ライフサイエンスコーパス: duct cell

1 rane exosomes from mouse cortical collecting duct cells.

2 Na(+) transport in mouse cortical collecting duct cells.

3 ion of surviving mature hepatocytes and bile duct cells.

4 ent ERK phosphorylation in benign pancreatic duct cells.

5 the apical membranes of mouse salivary gland duct cells.

6 capable to differentiate into SG acinar and duct cells.

7 ion on EP4 receptors expressed on collecting duct cells.

8 ession of Ascl3 is restricted to a subset of duct cells.

9 s of exosomes from mouse cortical collecting duct cells.

10 shed in P2X(7)(-/-) submandibular acinar and duct cells.

11 rin-2 (AQP2) trafficking in renal collecting duct cells.

12 ngII) type 1 receptor (AT(1)R) in collecting duct cells.

13 cells with similarities to mature pancreatic duct cells.

14 presence of RyR2 in the medullary collecting duct cells.

15 ERK and P38 in the cultured mouse collecting duct cells.

16 O(2) on c-Src expression in mouse collecting duct cells.

17 ize in the nuclei of mIMCD3 renal collecting duct cells.

18 human kidneys (NHK) and M-1 mouse collecting duct cells.

19 choline, whereas secretin receptors regulate duct cells.

20 n kinase and increased proliferation of bile duct cells.

21 elial Na(+) transport in cortical collecting duct cells.

22 al player to generate endocrine, acinar, and duct cells.

23 e adult is present only in some intercalated duct cells.

24 ivated protein kinase, and Src in pancreatic duct cells.

25 eton had no effect on P2X7R gating by ATP in duct cells.

26 and 18 in CFTR expression in some pancreatic duct cells.

27 PKbeta pathway in inner medullary collecting duct cells.

28 to generate hepatocytes and duct cells, only duct cells.

29 s functionally expressed in mouse pancreatic duct cells.

30 NHE3 was restricted to the apical region of duct cells.

31 e studied pNBC1 function in mouse pancreatic duct cells.

32 n autoimmune insult on the kidney collecting duct cells.

33 ductance in renal inner medullary collecting duct cells.

34 sufficient to confer activity in collecting duct cells.

35 r in cultured rat inner medullary collecting duct cells.

36 ells, whereas expression was not detected in duct cells.

37 n transport in M-1 mouse cortical collecting duct cells.

38 as located apically, toward the lumen in the duct cells.

39 on of epithelial cells as well as pancreatic duct cells.

40 ve target cells, i.e. in cortical collecting duct cells.

41 f NaKCl2 cotransporter protein were found in duct cells.

42 quaporin-2 water channel in renal collecting duct cells.

43 tered and became more characteristic of bile duct cells.

44 e of submandibular salivary gland acinar and duct cells.

45 lyol metabolism, in Capan-1 human pancreatic duct cells.

46 ancreatic acini and submandibular acinar and duct cells.

47 a subfraction of outer medullary collecting duct cells.

48 alpha-ENaC expression in cortical collecting duct cells.

49 ith autoantibodies against kidney collecting duct cells.

50 rier formation in Grhl2-deficient collecting duct cells.

51 amics in polarized mouse cortical collecting duct cells.

52 esmopressin stimulation of kidney collecting duct cells.

53 ater and Na(+) transport in renal collecting duct cells.

54 trastructural features of both endocrine and duct cells.

55 compartment differentiate into endocrine and duct cells.

56 ion and continue to generate both acinar and duct cells.

57 ctivity in aldosterone-stimulated collecting duct cells.

58 ldosterone-stimulated mpkCCD(c14) collecting duct cells.

59 thelial and mouse inner medullary collecting duct cells-3.

60 characterize [Ca2+]i signalling in salivary duct cells a procedure was developed for the rapid prepa

61 cellent approach for studying lacrimal gland duct cells about which relatively little is known at the

62 hypertonicity in inner-medullary collecting duct cells adapted to survive in hypertonic conditions.

63 Duct cells also expressed NHE2 and NHE3 in the luminal m

64 gans excretory (renal) system, the excretory duct cell and pore cell.

65 regulation of COX-2 expression in collecting duct cells and (ii) to assess the possible contribution

66 reatic cell types including endocrine cells, duct cells and endothelial cells.

67 and their subsequent differentiation to bile duct cells and hepatocytes.

