ライフサイエンスコーパス: TGN

1 TGN concentrations of >220 pmol/8 x 10(8) RBCs are assoc

2 It does not contain a 5'-TGN-extended -10 sequence, although mutants with mutatio

3 ed 6-MMP (6-methyl mercaptopurine) and low 6-TGN (6-thioguanine nucleotide) consistent with AZA-induc

4 GN and post-TGN cargo without the need for a TGN marker that universally cosegregates with all cargo.

5 P4a) and YIP4b (formerly YIP2), which form a TGN-localized complex with ECHIDNA (ECH) in Arabidopsis

6 Overall, our results reveal a TGN subdomain defined by ECH/YIP4 that is required for t

7 are detected in the trans-most cisternae and TGN compartments.

8 argeting mechanism of PI4KB to the Golgi and TGN membranes is unknown.

9 -Golgi network (TGN) to endosome traffic and TGN homotypic fusion.

10 plex mediate the transport of MIG-14/Wls and TGN-38/TGN38 cargo proteins from the recycling endosome

11 ing into AP1-coated vesicles for anterograde TGN-plasma membrane transport.

12 d composition to functional polar sorting at TGN subdomains remain unknown.

13 Furthermore, we find that retrograde cargo TGN-38 is trapped in early endosomes after depletion of

14 s, there was no association between red cell TGN levels and taking 6-MP with food versus without (206

15 LVs produced from TGN compartments (TGN-LVs) stained lighter than LVs and contained the cell

16 In contrast, TGN export of Frizzled 6, which localizes to the opposin

17 In addition, AtPep1 and different TGN/EE markers colocalized only rarely, implying that th

18 Are lipids also sorted into distinct TGN-derived carriers?

19 r polar domain of the plasma membrane and EE/TGN in root epidermal cells.

20 s to early endosomes/trans-Golgi network (EE/TGN) and is constitutively endocytosed through a monoubi

21 ncodes a trans-Golgi network/early endosome (TGN/EE)-localized E3 ubiquitin ligase.

22 ther the trans-Golgi network/early endosome (TGN/EE)-localized vacuolar H(+)-ATPase activity nor the

23 GLUT4 from a perinuclear recycling endosome/TGN compartment.

24 at the trans-Golgi network/early endosomes (TGN/EE) for vacuolar targeting.

25 the trans-Golgi network and early endosomes (TGN/EE) function as the central junction for major endom

26 Monthly erythrocyte TGN levels (pmol/8 x 108 erythrocytes) were measured ove

27 Thus yeast Gga adaptors facilitate TGN-PVC transport by direct binding of noncanonical phos

28 We propose that CLN3 facilitates TGN-to-plasma membrane transport of microdomain-associat

29 dosome/prevacuolar compartment (PVC) and for TGN homotypic fusion.

30 es the requirement of K33-ubiquitination for TGN-pool F-actin assembly and post-Golgi trafficking.

31 LVs produced from TGN compartments (TGN-LVs) stained lighter than LVs and

32 tion, silencing retromer or disrupting Golgi/TGN organization all impair efficient TSH-dependent cAMP

33 te coating events within the pre-Golgi/Golgi/TGN continuum.

34 inhibiting PKA II/interfering with its Golgi/TGN localization, silencing retromer or disrupting Golgi

35 protein kinase A (PKA) response at the Golgi/TGN.

36 c reticulum and, after passage through Golgi/TGN to the cell division plane, transformed into fusogen

37 findings support the notion that HCV hijacks TGN-endosome trafficking to facilitate particle assembly

38 disruption of Crn7-Eps15 interaction impairs TGN-pool F-actin assembly, a process essential for gener

39 HID-1 KO cells also exhibit defects in TGN acidification together with mislocalization of the G

40 s a link to a more general role of exomer in TGN organization.

41 minant negative (DN) Rab GTPases involved in TGN-endosome trafficking steps.

42 hat the ECH/YIP4 complex plays a key role in TGN-mediated secretion of pectin and hemicellulose to th

43 herers, high intra-individual variability in TGN levels contributed to increased relapse risk (hazard

44 in the cytoplasm that are unable to bud into TGN membranes.

45 gest that the virus perturbs a specific late TGN secretory pathway resulting in buildup of a key prot

46 se appear to be a subdomain of the mammalian TGN, showing only partial overlap with the TGN marker go

47 ns at the donor endosome membrane to mediate TGN trafficking.

