ライフサイエンスコーパス: trans-Golgi network

1 osphate receptors from late endosomes to the trans Golgi network.

2 nces of GPCR-mediated signaling at the Golgi/trans-Golgi network.

3 omology (PH) domains of FAPP proteins to the trans-Golgi network.

4 occurs even when ATP7B is restricted to the trans-Golgi network.

5 rane abundance of PAR1 by trapping it in the trans-Golgi network.

6 bidopsis also localized to the Golgi and the trans-Golgi network.

7 complex, involved in protein sorting at the trans-Golgi network.

8 internalizes and recycles slowly through the trans-Golgi network.

9 protein in complex with the viral DNA to the trans-Golgi network.

10 the maturation of dense-core vesicles at the trans-Golgi network.

11 in the Golgi stack and proper sorting at the trans-Golgi network.

12 tion and/or endosome recycling events at the trans-Golgi network.

13 ion of the rough endoplasmic reticulum-Golgi-trans-Golgi network.

14 bound oligosaccharides, and sorts it in the trans-Golgi network.

15 ograde transport from early endosomes to the trans-Golgi network.

16 addition, AP1M2 was localized at or near the trans-Golgi network.

17 where it is enriched in the trans-Golgi and trans-Golgi network.

18 tein involved in receptor retrieval from the trans-Golgi network.

19 onal organization and protein sorting at the trans-Golgi network.

20 hose stable MTs that form cluster around the trans-Golgi network.

21 returning secretory vesicle material to the trans-Golgi network.

22 l of L-selectin colocalizes with AP-1 at the trans-Golgi network.

23 he E3 glycoprotein is cleaved from E2 in the trans-Golgi network.

24 t sorts cargo from the early endosome to the trans-Golgi network.

25 ulates furin activation at pH~6.5 within the trans-Golgi network.

26 of retrograde cargo from the endosome to the trans-Golgi network.

27 that RabA2 localizes in Golgi stacks and the trans-Golgi network.

28 sulfotransferases (TPST-1 and TPST-2) in the trans-Golgi network.

29 osphate receptors from late endosomes to the trans-Golgi network.

30 that large pools of FcmuR accumulate in the trans-Golgi network.

31 um (ER) and the accumulation of gH/gL in the trans-Golgi network.

32 it was transported to late endosomes and the trans-golgi network.

33 vesicle transport between endosomes and the trans-Golgi network.

34 doplasmic reticulum (ER) and the trans-Golgi/trans-Golgi network.

35 led to a disruption in the structure of the trans-Golgi network.

36 red for wrapping, normally colocalize in the trans-Golgi network.

37 ked to cargo retrieval from endosomes to the trans-Golgi network.

38 t to traffic from the plasma membrane to the trans-Golgi network.

39 m the plasma membrane and trafficking to the trans-Golgi network.

40 plants, NRAMP2 is a resident protein of the trans-Golgi network.

41 uggesting that F13 uses another route to the trans-Golgi network.

42 teins, including the Na,K-ATPase, out of the trans-Golgi network.

43 full-length ATP7B, which is targeted to the trans-Golgi network, 1-4DeltaMBD-7B is targeted primaril

44 ocalized to endosomes was required for Golgi trans-Golgi network 46 (TGN46) recycling, exhibited Ca(2

45 ly activated form of proapoptotic BAX to the trans Golgi network, a previously unanticipated launch p

46 mpartment to facilitate PM targeting via the trans-Golgi network, a role that is most certainly criti

47 ity and proper localization to the Golgi and trans-Golgi network, although the EXS domain by itself c

48 nction leads to perturbed plasma membrane-to-trans Golgi network and Golgi-to-ER retrograde transport

49 pathways traffic cargo from endosomes to the trans-Golgi network and are a key part of the intracellu

50 that the fragmentation and dispersal of the trans-Golgi network and associated membranes render thes

51 host +TIPs that control MT formation at the trans-Golgi network and cortical capture, are specifical

52 In plants, the trans-Golgi network and early endosomes (TGN/EE) functio

53 ArfGAP3 localized to the trans-Golgi network and early endosomes.

54 n adaptor complexes to bud vesicles from the trans-Golgi network and endosomal compartments.

