ライフサイエンスコーパス: pancreatic acinar cell

1 or agonist-induced zymogen activation in the pancreatic acinar cell.

2 rt and exocytosis of zymogen granules in the pancreatic acinar cell.

3 ase relevant to the secretory process in the pancreatic acinar cell.

4 rn the differentiated phenotype of the adult pancreatic acinar cell.

5 the aberrant signaling of Ca(2+) within the pancreatic acinar cell.

6 ling and the pathogenesis of pancreatitis in pancreatic acinar cells.

7 dramatically modifies autophagy in infected pancreatic acinar cells.

8 n of the effects of intracellular trypsin on pancreatic acinar cells.

9 associated with zymogen granule membranes in pancreatic acinar cells.

10 of active trypsin determines its effects on pancreatic acinar cells.

11 we analyzed the Bmi1-labeled cell lineage of pancreatic acinar cells.

12 es that may maintain the stable phenotype of pancreatic acinar cells.

13 ng digestive enzyme and fluid secretion from pancreatic acinar cells.

14 P(3)-induced Ca(2+) release (IICR) to ATP in pancreatic acinar cells.

15 uated agonist-induced Ca(2+) signaling in WT pancreatic acinar cells.

16 ach to determine the plasticity potential of pancreatic acinar cells.

17 nges of NO concentration in acutely isolated pancreatic acinar cells.

18 focal microscopy of isolated perfused murine pancreatic acinar cells.

19 the pathologic activation of zymogens within pancreatic acinar cells.

20 exocytosis are highly polarized functions of pancreatic acinar cells.

21 s and the underlying signaling mechanisms in pancreatic acinar cells.

22 uring zymogen granule exocytosis in exocrine pancreatic acinar cells.

23 mechanism for mesotrypsinogen activation in pancreatic acinar cells.

24 on with membrane-bound secretory vesicles in pancreatic acinar cells.

25 Kras transgene, which targets expression to pancreatic acinar cells.

26 ns of [Ca(2+)](c) oscillations are shaped in pancreatic acinar cells.

27 ing protein we find prominently expressed in pancreatic acinar cells.

28 nts also may lead to NF-kappaB activation in pancreatic acinar cells.

29 g cascade of terminally differentiated mouse pancreatic acinar cells.

30 in regulating digestive enzyme secretion in pancreatic acinar cells.

31 nucleotide phosphate (NAADP) release Ca2+ in pancreatic acinar cells.

32 is selectively transcribed to high levels in pancreatic acinar cells.

33 toimmunity or in preserving the integrity of pancreatic acinar cells.

34 s and matrix metalloproteinase expression in pancreatic acinar cells.

35 cohol and accelerates disorders of the ER in pancreatic acinar cells.

36 fic phosphoregulation of Ca(2+) signaling in pancreatic acinar cells.

37 the exocyst in polarized Ca(2+) signaling in pancreatic acinar cells.

38 modification in secretagogue-stimulated rat pancreatic acinar cells.

39 published values for the volume of the ER in pancreatic acinar cells.

40 by Ins(1,4,5)P3, as originally discovered in pancreatic acinar cells.

41 R and CCK to induce cytosolic Ca2+ spikes in pancreatic acinar cells.

42 mice that over-express Rab3D specifically in pancreatic acinar cells.

43 , intestinal and bronchiolar epithelial, and pancreatic acinar cells.

44 cium concentration ([Ca2+]i) in isolated rat pancreatic acinar cells.

45 ores of submandibular salivary gland but not pancreatic acinar cells.

46 reactive oxygen species generation in mouse pancreatic acinar cells.

47 f almost all islet beta cells and subsets of pancreatic acinar cells.

48 nohistochemistry showed TNFalpha presence in pancreatic acinar cells.

49 after stimulation of secretion from isolated pancreatic acinar cells.

50 ccurs at the site of Ca2+ wave initiation in pancreatic acinar cells.

