ライフサイエンスコーパス: vesicular

1 croglial response is insufficient to prevent vesicular accumulation and photoreceptors of PRCD knocko

2 Blocking acetylcholine uptake and vesicular acetylcholine release by hemicholinium-3 also

3 ncoding choline acetyltransferase (ChAT) and vesicular acetylcholine transporter (VAChT) in specific

4 Vesicular acetylcholine transporter (VAChT) PET ligands

5 biopsies were stained for cholinergic marker vesicular acetylcholine transporter (VAChT).

6 herefore examined expression of ChAT and the vesicular acetylcholine transporter in the embryonic and

7 othelial basement membrane and enriched with vesicular activity.

8 e range suggestive of some impurities of non-vesicular aggregates.

9 ed to discriminate between subpopulations of vesicular and nonvesicular objects in the same sample an

10 mAb for tumor-specific antigens allow these vesicular antibodies (VAs) to selectively deliver a cyto

11 on caused a reduction in the number of multi-vesicular bodies (MVBs) targeted for lysosomal degradati

12 les' refers to a heterogeneous population of vesicular bodies of cellular origin that derive either f

13 ted activity of molecular motors trafficking vesicular cargo within a dynamic cytoskeletal network.

14 arriers that emanate from the TGN or through vesicular carriers that recruit GGA (Golgi-localized, ga

15 uncharacterized signaling cross-talk between vesicular compartments in CD8(+) T cells.

16 cial monolayer, plus a functionally attached vesicular complex, called the surface-associated surfact

17 We show that these vesicular condensates are stable at specific mixture com

18 ndocytosis is related to the Na(+)-dependent vesicular content change, we dialyzed glutamate into the

19 antitative comparison between exocytosis and vesicular content in intracellular vesicle impact electr

20 Our findings with VIEC reveal that the vesicular content increases with vesicle size.

21 of cell migration, cancer cell invasion, and vesicular content release, we sought to elucidate the si

22 tor availability with age, while presynaptic vesicular DA storage (as measured by DTBZ), which was si

23 trabenazine (DTBZ), a measure of presynaptic vesicular DA storage, and [11C]raclopride (RAC), an indi

24 such as alkanols, fatty acids, prodrugs, and vesicular delivery for steroids have been investigated.

25 To ensure vesicular delivery, motors need to navigate the microtub

26 ion with the vesicle size, implying that the vesicular dense core size determines the speed of each r

27 sponse to electrical stimulation of the VTA, vesicular depletion of dopamine, and amphetamine.

28 ves extensive membrane remodeling as well as vesicular discharge.

29 A (SVA) is a picornavirus that causes acute vesicular disease (VD), that is clinically indistinguish

30 g protocols provide an unprecedented view of vesicular dynamics near the plasma membrane in mouse egg

31 adaptor protein complex-2 (AP-2) involved in vesicular endocytosis.

32 p toward a molecular picture of caveolae and vesicular endocytosis.

33 dation of endosome-associated PTEN to induce vesicular enrichment of PI(3,4,5)P3 and sequential recru

34 hat M6PR binds PS-ASOs and facilitates their vesicular escape.

35 lular compartments and the directionality of vesicular exchange are intimately linked.

36 vo compartment generation, inter-compartment vesicular exchange, and biochemical conversion of membra

37 VAMP2 is essential for vesicular exocytosis and activity-dependent neurotransmi

38 pening of astrocyte CRAC channels stimulated vesicular exocytosis to mediate the release of gliotrans

39 under stress, both genes may be involved in vesicular export allowing allantoin translocation from r

40 ts, showing that tRNAs and Y RNAs in the non-vesicular extracellular compartment are released from ce

41 l extracellular vesicles and presence of non-vesicular extracellular matter have led to debate about

42 hat contain sorted receptors bud and undergo vesicular fission from the sorting endosomes remain elus

43 understudied virulence strategy resembles a vesicular form of intercellular trafficking that allows

44 ells isolated from white fat tissue (stromal vesicular fraction) produced the anti-inflammatory cytok

45 possibility that TSPAN5 might play a role in vesicular function in addition to regulating expression

46 t that ERICH3 may play a significant role in vesicular function in serotonergic and other neuronal ce

47 eavy chain which are known to play a role in vesicular function.