68 scence to consist of cytokeratin 19-positive duct cells and hormone-positive islet cells.

69 ching morphogenesis using primary pancreatic duct cells and identified a transient surge of Pdx1 expr

70 ndogenous ENaCs in mouse cortical-collecting duct cells and in primary cultures of human airway epith

71 transport had no effect on [Cl-]i changes in duct cells and inhibited only about 50% of Cl- uptake in

72 proximal cells are bipotent and give rise to duct cells and late-born endocrine cells, including the

73 uctures containing both parenchymal and bile duct cells and liver repopulation was extensive (60 to 8

74 acini, which undergo rapid reprogramming to duct cells and longer-term reprogramming to endocrine ce

75 polarized cultures of mouse renal collecting duct cells and mice treated with clinically relevant lit

76 ultured rat renal inner medullary collecting-duct cells and microarray analysis to identify genes aff

77 ongated in proximal tubule cells, collecting duct cells and parietal cells of the remaining kidney.

78 l protein expression is detected in salivary duct cells and peripheral nerve ganglia.

79 y treating immortalized mouse M-1 collecting duct cells and primary cultures of human kidney epitheli

80 re we provide evidence from renal collecting duct cells and serum- and glucocorticoid-induced kinase-

81 s process, we observed proliferation of bile duct cells and small epithelial cells, although transpla

82 arbonate and fluid secretion from pancreatic duct cells and suggested that cholecystokinin stimulatio

83 mulated COX-2 expression in mouse collecting duct cells and that 2) COX-2 may play a role in cell sur

84 te a progenitor-progeny relationship between duct cells and the acinar cell compartment, and identify

85 nction of receptors on pancreatic acinar and duct cells and the multiple intracellular signaling path

86 in the submandibular gland (SMG) acinar and duct cells and their regulation by basolateral and lumin

87 ) mouse to lineage-trace Hnf1beta(+) biliary duct cells and to assess their contribution to LPC expan

88 ries of studies suggest that neogenesis from duct cells and transdifferentiation of alpha-cells are p

89 the bestrophins are expressed in pancreatic duct cells and, more specifically, that hBest1 plays a r

90 n excretory cell, an excretory gland cell, a duct cell, and a pore cell.

91 ific immunolocalization of sAC in collecting duct cells, and immunoblots confirmed sAC expression in

92 f neonatal mice has a unique tropism to bile duct cells, and it triggers a hepatobiliary inflammation

93 he presence of human endothelial and biliary duct cells, and secreted human albumin that was detected

94 pression in mouse inner medullary collecting duct cells, and this effect was abrogated by AT(1)R bloc

95 ound to be restricted to a subset of biliary duct cells antigenically defined as CD45(-)/CD11b(-)/CD3

96 These results suggest that in parotid duct cells apical NHE2 and NHE3 do not play a major role

97 To test whether pancreatic duct cells are in vitro progenitors, they were purified

98 Adam10 in determining the fate of collecting duct cells are more complex than those of a simple upstr

99 HNF1beta(+) biliary duct cells are the origin of LPC.

100 n the pancreas, and reveals adult pancreatic duct cells as a latent multipotent cell type.

101 um stress as an early step and the status of duct cells as important entities in pancreatic injury.

102 ancreatic duct cells, challenges the role of duct cells as progenitors, and suggests a genetic mechan

103 murine pancreatic centroacinar and terminal duct cells, as visualized using fluorescent microscopy.

104 MPCs differentiate into hepatocytes and bile duct cells, as well as into fat, bone, cartilage, and en

105 In mature duct cells, Brg1 inhibits the dedifferentiation that pre

106 ated proliferation of mouse renal collecting duct cells but also increased the G2/S ratio, indicating

107 lpha 2 promoter activity in renal collecting duct cells but not in fibroblasts or in a medullary thic

108 n of activated LET-60/Ras in the neighboring duct cell, but not in the G1 or G2 cells, is sufficient

109 e were transplanted with cultured pancreatic duct cells, but no donor-derived hepatocytes were observ

110 nsplanted with cells enriched for pancreatic duct cells, but only three of the 34 (9%) recipients ana

111 ligation) and lineage-traced Ngn3-activated duct cells by labeling them through intraductal infusion

112 c analysis of rat inner medullary collecting duct cells by using a combination of phosphopeptide enri

113 n the secretion of bicarbonate by pancreatic duct cells, by transporting bicarbonate into the cell ac

114 ative signaling pathways in human pancreatic duct cells, cAMP-protein kinase A and mitogen-activated

115 and physiological features of the excretory duct cell, ces-2 and atf-2 mutants only exhibit anatomic

116 e specification of the intrahepatopancreatic duct cells, challenges the role of duct cells as progeni

117 re we showed that in mouse kidney collecting duct cells, claudin-4 functioned as a Cl(-) channel.