51 ation of fluid secretion and exocytosis from pancreatic acinar cells.

52 ial changes also underlie the paligenosis of pancreatic acinar cells.

53 amino acids, particularly L-Lys, on isolated pancreatic acinar cells.

54 d for taurocholate-induced necrosis in mouse pancreatic acinar cells.

55 led that CB2R protein was expressed in mouse pancreatic acinar cells.

56 A recruits KDM6A to genomic binding sites in pancreatic acinar cells.

57 Ca(2+) ([Ca(2+)]i) overload and necrosis of pancreatic acinar cells.

58 e pancreatic duct and subsequent exposure to pancreatic acinar cells.

59 ressed with KIAA1967 in the nuclei of normal pancreatic acinar cells.

60 rticipate in the regulation of exocytosis in pancreatic acinar cells.

61 uction of the neutrophil attractant CXCL1 in pancreatic acinar cells.

62 ed whether Bcl-2 affects Ca(2+) extrusion in pancreatic acinar cells.

63 ation and fibrosis-associated genes in adult pancreatic acinar cells.

64 d with atypical localization of claudin-2 in pancreatic acinar cells.

65 and carbachol-regulated Ca(2+) signaling in pancreatic acinar cells.

66 tor, thapsigargin, activated Ca2+ entry into pancreatic acinar cells, a process known as capacitative

67 In pancreatic acinar cells, acetylcholine and bombesin excl

68 In pancreatic acinar cells, acetylcholine evokes local Ca(2

69 Interestingly, in the pancreatic acinar cells, activation by cholecystokinin i

70 e key signalling events driving secretion in pancreatic acinar cells after stimulation by the secreta

71 of intracellular Ca(2+) signals may protect pancreatic acinar cells against Ca(2+) overload, intrace

72 receptor (CCKR) in its native milieu in the pancreatic acinar cell and in a Chinese hamster ovary (C

73 roteolytic activation of zymogens within the pancreatic acinar cell and initiate acute pancreatitis.

74 serves a major intracellular role within the pancreatic acinar cell and may be functionally active af

75 tionship between the events occurring in the pancreatic acinar cell and the vascular, neural, and imm

76 x-loop-helix transcription factor complex of pancreatic acinar cells and critical to acinar cell fate

77 CEL gene, which is specifically expressed in pancreatic acinar cells and encodes the digestive enzyme

78 GRP inhibited protein synthesis in AR42J rat pancreatic acinar cells and HuTu 80 human duodenal adeno

79 g/kg) induced a wave of DNA synthesis in the pancreatic acinar cells and in the proximal tubular epit

80 present in a subpopulation of self-renewing pancreatic acinar cells and is expressed in response to

81 lator of actin cytoskeleton and autophagy in pancreatic acinar cells and is potently protective again

82 s transfected with plasmids and in AR42J rat pancreatic acinar cells and isolated mouse pancreatic ac

83 on inside the endoplasmic reticulum store of pancreatic acinar cells and monitored the cytoplasmic Ca

84 has been described in considerable detail in pancreatic acinar cells and oocytes.

85 pancreatic ductal cannulas, and in isolated pancreatic acinar cells and pancreatic lobules in vitro.

86 genic mice showed increased proliferation of pancreatic acinar cells and severely perturbed acinar di

87 presence of ARC channels in both parotid and pancreatic acinar cells and shown that, again, they are

88 sitive palmitoyl-CoA-sensitive Ca2+ store in pancreatic acinar cells and suggest that palmitoyl-CoA m

89 that SHA can bind to normal murine and human pancreatic acinar cells and that SHA-binding glycans are

90 e advanced understanding of the functions of pancreatic acinar cells and the mechanisms by which thes

91 Bcl-2 regulates PMCA function in pancreatic acinar cells and thereby influences cell fate

92 n to play a role in amylase secretion by rat pancreatic acinar cells and to specifically dephosphoryl

93 sease that causes progressive destruction of pancreatic acinar cells and, ultimately, loss of pancrea

94 erleukin-6, interleukin-1, and chemokines by pancreatic acinar cells and/or transmigrated leukocytes.

