ライフサイエンスコーパス: apical membrane

1 2 translocation from storage vesicles to the apical membrane.

2 g at AREs and carrier vesicle docking at the apical membrane.

3 tween intracellular storage vesicles and the apical membrane.

4 riggers a reduction in CFTR abundance at the apical membrane.

5 recruitment of Yrt restricts the size of the apical membrane.

6 gulates the levels and asymmetry of D at the apical membrane.

7 e small GTPase Rab11a before arriving at the apical membrane.

8 al and CF donor lungs, CTSB localized to the apical membrane.

9 teins that would normally be targeted to the apical membrane.

10 , as well as physically anchoring Dia to the apical membrane.

11 basal to apical, forming the midbody at the apical membrane.

12 lular distribution of the channel toward the apical membrane.

13 umber, shape and positioning relative to the apical membrane.

14 of vesicles from their storage areas to the apical membrane.

15 cient and distinct restriction of Dia to the apical membrane.

16 zrin to continually bias its function to the apical membrane.

17 e migrating centrosome onto the lateral then apical membrane.

18 he rate at which ENaC was retrieved from the apical membrane.

19 ial for bile acid-dependent bile flow at the apical membrane.

20 ed JAM-A moved to the brain endothelial cell apical membrane.

21 was required to restrict its function to the apical membrane.

22 PDZK1 in the stabilization of NaPi-2c in the apical membrane.

23 GPR91 was expressed in RPE but only in the apical membrane.

24 alization using a specific marker of the RPE apical membrane.

25 ferential regulation and/or stability in the apical membrane.

26 rols, despite its normal localization to the apical membrane.

27 imulates the NKCC1 co-transporter at the CPE apical membrane.

28 storage pool than the lipid entering via the apical membrane.

29 l cyclase, colocalized with CFTR in the cell apical membrane.

30 rting or in maintaining the stability of the apical membrane.

31 thus recruiting the accumulated ENaC to the apical membrane.

32 possibly internalization of NaPi-2a from the apical membrane.

33 QP2), and increased abundance of AQP2 on the apical membrane.

34 the basolateral side and secrete them at the apical membrane.

35 icking pathways, including polar delivery to apical membrane.

36 xpressed at the basolateral membrane and the apical membrane.

37 KC/Cdc42 polarity complex to localize to the apical membrane.

38 cells and MTOC function is reassigned to the apical membrane.

39 ) transport by altering ENaC activity in the apical membrane.

40 ses the basolateral membrane en route to the apical membrane.

41 tabolism and normal GLUT5 trafficking to the apical membrane.

42 ches develop bubble-like cysts with enlarged apical membranes.

43 cell retained tight junctions and segregated apical membranes.

44 lateral membranes and the basolateral to the apical membranes.

45 trols anion secretion across epithelial cell apical membranes.

46 ional claudin molecules such as claudin-4 at apical membranes.

47 stability and confinement of the channel to apical membranes.

48 ed in transporting secretory vesicles to the apical membrane [5].

49 tion is part of a process that controls AQP2 apical membrane abundance in a vasopressin-dependent man

50 A2B purinergic P1 receptors induced V-ATPase apical membrane accumulation in medullary A-ICs but not

51 pididymal clear cells, cAMP induces V-ATPase apical membrane accumulation, which is linked to proton

52 Apical membrane Ag 1 (AMA1) is one of the leading candid

53 t is, merozoite surface protein 1 (MSP1) and apical membrane Ag 1 (AMA1).

54 nogenicity of vaccines against P. falciparum apical membrane Ag 1 in rhesus macaques (Macaca mulatta)

55 not affect the immunogenicity of the AdCh63 apical membrane Ag 1 vaccine.

56 the Plasmodium falciparum vaccine candidate apical membrane Ag-1 (AMA1) in HIV-infected and uninfect

57 Our simulations show how polyvalent apical membrane Ag-1 vaccination alters the selection pr

58 cation of the proton pump, HK-ATPase, to the apical membrane along with activation of apical chloride

59 tionally, Moe mutant cells lost Crb from the apical membrane and accumulated excess Crb at the MZ, su

60 s open in response to ATP stimulation at the apical membrane and allow K(+) flux to the airway surfac

61 of the sub-cellular components including the apical membrane and cytoplasm of the cell at the tissue

62 Internalized apical membrane and fluid were initially found in ZO-1-p

63 e stiffness of the intact, living urothelial apical membrane and found it to be highly deformable, ev

64 els of membrane raft-based biogenesis of the apical membrane and IFV envelope.