118 udy regulatory volume decrease (RVD) in bile duct cell clusters (BDCCs) from normal and cystic fibros

119 reduced RET activity, we find that Wolffian duct cells compete, based on RET signaling levels, to co

120 for ALGS ductal paucity.The hepatopancreatic duct cells connect liver hepatocytes and pancreatic acin

121 ssed in the apical membrane of submandibular duct cells, consistent with the significantly higher sal

122 yte-specific marker expression in pronephric duct cells correlates with loss of expression of the pro

123 Mouse renal proximal tubule and collecting duct cells, deficient in both pNBC1- and kNBC1-mediated

124 Furthermore, collecting duct cells derived from laminin-deficient kidneys and gr

125 actions of secretin on guinea-pig pancreatic duct cells described in this and the accompanying paper

126 in primary mouse inner medullary collecting duct cells did not detect ENaC activity but did detect a

127 the proper expression of genetic markers of duct cell differentiation.

128 In vitro, Grhl2-deficient collecting duct cells displayed increased paracellular flux of sodi

129 By contrast, P2X7Rs in duct cells displayed only rapid gating by ATP.

130 ncipal cells, and inner medullary collecting duct cells do not.

131 n the LIN-48/Ovo transcription factor in the duct cell during morphogenesis.

132 r cells (MPCs) produce acinar, endocrine and duct cells during organogenesis, but their existence and

133 ctivity for prolactin, TGF-beta1, and EGF in duct cells during pregnancy and after CI, most prominent

134 the HCO3- taken up by guinea-pig pancreatic duct cells during stimulation with secretin.

135 ate a parallel mechanism operative in mature duct cells during which functional cells undergo "ductal

136 In cultured collecting duct cells, enhanced apical Na(+) entry increased the ba

137 +) availability in cultured mouse collecting duct cells, enhanced apical Na(+) entry invariably led t

138 tely isolated rat inner medullary collecting duct cells ex vivo and ET-1 peptide in rat inner medulla

139 C2, NEK8-depleted inner medullary collecting duct cells exhibited a defective response to fluid shear

140 AngII-treated inner medullary collecting duct cells exhibited augmented intracellular calcium sig

141 In knockdown experiments with pancreatic duct cells exposed to UV light, RNF43 appeared to functi

142 Pancreatic islet and duct cells express 25(OH)D(3)-1alpha-hydroxylase that ge

143 elective conditions revealed that acinar and duct cells express at least five distinct Cl- channels;

144 rescence analysis showed that SMG acinar and duct cells expressed NHE1 in the basolateral membrane (B

145 es THM1) in mouse inner medullary collecting duct cells expressing an IFT88-enhanced yellow fluoresce

146 Collecting duct cells expressing this mutation had moderate abnorma

147 Only one of these, the duct cell fate, appears to be essential for viability.

148 zation, convergent extension of the cochlear duct, cell fate specification, synaptogenesis, and the e

149 In kidney collecting duct cells, filamentous actin (F-actin) depolymerization

150 Thus, purified duct cells from adult human pancreas can differentiate t

151 ethylation was significantly reduced in bile duct cells from BA patients compared to patients with ot

152 In contrast, duct cells from heterozygous patients with R117H/DeltaF5

153 Collecting duct cells from mutant mice have abnormal primary cilia

154 Duct cells from patients with DeltaF508 mutant CFTR show

155 ur previous conclusion that HCO3- entry into duct cells from the extracellular fluid requires Na+ but

156 ing pre-cystic renal tubule and hepatic bile duct cells from Tsc1, Tsc2 and Pkd1 heterozygous mice we

157 l NBCs in the HCO3- secreting SMG acinar and duct cells function as HCO3- salvage mechanisms at the r

158 ng integrin alpha3beta1-dependent collecting duct cell functions.

