ライフサイエンスコーパス: basolateral membrane

1 pithelial cells along the apical but not the basolateral membrane.

2 pical plasma membrane and Na/K-ATPase to the basolateral membrane.

3 with toxin translocation directly across the basolateral membrane.

4 the apical-lateral membrane, and EGFR at the basolateral membrane.

5 g duct, and increased AQP3 expression in the basolateral membrane.

6 in trafficking was internalization from the basolateral membrane.

7 he expression of SMCT1 was restricted to the basolateral membrane.

8 enin and integrin alpha6 were located at the basolateral membrane.

9 presence in chronically adapted cells at the basolateral membrane.

10 d that prestin is expressed at the whole OHC basolateral membrane.

11 ases in Na,K-ATPase protein abundance in the basolateral membrane.

12 reabsorption by CO2 and HCO3- sensors at the basolateral membrane.

13 ately 11-nM protein particles present in the basolateral membrane.

14 ely 11-nM particles in the outer hair cell's basolateral membrane.

15 tinal epithelium, both on the apical and the basolateral membrane.

16 fics between the trans-Golgi network and the basolateral membrane.

17 tion of the endogenous alpha1 subunit to the basolateral membrane.

18 to the apical membrane and MCT3/CD147 to the basolateral membrane.

19 e by the Na(+),K(+)-ATPase located along the basolateral membrane.

20 l for the exclusive targeting of NBC1 to the basolateral membrane.

21 showed strong and exclusive targeting on the basolateral membrane.

22 ine kidney cells, NIS mediates uptake at the basolateral membrane.

23 MCT1 to the apical membrane and MCT4 to the basolateral membrane.

24 it colocalizes with the Na+,K+-ATPase to the basolateral membrane.

25 parated from erbB2-4, which segregate to the basolateral membrane.

26 ng that Fyn mediates Ntcp retrieval from the basolateral membrane.

27 PMCA2z/b, and PMCA2z/a were confined to the basolateral membrane.

28 d 0 residues, respectively, localized to the basolateral membrane.

29 e the efflux of all-trans retinol at the RPE basolateral membrane.

30 whereas MCT3 labeling was restricted to the basolateral membrane.

31 MCT1 in the apical membrane and MCT3 in the basolateral membrane.

32 whereas IQGAP1 is mainly distributed to the basolateral membrane.

33 ents through patch pipette electrodes at the basolateral membrane.

34 odopsin-GFP and caused its missorting to the basolateral membrane.

35 f E-cadherin to a precise location along the basolateral membrane.

36 annels and its subsequent removal over their basolateral membrane.

37 eas synaptic transmission takes place at the basolateral membrane.

38 ting in concert to displace Bazooka from the basolateral membrane.

39 HBV enters hepatocytes via the basolateral membrane.

40 ssion of BCRP and PCFT was restricted to the basolateral membrane.

41 nt and restricting proteins to the apical or basolateral membrane.

42 -subunit is uniformly detected at the apical/basolateral membranes.

43 separation and maintenance of the apical and basolateral membranes.

44 a type II receptor (T2R) is localized at the basolateral membranes.

45 a1 subunits were detected on both apical and basolateral membranes.

46 s, while Crumbs3 localises to the apical and basolateral membranes.

47 vels and is localized at both the apical and basolateral membranes.

48 ized cells occurs from both their apical and basolateral membranes.

49 oordinates Na(+) transport across apical and basolateral membranes.

50 t AE1-M909T localized to both the apical and basolateral membranes.

51 transport and PAR-1-induced dispersion from basolateral membranes.

52 iched with PI(3,4,5)P(3), which localized to basolateral membranes.

53 receptor subtypes located in both apical and basolateral membranes.

54 Ca(2+)-dependent 4 h cycle of recruitment to basolateral membranes, activation, internalization, degr

55 est that RhCG contributes to both apical and basolateral membrane ammonia transport in the human kidn

56 resulted in targeting of the channels to the basolateral membrane and co-localization with SAP97 and

57 overcome resistor-capacitor filtering by the basolateral membrane and deliver sufficient mechanical e

58 Rho1 resulted in reduction of F-actin at the basolateral membrane and enrichment of apical F-actin, t

59 gnificant retention of integrin beta1 at the basolateral membrane and had tubular abnormalities.

60 2 and shows preferential localization to the basolateral membrane and hair bundle after P8.

