ライフサイエンスコーパス: dense-core

1 ace area only 37% of the high pH form with a dense core.

2 perimetral membrane surrounding an electron-dense core.

3 cell extension distinguished by an electron-dense core.

4 f a relatively hard shell and a softer, less dense core.

5 sma cell possesses a characteristic electron-dense core.

6 e, with enlargement in the volume around the dense core, a phenomenon that occurs to maintain constan

7 izes possible by accreting material around a dense core about one-third to one-half the present size

8 ost of components from their three granules: dense core, alpha, and lysosome.

9 terminal organelle having a central electron-dense core and adhesin-related proteins clustered at a t

10 in that most capsids in the nuclei lacked a dense core and most enveloped particles in the cytoplasm

11 ghts of pathways between the high-efficiency dense core and periphery.

12 In Syt IV knockouts, dense-core and microvesicle fusion was enhanced in cell-

13 nerve terminals making up each site possess dense-core and/or electron-lucent vesicles, suggesting d

14 ately 7 nm external diameter and an electron dense core, and to form channels of 50picoSiemens conduc

15 f the SP-NC junction, production of electron-dense cores, and cDNA synthesis but blocked retrotranspo

16 -like conformational changes of its electron-dense core are leveraged against a cytoplasmic anchor an

17 he cell membrane, and the peptide-containing dense cores are displayed.

18 This transformation from "dense core" at high pH to "dense shell" at low pH could

19 e physicochemical properties of the electron-dense core atrial gland vesicles from Aplysia californic

20 lts suggest that nanoparticles interrupt the dense-core biopolymer intragranular matrix and present t

21 nd display multilaminar, multivesicular, and dense-core bodies as well as mitochondria.

22 e their soluble content aggregates to form a dense core, but the mechanisms controlling biogenesis ar

23 ermination of the dimensions of the electron-dense core by transmission electron microscopy (TEM), wi

24 ion that displayed a clear halo around their dense cores (called active vesicles).

25 nhibitor-treated cells lacked DNA-containing dense-core capsids in the nucleus, and only incomplete v

26 l cycle, transitioning between an infectious dense-cored cell (DC) and a noninfectious reticulate cel

27 le, transitioning between a smaller electron dense-cored cell (DC), which has a dense nucleoid, and a

28 VLPT was localized on both reticulate and dense-core cells, and it was found extracellularly in th

29 a biphasic developmental cycle consisting of dense-cored cells (DCs) and reticulate cells (RCs).

30 e gp19 protein was present on reticulate and dense-cored cells, and it was found extracellularly in t

31 : the regulation of catecholamine-containing dense-core chromaffin granule biogenesis in the adrenal

32 focal microscopy demonstrated p47-expressing dense-cored (DC) ehrlichiae colocalized with PCGF5, FYN,

33 fectious reticulate cell (RC) and infectious dense-cored (DC) forms.

34 conversion to the extracellular, infectious "dense-core" (DC) form.

35 Neuropeptide-containing dense-core (DCVs) vesicles are trafficked in a polarized

36 Dense-core deposits that were not cleared were reduced i

37 ferentially expressed only on the surface of dense-cored ehrlichiae and detected in the Ehrlichia-fre

38 early steps in LDCV formation by controlling dense core formation at the TGN.

39 -SP processing, cDNA synthesis, and electron-dense core formation.

40 roperties, due to impaired cargo sorting and dense core formation.

41 The segregation of dense core-forming melts by porous flow is a natural mec

42 lcineurin b1 (Cnb1) in mouse islets impaired dense core granule biogenesis, decreased insulin secreti

43 Here, I investigate whether a single dense core granule can be loaded with both types of tran

44 expression of factors essential for insulin dense core granule formation and secretion and neonatal

45 haracteristic commonly associated with large dense core granule fusion pores.

46 I find that fusion of a single dense core granule releases both types of transmitters i

47 differentiation revealed that an increase in dense-core granule catecholamine content by exogenous ap

48 The secretion of the single dense-core granule of mammalian spermatozoa relies on th

49 Sperm contain a single large dense-core granule that is released by regulated exocyto

50 ophila, the polypeptides stored in secretory dense core granules (DCGs) are generated by proteolytic

51 The formation of dense core granules (DCGs) requires both the sorting of

52 ely in Paneth cells where they occur only in dense core granules and thus are secreted to function in

53 In neuroendocrine cells, whose dense core granules are strikingly similar to mast cell

54 apin co-localized with endogenous torsinA on dense core granules in PC12 cells and was recruited to p

55 t the trafficking of neuropeptide-containing dense core granules is markedly cell type specific and i

56 a secretory epithelial lineage that release dense core granules rich in host defense peptides and pr

57 f molecules from synaptic vesicles and large dense core granules through the process of exocytosis.