159 rogenitors that give rise to both acinar and duct cells, genetic ablation of SOX2 results in a failur

160 For example, sustentacular and duct cells give rise only to themselves after transplant

161 , PC1-depleted immortalized renal collecting duct cells had higher levels of integrin-beta1 and fibro

162 bud developed kidney agenesis and collecting duct cells had severe cytoskeletal, adhesion and polarit

163 Purified duct cells had slow expansion and poor aggregation, as w

164 Primary human pancreas duct cells harbouring oncogenic KRAS and induced mutatio

165 r sgk1-regulated ENaC activity in collecting duct cells has yet to be established.

166 ind that in mouse inner medullary collecting duct cells, high NaCl increases NTE mRNA within 8 h and

167 In cultured inner medullary collecting duct cells, HSP expression was maximal at 500 mOsm/kg, w

168 the constructs in inner medullary collecting duct cells (IMCD-3 cell line) and compared the subcellul

169 cal and functional features of the excretory duct cell in C. elegans result from the gain of expressi

170 o direct pathfinding of migrating pronephric duct cells in axolotl embryos by: (1) demonstrating that

171 Pax2 protein is present in collecting duct cells in both renal medulla and cortex and in thin

172 Strikingly, bile duct cells in cP(f/f)78(f/f) livers maintained wild-type

173 Dividing collecting duct cells in early stages of cyst formation fail to pro

174 Percentages of nonviable pancreatic duct cells in groups 1 to 5 were 3.8+/-2.7%, 59.7+/-4.4%

175 ells and in mouse inner medullary collecting duct cells in isotonic medium.

176 ructural and functional similarities to bile duct cells in normal liver.

177 Bile duct cells in pn demonstrated an accumulation of electro

178 plasma membrane of mouse cortical collecting duct cells in response to vasopressin.

179 tors in both pancreatic progenitor cells and duct cells in the adult pancreas.

180 nd that insulin(+) cells are continuous with duct cells in the epithelium that makes up the hyperplas

181 hepatocytes and proliferation of intra-islet duct cells in the pancreata of these mice evidently stem

182 TRIP13 in murine inner medullary collecting duct cells in the presence of hydrogen peroxide showed i

183 ein is predominantly localized to collecting duct cells in the rat kidney, with much lower expression

184 er medullary, and inner medullary collecting duct cells in vitro.

185 hing and cell cycle regulation in collecting duct cells in vivo Although in vitro data indicate that

186 nitors that produce exocrine, endocrine, and duct cells in vivo.

187 the apical plasma membrane of rat collecting duct cells, in contrast to the other three phospho-forms

188 rog3, MafA, Pdx1 and Pax6 converted exocrine duct cells into endocrine progeny with hallmark beta-cel

189 vasopressin signaling network of collecting duct cells, involving several kinases not generally acce

190 ed aquaporin protein abundance in collecting duct cells is a contributing factor in the increased uri

191 e molecule at the apical surface of PBC bile duct cells is a modified form of PDC-E2 or a cross-react

192 Therefore, Ngn3 activation in duct cells is not a signature for adult beta cell neogen

193 model, suggesting that activation of Ngn3 in duct cells is not sufficient to direct their transdiffer

194 changer at the apical membrane of pancreatic duct cells is now known to be SLC26A6.

195 of AQP2 in exosomes released from collecting duct cells is physiologically regulated and exosomal AQP

196 In mouse collecting duct cells, knockdown of KLHL3 profoundly increased the

197 Although cultured inner-medullary collecting duct cells lacked the gamma subunits, both variants gamm

198 a high resistance mouse cortical collecting duct cell line (94D).

199 scently loaded ECVs into a kidney collecting duct cell line (mCCDC11) and into primary cells.

200 terone in a mouse inner medullary collecting duct cell line and found that the transcript induced to

201 strated in the M-1 mouse cortical collecting duct cell line and in embryonic and adult mouse kidneys

202 lium in primary culture and a rat pancreatic duct cell line but had no effect on a hamster insulinoma

203 or Phe-340 in the inner medullary collecting duct cell line IMCD.

204 zed this system further using the collecting duct cell line Madin-Darby canine kidney (MDCK), which r

205 nnels expressed in either a mouse collecting duct cell line or primary cultures of human airway epith

206 (iii) silencing of ZBED6 in the human PANC-1 duct cell line reduced proliferation rates; and (iv) ZBE

207 re performed in a murine cortical collecting duct cell line that endogenously expresses ENaC.