48 mponents involved in these processes are the vesicular fusion machinery (SNARE proteins) and the regu

49 5-HT increased vesicular GABA release in naive and dependent rats but h

50 lation of MPOA neurons that express ESR1 and vesicular GABA transporter (VGAT) (MPOA(ESR1 VGAT) neuro

51 f two other inhibitory synapse constituents, vesicular GABA transporter (vGAT) and gephyrin, in the N

52 taken from male and female donors that lack vesicular GABA transporter (Vgat) expression disperse an

53 e expressing channelrhodopsin-(ChR2)-EYFP in vesicular GABA transporter (VGAT)-expressing neurons.

54 These data suggest a role for the vesicular GABA transporter in transplantation-mediated p

55 Rare co-localizations between pSTAT5 and vesicular GABA transporter or vasopressin were observed,

56 This neuron coexpresses the vesicular GABA transporter, the calcium-binding protein

57 ly and temporally target the deletion of the vesicular GABA transporter, Vgat, in developing neurons.

58 2 and does not involve presynaptic component vesicular GABA transporters.

59 -nm light stimulation via OPN5 and VGAT (the vesicular GABA/glycine transporter) in retinal ganglion

60 nduce ODP, demonstrating the pivotal role of vesicular GABAergic transmission for MGE transplantation

61 ne the interaction kinetics as a function of vesicular ganglioside content.

62 orted lipid bilayer (SLB) and MAG, we detect vesicular GD1a and GT1b binding and determine the intera

63 nhanced GFP (EGFP) in neurons expressing the vesicular glutamate (vGLUT2) or GABA transporter (vGAT),

64 docytosis was not affected by regulating the vesicular glutamate content.

65 lamic TH-immunoreactive (ir) neurons express vesicular glutamate or GABA transporters.

66 Vesicular glutamate receptor (VGLUT) 3 machinery orchest

67 complex proteins in Th17 cells that enable a vesicular glutamate release pathway that induces local i

68 eta42 caused the accumulation of presynaptic vesicular glutamate transporter (VGlut) and increased sp

69 opsin-2 (ChR2) is conditionally expressed in vesicular glutamate transporter 1 (Vglut1) sensory neuro

70 -ChR2) to optogenetically activate cutaneous vesicular glutamate transporter 1 (Vglut1)-positive LTMR

71 erminals were identified in both nuclei: (a) vesicular glutamate transporter 1 (vGluT1)-positive term

72 letion in glutamatergic neurons that express vesicular glutamate transporter 2 (VGlut2) and are locat

73 gmental area dopamine (DA) neurons expresses vesicular glutamate transporter 2 (VGluT2) and releases

74 eurons in the adult, healthy brain expresses vesicular glutamate transporter 2 (VGluT2) and thus rele

75 triatal terminals, which are associated with vesicular glutamate transporter 2 (Vglut2) expression, i

76 n) consecutive to previous expression of the vesicular glutamate transporter 2 (Vglut2) gene, coupled

77 ing mice expressing GFP under control of the vesicular glutamate transporter 2 (vGluT2) promoter.

78 ulation in the VP [VP neurons expressing the vesicular glutamate transporter 2 (VP(VGluT2))], whose a

79 he molecular layer, while immunostaining for vesicular glutamate transporter 2 and neurofilament H in

80 nsive cells in the PVH co-localized with the vesicular glutamate transporter 2.

81 bset of CCK neurons is composed of transient vesicular glutamate transporter 3 (tVGLUT3) neurons, whi

82 Vesicular glutamate transporter 3 (VGluT3) amacrine cell

83 Small-diameter vesicular glutamate transporter 3-lineage (Vglut3(lineag

84 an activity-dependent increase in Drosophila vesicular glutamate transporter expression.