95 ractivation, IgG-type autoantibodies against pancreatic acinar cells, and IgM-type autoantibodies aga

96 tophagy gene Atg5 is specifically deleted in pancreatic acinar cells, and show that coxsackievirus B3

97 GFR1/KLB) complexes expressed in adipocytes, pancreatic acinar cells, and the nervous system in mice.

98 ogen granule transport and exocytosis in the pancreatic acinar cell are not well defined.

99 ts show that key pathologic responses of the pancreatic acinar cell are regulated by PI3K gamma and s

100 Pancreatic acinar cells are a cell type of origin for pa

101 Pancreatic acinar cells are a classic model for the stud

102 Aberrant Ca(2+) signals within pancreatic acinar cells are an early and critical featur

103 Pancreatic acinar cells are commonly cotransplanted alon

104 Pancreatic acinar cells are involved in development of t

105 Pancreatic acinar cells are reprogrammed to a "ductal-li

106 nist-evoked cytosolic Ca(2+) spikes in mouse pancreatic acinar cells are specifically initiated in th

107 that adult intestinal cells, hepatocytes and pancreatic acinar cells are supplied physiologically fro

108 tant role in regulating protein secretion by pancreatic acinar cells, as does Rab3D.

109 inogen induced apoptosis of HEK293 cells and pancreatic acinar cells, as indicated by histology, DNA

110 duce Ca(2+) signals and necrosis in isolated pancreatic acinar cells but the effects of bile acids on

111 eak pathways in the endoplasmic reticulum of pancreatic acinar cells by directly measuring Ca(2+) in

112 1 mutant R122H (R122H_mPRSS1) is targeted to pancreatic acinar cells by fusion to the elastase promot

113 Pre-malignant transformation of pancreatic acinar cells by oncogenic Kras is dependent u

114 the regulation of potassium channels in rat pancreatic acinar cells by the cyclic AMP-mediated agoni

115 TP53(+/+) or TP53(f/f) specifically in adult pancreatic acinar cells by using a full-length pancreati

116 We investigated these processes in pancreatic acinar cells by using video-rate 2-photon mic

117 nduced cytosolic Ca2+ oscillations in single pancreatic acinar cells by whole-cell patch-clamp monito

118 One such factor is an excessive elevation in pancreatic acinar cell Ca(2+).

119 elevation of the Ca(2+) concentration inside pancreatic acinar cells ([Ca(2+)]i), due to excessive re

120 n conclusion, changes in intracellular pH in pancreatic acinar cells can profoundly alter cytosolic [

121 Alterations in calcium signaling in pancreatic acinar cells can result in pancreatitis.

122 It has been suggested that pancreatic acinar cells can serve as progenitors for pan

123 In response to inflammation, pancreatic acinar cells can undergo acinar-to-ductal met

124 Pancreatic acinar cell carcinoma (ACC) is an aggressive

125 We demonstrate that Piezo1 activation in pancreatic acinar cells caused a prolonged elevation in

126 In parotid and pancreatic acinar cells, changes in [Ca(2+)](c) and acti

127 ethyl Urea (NMU) results in abnormal foci in pancreatic acinar cells characterized by increased level

128 e previously reported phosphorylation of the pancreatic acinar cell cholecystokinin (CCK) receptor an

129 In pancreatic acinar cells, cholecystokinin (CCK) stimulate

130 e delivery to lysosomes critically regulates pancreatic acinar cell cholesterol metabolism.

131 close binding proximity of PTF1 and MIST1 in pancreatic acinar cell chromatin implies extensive colla

132 genetic memory of inflammatory injury in the pancreatic acinar cell compartment.

