquaporin-4 (AQP4), the most abundant water channel protein in the CNS, which is highly concen

251 ract more extensively with MAL than does the water channel protein not phosphorylated at this serine.

252 The water channel protein PvTIP3;1 (alpha-TIP) is a member o

253 Induction of an astrocytic water channel protein, Aquaporin 4 (AQP4), is known to p

254 2) in the mRNA and protein expression of the water channel protein, aquaporin 4 in these mice.

255 kidney collecting duct system including the water channel protein, Aquaporin-3 and the tight junctio

256 ted an upregulation of aquaporin-4 (AQP4), a water channel protein, following brain injury.

257 epithelial cell marker aquaporin 5 (AQP5), a water channel protein.

258 ck-polymer vesicles containing the bacterial water-channel protein Aquaporin Z (AqpZ) were investigat

259 mutations were identified in AQP5, encoding water-channel protein aquaporin-5 (AQP5).

260 Aquaporins (AQPs) are water channel proteins that are essential in biological

261 Aquaporins are water channel proteins that mediate the fine-tuning of c

262 uaporins represent a family of transmembrane water channel proteins that play a major role in trans-c

263 ical roles of aquaporins (AQPs), a family of water channel proteins, in the hepatobiliary system.

264 discusses the importance of the three brain water-channel proteins (AQP1, AQP4, AQP9) in brain physi

265 Aquaporins (AQPs) are integral membrane water channels, recognized for their importance in epith

266 The aquaporins are a family of membrane water channels, some of which also transport glycerol.

267 Aquaporin-4 (AQP4) water channel-specific IgG distinguishes neuromyelitis o

268 l as in individual thicker "ropes" that span water channels, suggesting that DNA could be imparting s

269 long parallel but otherwise randomly packed water channels surrounded by partially hydrophilic side

270 luorocarbon and the acidic groups lining the water channels than within the water channels.

271 r, it was found that there is a well-defined water channel that connects the interface between the su

272 aporin-2 (AQP2) is the vasopressin-regulated water channel that controls renal water reabsorption and

273 ce lacking aquaporin-4 (AQP4), an astroglial water channel that facilitates fluid movement between ce

274 breaks this ionic lock, forming a continuous water channel that leads to P2Y1 R activation.

275 uB induces the conformational changes of the water channel that stimulate the proton collection, and

276 d to the active site for water oxidation via water channels that lead from the surface of the protein

277 ar pulsation, and is dependent on astroglial water channels that line paravascular CSF pathways.

278 This also defines the proximal (presumably water) channel that opens in CYP46A1 upon substrate bind

279 The formation, or not, of a water channel, the distance between Sdelta(AdoMet) and N

280 Without a water channel, the substrate p53-Lys4-N(Me)H is not avai

281 aquaporin 2 followed by trafficking of this water channel to the apical membrane of principal cells

282 l gene transfer of human aquaporin-1 (hAQP1) water channels to the liver of 17alpha-ethinylestradiol-

283 ose cotransporter, and aquaporin 1 (AQP1), a water channel, to the attachment site.

284 e hypertonic challenge on AQP2 (aquaporin-2) water channel trafficking.

285 Aquaporins (AQPs) are transmembrane water channels ubiquitously expressed in mammalian tissu

286 restriction, and the abundance of renal AQP2 water channels was reduced, implying that vasopressin ac

287 ut the expression of endothelial aquaporin-1 water channels was unaltered.

288 iated with disrupted polarization of ion and water channels, we hypothesized that adhesion of astrocy

289 tassium buffering is often conducted through water channels, we studied the extent of a brain-specifi

290 The pores of these water channels were found to be critically narrow in thr

291 Full-length Aqp0a is a functional water channel when expressed in Xenopus oocytes and in y

292 e distinct aquaporin subfamily contains pure water channels, whereas a second subfamily contains chan

293 mbrane has a configuration consistent with a water channel, which we propose as a common feature unde

294 key histidine residue found in the lumen of water channels, which becomes a glycine residue in aquag

295 ar dynamics simulations revealed an extended water channel with additional water molecules bridging t

296 We report artificial imidazole-quartet water channels with 2.6 A pores, similar to AQP channels

297 of ECS properties in adult mice lacking AQP4 water channels with wild-type animals and demonstrates a

298 ion films, are elongated and parallel to the water channels, with cross-sections of approximately (5

299 is confirmed by the distribution of the AQP1 water channel within endothelial membranes.

300 mental results indicate that the size of the water channel within water swollen P(AM-co-IA) hydrogel