ライフサイエンスコーパス: chromaffin cell

1 ic vesicle, and a medium size vesicle in the chromaffin cell.

2 mice, we find that NPY is synthesized by all chromaffin cells.

3 es in a millisecond time resolution in mouse chromaffin cells.

4 successfully from multiple individual living chromaffin cells.

5 AP-25 x synaptotagmin-1 interaction in mouse chromaffin cells.

6 iNW-FET) to detect the K(+)-efflux from live chromaffin cells.

7 holamines released from small populations of chromaffin cells.

8 echolamines, exclusively, from fetal adrenal chromaffin cells.

9 iated fusion pore expansion in mouse adrenal chromaffin cells.

10 ippocampus, dorsal root ganglia, and adrenal chromaffin cells.

11 augmented T-type Ca2+ current in IH-treated chromaffin cells.

12 correlation, confirming similar findings in chromaffin cells.

13 stimulated catecholamine release in cultured chromaffin cells.

14 spatial distribution of calcium channels in chromaffin cells.

15 d released by exocytosis in PC12 and primary chromaffin cells.

16 adapted from a model for fast exocytosis in chromaffin cells.

17 typical transmitter storage and release from chromaffin cells.

18 nd neuronal cells, including sympathoadrenal chromaffin cells.

19 on with a D1-like receptor on bovine adrenal chromaffin cells.

20 omosyn-syntaxin 1A complexes in live adrenal chromaffin cells.

21 nced catecholamine loading of LDCVs in mouse chromaffin cells.

22 type/reporter plasmids were transfected into chromaffin cells.

23 receptors on exocytosis from bovine adrenal chromaffin cells.

24 se frequency of catecholamine in dissociated chromaffin cells.

25 matory effects that depend on NPY(+) adrenal chromaffin cells.

26 ant (>90%) mode of secretion in calf adrenal chromaffin cells.

27 calcium-triggered catecholamine release from chromaffin cells.

28 Ca) was produced by P2Y receptors in adrenal chromaffin cells.

29 motions related to the secretory response in chromaffin cells.

30 e in the Ca2+-cooperativity of exocytosis in chromaffin cells.

31 ficant reduction in DCG formation in adrenal chromaffin cells.

32 human embryonic kidney HEK293-S3 and adrenal chromaffin cells.

33 is a rare, but clinically important tumor of chromaffin cells.

34 18-1/syntaxin1A interaction in HEK293-S3 and chromaffin cells.

35 ive anion equilibrium potential, depolarizes chromaffin cells.

36 coupling after this peptidergic stimulus to chromaffin cells.

37 1-L61) were transiently expressed in adrenal chromaffin cells.

38 secretory response triggered by the toxin in chromaffin cells.

39 athetic neurons appears to represent adrenal chromaffin cells.

40 K"- or "Maxi K"-encoding Slo gene in adrenal chromaffin cells.

41 synapses as well as secretory cells, such as chromaffin cells.

42 d," was confirmed by immunohistochemistry at chromaffin cells.

43 in the exocytotic membrane fusion process in chromaffin cells.

44 ranscriptional activation of the VIP gene in chromaffin cells.

45 wo sequential priming steps in mouse adrenal chromaffin cells.

46 ease and extrusion from vesicles at mast and chromaffin cells.

47 ar calcium release, and elevation of cAMP in chromaffin cells.

48 e nerve and form postsynaptic neuroendocrine chromaffin cells.

49 nergic stimulated catecholamine release from chromaffin cells.

50 uptake at the synaptic terminals and adrenal chromaffin cells.

51 NPY(+) noradrenergic neurons and/or adrenal chromaffin cells.

52 ventional active zones and in neuroendocrine chromaffin cells.

53 le priming and secretory amplitude in living chromaffin cells.

54 ion is severely inhibited in Ophn1 knock-out chromaffin cells.

55 hn1 knock-out mice and OPHN1-silenced bovine chromaffin cells.

56 ipid microdomains at the exocytotic sites in chromaffin cells.

57 he nAChR subtypes expressed by human adrenal chromaffin cells.

58 and is also essential for vesicle docking in chromaffin cells.

59 med during catecholamine exocytosis in mouse chromaffin cells.

60 nk exocytosis to compensatory endocytosis in chromaffin cells.

61 duced bulk endocytosis also occurs in bovine chromaffin cells.

62 tivator (tPA) (over many seconds) in adrenal chromaffin cells.