65 late the trafficking of proteins between the apical membrane and intracellular vesicles.

66 sms leading to myosin II accumulation at the apical membrane and its exclusion from other membranes a

67 rotein Ve-cadherin disrupts formation of the apical membrane and lumen in a cell-autonomous manner.

68 portant signals for ion movement through the apical membrane and regulation of water secretion.

69 acidified resorption compartment between the apical membrane and the bone surface to solubilize hydro

70 nslocation to the renal proximal tubule cell apical membrane and the internalization of Na(+)-H(+) ex

71 that Cad99C serves as a link between the SG apical membrane and the secreted apical ECM component(s)

72 ecting sequestration of GUCY2C to intestinal apical membranes and segregation of mucosal and systemic

73 The active form of mDia1 localized to the apical membrane, and introduction of an active form of m

74 and displaced from M025alpha and NCC at the apical membrane, and redistributes to dense punctate str

75 he expression of FLVCR was restricted to the apical membrane, and the expression of BCRP and PCFT was

76 the host Madin-Darby canine kidney cell, its apical membrane, and the IFV budding from it.

77 Both receptors are located in A-IC apical membranes, and adenosine injection increased urin

78 centrosomes and nuclei move near the future apical membranes, and the postmitotic centrosomes lose a

79 CFTR is an apical membrane anion channel that regulates fluid homeo

80 host outer membrane and serve as ligands for apical membrane antigen (AMA) family surface proteins di

81 Higher levels of antibodies to apical membrane antigen 1 (AMA-1), but to none of the ot

82 iparum vaccine candidate antigens, including apical membrane antigen 1 (AMA-1), circumsporozoite prot

83 e that is based on the 3D7 clone sequence of apical membrane antigen 1 (AMA1) and formulated in Adjuv

84 A), a blood-stage candidate vaccine based on apical membrane antigen 1 (AMA1) from the 3D7 strain of

85 Apical membrane antigen 1 (AMA1) is a conserved transmem

86 Apical membrane antigen 1 (AMA1) is a leading malarial v

87 Apical membrane antigen 1 (AMA1) is a leading vaccine ca

88 The apical membrane antigen 1 (AMA1) protein was believed to

89 at includes a type I membrane protein called apical membrane antigen 1 (AMA1) to invade host cells.

90 ), erythrocyte binding antigen 175 (EBA175), apical membrane antigen 1 (AMA1), and parasite lysate.

91 rotein 2 (RON2) to the hydrophobic groove of apical membrane antigen 1 (AMA1), triggering junction fo

92 e P. falciparum blood-stage malaria antigen; apical membrane antigen 1 (AMA1).

93 entral player in this process is the protein apical membrane antigen 1 (AMA1).

94 orts, and that changes in antibody levels to Apical Membrane Antigen 1 suggested a decrease in transm

95 morphology (PhIL1), and host cell invasion (apical membrane antigen 1, AMA1).

96 e antigens from the P. falciparum 3D7 clone (apical membrane antigen 1, AMA1-3D7; merozoite surface p

97 phosphorylate downstream substrates such as apical membrane antigen 1.

98 CR), and a malaria surface antigen domain of apical membrane antigen AMA-1.

99 umsporozoite protein, liver-stage antigen-1, apical membrane antigen-1, and merozoite surface protein

100 e based on the highly polymorphic malaria Ag apical membrane antigen-1.

101 umsporozoite protein, liver-stage antigen 1, apical-membrane antigen 1 (AMA-1), and merozoite surface

102 es in both phosphorylation of serine-256 and apical membrane AQP2 trafficking.

103 Steady-state surface NKCC2 levels in the apical membrane are maintained by a balance between exoc

104 ntration and transmit the information to the apical membrane are not clear.

105 initial vascular cords of endothelial cells, apical membranes are established and become cleared of c

106 Drosophila ovarian follicle cell epithelium, apical membranes are specified by Crumbs (Crb), Stardust

107 that centrosomes are critical to specify the apical membrane as the new MTOC.