133 In isolated mouse pancreatic acinar cells, CRAC channels were activated by

134 Early events in the pancreatic acinar cell critical for development of pancr

135 TGF-beta isoforms in primary hepatocyte and pancreatic acinar cell cultures generated from transgeni

136 We show that in pancreatic acinar cells, CVB3 induces the formation of a

137 human SPINK1, die perinatally due to massive pancreatic acinar cell death, precluding investigation o

138 et effect of which is induction of apoptotic pancreatic acinar cell death.

139 rming growth factor alpha (TGF-alpha) in the pancreatic acinar cells develop tubular metaplasia, a po

140 k that is required to establish and maintain pancreatic acinar cell differentiation.

141 entify a rare TERT-positive subpopulation of pancreatic acinar cells dispersed throughout the exocrin

142 erved by fluorescence microscopy in isolated pancreatic acinar cells, dissociated hepatocytes, rod ph

143 Terminally differentiated pancreatic acinar cells do not have the innate capacity

144 These data indicate that human pancreatic acinar cells do not respond to CCK receptor a

145 dings include those demonstrating that human pancreatic acinar cells do not respond to cholecystokini

146 his study to measure total calcium loss from pancreatic acinar cells due to calcium extrusion.

147 ments of TNFalpha indicated its release from pancreatic acinar cells during incubation in primary cul

148 nvestigated by monitoring Ca(2+) dynamics in pancreatic acinar cells evoked by the flash photolysis o

149 gate the kinetics of ACh-evoked secretion in pancreatic acinar cells, exocytosis of zymogen granules

150 Zymogen secretory granules in pancreatic acinar cells express two vesicle-associated m

151 ed a direct function of insulin receptors on pancreatic acinar cells expressing a KRASG12D mutation i

152 Differentiated pancreatic acinar cells expressing endogenous levels of

153 mice, substance P levels in the pancreas and pancreatic acinar cell expression of NK1R are both incre

154 nd the Gbetagamma subunit of G proteins from pancreatic acinar cell extracts.

155 riptional network continuously maintains the pancreatic acinar cell fate.

156 hat ANO1/TMEM16A is a significant pathway in pancreatic acinar cells for HCO3 (-) secretion into the

157 ies of human pancreatitis, directly protects pancreatic acinar cells from oxidant-induced cytosolic C

158 nger RNA population and PTF1 target genes in pancreatic acinar cells from these and wild-type mice.

159 Pancreatic acinar cells from various species express cho

160 f epithelial cell polarity that is vital for pancreatic acinar cell function and viability and for th

161 The intracellular mechanisms regulating pancreatic acinar cell function are more complex than pr

162 eing made in understanding the regulation of pancreatic acinar cell function by receptor-activated in

163 Recent studies on pancreatic acinar cell function have led to a more detai

164 Recent investigations into the regulation of pancreatic acinar cell function have led to a more detai

165 Understanding the mechanisms that regulate pancreatic acinar cell function is contributing to knowl

166 Understanding the mechanisms that regulate pancreatic acinar cell function is contributing to our k

167 ding of molecular and cellular regulation of pancreatic acinar cell function.

168 rocess of acinar-to-ductal metaplasia (ADM), pancreatic acinar cells give rise to pancreatic intraepi

169 luding missense variants in genes related to pancreatic acinar cells (GP2) and insulin secretion (GLP

170 3-sulfate (TLC-S), on calcium signalling in pancreatic acinar cells has been investigated.

171 d cytosolic Ca(2+) ([Ca(2+)](i)) overload in pancreatic acinar cells have been implicated as the card

172 of the brain-gut peptide cholecystokinin on pancreatic acinar cells have indicated that NAADP and cA

173 ylene diamine (TPEN), we demonstrate that in pancreatic acinar cells, hepatocytes, and a variety of m

174 TG16L2, plays a critical role in maintaining pancreatic acinar cell homeostasis, whose dysregulation

175 hondrial alterations also occur in untreated pancreatic acinar cells; however, the underlying mechani

176 astase-Kras founder mice displayed perinatal pancreatic acinar cell hyperplasia and dysplasia.