63 large, dense core vesicles (LDCVs) in mouse chromaffin cells.

64 Adrenal chromaffin cells (ACCs), stimulated by the splanchnic ne

65 e changes in the surface membrane of adrenal chromaffin cells after stimulation of exocytosis with a

66 e via desensitization/down-regulation of the chromaffin cell alpha(2)-adrenergic receptors that norma

67 n of neural crest-derived catecholaminergic (chromaffin) cells already associated with blood vessels

68 Ganglion neurons and adrenal chromaffin cells also show strong expressions.

69 In addition to the catecholamines, chromaffin cells also synthesize a range of peptides, in

70 alogue enhances exocytosis in neuroendocrine chromaffin cells, altering the quantal release of catech

71 onitoring of exocytotic events from cultured chromaffin cells and adrenal slices.

72 in the purified large dense-core vesicles of chromaffin cells and associated with synaptotagmin-1.

73 yme, phenyl-N-methyl transferase, by adrenal chromaffin cells and changes in cell cycle dynamics.

74 an directly affect the secretory capacity of chromaffin cells and contribute, in part, to elevated ca

75 nsmission on sympathetic neurons and adrenal chromaffin cells and elevates cytosolic ROS.

76 the internal pH of the secretory vesicles of chromaffin cells and enteric neurons.

77 and vesicular catecholamine transporters of chromaffin cells and facilitates localization of the pri

78 investigated this question in mouse adrenal chromaffin cells and found that SNAP-25 inhibits Ca(2+)

79 nergic receptors are found on bovine adrenal chromaffin cells and have been implicated in the facilit

80 (APWs) using both native channels in adrenal chromaffin cells and heterologously expressed channels i

81 irst study of EP receptor signaling in mouse chromaffin cells and identifies a molecular mechanism fo

82 s, in vesicle docking and secretion in mouse chromaffin cells and in cell-free assays.

83 tory capacity measured amperometrically from chromaffin cells and in the expression of tyrosine hydro

84 nd [Ca2+]i responses in neonatal rat adrenal chromaffin cells and involves reactive oxygen species (R

85 ly, many imprinted genes are up-regulated in chromaffin cells and may play key roles in their develop

86 Using adrenal chromaffin cells and neurons, we now find that both over

87 th catecholamines from secretory vesicles in chromaffin cells and noradrenergic neurons.

88 repinephrine released from adrenal medullary chromaffin cells and norepinephrine released locally fro

89 mega-shaped structure in live neuroendocrine chromaffin cells and pancreatic beta-cells, visualized u

90 a restricted subset of cell types, including chromaffin cells and paraganglia.

91 and histamine H(1) receptor in mouse adrenal chromaffin cells and PC12 cells.

92 ibitor of catecholamine release from adrenal chromaffin cells and postganglionic sympathetic axons.

93 protein released from secretory granules of chromaffin cells and sympathetic nerves, triggers endoth

94 Adrenal chromaffin cells and sympathetic neurons synthesize and

95 ed genes differentially expressed by adrenal chromaffin cells and sympathetic neurons.

96 entiation and increased apoptosis in adrenal chromaffin cells and sympathetic neurons.

97 hrough voltage-gated Ca2+ channels in bovine chromaffin cells and the domain of this receptor variant

98 n the development of sympathetic neurons and chromaffin cells and the mechanisms involved in Lin28B-i

99 proximity to the surface of adherent bovine chromaffin cells and to amperometrically record single e

100 (TH) in catecholamine-producing neurons and chromaffin cells and tyrosinase in melanocytes.

101 at controls epinephrine release from adrenal chromaffin cells and, consequently, hepatic glucose prod

102 that is found in neurons, platelets, adrenal chromaffin cells, and a few other neurosecretory cells.

103 epinephrine is released from adrenomedullary chromaffin cells, and compensatory glucogenesis ensues.

104 ed transcriptional mechanisms in transfected chromaffin cells, and concluded with observations on blo

105 e into melanocytes, parasympathetic neurons, chromaffin cells, and dental mesenchymal populations.