108 DZK1 can both enhance the scaffolding at the apical membrane as well as augment EBP50's role in micro

109 s on trafficking to, and insertion into, the apical membrane, as well as on phosphorylation of conser

110 ppo kinase cascade, in turn, is regulated by apical membrane-associated proteins such as the FERM dom

111 Cad99C or SAS causes a dramatic increase in apical membrane at the expense of other membrane domains

112 ivation increased renal proximal tubule cell apical membrane AT2R protein (P<0.001) without changing

113 The intestines display villus fusion, apical membrane blebs, and disrupted microvilli.

114 arity by recruiting polarity proteins to the apical membrane, but how a change in protein localizatio

115 tightly packed arrays of microvilli in their apical membrane, but the fate of these microvilli is rel

116 ed that Crb did not constantly reside on the apical membrane, but was actively recycled.

117 ab27b and YFP-Rab27bQ78L translocated to the apical membrane, but YFPR-ab27bN133I did not.

118 l 3,4,5-trisphosphate (PI(3,4,5)P(3)) in the apical membrane by stimulating PI3K.

119 Accumulation of apical membrane ceramide is necessary and sufficient to

120 pressin-stimulated ENaC open probability and apical membrane channel number.

121 4 revealed the presence of subdomains on the apical membrane characterized by extensive exocytosis.

122 otease-activated receptor 2 activates airway apical membrane chloride permeability and increases cili

123 low-level nitric oxide production, increases apical membrane Cl(-) permeability approximately 3-5-fol

124 t the HAT-7 cells were polarized with a high apical membrane CO2 permeability and vigorous basolatera

125 arized acini lipids were more ordered at the apical membranes compared to basal membranes, and that a

126 nal crypt enterocytes PDK1 distributes to an apical membrane compartment comprising plasma membrane a

127 ila protein Crumbs (Crb), which nucleates an apical membrane complex that functionally interacts with

128 controlling the distribution and function of apical membrane complexes, regulating the small GTPase R

129 ns and decreased protein and activity on the apical membrane, confirming that GPI-anchored Hyal2 is e

130 ll as repressing Yki by recruiting Ex to the apical membrane, Crb promotes phosphorylation-dependent

131 iet showed elevated levels of both total and apical membrane Ctr1 protein in response to transient di

132 mental studies, however, have focused on the apical membrane, despite the fact that ion transport acr

133 also known as Mpp5), a core component of the apical membrane-determining CRB complex in the nephron.

134 n the renal outer medullary K(+) channel, an apical membrane distal nephron K(+) channel that is inte

135 P transporter protein to be expressed at the apical membrane domain of polarized epithelia.

136 1(+) vesicles containing PCP proteins to the apical membrane during the initiation of planar cell pol

137 n replenish the pool of DFV by internalizing apical membrane during voiding.

138 Conversely, AS160 knockdown increased apical membrane ENaC and I(sc) under basal conditions to

139 NaC expression 2.5-fold but did not increase apical membrane ENaC or amiloride-sensitive Na current (

140 ing, increases Cdc42 mobility and results in apical membrane enlargement.

141 Aldosterone-induced increases in apical membrane epithelial sodium channel (ENaC) density

142 also degrades old cuticle at molts, promotes apical membrane expansion in larval tracheae, and promot

143 b, a selective EGFR inhibitor, enhanced AQP2 apical membrane expression in collecting duct principal

144 hydrolase virulence factor that reduces the apical membrane expression of ABC transporters such as t

145 olves lateral membrane shortening coupled to apical membrane extension.

146 in-Expanded-Kibra complex is required at the apical membrane for Hippo activity.

147 oteins are important in epithelial polarity, apical membrane formation, and tight junction (TJ) assem

148 s like the hair bundle and ensuring that the apical membrane forms appropriately around the stereocil

149 increase or decrease ENaC expression at the apical membrane; forskolin increased the association of

150 multaneously targeting PI3K and Tiam1 to the apical membrane has a synergistic effect on membrane rem

151 or (FcRn) located at the brush border of the apical membrane has been implicated as the "receptor" me

152 Crumbs (Crb) is a conserved determinant of apical membrane identity that regulates epithelial morph

153 d to tight junctions, is sufficient to alter apical membrane identity through its interactions with p

154 n essential apical determinant which confers apical membrane identity.