58 ss a variety of beta-cell markers, including dense core granules visible by electron microscopy (EM).

59 Correct processing of human renin in dense core granules was confirmed by immunogold labeling

60 ere no differences in secretion of [3H]-5HT (dense core granules), platelet factor IV (alpha granules

61 ate that VAMP-8 is required for release from dense core granules, alpha granules, and lysosomes.

62 n microscopy revealed cytoplasmic, endocrine-dense core granules, analogous to those found in human n

63 mines and peptides are both contained within dense core granules, whether they are copackaged is less

64 mutant proteins were found in the same large dense core granules.

65 be FM4-64 and fluorescent proteins in single dense core granules.

66 Dense-core granules (DCGs) are organelles found in speci

67 is an important factor for the formation of dense-core granules by regulating the ability of CgA to

68 that a proportion of human TFH cells contain dense-core granules marked by chromogranin B, which are

69 trahymena thermophila, peptides secreted via dense-core granules, called mucocysts, are generated by

70 Recent work has established that, for dense-core granules, quantal size can be varied by stimu

71 g vesicles having the distinct morphology of dense-core granules.

72 ction with chemical models, we find that the dense core has been chemically processed for at least on

73 ck, but both results imply that star-forming dense cores have ages of about one million years, rather

74 plasmic and nuclear structures composed of a dense core inaccessible to nascent polypeptides surround

75 in, a second protein near the taper, forms a dense-core-like structure that is disrupted in the absen

76 TRP120 in HeLa cells and with E. chaffeensis dense-cored morulae and areas adjacent to morulae in the

77 W2 is the defining component of the electron-dense core of the terminal organelle.

78 membrane-bound cell extension is an electron-dense core of two segmented rods oriented longitudinally

79 plasma membrane, and then the membranes and dense cores of fused granules are internalized.

80 e star-forming regions are comparable to the dense cores of giant molecular clouds in the local Unive

81 n the Milky Way, high-mass stars form in the dense cores of interstellar molecular clouds, where gas

82 ctable on the surfaces of A. phagocytophilum dense core organisms bound at the HL-60 cell surface, bu

83 urfaces of intravacuolar reticulate cell and dense core organisms.

84 cellular morula fibers in morulae containing dense-cored organisms.

85 cations for secretory cargo condensation (or dense core "packing" structure) within the regulated pat

86 his technique is able to distinguish between dense-core particles, liquid-filled, bilayer-coated vesi

87 Aggregated Abeta accumulates as both dense core plaques and diffuse deposits in the brains of

88 ity (1.5 nM) for Abeta40 fibrils and labeled dense core plaques better than 6E10 as determined by imm

89 We observed fluorescence associated with dense core plaques, but not diffuse plaques, as determin

90 he non-immunized patients, neurites close to dense-core plaques (within 50 microm) were more abnormal

91 ial responses in the vicinity (</=50 mum) of dense-core plaques and tangles.

92 neurites close to and far from the remaining dense-core plaques did not differ, and both were straigh

93 Compared to non-immunized patients, dense-core plaques remaining after immunization had simi

94 Amyloid load and density of dense-core plaques were decreased in the immunized group

95 correlated with the loss of both diffuse and dense-core plaques within the cortex.

96 also occurs within the halo of the remaining dense-core plaques.

97 , and nine nondemented control subjects with dense-core plaques.

98 onstrating a dramatic synaptotoxic effect of dense-cored plaques.

99 ally less organized than an ION, possesses a dense core region consisting of multipolar neurons.

100 neous myocardial tissue (gray zone [GZ]) and dense core scar.

101 Processes underlying the formation of dense core secretory granules (DCGs) of neuroendocrine c

102 In some cells, the polypeptides stored in dense core secretory granules condense as ordered arrays

103 hat proinflammatory mediators in Paneth cell dense core secretory granules mediate tumor necrosis fac

104 granules, and the agonist-induced fusion of dense core secretory granules to the mast cell plasma me

105 nes and neuropeptides, through the fusion of dense core secretory granules with the cell surface.