106 n of individual secretory granules in living chromaffin cells, and related their mobilities to postfu

107 Adrenal chromaffin cells are an important part of the neuroendoc

108 Adrenal medullary chromaffin cells are innervated by the sympathetic splan

109 Chromaffin cells are known to express functional GABA(A)

110 onclude that sympathetic neurons and adrenal chromaffin cells are more vulnerable to diabetes than pa

111 findings demonstrate that the fetal adrenal chromaffin cells are the source for acute hypoxaemia-ind

112 y from neural crest precursors while adrenal chromaffin cells arise from neural crest-derived cells t

113 We demonstrate that large numbers of chromaffin cells arise from peripheral glial stem cells,

114 d catestatin is secreted from neuroendocrine chromaffin cells as an autocrine regulator of nicotine-s

115 hromocytoma cells and bovine adrenomedullary chromaffin cells as detected by Northern blotting, Weste

116 acitance measurements to probe exocytosis in chromaffin cells at low concentrations of intracellular

117 When secretion was measured from chromaffin cells, brief depolarizations triggered peptid

118 ion did not evoke action potential firing in chromaffin cells but did cause a persistent subthreshold

119 brane area through exocytosis does not swell chromaffin cells but may decrease membrane tension.

120 nt from mature secretory vesicles in adrenal chromaffin cells, but localizes to a compartment near th

121 ls (a rat insulinoma cell line) and cultured chromaffin cells, but not in AtT-20 cells (derived from

122 ediating SNARE-dependent exocytosis in mouse chromaffin cells, but the role of a closely related calc

123 or monitoring single vesicle exocytosis from chromaffin cells by constant potential amperometry as we

124 alin in secretory vesicles of neuroendocrine chromaffin cells by immunofluorescent confocal and immun

125 sponse element motif, an effect confirmed in chromaffin cells by site-directed mutagenesis on the tra

126 These results show that chromaffin cells can respond to depolarizing stimuli wit

127 ssociated with the effects of CIH on adrenal chromaffin cell catecholamine secretion.

128 Direct nicotinic stimulation of chromaffin cells caused catecholamine release and transg

129 e was measured from bovine adrenal medullary chromaffin cell (CC) cultures maintained over a period o

130 ty and reduced secretory activity in adrenal chromaffin cells (CCs).

131 In chromaffin cells, CHGA and KLKB1 proteins co-localized i

132 o shrink the Omega-profile in neuroendocrine chromaffin cells containing approximately 300 nm vesicle

133 are increased by Sp and that elevate 5-HT in chromaffin cell cultures, suggesting direct metabolic si

134 tailed structure-function analysis in murine chromaffin cells demonstrates that linker motifs play a

135 describes the primary culture of individual chromaffin cells derived by enzymatic digestion from the

136 We used amperometric recordings from chromaffin cells derived from mice that overexpress A30P

137 of NGF signaling for sympathetic neural and chromaffin cell development.

138 l sympathetic neuroblast hyperplasia, blocks chromaffin cell differentiation, and ultimately triggers

139 evoked secretion simultaneously from several chromaffin cells directly cultured on the device surface

140 owever, unlike hypothalamic nerve terminals, chromaffin cells do not display syntilla activation by d

141 synapses lacking Munc13s, the corresponding chromaffin cells do not exhibit a vesicle docking defect

142 surface membrane while secretory granules in chromaffin cells do not.

143 techolamine biosynthetic capacity of adrenal chromaffin cells during periods of sustained catecholami

144 rms, even upon high-frequency stimulation of chromaffin cells during stress responses.

145 Application of etomidate directly to the chromaffin cells elicited robust catecholamine secretion

146 Evidence suggests that chromaffin cells employ separate mechanisms for evoked e

147 e) Ca2+ and voltage-dependent K+ channels in chromaffin cells exhibit an inactivation that probably a

148 Thus chromaffin cells exhibit two kinetically and mechanistic

149 ously reported that N-type current in bovine chromaffin cells exhibits very little voltage-dependent

150 evious studies have shown that naive adrenal chromaffin cells express a nominal Ca(v)3.2-dependent co

151 d secretion from Munc18-1-null mouse adrenal chromaffin cells expressing Munc18-1 mutants designed to

152 residues, single exocytotic events in bovine chromaffin cells expressing R198Q, R198E, K201Q, or K201

153 Single exocytotic events in chromaffin cells expressing this mutant were characteriz

154 arge dense core vesicle (LDCV) exocytosis in chromaffin cells follows a well characterized process co

155 Stimulation of bovine chromaffin cells for 5 min with 6 mum free intracellular

156 at the plasma membrane and in the cytosol in chromaffin cells from adrenal medulla.