208 by using an unique mouse cortical collecting duct cell line that stably expresses functional mineralo

209 e developed an immortalized renal collecting duct cell line with inactive Pkd2; these cells had aberr

210 -mediated Na+ current in a kidney collecting duct cell line, although GILZ2 and GILZ3 also stimulated

211 vestigated in the cystic fibrosis pancreatic duct cell line, CFPAC-1.

212 In the mPEC pancreatic duct cell line, where endogenous pNBC1 functions with a

213 and WNK1 were observed in a human collecting duct cell line, while SPAK was unaltered.

214 ormal rat cholangiocyte (NRC) polarized bile duct cell line.

215 t Notch ligands Jagged1b and Jagged2b induce duct cell lineage in the liver and pancreas of the zebra

216 ption factors that maintain the exocrine and duct cell lineages.

217 of Period 1 (Per1) mRNA in renal collecting duct cell lines and in the rodent kidney.

218 sed in the majority of neoplastic pancreatic duct cell lines and VIP stimulates growth of VIP-1 recep

219 low, we generated inner medullary collecting duct cell lines that stably express enhanced green fluor

220 dent differentiation by infecting pancreatic duct cell lines with an Ngn3-expressing adenovirus.

221 table IMCD (mouse inner medullary collecting duct) cell lines, in which FPC was silenced by short hai

222 [Na+]i) were measured by microfluorometry in duct cells loaded with either the pH-sensitive fluoropro

223 odels of Ngn3 activation in adult pancreatic duct cells (low-dose alloxan treatment and pancreatic du

224 yzed using specific endocrine, exocrine, and duct cell markers as well as markers for dividing cells.

225 whether Ngn3 activation in adult pancreatic duct cells may lead to duct-to-beta cell transdifferenti

226 In vivo, inner medullary collecting duct cells may regulate urea uptake by altering UT-A1 gl

227 l tubular epithelial and cortical collecting duct cells mediates the antidiuretic and cytoprotective

228 later time points, showed reduced acinar-to-duct cell metaplasia.

229 5 was demonstrated in mouse renal collecting duct cells (mIMCD-3) by RT-PCR and by immunocytochemistr

230 ures of polarized inner medullary collecting duct cells (mIMCD-3).

231 egulated in renal inner medullary collecting duct cells (mIMCD3 cells) during exposure to hyperosmoti

232 is in mouse renal inner medullary collecting duct cells (mIMCD3) and increases GADD45 expression.

233 bination on mouse inner medullary collecting duct cells (mIMCD3).

234 cells, inhibition of ERK phosphorylation in duct cells mitigated TGFbeta-induced upregulation of gro

235 ultured outer and inner medullary collecting duct cells (mOMCD1 and mIMCD3).

236 PDAC resembles duct cells morphologically and, to some extent, at a mol

237 ake of exosomes by renal cortical collecting duct cells, most studies of human urinary exosomes have

238 tor-mediated response in cultured collecting duct cells (mpkCCD) from mouse.

239 in mouse kidney and mouse kidney collecting duct cells (mpkCCD14).

240 By contrast, duct cell NBC3 transported both OH(-) and HCO3-.

241 erentially expressed in the serous acini and duct cells of all major salivary glands.

242 95% in acinar cells and greater than 80% in duct cells of NHE1-deficient mice (Nhe1(-/-)).

243 lomerular cells and HIF-1alpha in collecting duct cells of the adult kidney.

244 transcript was found in islet cells but not duct cells of the healthy pancreas.

245 ne and endothelin-1 (ET-1) act on collecting duct cells of the kidney and are important regulators of

246 B(2) receptor in inner medullary collecting duct cells of the kidney.

247 d current was measured in parotid acinar and duct cells of wild type and P2X7R-/- mice and in HEK293

248 habditis briggsae, but acts in the excretory duct cell only in C. elegans.

249 hought able only to generate hepatocytes and duct cells, only duct cells.

250 Duct cell P2X7Rs are preassembled and therefore continua

251 this gene specifically in kidney collecting duct cells prevents cilia formation and promotes rapid p

252 es sodium absorption across renal collecting duct cells primarily by increasing the apical membrane e

253 of embryogenesis, Prox1 appears to regulate duct cell proliferation and morphogenesis.