177 1A on the specialized phenotype of the adult pancreatic acinar cell in vivo Transcriptome sequencing

178 at SEC23B is required for normal function of pancreatic acinar cells in adult mice.

179 based upon experiments with intact mice and pancreatic acinar cells in culture, that ZnT2 participat

180 cells of transgenic mice and in transfected pancreatic acinar cells in culture.

181 The role of pancreatic acinar cells in initiating fibrogenic respons

182 Rat PSTI-I expression was targeted to pancreatic acinar cells in transgenic mice by creating a

183 poptosis and death signaling pathways in rat pancreatic acinar cells, including caspase activation, c

184 We measured DeltaPsim in mouse pancreatic acinar cells incubated with ethanol alone and

185 ively inactivated CCK-evoked Ca2+ signals in pancreatic acinar cells, indicating that NAADP may funct

186 irst evidence that insulin directly protects pancreatic acinar cell injury induced by bona fide pancr

187 Bile acid exposure causes pancreatic acinar cell injury through a sustained rise i

188 In pancreatic acinar cells, inositol 1,4,5-trisphosphate (I

189 In isolated pancreatic acinar cells, insulin induced Akt-mediated ph

190 Protease activation within the pancreatic acinar cell is a key early event in acute pan

191 The pancreatic acinar cell is a valuable cell model for unde

192 The mature pancreatic acinar cell is dedicated to the production of

193 The pancreatic acinar cell is known to regulate exocytosis,

194 calcium-permeable ion channel Piezo1 in the pancreatic acinar cell is the initial step in pressure-i

195 unclear, phospholipase A2 (PLA2) produced by pancreatic acinar cells is a known pathogenic trigger.

196 dings indicate that signaling specificity in pancreatic acinar cells is aided by polarized expression

197 endocytosis at the apical plasma membrane in pancreatic acinar cells is coupled to ductal bicarbonate

198 cretion of luminal glycoprotein 2 (GP2) from pancreatic acinar cells is induced in a TNF-dependent ma

199 2Rs modulate intracellular Ca(2+) signals in pancreatic acinar cells is largely unknown.

200 ed that cholecystokinin stimulation of human pancreatic acinar cells is likely regulated by an indire

201 uggest that the fibroinflammatory program in pancreatic acinar cells is suppressed under normal physi

202 s of nicotine were also evaluated in primary pancreatic acinar cells isolated from wild-type, nAChR7a

203 A but not wild-type K18-overexpressing mice, pancreatic acinar cell keratin filaments retracted from

204 own to activate signaling kinase cascades in pancreatic acinar cells, leading to the activation of ex

205 Overexpression of Bcl-2 in the pancreatic acinar cell line AR42J decreased Ca(2+) extru

206 Despite its presence within a pancreatic acinar cell line, reg I gene expression is no

207 d gastrin (Gly-G) stimulates growth of a rat pancreatic acinar cell line; however, the effect of Gly-

208 inct groups of mitochondria in normal living pancreatic acinar cells, located (i) in the peripheral b

209 In pancreatic acinar cells, low concentrations of acetylcho

210 In pancreatic acinar cells, low-phosphate conditions increa

211 Secretory pancreatic acinar cells mature postnatally to synthesize

212 eurotransmitter cholecystokinin (CCK) in rat pancreatic acinar cells may be an important signaling ca

213 with cholecystokinin were noted in a primary pancreatic acinar cell model.

214 eutrophil sequestration in the pancreas, and pancreatic acinar cell necrosis were significantly reduc

215 However, in pancreatic acinar cells, neither messenger can explain t

216 Pancreatic acinar cells normally do not express K19, but

217 PKD phosphorylation in pancreatic acinar cells occurs viaaCa2+-independent, dia

218 Inactivation of Sec23b exclusively in the pancreatic acinar cells of adult mice results in decreas

219 or the inhibitor of kappaB kinase (IKK)2 in pancreatic acinar cells of mice.