157 ally occurring splice variants of CAPS2 into chromaffin cells from CAPS1/CAPS2 double-deficient mice

158 A30P or wild-type (WT) alpha-syn, as well as chromaffin cells from control and alpha-syn null mice, t

159 We show that adrenal chromaffin cells from CPX II knockout mice exhibit marke

160 Additionally, mRNA analyses of purified chromaffin cells from Gata3 mutants show that levels of

161 e have examined the kinetics of secretion in chromaffin cells from mice lacking phosphatidylinositol

162 ime and characterized in freshly dissociated chromaffin cells from mouse.

163 SCR-1 calcium-insensitive mutant or by using chromaffin cells from PLSCR-1(-)/(-) mice prevents outwa

164 ar mechanisms by which PGE(2) might modulate chromaffin cell function.

165 grams down-regulate SCP-gene and up-regulate chromaffin cell-gene networks.

166 s highly expressed in bovine adrenomedullary chromaffin cells, human pheochromocytoma tissue, PC12 ph

167 euroblastoma at single-cell level and find a chromaffin cell identity of neuroblastoma.

168 We electrically stimulated chromaffin cells in adrenal tissue slices at the sympath

169 ime-lapse imaging of Lifeact-GFP-transfected chromaffin cells in combination with fluorescent 70 kDa

170 lar sites expressed in intact bovine adrenal chromaffin cells in culture.

171 small and different subpopulations of bovine chromaffin cells in culture.

172 -R(KT) mAb was observed in adrenal medullary chromaffin cells in murine and human tissue.

173 es and other hormones, released from adrenal chromaffin cells in response to Ca(2+) influx through vo

174 to the extent of catecholamine release from chromaffin cells in response to stimulation by carbachol

175 s on T-type Ca(v)3.2 calcium influx in mouse chromaffin cells in situ.

176 umor entity originating from adrenomedullary chromaffin cells in the adrenal medulla or in sympatheti

177 The number of chromaffin cells in the adrenal medulla was also decreas

178 catecholamines and a neuropeptide from mouse chromaffin cells in vitro.

179 0 were colocalized to the Golgi apparatus of chromaffin cells in vivo and shared localization with CH

180 We hypothesize that Slo splicing in adrenal chromaffin cells in vivo is differentially regulated by

181 ociated with distinctive membrane changes of chromaffin cells including increased electron density, a

182 evealed decreased LDCV size in noradrenergic chromaffin cells, increased adrenal norepinephrine and e

183 ated exocytic function in Mecp2(-/y) adrenal chromaffin cells, indicating that the Mecp2 null mutatio

184 ially regulate fusion pore dynamics in mouse chromaffin cells, indicating TMD flexibility as a mechan

185 pression of Ca(v)3.2 channels in MPC 9/3L-AH chromaffin cells induced low-threshold secretion that co

186 In chromaffin cells, inhibition of H(+)-ATPase diverted CHG

187 In chromaffin cells, IRM detects the fusion of individual g

188 ominant calcium signal regulating release in chromaffin cells is generated by the cooperative action

189 Transient stimulation of secretion in calf chromaffin cells is invariably followed by rapid endocyt

190 Exocytosis in adrenal chromaffin cells is strongly influenced by the pattern o

191 heteromeric nAChR expressed by human adrenal chromaffin cells is the alpha3beta4* subtype (asterisk i

192 on of neurotransmitters and neuropeptides in chromaffin cells, is poorly understood.

193 In chromaffin cells isolated from a PICK1 knockout (KO) mou

194 Chromaffin cells isolated from transgenic mice that over

195 analyzed their role in LDCV exocytosis using chromaffin cells lacking individual isoforms.

196 equently, the absence of Snapin in embryonic chromaffin cells leads to a significant reduction of cal

197 We provide evidence that chromaffin cell malfunction derives from altered Cav1.2

198 These findings suggest one way in which chromaffin cells may regulate cargo release is via diffe

199 Thus, chromaffin cells may regulate release of different trans

200 Mouse chromaffin cells (MCCs) fire spontaneous action potentia

201 We show that loss of SDH activity in a chromaffin cell model does not perturb complex I functio

202 SDH deficiency based on epithelial cells, a chromaffin cell model retains aspects of metabolic "heal

203 letion of a gene highly expressed by adrenal chromaffin cells, NIK-related kinase, a gene on the X-ch

204 e docking, neither synchronized secretion in chromaffin cells nor Ca(2+)-triggered SUV-GUV fusion was