254 Additionally, significant intra-islet duct cell proliferation in the pancreata of transgenic K

255 nt of Ilotropin and is capable of initiating duct cell proliferation, a prerequisite for islet neogen

256 d molecular changes that occur in acinar and duct cell properties on Kras(G12D) expression, we took a

257 ilic cell, chromophobic cell, and collecting duct cell RCCs), metastatic RCCs, and non-renal cell cle

258 located on the apical membrane of collecting duct cells, regulates water reabsorption under the contr

259 in pancreatic acinar and submandibular gland duct cells, respectively, evoke a Ca2+ signal by a mecha

260 raged 56 +/- 8 and 26 +/- 7 mM in acinar and duct cells, respectively.

261 II receptor deletion in cultured collecting duct cells resulted in excessive integrin alphavbeta6-de

262 ement of CFTR current in WT and slc26a6(-/-) duct cells revealed that deletion of slc26a6 resulted in

263 rane of aldosterone-stimulated A6 collecting duct cells revealed that the open probability of ENaC wa

264 g (Affymetrix) in mouse mpkCCDc14 collecting duct cells, revealing expression of 25 TRs that are also

265 ranes is consistent with the hypothesis that duct cells secrete the relatively high K+ in lacrimal fl

266 columnar epithelial cells, these pancreatic duct cells secreted mucin constitutively and responded t

267 transport (NBC) activities in SMG acinar and duct cells showed separate DIDS-sensitive/EIPA-insensiti

268 We also show that SER in the duct cells signals to the adjacent secretory cells to sp

269 d mouse principal kidney cortical collecting duct cells significantly decreases cell motility.

270 tochemistry, however, showed that pancreatic duct cell-specific differentiation (carbonic anhydrase I

271 AMP, cytosolic pH, and Ca2+ in isolated bile duct cells suggest that glybenclamide directly activates

272 n obligatory component in the maintenance of duct cell survival, proliferation, and migration during

273 K(ATP) channel is present in salivary gland duct cells that is regulated by extracellular ATP and po

274 human liver (including hepatocytes and bile duct cells), the major enzyme is ACAT1, rather than ACAT

275 In the collecting duct cells, the assembly of claudin-4 into TJ strands re

276 -:1 Na+ stoichiometry, whereas in collecting duct cells, they have a 2:1 stoichiometry.

277 ppeared to relocate from an apical region of duct cells to an unidentified cytoplasmic compartment.

278 use deep DNA sequencing in mouse collecting duct cells to ask whether vasopressin signaling selectiv

279 d in isolated submandibular gland acinar and duct cells to characterize and localize the purinergic r

280 he transcellular Cl- transport by acinar and duct cells to determine the final electrolyte compositio

281 Here we used parotid acinar and duct cells to reveal the unique cell-specific assembly a

282 iates its effects in one cell (the excretory duct cell) together with another bZip protein, ATF-2.

283 ells, which can give rise to both acinar and duct cell types in the murine salivary glands.

284 n in the thick ascending limb and collecting duct cell types.

285 n mouse principal kidney cortical collecting duct cells using a GST-SNX27 fusion construct as bait.

286 thylated in microdissected normal pancreatic duct cells using bisulfite-modified sequencing and in tw

287 s was detected within the graft's collecting duct cells using quantitative polymerase chain reaction

288 3- across the luminal membrane of pancreatic duct cells was studied by monitoring the luminal pH of i

289 alivary submandibular gland (SMG) acinar and duct cells was used to evaluate the role of Cl- channels

290 ll mice, which consists of only exocrine and duct cells, was subtracted from fetal wild-type pancreas

291 e apical plasma membrane of renal collecting duct cells, we have carried out immunoblotting, immunocy

292 inuous cultures of intermedullary collecting duct cells were exposed to various levels of oxalate, a

293 ure cotransporter activity, mouse pancreatic duct cells were grown to confluence on a porous substrat

294 ermore, ptip null inner medullary collecting duct cells were sensitive to hyperosmolality in vitro.

295 m-specific, renal inner medullary collecting duct cells were stably transfected with cDNA's encoding

296 in is expressed in cultured mouse collecting duct cells, where apical Na(+) transport is mediated by

297 are expressed on the basolateral membrane of duct cells, whereas KCC1, IK(Ca)1, CFTR, and ClC3 are ap

298 NHE2 to apical membranes of both acinar and duct cells, whereas NHE3 was restricted to the apical re

299 ch are responsible for saliva formation, and duct cells, which modify the saliva and conduct it to th

300 omplete loss of canonical Notch activity and duct cells within the liver and exocrine pancreas, where