85 Labeling for vesicular glutamate transporter is evident at the motor

86 Molecular identification of vesicular glutamate transporter three and cholecystokini

87 We demonstrate that the vesicular glutamate transporter VGLUT2 may be exploited

88 y express an excitatory neuronal marker, the vesicular glutamate transporter, expanding the possible

89 ase in Syt2 signals alongside an increase in vesicular glutamate transporter-2 signals on PV+ cells i

90 ochlear inner hair cells in mice lacking the vesicular glutamate transporter-3 (Vglut3(KO) ), at 9-11

91 Vesicular Glutamate Transporters (VGLUT) accumulate glut

92 The vesicular glutamate transporters (VGLUTs) concentrate th

93 glutamate release machinery mediated through vesicular glutamate transporters (VGLUTs) that ultimatel

94 , these glutamatergic terminals express both vesicular glutamate transporters 1 and 2 denoting a spec

95 into the presynaptic cytosol or blocked the vesicular glutamate uptake with bafilomycin and found th

96 We propose that these vesicular hexosomes do not form via a conventional nucle

97 The topological defects of these so-called "vesicular hexosomes" are enticing as they could serve as

98 ibitor ("5b") that prevented alphaS-positive vesicular inclusions and cytotoxicity in cultured human

99 ing attention as important platforms for non-vesicular, inter-organellar communication.

100 many organelles are ill-defined because the vesicular intermediates are transient, low-abundance and

101 ites innervated by infected neurons, causing vesicular lesions.

102 , while the hollow cylindrical shell and the vesicular lumen could spatially accommodate cargoes with

103 mission EM and showed high levels of mRNA of vesicular markers in the oviduct segments where eggshell

104 principle gliotransmitter and is released by vesicular mechanisms blocked by dnSNARE expression.

105 individual vesicles after disruption of the vesicular membrane by an applied electrical potential.

106 ial by forming the SNARE complex that drives vesicular membrane fusion.

107 amphiphilic lipids, these nucleoprotein-RNA vesicular membranes exhibit local ordering, size-depende

108 fluorescence confirmed the presence of major vesicular, mineralization-specific and eggshell matrix p

109 droxyphenylacetic acid (DOPAC)/DA ratio, and vesicular monoamine transporter 2 (VMAT2) protein.

110 rough the coordinated activity of astroglial vesicular monoamine transporter 2 (VMAT2) together with

111 The vesicular monoamine transporter type 2 (VMAT2), an impor

112 hinese hamster ovary cells expressing either vesicular monoamine transporter.

113 his exon leads to increased activity of both vesicular monoamine transporters.

114 lts: Thirty-five studies (29 DAT, 6 AADC, no vesicular monoamine type 2 studies) with 356 MSA-P patie

115 (11)C-dihydrotetrabenazine ((11)C-DTBZ) is a vesicular monoamine type 2 transporter PET ligand that a

116 a(+) accumulated in the terminals, activated vesicular Na(+)/H(+) exchanger, and regulated glutamate

117 duced elevation of cytosolic Na(+) activated vesicular Na(+)/H(+) exchanger, facilitated glutamate lo

118 Our findings suggest that RAB11-dependent vesicular nephrin trafficking plays a role in the pathog

119 iform nanostructured hydrogels of spherical, vesicular, or cylindrical morphologies.

120 Vesicular- or vacuolar-type adenosine triphosphatases (V

121 tic vesicles uses energy from proton-pumping vesicular- or vacuolar-type adenosine triphosphatases (V

122 Upon nutrient limitation, ANKRD9 loses its vesicular pattern and assembles with IMPDH2 into rodlike

123 ected cells with wild-type AP1B1 rescues the vesicular phenotype, conclusively establishing that loss

124 nding the release of this specific drug from vesicular phospholipid gel formulations but describe a g

125 d recycles DA for storage in the presynaptic vesicular pool.

126 stribution of dopamine between cytosolic and vesicular pools, leading to increased accumulation of ne

127 Additionally, for each species vesicular proteins were categorized based on biological

128 Slp-4 binds vesicular Rab proteins via an N-terminal Slp homology do

129 We recently proposed that the tubular-vesicular recycling endosome membranes were a core platf

130 between TBC1D8B and Rab11b, a key protein in vesicular recycling in cells.