205 exhibiting differential mobility shifting to chromaffin cell nuclear proteins during EMSA, binding of

206 own to accumulate mainly in association with chromaffin cells, occasional nerve endings and macrophag

207 also expressed in neonatal adrenal medullary chromaffin cells of rats and mice whose hypoxia-evoked c

208 To specifically delete GRK2 in the chromaffin cells of the adrenal gland, we crossed PNMTCr

209 Chromaffin cells of the adrenal medulla (AM) represent t

210 Chromaffin cells of the adrenal medulla are a primary ne

211 Chromaffin cells of the adrenal medulla are innervated b

212 c neurons are severely depleted in CIPA, but chromaffin cells of the adrenal medulla are spared.

213 ium channels are expressed in neurosecretory chromaffin cells of the adrenal medulla.

214 opening of a narrow fusion pore, in adrenal chromaffin cells of wild-type and Rab3A(-/-) mice.

215 gs of quantal exocytosis from bovine adrenal chromaffin cells on the device.

216 By culturing chromaffin cells on the VAL-PVC/SiNW-FET, the conductanc

217 ak amplitude of nicotine-induced currents in chromaffin cells or in human embryonic kidney cells ecto

218 cement of exocytosis by PMA in either bovine chromaffin cells or the INS-1 insulin-secreting cell lin

219 ytomas and paragangliomas are rare tumors of chromaffin cell origin.

220 Thus, in chromaffin cells, PKC enhances exocytosis both by increa

221 Internalisation of PrP(d) from the chromaffin cell plasma membrane occurred in association

222 suggest that PROG inhibits CA secretion from chromaffin cells predominantly by rapidly inhibiting nAC

223 The bovine chromaffin cell procedure should yield approximately 10-

224 Pheochromocytomas, arising from chromaffin cells, produce catecholamines, epinephrine an

225 In cultured chromaffin cells, reducing endogenous CHGA expression by

226 Adrenal chromaffin cells release hormones and neuropeptides that

227 est that a spontaneous syntilla, at least in chromaffin cells, releases Ca2+ into a cytosolic microdo

228 wise, inactivation of the V0 a1-I subunit in chromaffin cells resulted in a decreased frequency and p

229 comparable with those of bPAC1hop in bovine chromaffin cells resulted in acquisition by PC12-G cells

230 hat overexpression of neuronal AP-3 in mouse chromaffin cells results in a striking decrease in the n

231 rometric measurements of exocytosis in mouse chromaffin cells revealed that syb2 TMD mutations altere

232 medullary slices that permit separating the chromaffin cell secretion from sympathetic input.

233 Stimulation of chromaffin cell secretion in vitro triggers not only sec

234 CG10 by synthetic siRNAs virtually abolished chromaffin cell secretion of a transfected CHGA-EAP chim

235 revented the effects of IH on hypoxia-evoked chromaffin cell secretion.

236 extraordinary accumulation of solutes inside chromaffin cell secretory vesicles, although this has ye

237 r with time, that vesicles in bovine adrenal chromaffin cells segregate into distinct populations, ba

238 We provide data to show that chromaffin cells selectively release catecholamine under

239 l firing rates, set by the sympathetic tone, chromaffin cells selectively release catecholamines at a

240 Neuroendocrine chromaffin cells selectively secrete a variety of transm

241 of this phenomenon in neuroendocrine adrenal chromaffin cells show that a single 2-ns, 16 MV/m unipol

242 In summary, PAI-1 is expressed in chromaffin cells, sorted into the regulated pathway of s

243 e mice, expressing Cre recombinase under the chromaffin cell-specific phenylethanolamine N-methyltran

244 Chromaffin cells stimulated with high KCl showed both sl

245 ndogenous proteins are expressed in separate chromaffin cell subpopulations.

246 gnals was severalfold faster than in adrenal chromaffin cells, suggesting profound differences in the

247 eterogeneous release of catecholamine at the chromaffin cell surface.

248 ltered transmission at the preganglionic --> chromaffin cell synapse.

249 In bovine chromaffin cells, syntaxin and SNAP-25 colocalize in def

250 Two Syt isoforms are expressed in chromaffin cells: Syt-1 and Syt-7.

251 medulla gland and of cultured human adrenal chromaffin cells that demonstrated prominent expression

252 chains supported secretion in permeabilized chromaffin cells that had been allowed to rundown.

