ライフサイエンスコーパス: trans-Golgi network

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

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

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

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

5 were reduced while ATG9A accumulated in the trans-Golgi network.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

22 , where they regulate vesicle budding at the trans-Golgi network.

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

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

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

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

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

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

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

30 lipid homeostasis and trafficking across the trans-Golgi network.

31 lpha(2B)-AR and to recruit clathrin onto the trans-Golgi network.

32 point that delays the export of DOR from the trans-Golgi network.

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

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

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

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

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

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

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

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

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

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

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

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

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

46 carboxypeptidase E (CPE) accumulate near the trans-Golgi network and are not retained in mature DCVs

47 ure virions due to a wrapping process at the trans-Golgi network and are required for cell-to-cell sp

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

66 hat associate with the cytosolic face of the trans-Golgi network and recycling endosomes, respectivel

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

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

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

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

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

72 ent of VZV capsids by altering the pH of the trans-Golgi network and thereby preventing the correct f

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

74 e autophagy protein ATG9A accumulated in the trans-Golgi network and was depleted from peripheral com

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

76 687 residue that accumulates APP in the TGN (Trans-Golgi Network) and diminishes its amyloidogenic cl

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

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

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

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

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

82 asizes the importance of the Golgi apparatus/trans-Golgi network as a platform in the alphaherpesviru

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

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

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

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

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

88 sortilin, is retrieved from endosomes to the trans-Golgi network by retromer.

89 profile of the SYNTAXIN OF PLANTS61 (SYP61) trans-Golgi network compartment in Arabidopsis (Arabidop

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

91 tures and show that its incorporation at the trans-Golgi network depends on cellular abundance of OSB

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

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

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

95 The dynamic trans-Golgi network/early endosome (TGN/EE) facilitates

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

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

98 the AtUPS5L variant was also detected in the trans-Golgi network/early endosome and at the plasma mem

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

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

101 CERBERUS colocalized with the trans-Golgi network/early endosome markers.

102 ERUS stabilizes LjVPY1 and LjVPY2 within the trans-Golgi network/early endosome, where they might fun

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

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

105 ated vesicles (CCVs) that form at the PM and trans-Golgi network/early endosomes have emerged as the

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

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

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

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

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

111 cleave at specific basic residues within the trans-Golgi network, granules, or at the cell surface/en

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

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

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

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

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

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

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

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

127 into the function of XP revealed plasma and trans Golgi network membrane-associated roles in virus a

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

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

130 y envelopment of capsids was not seen in the trans-Golgi network, nor were prototypical enveloped par

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

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

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

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

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

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

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

138 numerous protein cargos from the endosome to trans-Golgi network or the cell surface.

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

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

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

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

143 ally, we mapped subapical F-actin fringe and trans-Golgi network positioning relative to sites of bul

144 t for 1-3 hours, TPD52 co-localised with the trans-Golgi network protein syntaxin 6, but after 5 hour

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

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

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

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

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

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

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

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

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

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

157 nd targeting it for sequestration within the trans- Golgi network (TGN).

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

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

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

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

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

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

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

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

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

167 plasma membrane and in pathways between the trans-Golgi network (TGN) and endosomes.

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

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

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

171 apparatus, with prominent enrichment in the trans-Golgi network (TGN) and post-Golgi vesicles.

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

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

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

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

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

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

178 doplasmic reticulum, KOR1 cycles between the trans-Golgi network (TGN) and the plasma membrane (PM).

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

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

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

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

183 S1426I-do not affect ATP7B targeting to the trans-Golgi network (TGN) but reduce its Cu-transport ac

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

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

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

187 4B is recruited to vesicles that emerge from trans-Golgi network (TGN) compartments and regulates pol

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

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

190 endosome-derived transport carriers with the trans-Golgi network (TGN) depends on the concerted actio

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

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

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

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

195 the nuclear periphery, suggesting a role for trans-Golgi network (TGN) functions and retrograde trans

196 rting of integral membrane proteins from the trans-Golgi network (TGN) has been shown to occur throug

197 distinct vesicle classes at the level of the trans-Golgi network (TGN) has remained elusive.

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

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

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

201 The plant trans-Golgi network (TGN) is a central trafficking hub w

202 The trans-Golgi network (TGN) is a major site for sorting of

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

204 idylinositol 4-phosphate (PI4P) in the yeast trans-Golgi network (TGN) is dependent on intracellular

205 The integrity of the Golgi and trans-Golgi network (TGN) is disrupted by brefeldin A (B

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

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

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

209 Previously, we showed that the trans-Golgi network (TGN) membrane tether/golgin, GCC88,

210 ing of vesicular transport carriers from the trans-Golgi network (TGN) must coordinate specification

211 ocessed by endogenous alpha-secretase at the trans-Golgi network (TGN) of both transfected HeLa cells

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

213 nctions to control GLUT4 mobilization from a trans-Golgi network (TGN) storage compartment, establish

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

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

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

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

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

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

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

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

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

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

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

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

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

227 phosphatidylinositol 4-phosphate [PI(4)P] on trans-Golgi network (TGN) vesicles were recruited to mit

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

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

230 Formation of SGs occurs at the trans-Golgi network (TGN) where their soluble cargo aggr

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

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

233 transport of vesicles from endosomes to the trans-Golgi network (TGN), and its mutation leads to sev

234 M protein is retained intracellularly in the trans-Golgi network (TGN), and we identified two motifs

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 thways including retrograde transport to the trans-Golgi network (TGN), is involved in the presentati

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

239 in clathrin-coated vesicle formation at the trans-Golgi network (TGN), likely aiding the transport o

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

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

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

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

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

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

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

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

255 showed that the L-type lectin, LMAN2, limits trans-Golgi Network (TGN)-to-endosomes traffic of GPRC5B

256 t endosome-derived vesicles destined for the trans-Golgi network (TGN).

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

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

259 ployed, such as one that intersects with the trans-Golgi network (TGN).

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

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

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

263 ponent of a protein coat associated with the trans-Golgi network (TGN).

264 d in swollen trans cisternal margins and the Trans-Golgi network (TGN).

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

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

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

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

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

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

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

278 The distribution of the M6PR pathway (trans-Golgi network to late endosomes) was constrained i

279 tracellular envelopment of poxviruses at the trans-Golgi network to release infectious extracellular

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

281 uttling of rnf-145 from the cis-Golgi to the trans-Golgi network to stop glial growth.

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

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

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

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

286 , we show that BACE1 is transported from the trans-Golgi network to the plasma membrane in an AP-1- a

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

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

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

300 of single enveloped viral particles from the trans-Golgi network within small vacuoles to the plasma