61 HCO(3)(-) exchanger that is expressed on the basolateral membrane and in the cytoplasm of two distinc

62 er NHX-7 (PBO-4) extrudes protons across the basolateral membrane and is necessary for both acute aci

63 AR is a component of tight junctions and the basolateral membrane and is normally excluded from the a

64 ansporter NBC1 is located exclusively on the basolateral membrane and mediates vectorial transport of

65 In fact, the ion permeabilities of the basolateral membrane and paracellular pathway remain lar

66 receptor Type II is predominantly located on basolateral membrane and receptor stimulation activates

67 rentially infected the epithelia through the basolateral membrane and released viral progeny across t

68 requirement of syntaxin 4 in the delivery of basolateral membrane and secretory proteins, the basolat

69 water permeation barrier as the endothelial basolateral membrane and show that the apical membrane i

70 derived iPSC-RPE, BEST1 was expressed at the basolateral membrane and the apical membrane.

71 pressed v-SNARE cellubrevin localizes to the basolateral membrane and to recycling endosomes, where i

72 ne of the small intestine and the hepatocyte basolateral membrane and transports structurally diverse

73 )-ATPase pump (NKA) was less abundant in the basolateral membrane and was mislocalized to apical bund

74 Unstimulated NKCC1 was expressed on basolateral membranes and exhibited a topological expres

75 nal and colonic epithelia, NBC1 localizes to basolateral membranes and is thought to function in anio

76 nuclei and contains markers associated with basolateral membranes and junctions.

77 pithelial cells that separate the apical and basolateral membranes and may also be important in the e

78 ne promoted dramatic recruitment of NKCC1 to basolateral membranes and prolonged the cycle of co-tran

79 bidirectionally, from both the apical to the basolateral membranes and the basolateral to the apical

80 ect NHERF-1 from the apical cytoplasm to the basolateral membrane, and internal deletion of residues

81 plasma membrane, PMCA2 was localized to the basolateral membrane, and PMCA4 was localized to the api

82 The virus can infect via the apical or basolateral membrane, and progeny virus particles are se

83 by two mechanisms: passive uptake across the basolateral membrane, and temperature-dependent transcel

84 We show that the basolateral membrane aquaporin (AQP)-3, but not the equi

85 cylglycerols entering the enterocyte via the basolateral membrane are also incorporated into triacylg

86 Basolateral membranes are specified by Lethal giant larv

87 olves a intermediate stop at the ab-luminal (basolateral) membrane, as in hepatocytes.

88 lls are polarized upon insertion of distinct basolateral membrane at the first division.

89 Type I hair cells are characterized by their basolateral membrane being enveloped in a single large a

90 embranes, whereas prestin is confined to the basolateral membrane below the junctions.

91 are expressed in BCEC on both the apical and basolateral membrane (BL) surfaces consistent with niflu

92 mber of Na,K-ATPase alpha(1) subunits at the basolateral membrane (BLM), without changing its total c

93 Vesicles from +/b basolateral membranes (BLM) showed similar activity to B

94 latory movement toward either canalicular or basolateral membranes, but only fused with the canalicul

95 reted in equal amounts across the apical and basolateral membranes, but the apical membrane was more

96 rafficked efficiently across the cell to the basolateral membrane by transcytosis.

97 GM1 sphingolipids can traffic from apical to basolateral membranes by transcytosis in the absence of

98 ilbene-2,2'-disulfonic acid (DNDS)-sensitive basolateral membrane conductance (GDS) of cells expressi

99 receptor 1 distribution was shifted from the basolateral membrane (control) to a predominantly intrac

100 brake in their development, such that their basolateral membrane currents and synaptic machinery ret

101 brake in their development, such that their basolateral membrane currents and synaptic machinery ret

102 CARTS appear to be basolateral membrane-directed carriers that use myosin f

103 ains EGF secretion to the apical but not the basolateral membrane, disrupting this cascade and causin

104 laudin-7 is unique in that it has a stronger basolateral membrane distribution than other claudins, w

105 We tested whether establishment of the basolateral membrane domain and E-cadherin-mediated epit

106 nction, transcytosing from the apical to the basolateral membrane domain or inducing cell movement su

107 ncreased level of phosphorylated mTOR in the basolateral membrane domain.

108 lia from stem cells by developing apical and basolateral membrane domains and form sheets of cells co

109 sort transmembrane proteins to the apical or basolateral membrane domains during biosynthetic deliver

110 3 overexpression depletes uPAR from distinct basolateral membrane domains in breast cancer cells, res

111 ytes in control rats and on brush-border and basolateral membrane domains in iron-deprived rats.