253 Src family kinases (SFKs) are abundant in chromaffin cells that reside in the adrenal medulla and

254 In cultured chromaffin cells, the total cytosolic catechol concentra

255 irectly activated GABA(A) receptors found in chromaffin cells thereby elevating [Ca(2+)](i).

256 , high-affinity nAChRs expressed in cultured chromaffin cells, they do not appear to be involved in f

257 hape of the bipolar pulse, Ca(2+) entry into chromaffin cells through electropores could be attenuate

258 Stimulation causes chromaffin cells to fire action potentials, leading to t

259 We used bovine chromaffin cells to investigate the effects of PROG on C

260 tentials delivered at 0.5 Hz) causes adrenal chromaffin cells to selectively release catecholamines t

261 hetic tone, basal synaptic excitation drives chromaffin cells to selectively secrete modest levels of

262 Exposing adrenal chromaffin cells to single 150 to 400 ns electric pulses

263 CPE and PC activity in extracts of cultured chromaffin cells; total protein levels were unaltered fo

264 In a chromaffin cell-transfected CHGA 3'-UTR/luciferase repor

265 ies have demonstrated that adrenal medullary chromaffin cells transplanted into the spinal subarachno

266 ection of catecholamine release from adrenal chromaffin cells trapped in a microfluidic network.

267 ificity for the diagnosis of adrenomedullary chromaffin cell tumors can be jeopardized by physiologic

268 PC12 cells, like endocrine chromaffin cells, undergo neuronal-like differentiation

269 We studied insertion of granules in bovine chromaffin cells using capacitance as a measure of plasm

270 ne release in individual quantal events from chromaffin cells using cell-attached patch amperometry.

271 s of exocytosis from populations of mast and chromaffin cells using chemoreceptive neuron MOS (CnuMOS

272 We investigated its role in chromaffin cells using Doc2b knock-out mice and high tem

273 Experiments on diI-stained bovine adrenal chromaffin cells using polarized TIRFM demonstrate rapid

274 strate that CIH increases the RRP in adrenal chromaffin cells via ROS-mediated activation of PKC and

275 punctate staining of norepinephrine-enriched chromaffin cells visualized using confocal microscopy in

276 Secretion of catestatin intermediates from chromaffin cells was accompanied by the cosecretion of c

277 histamine in H(1) receptor/TRPC4-expressing chromaffin cells was comparable with that triggered by a

278 ing of individual exocytotic fusion pores in chromaffin cells was imaged electrochemically with high

279 eover, regulated secretion of endopin 2 from chromaffin cells was induced by nicotine and KCl depolar

280 lamines, measured by amperometry in cultured chromaffin cells, was found to be increased either by pr

281 In Cplx 2-null adrenal chromaffin cells, we also find decreased and desynchroni

282 In bovine adrenal chromaffin cells, we found Rac1, but not Cdc42, to be ra

283 ophysiological measurements in mouse adrenal chromaffin cells, we show that PI(4,5)P2 uncaging potent

284 In individual chromaffin cells, we tracked conformational changes in S

285 these mutations on the exocytotic process in chromaffin cells were assessed using capacitance measure

286 We show that bovine adrenal chromaffin cells were excited by etomidate at clinically

287 Bovine adrenal chromaffin cells were induced to express Rab3AQ81L and g

288 egulates stimulus-secretion coupling, bovine chromaffin cells were infected with Semliki Forest virus

289 Bovine adrenal chromaffin cells were loaded into the microfluidic chann

290 Bovine adrenal chromaffin cells were superfused with a variety of GABA(

291 Small populations of chromaffin cells were trapped in the microfluidic device

292 red how alpha-syn overexpression in PC12 and chromaffin cells, which exhibit low endogenous alpha-syn

293 s to hypoxia by the carotid body and adrenal chromaffin cells, which regulate cardio-respiratory func

294 Combined treatment of chromaffin cells with 40 mm KCl, which elevates intracel

295 y monitoring CME of single vesicles in mouse chromaffin cells with cell-attached capacitance measurem

296 Stimulation of chromaffin cells with lysophosphatidic acid, a nonsecret

297 s and whole-cell recordings from rat adrenal chromaffin cells with parallel experiments on inactivati

298 Treatment of cultured bovine adrenal chromaffin cells with the catecholamine transport blocke

299 monstrate that electrostimulation of adrenal chromaffin cells with ultrashort pulses can be modulated

300 foundly impairs priming of granules in mouse chromaffin cells without altering catecholamine release