55 Clathrin-mediated traffic between the trans-Golgi network and endosomes mediates responses to

56 ons in clathrin-mediated traffic between the trans-Golgi network and endosomes, linking clathrin adap

57 x (AP-1), which transports cargo between the trans-Golgi network and endosomes, plays a role in the t

58 adaptor complex that sorts cargo between the trans-Golgi network and endosomes.

59 l relocalization of clathrin adaptors at the trans-Golgi network and endosomes.

60 lathrin-mediated protein sorting between the trans-Golgi network and endosomes.

61 re, we show that Rab29 recruits LRRK2 to the trans-Golgi network and greatly stimulates its kinase ac

62 GPR107 localizes to the trans-Golgi network and is essential for retrograde tran

63 from intracellular organelles, including the trans-Golgi network and late endosomes.

64 mbrane-bound compartment associated with the trans-Golgi network and microtubule-organizing center.

65 In high copper, ATP7B exits the trans-Golgi network and moves to the apical domain of he

66 usion protein localized to the Golgi and the trans-Golgi network and not the plasma membrane when exp

67 egral membrane endo-beta1,4-glucanase in the trans-Golgi network and plasma membrane that is essentia

68 aintains a constant lipid composition in the trans-Golgi network and post-Golgi compartments, thus co

69 artments containing aleurain, as well as the trans-Golgi network and prevacuolar compartments, were s

70 r sorting receptor (VSR), which includes the trans-Golgi network and prevacuoles.

71 retory products no longer accumulated in the trans-Golgi network and secretory granule exocytosis was

72 ized, whereas cKalSec14-GFP localized to the trans-Golgi network and secretory granules.

73 ficked in axons together with markers of the trans-Golgi network and synaptic vesicles.

74 t promotes vesicular trafficking between the trans-Golgi network and the endosomes.

75 es transmembrane cargo from endosomes to the trans-Golgi network and the plasma membrane.

76 ritical checkpoint to regulate exit from the trans-Golgi network and thus control BK channel cell sur

77 ponents of protein coats associated with the trans-Golgi network and/or recycling endosomes.

78 ilitates choline transport, localizes to the trans-Golgi network, and during cytokinesis is associate

79 porters NHX5 and NHX6 localize to the Golgi, trans-Golgi network, and prevacuolar compartments and ar

80 tions, including the plasma membrane, Golgi, trans-Golgi network, and small CESA-containing compartme

81 alized to Rab5-positive early endosomes, the trans-Golgi network, and subsequently Rab11-positive rec

82 ng HLA-I at the endoplasmic reticulum, Golgi/trans-Golgi network, and the plasma membrane (PM) was as

83 t, through endocytic trafficking towards the trans-Golgi network, and, ultimately, the entry into the

84 uggest that HSV-1 has evolved to exploit the trans-Golgi network as an alternate MT organizing center

85 However, furin activates in the trans-golgi network at a pH of 6.5 while a paralog, prop

86 somal system, and from late endosomes to the trans-Golgi-network, before nuclear delivery.

87 Inp53 normally promotes sorting at the trans-Golgi network but localizes to cortical actin patc

88 afficking, mediating late secretion from the trans-Golgi network but not recycling of endocytosed pro

89 e conditions, PC7 is mainly localized in the trans-Golgi network, but a small fraction is found at th

90 tants) from the endoplasmic reticulum to the trans-Golgi network compartment, in recovery of its Cu-d

91 etained outside of lysosomal compartments in trans-Golgi network-derived transport vesicles.

92 und the pre-DMS, and fusion profiles between trans-golgi network-derived vesicles and the DMS were ob

93 ecretion of PAUF, a protein carried in small trans-Golgi network-derived vesicles.

94 fusions, we determined that KEG localizes to trans-Golgi network/early endosome (TGN/EE) vesicles.