131 This multi-vesicular release (MVR) occurs at most synapses, but its

132 , MVR events preferentially overlap with uni-vesicular release (UVR) events at sites closer to an AZ

133 The majority of ribbon markers, presynaptic vesicular release and postsynaptic neurotransduction-rel

134 proteins that allow dendrites to respond to vesicular release at synapses, suggesting that axon-myel

135 Vesicular release from neurons promotes myelin sheath gr

136 ehaving animals blockade of Ca(2+)-dependent vesicular release mechanisms in NTS astrocytes by virall

137 Here, we report non-vesicular release of glutamate through the glutamate-per

138 erogeneous, resulting in a broad spectrum of vesicular release probabilities within synapses.

139 operating via activity-dependent changes of vesicular release probability (e.g. by a facilitation fu

140 ase by promoting vesicle docking/priming and vesicular release probability via stabilization of Munc1

141 ns in the neuroendocrine system translate to vesicular release toward the pituitary and identify how

142 emains unresolved how sorting into diverging vesicular routes is spatially organized.

143 isms of effects of ketamine and [cAMP](i) on vesicular secretion: a rise in [cAMP](i) facilitated, wh

144 Here we examined the role of vesicular SOCS3 secretion as a mechanism by which AMs re

145 cle-associated membrane protein 4 (VAMP4), a vesicular soluble N-ethylmaleimide-sensitive factor atta

146 In this study, we identify the vesicular soluble N-ethylmaleimide-sensitive factor atta

147 estinal media was determined, as well as the vesicular stability.

148 uenza A (IAV), measles (MV), Sendai (SV), or vesicular stomatitis (VSV) virus.

149 of vesiculovirus-based therapies.IMPORTANCE Vesicular stomatitis Indiana virus (VSIV) is a veterinar

150 Vesicular stomatitis Indiana virus (VSIV), formerly know

151 hanced ISG expression and protection against vesicular stomatitis Indiana virus infection compared wi

152 rms, methyltransferase-defective recombinant vesicular stomatitis virus (mtdVSV) and a DNA vaccine.

153 The recombinant vesicular stomatitis virus (rVSV) Ebola vaccine was show

154 ion of VesiculoVax that contains recombinant vesicular stomatitis virus (rVSV) vectors expressing fil

155 immunostimulatory properties of recombinant vesicular stomatitis virus (rVSV)-based vaccines make th

156 Vesicular stomatitis virus (VSV) (a rhabdovirus) and its

157 een shown to induce G(2)/M arrest.IMPORTANCE Vesicular stomatitis virus (VSV) (a rhabdovirus) and its

158 ), only HuMxA is considered antiviral toward vesicular stomatitis virus (VSV) (a rhabdovirus).

159 t on the replication of the (-)ssRNA viruses vesicular stomatitis virus (VSV) (Rhabdoviridae family)

160 The L proteins of rhabdoviruses, such as vesicular stomatitis virus (VSV) and rabies virus (RABV)

161 Vesicular stomatitis virus (VSV) based oncolytic viruses

162 we generate a highly infectious recombinant vesicular stomatitis virus (VSV) bearing the SARS-CoV-2

163 on content release and infection by chimeric vesicular stomatitis virus (VSV) containing the envelope

164 iously, we developed a replication-competent vesicular stomatitis virus (VSV) expressing a modified f

165 Using an infectious molecular clone of vesicular stomatitis virus (VSV) expressing eGFP as a ma

166 of neurotropism, we asked whether a chimeric vesicular stomatitis virus (VSV) expressing the EBOV gly

167 oV HKU5 expressing the SARS-CoV-1 spike, and vesicular stomatitis virus (VSV) expressing the SARS-CoV

168 itis Indiana virus (VSIV), formerly known as vesicular stomatitis virus (VSV) Indiana (VSV(IND)), is

169 Vesicular stomatitis virus (VSV) infection downregulates

170 impaired IFN production in macrophages after vesicular stomatitis virus (VSV) infection, and HIPK2-de

171 Vesicular stomatitis virus (VSV) is an archetypical memb

172 polymerases since the first structure of the vesicular stomatitis virus (VSV) L protein determined in

173 The complex closely resembles the vesicular stomatitis virus (VSV) L-P, the one other know

174 obial molecule against infection with either vesicular stomatitis virus (VSV) or influenza was demons

175 Vesicular stomatitis virus (VSV) P is dimeric with an ol

176 yped HIV-1, murine leukemia virus (MLV), and vesicular stomatitis virus (VSV) particles.