48 al compartments and the trans-Golgi network (TGN) [including the retromer complex (Vps35, Vps26) and

49 ansport of BACE1 to the trans-Golgi network (TGN) and a delayed delivery of BACE1 to the lysosomes, t

50 fic retrogradely to the trans-Golgi network (TGN) and activate endogenous Gs-proteins in the retromer

51 ompartmentalized to the Trans-Golgi Network (TGN) and also to milk.

52 n transport between the trans-Golgi network (TGN) and early endosome (EE) requires Drs2, a phospholip

53 action enriched for the trans-Golgi network (TGN) and endosomal compartments.

54 pid trafficking through trans-Golgi network (TGN) and endosomal systems.

55 ein sorting between the trans-Golgi network (TGN) and endosomes.

56 lathrin adaptors to the trans-Golgi network (TGN) and endosomes.

57 ed cupro-enzymes in the trans-Golgi network (TGN) and exports excess copper out of cells by trafficki

58 L20 is localized to the trans-Golgi network (TGN) and is important for post-Golgi trafficking by prom

59 t CLN3 localizes to the trans-Golgi network (TGN) and partitions with buoyant microdomain fractions.

60 rade trafficking to the trans-Golgi network (TGN) and reaches a steady-state distribution in the TGN

61 FR/RTK anchoring on the trans-Golgi network (TGN) and recycling back to the plasma membrane, leading

62 ves sequentially to the trans-Golgi network (TGN) and recycling endosomes before nuclear translocatio

63 predominantly from the trans-Golgi network (TGN) and recycling endosomes, respectively.

64 ograde transport to the trans-Golgi network (TGN) and recycling to the plasma membrane.

65 trafficking toward the trans-Golgi network (TGN) and the Golgi apparatus correlates with transductio

66 7B was localized to the trans-Golgi network (TGN) and the plasma membrane of the soma and dendrites b

67 ins transit through the trans-Golgi network (TGN) and the prevacuolar compartment (PVC) en route to t

68 somal hydrolases at the trans-Golgi network (TGN) are well understood.

69 n forms clusters in the trans-Golgi network (TGN) but not at the plasma membrane.

70 rade transport from the trans-Golgi network (TGN) by facilitating localized actin assembly at the TGN

71 f SM homeostasis at the trans-Golgi network (TGN) by treatment of HeLa cells with d-ceramide-C6, whic

72 ciated with a subapical trans-Golgi network (TGN) compartment, whose cytoplasmic position at the poll

73 sicles that emerge from trans-Golgi network (TGN) compartments and regulates polarized membrane traff

74 the trans cisternae and trans-Golgi network (TGN) compartments.

75 of ARF1 and BIG4 at the trans-Golgi network (TGN) depends on ECHIDNA (ECH), a plant homolog of yeast

76 ightly regulated at the trans-Golgi network (TGN) during constitutive secretion.

77 me and L2 travel to the trans-Golgi network (TGN) following exit from the LE, while L1 is retained.

78 of cargo sorting at the trans-Golgi network (TGN) for secretion is poorly understood.

79 a complex to reach the trans-Golgi network (TGN) for subsequent ciliary targeting.

80 otein, Vangl2, from the trans Golgi network (TGN) in mammalian cells.

81 V16 pseudogenome in the trans-Golgi network (TGN) in Pyk2-depleted cells, suggesting that the kinase

82 early endosomes and the trans-Golgi network (TGN) in unstimulated human colonic epithelial cells.

83 post-Golgi compartment trans-Golgi Network (TGN) is a central hub divided into multiple subdomains h

84 c vesicles at the yeast trans-Golgi network (TGN) is believed to be mediated by their coalescence wit

85 saccharides through the trans-Golgi network (TGN) is required for plant cell elongation.

86 ncipal functions of the trans Golgi network (TGN) is the sorting of proteins into distinct vesicular

87 at colocalizes with the trans-Golgi network (TGN) marker TGN46 in KSHV-infected PEL cells.

88 enance of the Golgi and trans Golgi network (TGN) PI4P pools, however, the actual targeting mechanism

89 differentially affected trans-Golgi network (TGN) pools of PI(4)P and post-TGN traffic.