106 ic pathway function, biogenesis of mast cell dense core secretory granules, and the agonist-induced f

107 1 nonetheless activates at pH~5.5 within the dense core secretory granules.

108 n of the protein architecture of the 'human' dense core secretory vesicles (DCSV) to understand mecha

109 protein tyrosine phosphate family located in dense core secretory vesicles and a major autoantigen in

110 Dense-core secretory granule (DCG) biogenesis is a prere

111 Sperm contain a large dense-core secretory granule (the acrosome) whose conten

112 family of prohormones widely distributed in dense-core secretory granules (DCGs) of endocrine, neuro

113 The biogenesis of dense-core secretory granules (DCGs), organelles respons

114 layed very minor overlaps with lysosomes and dense-core secretory granules and were similar to lysoso

115 peptides, which are stored and released from dense-core secretory granules of neuroendocrine cells, h

116 rotid secretory proteins are stored in large dense-core secretory granules that undergo stimulated se

117 localizes to synaptic vesicles and to large dense-core secretory vesicles as reported previously, wh

118 ates, is stored in, and secreted from, large dense-core secretory vesicles in nerve terminals in the

119 Bioactive peptides are packaged in large dense-core secretory vesicles, which mediate regulated s

120 yrosine phosphatase family and is located in dense-core secretory vesicles.

121 network; the only known role of clathrin in dense-cored secretory granules formation is to remove mi

122 In contrast, formation of much larger dense-cored secretory granules is driven by selective ag

123 in the final stages of star formation, where dense cores (size approximately 0.1 parsecs) inside mole

124 Although vesicles with a dense core still form in the absence of AP-3, they conta

125 00 km MCF, offering flexibility to fabricate dense core structures with same cladding diameter.

126 ll is defined by the presence of an electron-dense core that appears as paired, parallel bars oriente

127 ions of the brain, which collectively form a dense core that enhances the functional integration of a

128 sufficient to create a mass distribution of dense cores that resembles, and sets, the stellar initia

129 ns regarding the composition of the electron-dense core, the means by which the terminal organelle is

130 (+) activated microglia in randomly selected dense-core (Thioflavin-S(+)) plaques from the temporal n

131 PC12 cells are used to test whether altering dense core vesicle (DCV) motion affects neuropeptide rel

132 Large dense core vesicle (LDCV) exocytosis in chromaffin cells

133 for secretion (CAPS) protein is required for dense core vesicle docking but not synaptic vesicle dock

134 Here, we describe a mechanism for dense core vesicle docking in neurons.

135 CAPS function in dense core vesicle docking parallels UNC-13 in synaptic

136 for synaptic vesicles, is not essential for dense core vesicle docking.

137 taxin can bypass the requirement for CAPS in dense core vesicle docking.

138 PI(4,5)P2 localizes to sites of dense core vesicle exocytosis in neuroendocrine cells an

139 have been analyzed for biological effects on dense core vesicle exocytosis in neuroendocrine PC12 cel

140 fferent systems as follows: Ca(2+)-triggered dense core vesicle exocytosis, spontaneous synaptic vesi

141 sible roles of the CAPS protein in mediating dense core vesicle fusion and modulating synaptic vesicl

142 nal is transmitted through calcium-activated dense core vesicle neurosecretion.

143 eta cells, IA-2 is an important regulator of dense core vesicle number and glucose-induced and basal

144 Importantly, dense core vesicle release and secretion of the neurotra

145 d SSLV fusion events without affecting large dense core vesicle secretion.

146 signal peptide-containing domain, for large dense core vesicle sorting and regulated secretion from

147 he formation and/or maintenance of the small dense core vesicle subpool in PC12 cells.

148 w that the presence and release of the small dense core vesicle subpool is dependent on synaptotagmin

149 of dense core vesicles, a small and a large dense core vesicle subpool.

150 ficial peptide neurotransmitter containing a dense core vesicle targeting domain, a NMDA NR1 subunit

151 Neither large dense core vesicle terminals nor type I synaptic glomeru

152 o suggested to play a role in Ca2+-dependent dense-core vesicle (DCV) exocytosis in neuroendocrine ce

153 Dense-core vesicle (DCV) exocytosis is a SNARE (soluble

154 unknown whether the molecular steps of large dense-core vesicle (LDCV) docking and priming are identi

155 The six targets include several large dense-core vesicle (LDCV) proteins, but also proteins in

156 We propose that dense-core vesicle acidification controlled by the evolu

157 UNC-13 serve parallel and dedicated roles in dense-core vesicle and synaptic vesicle exocytosis, resp

158 st that CeIA-2 may be an important factor in dense-core vesicle cargo release with parallels to insul

159 has been shown in other systems to regulate dense-core vesicle cargo release.