112 x32) gap junctions specifically localized to basolateral membrane domains of hepatocytes, the precise

113 of the full-length hFcRn from the apical or basolateral membrane domains, however, are equal.

114 of polarized cells with distinct apical and basolateral membrane domains.

115 t release of ATP or UTP across the apical or basolateral membrane elicits qualitatively different eff

116 f this newly delivered protein traverses the basolateral membrane en route to the apical membrane.

117 a transcellular route in which internalized, basolateral-membrane enclosed bacteria are trafficked to

118 Interestingly, the basolateral membrane entry pathways for both serotypes w

119 -/-) mice and protein levels for the hepatic basolateral membrane export transporters, multidrug resi

120 EGFP-EAAT2a or EGFP-EAAT2b and found robust basolateral membrane expression of the EAAT2b isoform.

121 ency results in a redistribution of CUA-1 to basolateral membranes for copper efflux to peripheral ti

122 Whereas TfR recycles to the basolateral membrane from CRE, Megalin, like pIgR, traff

123 ATPase activity and protein abundance in the basolateral membranes from peripheral lung tissue of hyp

124 al release apparently resulted from endosome-basolateral membrane fusion (i.e., exocytosis).

125 ude that Munc18c's role in mediating ectopic basolateral membrane fusion of ZGs contributes to the in

126 Core regulators of epithelial basolateral membrane identity localize to T-tubules, and

127 SLC4A11 is localized to the basolateral membrane in BCEC.

128 ting information that cotargets CD147 to the basolateral membrane in both epithelia.

129 with the Na,K-ATPase alpha(1) subunit to the basolateral membrane in MDCK cells may determine the dif

130 and the other half from transcytosis via the basolateral membrane in MDCK cells.

131 ne in normal rats while overexpressed at the basolateral membrane in PCK rats.

132 es exist for transport from the Golgi to the basolateral membrane in polarized epithelial cells.

133 athway in nonpolarized cells, cycles via the basolateral membrane in polarized MDCK cells.

134 and tubular delivery to and fusion with the basolateral membrane in S1 proximal tubule cells.

135 ns, and is achieved by directed insertion of basolateral membrane in the cleavage furrow.

136 d in the generation of endolymph, and on the basolateral membrane in the distal nephron.

137 s epidermal growth factor receptor (EGFR) to basolateral membranes in Caenorhabditis elegans.

138 that Wrch-1 distributes along the apical and basolateral membranes in MDCK cells and binds the cell p

139 nct protein compositions in their apical and basolateral membranes in order to perform their transpor

140 ily of scaffolding proteins, CASK resides at basolateral membranes in polarized epithelia.

141 ocalize in bands just beneath the apical and basolateral membranes in two different cortical collecti

142 Additionally, localization of sgk1 to the basolateral membrane indicates that the effects mediated

143 topic rhabdomeres inappropriately located in basolateral membrane, indicating a role for MyoV in phot

144 ns that are involved in extracellular matrix-basolateral membrane interactions, CD63, MMP-3 and Cdc42

145 transporting bile acids across the ileocyte basolateral membrane into the portal circulation have no

146 that FcRn traffics IgG from either apical or basolateral membranes into the recycling endosome (RE),

147 also acquired an extensive brush border and basolateral membrane invaginations resembling those obse

148 L and indicate the involvement of apical and basolateral membrane ion transporters in maintaining a h

149 nal domain is targeted constitutively to the basolateral membrane irrespective of dietary copper conc

150 Cl(-) influx across the basolateral membrane is a limiting step in fluid product

151 We know that HCO3- uptake at the basolateral membrane is achieved by Na+-HCO3- cotranspor

152 esent in endosomes, and its targeting to the basolateral membrane is increased in hypertonicity and p

153 Basolateral membranes isolated from peripheral lung tiss

154 k cAMP-mediated Ca(2+) signaling to activate basolateral membrane K(+) conductance, resulting in weak

155 t SMase acts by down-regulating a cAMP-gated basolateral membrane K(+) conductance.

156 naesthetic MS-222, which reduces the size of basolateral membrane K(+) currents.