95 s in the KEEP ON GOING gene, which encodes a trans-Golgi network/early endosome (TGN/EE)-localized E3

96 omplexes to the vacuole required neither the trans-Golgi network/early endosome (TGN/EE)-localized va

97 sis AtPAT10 is localized in the Golgi stack, trans-Golgi network/early endosome and tonoplast.

98 redominantly distinct from the Golgi and the trans-Golgi network/early endosome in the seed coat epid

99 Both AtMIN7 and HopM1 are localized to the trans-Golgi network/early endosome, a subcellular compar

100 Thus, blocking pathogen degradation of trans-Golgi network/early endosome-associated AtMIN7 is

101 g to a so far undetected contribution of the trans-Golgi network/early endosome-localized V-ATPase to

102 BEX5/RabA1b localizes to trans-Golgi network/early endosomes (TGN/EE) and acts on

103 and is essential for its recognition at the trans-Golgi network/early endosomes (TGN/EE) for vacuola

104 he IRT1 protein localizes to early endosomes/trans-Golgi network (EE/TGN) and is constitutively endoc

105 nce of an extensive reservoir of Chs3 at the trans-Golgi network/EE, which allows for the timely deli

106 igomers results in alpha-SYN deposits in the trans-Golgi network followed by endoplasmic reticulum sw

107 gh the binding of regulatory proteins in the trans-Golgi network, followed by full activation by PI4P

108 termediate compartment, Golgi apparatus, and trans-Golgi network form a ring that outlines the cVAC.

109 olocalization experiments, we found that the trans-Golgi network had an acidic pH of 6.1, while the p

110 ociated largely but not exclusively with the trans-Golgi network in central neurons.

111 rs and restores the discrete identity of the trans-Golgi network in nev abscission zones.

112 phosphate transporter mutants implicates the trans-Golgi network in phosphate transporter secretion.

113 ted at the Golgi stack, and the entry of the trans-Golgi network in secretory pathway could be signal

114 mply that AP-1 normally tethers ATP7A at the trans-Golgi network in the somatodendritic segments of m

115 ionophore monensin shifted APP away from the trans-Golgi network into early and recycling endosomes i

116 cargo adaptor known to sort proteins at the trans-Golgi network into secretory vesicles.

117 that retrograde transport of capsids to the trans-Golgi network is necessary for gene delivery.

118 ograde transport from early endosomes to the trans-Golgi network is required for the membrane-wrappin

119 Although localized largely to the trans-Golgi network, it shares common guanine nucleotide

120 , GFP-VPS16B colocalized with markers of the trans-Golgi network, late endosomes and alpha-granules.

121 ing determinants responsible for recognizing trans-Golgi network-like bicelles including phosphoinosi

122 t for the internalization of PC7 but not for trans-Golgi network localization.

123 tion of CESAs with vesicles decorated by the trans-Golgi network-localized protein SYNTAXIN OF PLANTS

124 ffinity pulldown analyses, and the primarily trans-Golgi network-localized Rab31 has increased coloca

125 d was secreted via the endoplasmic reticulum-trans-Golgi network machinery into the locule.

126 cle-like structures that colocalize with the trans-Golgi network marker TGN38 upon deletion of either

127 , capsids did not colocalise with either the trans-Golgi network marker TGN46 or late endosomal marke

128 e endosomal/lysosomal pathway but not with a trans-Golgi network marker.

129 feldin A, that colocalize to known Golgi and trans-Golgi network markers.

130 affected intracellular transport of UL20p to trans-Golgi network membranes.

131 y, Dlg1 depletion by siRNA duplexes disrupts trans-Golgi network morphology and WPB formation.

132 in the cell cytosol but associates with the trans-Golgi network, nucleus and plasma membrane.

133 nd here that FcmuR was also expressed in the trans-Golgi network of developing B cells, where it cons

134 trograde transport from the endosomes to the trans-Golgi network of endogenous CIMPR, but not truncat

135 at Piccolo, Bassoon, and ELKS2/CAST exit the trans-Golgi network on a common vesicle that requires Pi

136 and ABI5 were observed in the cytoplasm and trans-Golgi network only when the RING domain of KEG was

137 ore it reaches the acidic environment of the trans-Golgi network or its final destination in the cell

138 in recycling proteins from endosomes to the trans-Golgi network or plasma membrane.