160 defects in sorting soluble and transmembrane dense-core vesicle cargos.

161 n were defective for anterograde movement of dense-core vesicle components, including egl-3 PC2, egl-

162 oposed to be an important regulator of large dense-core vesicle exocytosis from neuroendocrine tissue

163 " Rab3 and Rab27, regulate late steps during dense-core vesicle exocytosis in neuroendocrine cells.

164 Essential prefusion steps in dense-core vesicle exocytosis involve sequential ATP-dep

165 Novel assays for dense-core vesicle exocytosis were developed by expressi

166 esynaptic UNC-31 activity, likely acting via dense-core vesicle exocytosis, is required to locally ac

167 Rab27/Rab3A constitutes a Rab-GEF cascade in dense-core vesicle exocytosis.

168 ut is generally required for and specific to dense-core vesicle exocytosis.

169 to be essential for synaptic vesicle but not dense-core vesicle exocytosis.

170 7 to examine how synaptotagmins function in dense-core vesicle exocytosis.

171 the primary determinant of Ca(2+)-triggered dense-core vesicle exocytosis.

172 rface with three other proteins required for dense-core vesicle exocytosis: phospholipase D1 (PLD1),

173 norhabditis elegans for mutants defective in dense-core vesicle function.

174 osphate synthesis in the regulation of large dense-core vesicle fusion dynamics.

175 on was enhanced in cell-attached patches and dense-core vesicle fusion pores had conductances that we

176 C. elegans mutants lacking the dense-core vesicle priming protein UNC-31 (CAPS) share h

177 changes were correlated with alterations in dense-core vesicle size.

178 ed family member) and determined its role in dense-core vesicle-mediated peptide secretion and in syn

179 rs are released from a unique organelle: the dense-core vesicle.

180 d a lower frequency of synapse formation and dense-cored vesicle content than CHT-labeled profiles in

181 the receptor is concentrated on peptidergic dense core vesicles (DCVs) and is notably absent from th

182 pported bilayers and purified neuroendocrine dense core vesicles (DCVs) as fusion partners, and we ex

183 ion requires anterograde axonal transport of dense core vesicles (DCVs) containing neuropeptides and

184 Cmpy first delivers Gbb to dense core vesicles (DCVs) for activity-dependent releas

185 Despite a key role for dense core vesicles (DCVs) in neuronal function, there a

186 The dense core vesicles (DCVs) of neuroendocrine cells are a

187 nctional relationships of axonal kinesins to dense core vesicles (DCVs) that were filled with a GFP-t

188 Neurons secrete neuropeptides from dense core vesicles (DCVs) to modulate neuronal activity

189 beta cells to form crystalline aggregates in dense core vesicles (DCVs), which are released in respon

190 another form of neuronal signaling, that of dense core vesicles (DCVs), whose contents can include n

191 el of neuropeptide release from motor neuron dense core vesicles (DCVs).

192 cargos derived from neuronal and intestinal dense core vesicles (DCVs).

193 esting the existence of a refractory pool of dense core vesicles (DCVs).

194 isms responsible for production of the large dense core vesicles (LDCVs) capable of regulated release

195 e role for PICK1 in the biogenesis of large, dense core vesicles (LDCVs) in mouse chromaffin cells.

196 of proteins and neurotransmitters from large dense core vesicles (LDCVs) is a highly regulated proces

197 Large dense core vesicles (LDCVs) mediate the regulated releas

198 Neuroendocrine (NE) cells use large dense core vesicles (LDCVs) to traffic, process, store a

199 , hormones and neuropeptides stored in large dense core vesicles (secretory granules) are released th

200 nce that CKA facilitates axonal transport of dense core vesicles and autophagosomes in a PP2A-depende

201 ontacts; 2) small, round vesicles plus a few dense core vesicles and forming asymmetric contacts; or

202 Here, we demonstrate that dense core vesicles and lysosomal trafficking dynamics a

203 es, endomorphin-2 was contained primarily in dense core vesicles and MOR1 was located primarily at no

204 syt I and VII partially colocalize on large dense core vesicles and that upregulation of syt VII pro

205 eptide precursor VGF that is stored in large dense core vesicles and undergoes regulated secretion.