155 al recycling endosomes (ARE) and reaches the apical membrane in a microtubule- and Rab11-dependent ma

156 pressed at the ATP release site, such as the apical membrane in airway epithelial cells; (3) the phar

157 ssigned to non-centrosomal sites such as the apical membrane in epithelial cells, the nuclear envelop

158 y, we demonstrate that Ctr1 localizes to the apical membrane in intestinal epithelial cells of the mo

159 r apical polarity factors disappear from the apical membrane in mitosis.

160 ive network of filaments spanning the entire apical membrane in nonconfluent ECs.

161 duces translocation of alpha-ENaC toward the apical membrane in situ.

162 MPP3 localizes at the apical membrane in which it shows partial colocalization

163 Hair bundles and apical membranes in mice with mutations in the Elmod1 ge

164 H/K-ATPase-rich tubulovesicles (TVs) toward apical membranes in response to histamine stimulation vi

165 ectively, in maturation and targeting to the apical membrane, in polarized Madin-Darby Canine Kidney

166 in the RPE with specific localization to the apical membrane, indicating that succinate in the subret

167 e differences in sampling of the ciliary and apical membranes inherent to confocal microscopes.

168 eting of apical endosomes to the midbody and apical membrane initiation site (AMIS) during lumenogene

169 urface and initiating its transcytosis to an apical membrane initiation site for lumen formation.

170 or the sorting marker SNX18 and derived from apical membrane internalization.

171 rtures are formed by fusion of the basal and apical membranes into a tunnel that spans the height of

172 ent of MTOC function from centrosomes to the apical membrane is associated with a physical hand-off o

173 elial basolateral membrane and show that the apical membrane is highly permeable.

174 icrobial particles; M cells display a unique apical membrane lacking microvilli.

175 Cholesterol depletion from the apical membrane leads to DAF aggregation and, presumably

176 initially developed normally, but the cell's apical membrane lifted away from the cuticular plate, an

177 he role of AP-2 in the maintenance of proper apical membrane lipid and cell wall composition is furth

178 rt carriers before reaching its steady-state apical membrane localization in mature lumen.

179 Furthermore, knockdown of PHLPP altered the apical membrane localization of aPKCs and reduced the fo

180 ly reduced colocalization of KCNN4c with the apical membrane marker wheat germ agglutinin in T84WT ce

181 n caused by defective anion transport at the apical membrane may contribute to the excessive and pers

182 osomal microtubules, and its delivery to the apical membrane mediated by the small GTPase rab11a.

183 cking component mislocalizes the same set of apical membrane molecules basolaterally, including the p

184 he cell's epithelial features and associated apical membrane morphogenesis.

185 a a cyclic AMP-independent process involving apical membrane Na-H, SCFA-HCO(3), and Cl-SCFA exchanges

186 The main apical membrane neutral amino acid transporters in mouse

187 oteins are more effectively processed to the apical membrane of airway epithelia than human DeltaF508

188 K channels are present and functional at the apical membrane of airway epithelial cells.

189 dings of excised inside-out patches from the apical membrane of aldosterone-stimulated A6 collecting

190 cretory sorting of the auxin carrier PIN2 to apical membrane of Arabidopsis root epithelial cells.

191 Cl(-) channels in the apical membrane of biliary epithelial cells (BECs) provi

192 es bile secretion and other functions at the apical membrane of biliary epithelial cells (i.e., chola

193 alyze how MTOC function is reassigned to the apical membrane of C. elegans intestinal cells.

194 ize in unique and overlapping domains at the apical membrane of ciliated surface cells.

195 ast to wild-type Ncc, which localized to the apical membrane of distal convoluted tubule cells, T58M

196 potential vanilloid 5 (TRPV5) channel on the apical membrane of distal tubule epithelial cells.

197 topic transmembrane protein localized at the apical membrane of enterocytes and the canalicular membr

198 ce regulator (CFTR) acts as a channel on the apical membrane of epithelia.

199 CFTR controls the flow of anions through the apical membrane of epithelia.

200 nt its proper folding and trafficking to the apical membrane of epithelial cells.

201 AMP-activated Cl(-) channel expressed in the apical membrane of fluid-transporting epithelia.

202 DUOX2), a hydrogen-peroxide generator at the apical membrane of gastrointestinal epithelia, is up-reg

203 tivity of K(Ca)3.1 channels expressed in the apical membrane of HME cells.

204 osa that reduces the quantity of CFTR in the apical membrane of human airway epithelial cells.

205 egulation by GPCRs that are expressed at the apical membrane of intestinal and airway epithelia.