157 ATP11C is essential for basolateral membrane localization of multiple bile salt

158 urfaces, consistent with an observed loss of basolateral membrane localization of Munc18c, which norm

159 t epithelia, this entails HCO3- entry at the basolateral membrane, mediated by the Na+-HCO3- cotransp

160 ; (ii) by entry of cell-free virions through basolateral membranes, mediated in part through an inter

161 dings support the model that ABCC6 is in the basolateral membrane, mediating the sinusoidal efflux of

162 We found that TIP-1 competes with the basolateral membrane mLin-7/CASK complex for interaction

163 x across the jejuna of CFTR(+), CFTR(-), the basolateral membrane Na(+)/K(+)/2Cl(-) co-transporter pr

164 he co-localization of AE1 and SLC26A7 on the basolateral membrane of A-IC cells in OMCD.

165 hloride transporter that is expressed on the basolateral membrane of acid-secreting cells in the rena

166 exchanger that co-localizes with AE1 on the basolateral membrane of Alpha intercalated cells (A-IC)

167 sporter inebriated (ine) is expressed in the basolateral membrane of anterior hindgut epithelial cell

168 vity and abundance of the Na,K-ATPase in the basolateral membrane of ATII cells.

169 e presence of its influx transporters at the basolateral membrane of BBB served as the basis for our

170 Lgl2 localises to the basolateral membrane of blastomeres, while Crumbs3 local

171 ATP11C localized to the basolateral membrane of central hepatocytes in the liver

172 in the turnover of intracellular cAMP at the basolateral membrane of columnar epithelial cells, while

173 (DCT) via engagement of its receptor on the basolateral membrane of DCT cells and activation of the

174 M3 cholinergic receptor are expressed on the basolateral membrane of duct cells, whereas KCC1, IK(Ca)

175 4.1R is located on the basolateral membrane of enterocytes, where it co-localiz

176 al glucose transporter GLUT1 appeared at the basolateral membrane of enterocytes.

177 MRP3 is an ABC transporter localized in the basolateral membrane of epithelial cells such as hepatoc

178 /H+ exchanger is abundantly expressed on the basolateral membrane of gastric parietal cells.

179 tions revealed that AQP9 is most abundant in basolateral membrane of hepatocytes adjacent to the sinu

180 ults unequivocally show that ABCC6 is in the basolateral membrane of hepatocytes and is not associate

181 ociated gene family that is expressed on the basolateral membrane of hepatocytes and undergoes adapti

182 ted bile acids (BAs) and is localized at the basolateral membrane of hepatocytes.

183 V2/5, rAAV2/1 transduced both the apical and basolateral membrane of human airway epithelia with simi

184 al space can provide such an activity to the basolateral membrane of intestinal enterocytes in trans.

185 amino acid transporter) is expressed in the basolateral membrane of intestinal epithelia and is asso

186 ptor Type II is predominantly present in the basolateral membrane of intestinal epithelial cells.

187 gene confirmed that ATP7 is expressed at the basolateral membrane of larval midgut copper cells and t

188 erin and other proteins to their site in the basolateral membrane of MDCK cells, consistent with RalA

189 dhesion molecule (EpCAM) is expressed at the basolateral membrane of most normal epithelial cells but

190 oscopy localized OSTalpha and OSTbeta to the basolateral membrane of mouse, rat, and human ileal ente

191 munostaining revealed Best2 localized to the basolateral membrane of mucin-secreting colonic goblet c

192 olute carrier family 26, is expressed in the basolateral membrane of outer hair cells.

193 s receptor activation and trafficking to the basolateral membrane of polarized epithelia through a pr

194 mes, lysosome-related organelles, and/or the basolateral membrane of polarized epithelial cells.

195 Exogenous bacterial SMase acts on the basolateral membrane of polarized human intestinal epith

196 und that mZip5 localizes specifically to the basolateral membrane of polarized Madin-Darby canine kid

197 Wild-type GFP-tagged AE1 localized to the basolateral membrane of polarized MDCK cells, but AE1-M9

198 SHIP2 is mainly localized at the basolateral membrane of polarized MDCK cells.

199 started the infection preferentially at the basolateral membrane of polarized MDCK II cells; however

200 reduced accumulation of NBCe1 protein in the basolateral membrane of proximal-tubule epithelia is the

201 cotransports Na(+) and HCO(3)(-) across the basolateral membrane of renal proximal tubule cells.