206 in the density of both synaptic vesicles and dense core vesicles at presynaptic terminals.

207 5-HT secreted by both synaptic vesicles and dense core vesicles diffuse readily to the extrasynaptic

208 In Caenorhabditis elegans motor neurons, dense core vesicles dock at the plasma membrane but are

209 vesicles but not in insulin-containing large dense core vesicles in beta-cells.

210 h BDNF or its pro-peptide both stained large dense core vesicles in excitatory presynaptic terminals

211 in nerve terminals or the movement of large dense core vesicles in growth cones and endocrine cells.

212 extracellularly applied HRP (0.1%) perturbs dense core vesicles in the synaptic processes of leech n

213 In sensory afferents, the number of dense core vesicles increases 5-fold, while there is onl

214 dorsal horn are localized exclusively within dense core vesicles of synaptic terminals.

215 SgII-containing dense core vesicles share morphological and physical pro

216 th full exocytotic fusion of small clear and dense core vesicles shown in previous morphometric studi

217 at neuronal exocytosis of neuropeptides from dense core vesicles suppressed the survival of Caenorhab

218 at both calcium-regulated exocytic vesicles (dense core vesicles) and endocytic structures (clathrin-

219 ude small clear vesicles and two subpools of dense core vesicles, a small and a large dense core vesi

220 trinsic neurons, afferent neurons containing dense core vesicles, and systems of serial synaptic comp

221 Secretory granules, such as neuronal dense core vesicles, are specialized for storing cargo a

222 l size was much less than expected for large dense core vesicles, suggesting that release originated

223 the open state of syntaxin, which then docks dense core vesicles.

224 s also exhibit enhanced peptide release from dense core vesicles.

225 bpools of vesicles: small clear vesicles and dense core vesicles.

226 Here, green fluorescent protein-tagged dense-core vesicles (DCVs) are imaged in Drosophila moto

227 Dense-core vesicles (DCVs) are regulated secretory organ

228 ned by constitutive bidirectional capture of dense-core vesicles (DCVs) as they circulate in and out

229 Neuronal dense-core vesicles (DCVs) contain diverse cargo crucial

230 imaging of Drosophila and hippocampal neuron dense-core vesicles (DCVs) containing a neuropeptide or

231 ants revealed a 50% reduction in presynaptic dense-core vesicles (DCVs) corresponding to enhanced neu

232 ized distribution of neuropeptide-containing dense-core vesicles (DCVs) in Caenorhabditis elegans cho

233 Neuropeptides released from dense-core vesicles (DCVs) modulate neuronal activity, b

234 indicating that both microvesicles (MVs) and dense-core vesicles (DCVs) undergo fusion.

235 n essential for the Ca2+-dependent fusion of dense-core vesicles (DCVs) with the plasma membrane and

236 tinct organelles-synaptic vesicles (SVs) and dense-core vesicles (DCVs), respectively.

237 phins depends on presynaptic accumulation of dense-core vesicles (DCVs).

238 enzymes, and neurotrophins by exocytosis of dense-core vesicles (DCVs).

239 store, and release neuropeptides packaged in dense-core vesicles (DCVs).

240 eins depends on their inclusion within large dense-core vesicles (LDCVs) capable of regulated exocyto

241 the function of syb in the docking of large dense-core vesicles (LDCVs) in live PC12 cells using tot

242 presence of estrogen receptor-alpha on large dense-core vesicles (LDCVs) in the hippocampus suggests

243 bly, we found that TRPV1 is present in large dense-core vesicles (LDCVs) that were mobilized to the n

244 cells, VMAT2 localizes exclusively to large dense-core vesicles (LDCVs), and we now show that cytopl

245 quired for release at the synapse, and large dense-core vesicles (LDCVs), which mediate extrasynaptic

246 otransmitters and peptide hormones via large dense-core vesicles (LDCVs).

247 artially colocalized with CGRP in some large dense-core vesicles (LDCVs).