177 ent cell-to-cell fusion assays, and chimeric vesicular stomatitis virus (VSV) recombinants expressing

178 an immunodeficiency virus type 1 (HIV-1) and vesicular stomatitis virus (VSV) to measure the neutrali

179 resses cytosolic poly(I:C), 5'ppp-dsRNA, and vesicular stomatitis virus (VSV) triggers IFN-I expressi

180 e, three papers describe the pseudotyping of vesicular stomatitis virus (VSV) with the SARS-CoV-2 spi

181 ks with DNA, modified vaccinia Ankara (MVA), vesicular stomatitis virus (VSV), adenovirus type 5 (Ad5

182 n immunodeficiency virus type-1 (HIV-1), and vesicular stomatitis virus (VSV), as well as a replicati

183 Within 2-6 hours after infection by vesicular stomatitis virus (VSV), newly assembled VSV pa

184 y, PGAM5 deficient MEFs, upon infection with vesicular stomatitis virus (VSV), revealed diminished IF

185 prototype of NNS RNA virus gene expression, vesicular stomatitis virus (VSV), we determined the impo

186 us (EBOV) crisis of 2013-2016, a recombinant vesicular stomatitis virus (VSV)-based EBOV vaccine was

187 binants carrying large transgenes.IMPORTANCE Vesicular stomatitis virus (VSV)-based oncolytic viruses

188 To address these limitations, we devised a vesicular stomatitis virus (VSV)-based probe to display

189 ferent turns, as is observed for the related Vesicular stomatitis virus (VSV).

190 nuclear cells were infected with recombinant vesicular stomatitis virus encoding EBOV antigens.

191 pressing influenza, measles, Ebola, Lassa or vesicular stomatitis virus envelope glycoproteins enable

192 tion activity in vitro against a recombinant vesicular stomatitis virus expressing MACV GPC (VSV-MACV

193 transfected secretory membrane glycoprotein, vesicular stomatitis virus G (VSVG) glycoprotein, was re

194 While MMLV pseudotyped the vesicular stomatitis virus G glycoprotein (VSV-G) effici

195 "Gectosomes," are designed to co-encapsulate vesicular stomatitis virus G protein (VSV-G) with bioact

196 g human GBA to an exosome-anchoring protein: vesicular stomatitis virus glycoprotein (VSVG), we demon

197 related class III fusion proteins, including vesicular stomatitis virus glycoprotein G (VSV-G) or bac

198 uster activates the IFN pathway and inhibits vesicular stomatitis virus infection by directly targeti

199 V virus-like particle, and EBOV glycoprotein/vesicular stomatitis virus pseudovirion.

200 By in situ analyses of vesicular stomatitis virus RNA synthesis, specific activ

201 A replication-competent vesicular stomatitis virus vaccine expressing the Ebola

202 rabies virus) and heterologous (inactivated vesicular stomatitis virus) antigens and acceptable accu

203 vity of alpha interferon (IFN-alpha) against vesicular stomatitis virus, Indiana serotype (VSV(IND)),

204 neurotropic viruses, including rabies virus, vesicular stomatitis virus, Semliki Forest virus, and he

205 used a vesicular stomatitis virus-based probe to isolate B cell

206 A live, recombinant vesicular stomatitis virus-based vaccine has been deploy

207 for rapid expanded access to the recombinant vesicular stomatitis virus-Zaire Ebola virus (rVSV-ZEBOV

208 Recombinant vesicular stomatitis virus-Zaire Ebola virus (rVSV-ZEBOV

209 , lot consistency, and safety of recombinant vesicular stomatitis virus-Zaire Ebola virus envelope gl

210 reovirus, HIV-1, human metapneumovirus, and vesicular stomatitis virus.