206 The apical membrane of intestinal epithelia expresses interm

207 ated by the NaDC1 transporter located on the apical membrane of kidney proximal tubule and small inte

208 Unlike in the DCT, OSR1 remains at the TAL apical membrane of KO mice where it is accompanied by an

209 , antenna-like structures extending from the apical membrane of most mammalian cells.

210 imary cilia, which are positioned within the apical membrane of neuroepithelial progenitors, we hypot

211 ssociated with a multiprotein complex at the apical membrane of normal mouse cholangiocytes, with pro

212 response to acid stimuli, is enriched in the apical membrane of PKD2L1-expressing taste cells and is

213 cumulation and virus release occurred at the apical membrane of polarized Caco-2 cells.

214 t IL-10R1 was expressed predominantly on the apical membrane of polarized epithelial cells.

215 receptors mediated Smad3 signaling from the apical membrane of polarized epithelial cells.

216 with polar secretory trafficking of PIN2 to apical membrane of polarized epithelial cells.

217 al disease by binding ganglioside GM1 on the apical membrane of polarized intestinal epithelial cells

218 nase A (PKA)-activated Cl(-) channels in the apical membrane of principal cells from the cortical col

219 a significant redistribution of AQP2 to the apical membrane of principal cells in cortical collectin

220 creased expression of NaPi-2a protein in the apical membrane of proximal tubules but impaired up-regu

221 with clathrin, but not with caveolin, at the apical membrane of PTECs, which determines clathrin-medi

222 sphorylation of the Gas6 receptor Axl in the apical membrane of renal tubular cells.

223 omolecular complex within lipid rafts at the apical membrane of surface and glandular airway epitheli

224 arrier to CO(2) resides in the umbrella cell apical membrane of the bladder with its dense array of u

225 increased the ROMK channel intensity in the apical membrane of the collecting tubule in Romk1(+/+),

226 c lines showed that Cftr is localized to the apical membrane of the epithelial cells in KV during lum

227 tood, nonheme iron is transported across the apical membrane of the intestinal enterocyte by divalent

228 ely activate type 2 chloride channels in the apical membrane of the intestinal epithelial cells leadi

229 ) is the major salt transport pathway of the apical membrane of the mammalian thick ascending limb of

230 unctional SGLT2 transporters detected in the apical membrane of the proximal tubule but not detected

231 NCCbeta is present in the apical membrane of the rectum.

232 P) 2B1 (OATP-B; SLCO2B1) is expressed in the apical membrane of the small intestine and the hepatocyt

233 regulatory molecule, Cab39/MO25alpha, at the apical membrane of the thick ascending limb (TAL) and di

234 stry, aquaporin 2 was concentrated along the apical membrane of tubular cells with ET but not PA, and

235 kidney tissue showed expression of 24p3R in apical membranes of distal tubules and collecting ducts,

236 y normal localization, PIN2 is depleted from apical membranes of epidermal cells and shows basal to a

237 g assembly before they are inserted into the apical membranes of epithelial cells, and maximal activi

238 tor (CFTR), an anion channel found mainly in apical membranes of epithelial cells.

239 f PC2 channel function from a preparation of apical membranes of human syncytiotrophoblast (PC2hst) r

240 ither NHE2 nor NHE3 expression is altered in apical membranes of inflamed colon.

241 CD36 was immunodetected on apical membranes of secretin- and CCK-positive EECs and

242 2 is expressed in several tissues, including apical membranes of small intestinal epithelial cells.

243 in is reduced 23%, NHE2 remains localized to apical membranes of surface epithelium, and NHE1 protein

244 Here we reconstituted apical membranes of term human syncytiotrophoblast (hST)

245 iltered by the kidney, binds to SGLT2 in the apical membranes of the early proximal tubule, and is su

246 d cellular mechanism to create and model the apical membranes of the two fundamental types of photore

247 ngl2 is enriched in the basolateral, but not apical, membranes of floor plate cells.