248 Furthermore, we describe two types of dense-core vesicles and quantify a filamentous network o

249 three ultrastructural types, with clear- or dense-core vesicles and those with a dark cytoplasm havi

250 Dense-core vesicles are generated at the trans-Golgi and

251 Large dense-core vesicles are unaffected by clathrin knock dow

252 In both cases, dense-core vesicles associated with DOR labeling were of

253 onserved proteins controls the maturation of dense-core vesicles at the trans-Golgi network.

254 Our results indicate that dense-core vesicles carry CAPS to sites of exocytosis, w

255 Moreover, after a CWSS, dense-core vesicles containing DOR immunoreactivity coul

256 packing of peptide hormones/neuropeptides in dense-core vesicles do not necessarily require a special

257 ATP release and the number of ATP-containing dense-core vesicles docking are decreased in HD astrocyt

258 een suggested to trigger exocytosis of large dense-core vesicles from neuroendocrine cells.

259 y that regulates the exocytic fusion pore of dense-core vesicles in cultured endocrine beta cells.

260 The Ca(2+)-dependent exocytosis of dense-core vesicles in neuroendocrine cells requires a p

261 mponent for the Ca2+-dependent exocytosis of dense-core vesicles in neuroendocrine cells.

262 We found Syt IV on both micro- and dense-core vesicles in posterior pituitary nerve termina

263 Proneuropeptides are packaged into dense-core vesicles in which they are processed into act

264 strocytes, suggesting that the exocytosis of dense-core vesicles is impaired by mHtt in HD astrocytes

265 By 5 minutes, small dense-core vesicles known to transport active zone prote

266 is relatively enriched in the purified large dense-core vesicles of chromaffin cells and associated w

267 e, substance P, are colocalized in the large dense-core vesicles of pain-sensing neurons.

268 hormones are stored in the amyloid state in dense-core vesicles of secretory cells.

269 w that these isoforms sort to populations of dense-core vesicles that differ in size.

270 a decrease in immunolabeling associated with dense-core vesicles that were near the plasma membrane a

271 ion and participates in the docking of large dense-core vesicles to the plasma membrane.

272 y the local changes of 27 proteins at single dense-core vesicles undergoing calcium-triggered fusion.

273 When the dense-core vesicles were near the plasma membrane, somet

274 S-1 is required for Ca2+-triggered fusion of dense-core vesicles with the plasma membrane, but its si

275 on-lucent vesicles and, occasionally, large, dense-core vesicles) and symmetrical (with small, flatte

276 ar, spherical vesicles and a few granular or dense-core vesicles, and (4) specialization in the last

277 in neurons, are associated with synaptic and dense-core vesicles, and control vesicle acidification a

278 ect in which a portion of synaptic vesicles, dense-core vesicles, and presynaptic cytomatrix proteins

279 3a, a small GTPase localized on membranes of dense-core vesicles, and prevents GTP-Rab3a from binding

280 re integral membrane components of the large dense-core vesicles, and that they are closely regulated

281 Labeled boutons contain dense-core vesicles, and they resemble a population of t

282 addition to being a resident on cytoplasmic dense-core vesicles, CAPS was present in clusters of app

283 ory organelles (synaptic-like microvesicles, dense-core vesicles, lysosomes, exosomes and ectosomes),

284 ted emission depletion microscopy imaging of dense-core vesicles, we find that fusion-generated Omega

285 alized to the membrane of insulin-containing dense-core vesicles.

286 ffiliated with either endomembranes or large dense-core vesicles.

287 ptic vesicles and a smaller number of larger dense-core vesicles.

288 thought to mediate Ca2+-triggered fusion of dense-core vesicles.

289 immunolabeling was particularly enriched in dense-core vesicles.

290 eals a substantial decrease in the number of dense-core vesicles.

291 toplasmic compartment, often associated with dense-core vesicles.

292 -dependent manner by virtue of transport via dense-core vesicles.

293 a membranes, but neither is present on large dense-core vesicles.

294 with small clear vesicles and also contained dense-core vesicles.

295 ium, which is the main mechanism to retrieve dense-core vesicles.

296 ry afferent synapses (C-type), synapses with dense-cored vesicles (D, mostly primary afferents), and

297 nly in presynaptic cells and may account for dense-cored vesicles previously seen in some taste cells

298 ts are suggested by the presence of numerous dense-cored vesicles.

299 ose contacts were smaller in size and lacked dense-cored vesicles.

300 on; in the clade of filamentous ascomycetes, dense-core Woronin bodies bud from peroxisomes to gate c