211 Recombinant vesicular stomatitis viruses (rVSV) expressing foreign g

212 RhIVs are based on vesicular stomatitis viruses (VSV), but viral entry is m

213 Chimeric vesicular stomatitis viruses with the EBOV glycoprotein

214 d infectivity assays with BCoV-S-pseudotyped vesicular stomatitis viruses.

215 city, which helps to evolve various kinds of vesicular structure.

216 TLR7/8 agonist that in aqueous medium forms vesicular structures of 200 nm.

217 chondria, peroxisomes, and other cytoplasmic vesicular structures.

218 s not invoke long-range trafficking of large vesicular structures.

219 pic investigations of weak acid transport in vesicular suspensions.

220 orescence spectroscopy methods, we find that vesicular synaptobrevin-2 (syb-2) in its monomeric prefu

221 cally fuelled self-replicating micelles, our vesicular system was too stable to surfactant degradatio

222 Using GZnP3 as well as GZnP3-derived vesicular targeted probes, we provide the first direct e

223 meric Golgi (COG) complex, a Golgi apparatus vesicular tether.

224 rt through MFB, although the contribution of vesicular traffic can be significant in a population of

225 plex II (COPII) are the primary mediators of vesicular traffic from the endoplasmic reticulum to the

226 TRAPP subunit, TRAPPC4 that associates with vesicular trafficking and autophagy defects.

227 dc42 are central regulators of intracellular vesicular trafficking and of the actin cytoskeleton, the

228 n of the MAP1B binding domain did not impair vesicular trafficking and preferential delivery of Na(v)

229 ement from STRIC is independent of canonical vesicular trafficking but requires Arp2/3, suggesting a

230 ne protein complex that coordinates multiple vesicular trafficking events within the endolysosomal sy

231 copy, we demonstrated that ARF4 enhanced NIS vesicular trafficking from the Golgi to the plasma membr

232 Thus, transfer routes orthogonal to vesicular trafficking govern the flow of sterols in the

233 migration, cytoskeletal rearrangements, and vesicular trafficking in epithelial cells.

234 e small GTPase, Rab27, a protein involved in vesicular trafficking in immune cells.

235 Viruses are considered to use vesicular trafficking in infected cells, but the details

236 d role of INF2 in regulating dynein-mediated vesicular trafficking in podocytes.

237 les and the dynein motor, in connection with vesicular trafficking involving RAB11 and IKK-related ki

238 d synthesis and underscore the importance of vesicular trafficking of PM cholesterol for steroidogene

239 hat starvation induces rapid Rab11-dependent vesicular trafficking of Rabin8, a Rab8 guanine-nucleoti

240 a phosphorylation event participating in the vesicular trafficking pathway downstream of G protein si

241 yt11 is an essential component of a neuronal vesicular trafficking pathway that differs from the well

242 cific mode of action, targeting Sec14 of the vesicular trafficking pathway.

243 ximal host factor demonstrated importance of vesicular trafficking pathways, ubiquitin-dependent and

244 ated proteins work at the interface of other vesicular trafficking pathways.

245 Here, we report that the vesicular trafficking protein Rab39a is needed for optim

246 that requires emerin's LEM domain to mediate vesicular trafficking to lysosomes.

247 dramatic shape changes such as endocytosis, vesicular trafficking, and cell division.

248 nt suggests its involvement in modulation of vesicular trafficking, and it might serve as a putative

249 olarity, cell junction, cilia, cytoskeleton, vesicular trafficking, and regulation of beta-cell epige

250 ynamic processes, such as nuclear transport, vesicular trafficking, and virus entry and egress.

251 373 proteins implicated in the regulation of vesicular trafficking, cytoskeletal organization, autoph

252 plant cells reprogram their cell surface is vesicular trafficking, including secretion and endocytos

253 results highlight functional enrichments of vesicular trafficking, ion transport/homeostasis and oxi

254 l protein synthesis or on intact host actin, vesicular trafficking, or microtubules.