220 Pancreatic acinar cells of patients with CP have increas

221 enhancer drives high level transcription to pancreatic acinar cells of transgenic mice and in transf

222 Ca(2+) release-activated Ca(2+) currents in pancreatic acinar cells offers remarkable protection aga

223 we show that microRNA-26a (miR-26a) inhibits pancreatic acinar cell (PAC) store-operated Ca(2+) entry

224 nd 19 were tested in freshly isolated murine pancreatic acinar cells (PACs) to determine inhibition o

225 ated current has been previously reported in pancreatic acinar cells (PACs), the role of TRPM4 in the

226 Epithelial pancreatic acinar cells perform crucial functions in foo

227 Within isolated mouse pancreatic acinar cells, PKD3 undergoes rapid membrane t

228 alpha- and beta-cells but is abundant in the pancreatic acinar cell plasma membrane.

229 Pancreatic acinar cells possess very high protein synthe

230 perimental approaches with acute dissociated pancreatic acinar cells prepared from wild type, CB1R-kn

231 The results indicate that pancreatic acinar cells produce, release, and respond to

232 The effects of aging on pancreatic acinar cell proliferation have not been clear

233 the critical role of the PI3K/Akt pathway in pancreatic acinar cell proliferation, IGF-1-mediated cel

234 I and PNA appear to be excellent lectins for pancreatic acinar cell purification.

235 To study the role of palmitoyl-CoA in the pancreatic acinar cell, rat pancreatic acini were isolat

236 lysis of fecal samples from 1795 volunteers, pancreatic acinar cell, rather than duct cell, function

237 aracterized the pH-dependent interactions of pancreatic acinar cell-regulated secretory proteins (zym

238 ressed in the exocrine pancreas, and whether pancreatic acinar cells release and respond to TNFalpha.

239 Pancreatic acinar cells rely on PTF1 and other transcrip

240 However, the tumorigenic potential of human pancreatic acinar cells remains under debate.

241 ent with high levels of IL-22RA1 expression, pancreatic acinar cells responded to IL-22 signaling via

242 tor kappaB transcriptional program in normal pancreatic acinar cells, resulting in acinar-ductal meta

243 Functional mapping of Ca2+ signaling in pancreatic acinar cells revealed that the M3, cholecysto

244 Pancreatic acinar cells secreted physiological concentra

245 in 2 (VAMP 2) and VAMP 8 in Ca(2+)-regulated pancreatic acinar cell secretion, however, their coordin

246 stress has not been studied in CP, although pancreatic acinar cells seem to be especially vulnerable

247 n cerulein-induced pancreatitis samples from pancreatic acinar cell-specific Kras knock-in (Ptf1aCre(

248 We generated mice with tamoxifen-inducible, pancreatic acinar cell-specific Sec23b deletion.

249 Perturbation of pancreatic acinar cell state can lead to acinar-to-ducta

250 nals and NADH responses were investigated in pancreatic acinar cells stimulated with calcium-releasin

251 and intracellular chymotrypsin activation in pancreatic acinar cells, suggesting that the modulation

252 Orai complexes contributes to the disease in pancreatic acinar cells, supporting a role for endoplasm

253 ults provide insights into the mechanisms in pancreatic acinar cells that link tumor necrosis factor

254 induced by muscarinic receptor activation of pancreatic acinar cells that reside within intact pancre

255 Menadione caused apoptosis of pancreatic acinar cells that was significantly potentiat

256 ool of heavy metal ions (> or = 12 microM in pancreatic acinar cells) that does not rapidly exchange

257 In pancreatic acinar cells the activity of the B element re

258 In pancreatic acinar cells the fusion pore remains open muc

259 In pancreatic acinar cells, the HOX-like factor PDX1 acts a

260 Thus, infusion of purified Gbetagamma into pancreatic acinar cells through a patch pipette evokes [

261 s suggest that acid challenge sensitizes the pancreatic acinar cell to secretagogue-induced zymogen a

262 The transdifferentiation of pancreatic acinar cells to a ductal phenotype (acinar-to

263 s, Ngn3, Mafa, and Pdx1, directly reprograms pancreatic acinar cells to beta-cells.