139 e budding of the somatic organelles from the trans-Golgi network or the retrieval of the vesicular me

140 lls, but localizes to a compartment near the trans-Golgi network, partially overlapping with syntaxin

141 ular vesicle trafficking and a dysfunctional trans-Golgi network phenotype in patient-derived fibrobl

142 ective vesicle trafficking and dysfunctional trans-Golgi network phenotypes were reversed, suggesting

143 eus, endoplasmic reticulum, Golgi apparatus, trans-Golgi network, plasma membrane, apoplast, late end

144 NAs linked to VPg revealed that the cellular trans-Golgi network protein 2 (TGOLN2) mRNA was the temp

145 ide encoding a YXXO signal (SDYQRL) from the trans-Golgi network protein TGN38.

146 holesterol and sphingolipid transport to the trans-Golgi network, PtdIns(4)P consumption interrupts t

147 Further, the trans-Golgi network Rab Ypt31/32p and secretory vesicle

148 irus DNA bound to L2 is recycled through the trans-Golgi network rather than back to the plasma membr

149 o distinct carrier vesicles can occur at the trans-Golgi network, recycling endosomes, or a growing a

150 lpha-SYN that are subsequently stored in the trans-Golgi network region.

151 ne/threonine kinase that associates with the trans-Golgi network, regulating fission of transport car

152 AP-1 complex, leading to the formation of a trans-Golgi network reserve pool and that phosphorylatio

153 almitoylated BK channels are retarded in the trans-Golgi network, reversible protein palmitoylation p

154 ps of the formation of these granules at the trans-Golgi network specifically require VWF aggregation

155 become separated from one another within the trans-Golgi network, suggesting that they are sorted int

156 one PCP signaling protein, Vangl2, from the trans Golgi network (TGN) in mammalian cells.

157 One of the principal functions of the trans Golgi network (TGN) is the sorting of proteins int

158 ritical for the maintenance of the Golgi and trans Golgi network (TGN) PI4P pools, however, the actua

159 table complexes can exchange peptides in the Trans Golgi Network (TGN).

160 cking between endosomal compartments and the trans-Golgi network (TGN) [including the retromer comple

161 BBLF1 is shown to localize to the trans-Golgi network (TGN) along with gp350/220, a site w

162 delayed retrograde transport of BACE1 to the trans-Golgi network (TGN) and a delayed delivery of BACE

163 us TSH receptors traffic retrogradely to the trans-Golgi network (TGN) and activate endogenous Gs-pro

164 R and therefore was compartmentalized to the Trans-Golgi Network (TGN) and also to milk.

165 B has a dual intracellular localization: the trans-Golgi network (TGN) and cytosolic vesicles.

166 the cell surface, but instead returns to the trans-Golgi network (TGN) and does not re-enter the ER.

167 budding yeast, protein transport between the trans-Golgi network (TGN) and early endosome (EE) requir

168 acellular membrane fraction enriched for the trans-Golgi network (TGN) and endosomal compartments.

169 ed in membrane and lipid trafficking through trans-Golgi network (TGN) and endosomal systems.

170 ell polarity and translation, traffic at the trans-Golgi network (TGN) and endosomes is regulated by

171 nd receptors and protein sorting between the trans-Golgi network (TGN) and endosomes.

172 recruit AP1 and GGA clathrin adaptors to the trans-Golgi network (TGN) and endosomes.

173 infected cells leads to gB enrichment in the trans-Golgi network (TGN) and enhances the relocalizatio

174 onto newly synthesized cupro-enzymes in the trans-Golgi network (TGN) and exports excess copper out

175 r SYP41 is involved in vesicle fusion at the trans-Golgi network (TGN) and interacts with AtVPS45, SY

176 substrate adaptor KLHL20 is localized to the trans-Golgi network (TGN) and is important for post-Golg

177 Last, we show that CLN3 localizes to the trans-Golgi network (TGN) and partitions with buoyant mi

178 llular copper homeostasis by activity at the trans-Golgi network (TGN) and plasma membrane (PM), with