202 thought to function as an ion channel in the basolateral membrane of retinal pigment epithelial (RPE)

203 PrP(C) is expressed on the basolateral membrane of retinal-pigment-epithelial (RPE)

204 interacting proteins, TfR1 and TfR2, at the basolateral membrane of RPE is relevant to the regulatio

205 protein was specifically associated with the basolateral membrane of RPE.

206 e data showed that NBCe1 is expressed at the basolateral membrane of secretory ameloblasts, whereas A

207 Expression of ClC-2 was higher in the basolateral membrane of surface cells in the EDC compare

208 er AE1, away from its normal position on the basolateral membrane of the alpha-intercalated cell caus

209 s on an assembly of 'motor' molecules in the basolateral membrane of the cell.

210 transporters in its dual localization at the basolateral membrane of the choroid plexus epithelium an

211 orter family reported to be expressed in the basolateral membrane of the cortical collecting duct and

212 anged, but this protein was removed from the basolateral membrane of the enterocyte.

213 tributed to a residual calyx attached to the basolateral membrane of the hair cells.

214 tative Na+/H+ ion exchanger expressed on the basolateral membrane of the intestine, juxtaposed to the

215 transports sodium and bicarbonate across the basolateral membrane of the renal proximal tubule.

216 transporter preferentially expressed in the basolateral membrane of the retinal pigment epithelium (

217 ophin-1, encoded by BEST1, is located at the basolateral membrane of the retinal pigment epithelium i

218 trophin-1 is preferentially expressed at the basolateral membrane of the retinal pigmented epithelium

219 MCT3, which is expressed in the basolateral membrane of the RPE wild-type mouse, was exp

220 we have shown that Mct8 is localized at the basolateral membrane of thyrocytes and that the serum TH

221 We found that, whereas the basolateral membrane of vestibular hair cells from the f

222 tein abundance and activity decreased at the basolateral membranes of alveolar epithelial type II cel

223 ng receptor is expressed on both luminal and basolateral membranes of colonocytes, and, in other cell

224 Basolateral membranes of DCT cells were depolarized, nea

225 ATPase activity and protein abundance at the basolateral membranes of distal airspaces.

226 ence identity yet localize in the apical and basolateral membranes of epithelial cells, respectively.

227 Oct1 is expressed at the basolateral membranes of hepatocytes and proximal renal

228 sma membrane, was detected in the apical and basolateral membranes of human RPE in situ and ARPE-19 c

229 , conversion of sphingomyelin to ceramide in basolateral membranes of intestinal cells rapidly activa

230 ory" NKCC1 cotransporter is localized in the basolateral membranes of many epithelia.

231 The P2X7R was expressed on apical and basolateral membranes of mouse RPE; mRNA expression of P

232 OAT1 and OAT3 localized to basolateral membranes of nonpigmented epithelial cells a

233 of nonpigmented epithelial cells and MRP4 to basolateral membranes of pigmented cells in the human ey

234 Caveolae were detected in the basolateral membranes of polarized human oral epithelial

235 .Glu143Lys missense variant localized to the basolateral membranes of polarized Madin-Darby canine ki

236 nt-dependent NBC activity is present only in basolateral membranes of proximal colon.

237 co-localized with PG intracellularly and on basolateral membranes of proximal crypt cells, providing

238 mbranes of periportal hepatocytes and in the basolateral membranes of proximal tubules in the renal c

239 2 in the kidney and found that it resides on basolateral membranes of proximal tubules.

240 ed at very low levels in both the apical and basolateral membranes of the Bsg(-/-) mouse.

241 M(3) and GD(3) are located in the apical and basolateral membranes of the Caco-2 cells.

242 ted on d16 of gestation and localized to the basolateral membranes of the single-layered epithelium.

243 t highly expressed subunit, localized to the basolateral membranes of type I and type II hair cells.

244 lucose uptake across the apical, but not the basolateral, membrane of H441 and HBE monolayers.

245 transcytosis, but regulates recycling to the basolateral membrane only.

246 Basolateral membrane permeability to NH(3) was reduced i

247 lial cells are not separated into apical and basolateral membranes ('polarized'), or when tight junct

248 Spontaneous oscillations in basolateral membrane potential suggested that Ca2+ oscil

249 Hepatic expression of this basolateral membrane protein is increased in cholestasis

250 Newly synthesized apical and basolateral membrane proteins are sorted from one anothe

251 ponsible for the polarized transport of many basolateral membrane proteins in epithelial cells.