264 tically, IL-22 acts directly at the level of pancreatic acinar cells to decrease expression of the pa

265 th the CHO-CCKR cells and agonist-stimulated pancreatic acinar cells to provide direct evidence for t

266 r level acute alcohol exposure can sensitize pancreatic acinar cells to secretagogue stimulation, res

267 tic duct cells connect liver hepatocytes and pancreatic acinar cells to the intestine, but the mechan

268 mal studies have demonstrated the ability of pancreatic acinar cells to transform into pancreatic duc

269 method for in vivo conversion of adult mouse pancreatic acinar cells toward beta cells, we show that

270 e transgenes is activated by doxycycline the pancreatic acinar cells turn into duct-like cells.

271 PDAC can arise when pancreatic acinar cells undergo acinar-to-ductal metapla

272 resent study describes a novel phenomenon in pancreatic acinar cells undergoing regulated exocytosis.

273 Phosphorylation of rpS6 was increased in pancreatic acinar cells upon implantation of the chemica

274 R sensitivity of different regions of intact pancreatic acinar cells using local uncaging of caged Ca

275 W) in agonist-induced Ca(2+) oscillations in pancreatic acinar cells using multiple experimental appr

276 small fluorescent probes in the ER lumen of pancreatic acinar cells, using confocal microscopy, loca

277 in InsP3-evoked Ca2+ release in single mouse pancreatic acinar cells, using high-speed (approximately

278 Marked apoptosis of pancreatic acinar cells was observed during embryogenesi

279 rise in the cytosolic Ca2+ concentration of pancreatic acinar cells was triggered by stimulation wit

280 In pancreatic acinar cells we have therefore found a differ

281 Since CEL is expressed mainly in pancreatic acinar cells, we asked whether we could find

282 oreover, using 3D explant culture of primary pancreatic acinar cells, we show that PKD1 acts downstre

283 Pancreatic acinar cells were able to generate fast calci

284 Isolated rat pancreatic acinar cells were exposed to cholecystokinin

285 Finally, NAADP-evoked Ca(2+) oscillations in pancreatic acinar cells were identical in wild-type and

286 Rat pancreatic acinar cells were isolated by collagenase dig

287 Isolated mouse or rat pancreatic acinar cells were treated with high concentra

288 Mouse pancreatic acinar cells were whole-cell patch clamped to

289 In pancreatic acinar cells where intracellular infusion of

290 microsomes [5] and triggers Ca2+ signals in pancreatic acinar cells, where it is proposed to mediate

291 This is in marked contrast to the related pancreatic acinar cells, where the distribution of mitoc

292 fication had no effect on [Ca2+]i in resting pancreatic acinar cells, whereas cytosolic alkalinizatio

293 e primary receptors for basement membrane in pancreatic acinar cells, which function to synthesize an

294 ced enhancement of Ca(2+) signaling in mouse pancreatic acinar cells, which suggests a potential cell

295 Stimulation of pancreatic acinar cells with acetylcholine (ACh) and cho

296 te pancreatitis: supramaximal stimulation of pancreatic acinar cells with cholecystokinin.

297 calcium dependence of calcium extrusion from pancreatic acinar cells with preserved intracellular env

298 rincipal component of the UPR) in most adult pancreatic acinar cells (Xbp1fl/fl).

299 re-lox recombination strategy in adult mouse pancreatic acinar cells (Yap1fl/fl;Tazfl/fl;Ela1-CreERT2

300 A key event leading to exocytosis of pancreatic acinar cell zymogen granules is the inositol