248 ing Cdc42 clustering, by tethering it to the apical membrane or lowering its diffusion, restores norm

249 e cell surface, but fails to localize at the apical membrane patch specialized for fusion and fails t

250 ss of the shell generated by adhesion of the apical membrane patches to the pore rim and the apparent

251 in the facilitated iodide efflux across the apical membrane (PDS), the organification of iodide with

252 ndings, we propose a trafficking pathway for apical membrane polarity and lumen morphogenesis that im

253 daptor protein 1 (AP-1)-dependent intestinal apical membrane polarity and polarity-dependent localiza

254 TORC1 activity at least partly by regulating apical membrane polarity.

255 , this network regulates lateral mobility of apical membrane probes such as integrins or epidermal gr

256 ested this model using the Toxoplasma gondii apical membrane protein 1 (TgAMA1), which binds to aldol

257 th and modulate the activity of a variety of apical membrane proteins, including the renal outer medu

258 o ring-like structures, which is followed by apical membrane protrusion.

259 of the endothelium through the formation of apical membrane protrusions that embrace adherent leukoc

260 PI(4,5)P2 levels at the apical membrane regulate Dia localization in both the MD

261 XOR mediates apical membrane reorganization during milk lipid secreti

262 ficial mistargeting of endogenous LGN to the apical membrane results in a near 90 degrees rotation of

263 ll-attached patch recording on the hair-cell apical membrane revealed, after BAPTA treatment or durin

264 ngly, patch clamp studies on cortical tubule apical membranes revealed that mTOR inhibition markedly

265 ase in focal adhesions, and the formation of apical membrane ruffles.

266 re, we scrutinized the elastic properties of apical membranes separated from living cells and attache

267 bacterial adherence, from basolateral to the apical membrane sides in a microtubule- and Stim1-depend

268 e or lowering its diffusion, restores normal apical membrane size in ATP8B1-depleted cells.

269 Loss of this regulation results in increased apical membrane size with scattered apical recycling end

270 n belt and crumbs overexpression expands the apical membrane size.

271 that the small GTPase Rab14 is required for apical membrane specification.

272 'bare zone', a microvilli-free sub-region of apical membrane specified by the Insc-LGN-Galphai protei

273 del intestinal epithelium, the conversion of apical membrane sphingomyelin to ceramide by exogenous b

274 ppeared more dispersed, and the intensity of apical membrane staining for AQP2 was reduced significan

275 letal polarization to control the developing apical membrane surface during blood vessel tubulogenesi

276 AQP2-S256E, which fits well with its role in apical membrane targeting.

277 nge factor that is recruited by ezrin to the apical membrane, that is enriched at a marginal zone api

278 s TRPV4 trafficking and translocation to the apical membrane, the PKC-dependent pathway increases the

279 nating abscission with delamination from the apical membrane; timing of neurogenesis and its indirect

280 have evolved unique structures to expand the apical membrane to accommodate the phototransduction mac

281 in concert with a Cl:HCO3- exchanger in the apical membrane to affect transcellular HCO3- transport.

282 binds to Ex and co-localises with it at the apical membrane to antagonise Yki activity.

283 tion permits ENaC forward trafficking to the apical membrane to augment Na absorption.

284 We found the apical membrane to be enriched in sphingolipids (SPs) an

285 n of syntaxin 2 and 5' nucleotidase from the apical membrane to subapical puncta, whereas multidrug r

286 orphogenesis and plays a role in linking the apical membrane to the underlying ezrin-containing cytos

287 initiation, but rather the inability of the apical membrane to transform and elaborate into a rhabdo

288 caused localization of intestinal SR-B1 from apical membranes to intracellular organelles and reduced

289 RISAP overexpression interferes with apical membrane traffic and blocks tip growth.

290 helial cyst cultures, Myo5B was required for apical membrane trafficking and de novo lumen formation,

291 ML1 is an important protein in parietal cell apical membrane trafficking.

292 sporter and collectrin, which is involved in apical membrane vesicle trafficking.

293 In these cells, Na(+) crosses the apical membrane via epithelial Na(+) channels (ENaC) and

294 e (KHK), as well as GLUT5 trafficking to the apical membrane via the Ras-related protein-in-brain 11

295 he apical and basolateral membranes, but the apical membrane was more active in endocytosing and degr

296 r Cl(-) /HCO3(-) exchange via SLC26A6 at the apical membrane were able to support a HCO3(-) -rich sec

297 than threefold brighter than the surrounding apical membrane when the densities of fluorescently labe

298 of KCNE2 to be markedly enriched in the CPe apical membrane, where we also discovered expression of

299 ts in dividing cells become localized to the apical membrane, which becomes highly enriched in microt

300 roscopy examination revealed that hepatocyte apical membrane with microvilli substantially extended i