179 that regulates retrograde trafficking to the trans-Golgi network (TGN) and reaches a steady-state dis

180 adaptor to assist EGFR/RTK anchoring on the trans-Golgi network (TGN) and recycling back to the plas

181 endosomes and then moves sequentially to the trans-Golgi network (TGN) and recycling endosomes before

182 e basolateral sorting predominantly from the trans-Golgi network (TGN) and recycling endosomes, respe

183 vents, including retrograde transport to the trans-Golgi network (TGN) and recycling to the plasma me

184 re, we show that AAV2 trafficking toward the trans-Golgi network (TGN) and the Golgi apparatus correl

185 u(2+) conditions, ATP7B was localized to the trans-Golgi network (TGN) and the plasma membrane of the

186 ates vesicular protein transport between the trans-Golgi network (TGN) and the plasma membrane, in th

187 Many soluble proteins transit through the trans-Golgi network (TGN) and the prevacuolar compartmen

188 Gly(875) variant of ATP7B is targeted to the trans-Golgi network (TGN) and transports copper into the

189 rane cargoes and lysosomal hydrolases at the trans-Golgi network (TGN) are well understood.

190 en fluorescent protein forms clusters in the trans-Golgi network (TGN) but not at the plasma membrane

191 lates protein anterograde transport from the trans-Golgi network (TGN) by facilitating localized acti

192 Ca(2+) import into the lumen of the trans-Golgi network (TGN) by the secretory pathway calci

193 how that disruption of SM homeostasis at the trans-Golgi network (TGN) by treatment of HeLa cells wit

194 h F-actin and is associated with a subapical trans-Golgi network (TGN) compartment, whose cytoplasmic

195 4B is recruited to vesicles that emerge from trans-Golgi network (TGN) compartments and regulates pol

196 rnae and swelling of the trans cisternae and trans-Golgi network (TGN) compartments.

197 hat the localization of ARF1 and BIG4 at the trans-Golgi network (TGN) depends on ECHIDNA (ECH), a pl

198 ion and fission are tightly regulated at the trans-Golgi network (TGN) during constitutive secretion.

199 the viral pseudogenome and L2 travel to the trans-Golgi network (TGN) following exit from the LE, wh

200 The mechanism of cargo sorting at the trans-Golgi network (TGN) for secretion is poorly unders

201 ust interact and form a complex to reach the trans-Golgi network (TGN) for subsequent ciliary targeti

202 Recently, the trans-Golgi network (TGN) has been implicated as a key c

203 d retention of the HPV16 pseudogenome in the trans-Golgi network (TGN) in Pyk2-depleted cells, sugges

204 e localized AFTPH to early endosomes and the trans-Golgi network (TGN) in unstimulated human colonic

205 The post-Golgi compartment trans-Golgi Network (TGN) is a central hub divided into

206 proteins into exocytic vesicles at the yeast trans-Golgi network (TGN) is believed to be mediated by

207 ion of cell wall polysaccharides through the trans-Golgi network (TGN) is required for plant cell elo

208 e perinuclear structures colocalize with the trans-Golgi network (TGN) marker TGN38 and to a lesser d

209 to 24-kDa species that colocalizes with the trans-Golgi network (TGN) marker TGN46 in KSHV-infected

210 hen undergo secondary envelopment, involving trans-Golgi network (TGN) membranes.

211 PI4KII isoforms also differentially affected trans-Golgi network (TGN) pools of PI(4)P and post-TGN t

212 Previous studies showed that CHV1 utilizes trans-Golgi network (TGN) secretory vesicles for replica

213 fine a signaling-regulated checkpoint at the trans-Golgi network (TGN) that controls the surface deli

214 a long coiled-coil protein localized to the trans-Golgi network (TGN) that functions in maintaining

215 rtner, the calcium-binding centrin Cdc31, in trans-Golgi network (TGN) to endosome traffic and TGN ho

216 tion that mediates transport of APP from the trans-Golgi network (TGN) to endosomes, thereby reducing