255 thelial cells are caused by dysregulation of vesicular trafficking.

256 -SCAM, a protein that has been implicated in vesicular trafficking.

257 f membrane remodeling, membrane fission, and vesicular trafficking.

258 tanding of mechanisms by which viruses coopt vesicular trafficking.

259 us and is thought to play a critical role in vesicular trafficking.

260 dependent signalling pathways and defects in vesicular trafficking.

261 e nucleotide Exchange Factors) that regulate vesicular trafficking.

262 y human intestinal epithelium (SMI-100) by a vesicular transcytosis process, activate hIL-10 receptor

263 rocess that takes place by dynamin-dependent vesicular transcytosis through the lymphatic endothelial

264 The release kinetics of vesicular transmitters and dense core size have the same

265 rotein tyrosine kinase, but independent from vesicular transport and chloride channels.

266 Coat proteins have a central role in vesicular transport by binding to cargoes for their sort

267 ment network presents numerous challenges to vesicular transport by teams of myosin Va (MyoVa) molecu

268 In the secretory pathway, budding of vesicular transport carriers from the trans-Golgi networ

269 inflammation, neuronal injury, autophagy and vesicular transport genes are observed in PD with and wi

270 membrane with only a limited contribution of vesicular transport in recycling endosomes.

271 contributed to a basic understanding of how vesicular transport is initiated.

272 dmilling and selective recycling by internal vesicular transport of cortex-bound transmembrane protei

273 ically imaged, in pairwise combinations, the vesicular transport of fluorescently tagged components o

274 findings are challenging long-held models of vesicular transport of large matrix proteins, such as pr

275 ane traffic at the Golgi, is involved in the vesicular transport of LAT to the immune synapse.

276 of different cells types where it regulates vesicular transport of proteins and membrane components.

277 tions as a carrier for the sequestration and vesicular transport of the potent eosinophil granule cat

278 ly by inhibiting KRAS proximity to the SNARE vesicular transport proteins SNAP23, SNAP29, and VAMP3.

279 iew we discuss the function of intracellular vesicular transport systems in reovirus entry, trafficki

280 0 years ago, such basic questions as whether vesicular transport through the Golgi occurs in an anter

281 We have previously proposed a model of vesicular transport to provide stabilized ACC in chicken

282 experimental evidence for the components of vesicular transport to supply ACC in a vertebrate model

283 s were found to remain largely intact during vesicular transport to the nucleus.

284 s cycles of endocytosis, solubilization, and vesicular transport to the PM.

285 any proteins that regulate the cytoskeleton, vesicular transport, and physiology of the narrow canals

286 l parasites, supports long, multidirectional vesicular transport, and regulates transport, density an

287 F1, relevant for COPI/Arf1-mediated cellular vesicular transport, participates in the replication cyc

288 r, we also uncovered evidence for selective, vesicular transport-mediated turnover of a single INM pr

289 llular processes, from muscle contraction to vesicular transport.

290 processes such as chromosome segregation and vesicular transport.

291 CteG might function by subverting host cell vesicular transport.

292 ts apical actin placement and RAB-8-mediated vesicular transport.

293 d DRD5), the dopamine transporter (DAT), and vesicular transporters (VMAT1 and VMAT2).

294 These interneurons express vesicular transporters for acetylcholine (VAChT) and glu

295 We show that anterograde or retrograde vesicular transports are asymptotic behaviors of a much

296 exits the compartment on syntaxin-6-positive vesicular/tubular carriers that depend on Rab10 for thei

297 EHD1 and RUSC2 colocalize with EGFR in vesicular/tubular structures and at the Golgi compartmen

298 Vesicular, urticarial, and maculopapular eruptions and l

299 formation of SNARE complexes composed of the vesicular (v)-SNARE synaptobrevin and the target (t)-SNA

300 third type of Golgi-derived carrier that is vesicular, yet clathrin independent.