252 he transport of newly synthesized apical and basolateral membrane proteins in fully polarized filter-

253 1b1 mutants, we examined the localization of basolateral membrane proteins in hair cells.

254 to intracellular accumulation of apical and basolateral membrane proteins, and loss of vertically or

255 ce, or the polarized targeting of apical and basolateral membrane proteins.

256 ctly affecting the distribution of apical or basolateral membrane proteins.

257 rized transport of tyrosine motif containing basolateral membrane proteins.

258 hich has been implicated in the targeting of basolateral membrane proteins.

259 newly synthesized proteins to the apical or basolateral membrane remain largely unknown.

260 Thus, elements of the basolateral membrane render epithelial cells highly sens

261 nvades the large intestine epithelium at the basolateral membrane, replicates, and spreads cell to ce

262 n of monomeric beta subunits detected in the basolateral membrane represents a transient pool of the

263 adherin levels at the adherens junctions and basolateral membrane, respectively, through Rab5- and Dy

264 cin to increase [Ca(2+)]i near the apical or basolateral membrane, respectively.

265 ation of P2X(2) and P2Y(2) to the apical and basolateral membranes, respectively.

266 loses PIPKIgamma binding and shows disrupted basolateral membrane targeting no longer forms AJs and l

267 and AP-1B in TGN to endosome or endosome to basolateral membrane targeting, respectively.

268 The subsequent increase in basolateral membrane tension had the opposite effect and

269 TfR utilizes a direct route from Golgi to basolateral membrane that is established as the epitheli

270 m for HCO3- efflux and Cl- influx across the basolateral membrane that is needed for acid secretion.

271 of polarized cells with distinct apical and basolateral membranes that serve as functional and physi

272 t-SNARE syntaxin 4 has been localized to the basolateral membrane, the v-SNARE operative in the AP-1B

273 involves ATP release across the macula densa basolateral membrane through a maxi-anion channel.

274 ating F-actin distribution at the apical and basolateral membranes through Rho kinase.

275 insertion of vacuolar proton pumps into the basolateral membrane to absorb H(+) into the blood.

276 uitination of Stx3 leads to removal from the basolateral membrane to achieve apical polarity, that St

277 Exposure of the cholangiocyte basolateral membrane to CFTR inhibitors [5-nitro-2-(3-ph

278 se of the need for K(+) recycling across the basolateral membrane to enable normal activity of the Na

279 istribution of NKCC1 immunostaining from the basolateral membrane to intracellular vesicles in both s

280 sed mislocalization of bestrophin-1 from the basolateral membrane to the cytoplasm.

281 gest that cellubrevin and AP-1B cooperate in basolateral membrane trafficking.

282 Localization of the basolateral membrane transporter, organic anion transpor

283 tion of PAH transport by probenecid in renal basolateral membrane vesicles (5.2-fold).

284 e dramatically increased in brush-border and basolateral membrane vesicles isolated from iron-deficie

285 ssed in the Golgi and are transported to the basolateral membrane via a separate vesicular system for

286 ndent transporter, SGLT, and exit across the basolateral membrane via facilitative, GLUT-mediated, tr

287 a Na(+) pump, with recycling of K(+) at the basolateral membrane via K(+)-permeable channels.

288 ver, LPS-induced recruitment of MyD88 to the basolateral membrane was impaired in TLR2(-/-) MTALs.

289 abundance of AQP1 in brush border apical and basolateral membranes was augmented >2-fold by increasin

290 helial integrity allows ligand access to the basolateral membrane where it immediately binds to and a

291 T/CD147 heterocomplexes are localized in the basolateral membrane where they transport lactate out of

292 -tagged PMCA4b construct was targeted to the basolateral membrane, whereas a green fluorescent protei

293 canine kidney cells, GLUT9 trafficked to the basolateral membrane, whereas GLUT9DeltaN localized to t

294 In epithelial cells, Cadm1 was enriched in basolateral membranes, whereas, in fiber cells, expressi

295 ced a significant retrieval of Ntcp from the basolateral membrane, which was accompanied by an activa

296 that direct the targeting of kidney NBC1 to basolateral membrane, wild type and various carboxyl-ter

297 omolar concentrations of ACT when applied to basolateral membranes, with little or no response to tox

298 ial cells that also separates the apical and basolateral membranes within these cells.

299 the endoplasmic reticulum and sorting to the basolateral membrane without altering other properties o

300 Wild-type AE1 trafficked directly to the basolateral membrane without apical passage, whereas AE1