217 rnalized APP molecules from endosomes to the trans-Golgi network (TGN) to prevent proteolytic process

218 protein chitin synthase III (Chs3p) from the trans-Golgi network (TGN) to the cell surface and to and

219 y reported that PAUF is transported from the trans-Golgi network (TGN) to the cell surface in specifi

220 ling of active alpha5beta1 integrin from the trans-Golgi network (TGN) to the EC surface, thus allowi

221 tor protein that sorts cargo proteins at the trans-Golgi network (TGN) to the endosome/lysosome pathw

222 irectly required both for transport from the trans-Golgi network (TGN) to the late endosome/prevacuol

223 ort of a selected number of cargoes from the trans-Golgi network (TGN) to the plasma membrane in Sacc

224 TION3 (PEN3) outer membrane protein from the trans-Golgi network (TGN) to the plasma membrane in the

225 ct transport of a subset of cargoes from the trans-Golgi network (TGN) to the plasma membrane.

226 APP1) regulates secretory transport from the trans-Golgi network (TGN) to the plasma membrane.

227 In yeast, Vps10 transports enzymes from the trans-Golgi network (TGN) to the vacuole.

228 ence that Mn-induced exit of GPP130 from the trans-Golgi network (TGN) toward lysosomes is mediated b

229 tromer in the sequence-dependent endosome-to-trans-Golgi network (TGN) transport of the cation-indepe

230 For several decades, the trans-Golgi network (TGN) was considered the most distal

231 ic reticulum (ER) and its trafficking to the trans-Golgi network (TGN) were unaffected, indicating th

232 absorption and provides cuproenzymes in the trans-Golgi network (TGN) with copper.

233 ng retrograde through sorting endosomes, the trans-Golgi network (TGN), and into the endoplasmic reti

234 LDCVs form at the trans-Golgi network (TGN), but the mechanism for protein

235 Here, we show that ANK localizes to the trans-Golgi network (TGN), clathrin-coated vesicles and

236 E3/49K is localized in the Golgi/trans-Golgi network (TGN), in the early endosomes, and o

237 hate receptor (CI-MPR) from endosomes to the trans-Golgi network (TGN), is thought to consist of a ca

238 At the trans-Golgi network (TGN), phosphatidylinositol 4-phosph

239 er-like 1 (CTL1) protein is localized to the trans-Golgi network (TGN), prevacuolar compartment (PVC)

240 ain transmembrane proteins from endosomes to trans-Golgi network (TGN), regulated Crb in epithelial c

241 and late endosomes, and associated with the trans-Golgi network (TGN), suggesting that FgVps35 funct

242 BACE1 cycles between the trans-Golgi network (TGN), the plasma membrane, and endo

243 ck away from the plasma membrane (PM) to the trans-Golgi network (TGN), thereby preventing the recrui

244 ST leads to retention of the receptor in the trans-Golgi network (TGN), to the effect that overexpres

245 and were colocalized with PI4KIIalpha in the trans-Golgi network (TGN), were characterized in detail.

246 This new step takes place at the trans-Golgi network (TGN), where Rod1 localizes dynamica

247 They form at the trans-Golgi network (TGN), where their soluble content a

248 llomavirus (HPV) capsid is trafficked to the trans-Golgi network (TGN), whereupon it enters the nucle

249 elease of SGLT1-containing vesicles from the trans-Golgi network (TGN), which is regulated by a domai

250 go adaptor that sorts specific proteins into trans-Golgi network (TGN)-derived vesicles in response t

251 Here, we show a critical role of trans-Golgi network (TGN)-endosome trafficking during th

252 erization of a functional Golgi Arf-GEF, the trans-Golgi network (TGN)-localized Sec7 protein from ye

253 ECH protein is required for the trans-Golgi network (TGN)-mediated trafficking of the au

254 cking of Kex2p both in vivo and in cell-free trans-Golgi network (TGN)-prevacuolar compartment (PVC)

255 ocation of Abeta production-endosomes or the trans-Golgi network (TGN)-remains uncertain.

256 hrin coat involved in protein sorting at the trans-Golgi network (TGN).

257 most cases leading to cargo fusion with the trans-Golgi network (TGN).

258 uit that controls sphingolipid levels at the trans-Golgi network (TGN).

259 into cytoplasmic membranes derived from the trans-Golgi network (TGN).

260 pendent sorting of secretory proteins at the trans-Golgi network (TGN).

261 mately resulting in vesicle fission from the trans-Golgi network (TGN).

262 etrograde transport from the endosome to the trans-Golgi network (TGN).

263 The L2/DNA complex traffics to the trans-Golgi network (TGN).

264 endoplasmic reticulum, Golgi apparatus, and trans-Golgi network (TGN).

265 e endoplasmic reticulum (ER) rather than the trans-Golgi network (TGN).

266 tinuous endocytic cycling from the PM to the trans-Golgi network (TGN).

267 HLB1 associated with the trans-Golgi network (TGN)/early endosome (EE) and tracke

268 Here, we identify the trans-Golgi network (TGN)/endosomally localized adaptor

269 brane-trafficking machinery operating at the trans-Golgi network (TGN)/endosome interface.

270 a viral nucleocapsid buds into a vesicle of trans-Golgi network (TGN)/endosome origin, acquiring an

271 , a copper transporting P-type ATPase in the trans-Golgi network that is required for copper acquisit

272 SPCA1 regulates proteases within the trans-Golgi network that require calcium for their activ

273 es in the slightly acidic environment of the trans-Golgi network, thereby allowing cellular furin to

274 WF quanta within the continuous lumen of the trans-Golgi network, thereby generating organelles of di

275 l modulation of membrane organization at the trans-Golgi network through interacting with the effecto

276 proteins travel in carrier vesicles from the trans Golgi network to the apical or basolateral plasma

277 facilitating the transport of V-ATPases from trans-Golgi network to early endosomes.

278 and as an intracellular sorting receptor for trans-Golgi network to endosome traffic.

279 livery of nascent lysosomal enzymes from the trans-Golgi network to endosomes, we evaluated their rol

280 g is required for trafficking of Rh from the trans-Golgi network to rhabdomere membranes via a Rab11-

281 nosine triphosphatase that traffics from the trans-Golgi network to the canalicular area of hepatocyt

282 , from the endoplasmic reticulum through the trans-Golgi network to the cell surface, is utilized by

283 1) mediates trafficking of Ca(V)2.2 from the trans-Golgi network to the cell surface.

284 and other organisms known to signal from the trans-Golgi network to the endosomal compartment.

285 ncated sortilin redistributes BACE1 from the trans-Golgi network to the endosomes and substantially r

286 tes signal-mediated export of ATG9A from the trans-Golgi network to the peripheral cytoplasm, contrib

287 ATP7A relocalization from the trans-Golgi network to the plasma membrane in response t

288 s function in trafficking of ABCB19 from the trans-Golgi network to the PM.

289 ch intracellular CTLA-4 is shuttled from the trans-Golgi network to the surfaces of T cells.

290 on of multiple trafficking pathways from the trans-Golgi network to the vacuole and to the plasma mem

291 as PS2-containing ones were addressed to the trans-Golgi network, to recycling endosomes, and, depend

292 rence with the adaptor protein GGA1-mediated trans Golgi network-to-endosome transport of GPRC5B.

293 regulated during cyst formation, as are some trans-Golgi network-to-endosome trafficking genes.

294 SNAP-47 preferentially interacted with the trans-Golgi network VAMP4 and post-Golgi VAMP7 and -8.

295 PP-C-terminal fragment (CTF) delivery to the trans-Golgi network where gamma-secretase cleavage occur

296 AP-1 is a clathrin adaptor recruited to the trans-Golgi Network where it can interact with specific

297 serine/threonine kinase, is recruited to the trans-Golgi network where it influences vesicular traffi

298 port of the propeptide-enzyme complex to the trans-Golgi network, where it promotes cleavage and rele

299 ition, localization studies place KEG at the trans-Golgi network, whereas ABI5 is nuclear.

300 d that the wrapping membrane arises from the trans-Golgi network, whereas others suggested an origin