90 lated checkpoint at the trans-Golgi network (TGN) that controls the surface delivery of the delta opi

91 nding centrin Cdc31, in trans-Golgi network (TGN) to endosome traffic and TGN homotypic fusion.

92 s from endosomes to the trans-Golgi network (TGN) to prevent proteolytic processing or by directing n

93 se III (Chs3p) from the trans-Golgi network (TGN) to the cell surface and to and from the early endos

94 is transported from the trans-Golgi network (TGN) to the cell surface in specific carriers called CAR

95 beta1 integrin from the trans-Golgi network (TGN) to the EC surface, thus allowing FN fibrillogenesis

96 s cargo proteins at the trans-Golgi network (TGN) to the endosome/lysosome pathway.

97 for transport from the trans-Golgi network (TGN) to the late endosome/prevacuolar compartment (PVC)

98 ber of cargoes from the trans-Golgi network (TGN) to the plasma membrane in Saccharomyces cerevisiae

99 mbrane protein from the trans-Golgi network (TGN) to the plasma membrane in the root epidermis of Ara

100 sports enzymes from the trans-Golgi network (TGN) to the vacuole.

101 exit of GPP130 from the trans-Golgi network (TGN) toward lysosomes is mediated by the sorting recepto

102 e-dependent endosome-to-trans-Golgi network (TGN) transport of the cation-independent mannose 6-phosp

103 or several decades, the trans-Golgi network (TGN) was considered the most distal stop and hence the u

104 its trafficking to the trans-Golgi network (TGN) were unaffected, indicating that the decreased intr

105 des cuproenzymes in the trans-Golgi network (TGN) with copper.

106 sorting endosomes, the trans-Golgi network (TGN), and into the endoplasmic reticulum.

107 at ANK localizes to the trans-Golgi network (TGN), clathrin-coated vesicles and the plasma membrane.

108 localized in the Golgi/trans-Golgi network (TGN), in the early endosomes, and on the plasma membrane

109 ) from endosomes to the trans-Golgi network (TGN), is thought to consist of a cargo-selective VPS26-V

110 At the trans-Golgi network (TGN), phosphatidylinositol 4-phosphate (PtdIns4P) plays

111 ein is localized to the trans-Golgi network (TGN), prevacuolar compartment (PVC), and plasma membrane

112 and associated with the trans-Golgi network (TGN), suggesting that FgVps35 functions at the donor end

113 of the receptor in the trans-Golgi network (TGN), to the effect that overexpressed PIST reduces acti

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

115 step takes place at the trans-Golgi network (TGN), where Rod1 localizes dynamically upon triggering e

116 They form at the trans-Golgi network (TGN), where their soluble content aggregates to form a d

117 id is trafficked to the trans-Golgi network (TGN), whereupon it enters the nucleus during mitosis.

118 ining vesicles from the trans-Golgi network (TGN), which is regulated by a domain of protein RS1 (RSC

119 show a critical role of trans-Golgi network (TGN)-endosome trafficking during the assembly, but princ

120 onal Golgi Arf-GEF, the trans-Golgi network (TGN)-localized Sec7 protein from yeast.

121 ein is required for the trans-Golgi network (TGN)-mediated trafficking of the auxin influx carrier AU

122 n vivo and in cell-free trans-Golgi network (TGN)-prevacuolar compartment (PVC) transport.

123 protein sorting at the trans-Golgi network (TGN).

124 o cargo fusion with the trans-Golgi network (TGN).

125 branes derived from the trans-Golgi network (TGN).

126 cretory proteins at the trans-Golgi network (TGN).

127 ingolipid levels at the trans-Golgi network (TGN).

128 esicle fission from the trans-Golgi network (TGN).

129 rom the endosome to the trans-Golgi network (TGN).

130 complex traffics to the trans-Golgi network (TGN).

131 ling from the PM to the trans-Golgi network (TGN).

132 LB1 associated with the trans-Golgi network (TGN)/early endosome (EE) and tracked along filamentous a

133 hinery operating at the trans-Golgi network (TGN)/endosome interface.

134 adherence, red cell thioguanine nucleotide (TGN) levels, and risk of relapse in children with TMPT w

135 formation of active thioguanine nucleotide (TGN) metabolites varies widely.

136 sured as erythrocyte thioguanine nucleotide [TGN] levels) in children with acute lymphoblastic leukem

137 i trafficking by promoting the biogenesis of TGN-derived transport carriers.

138 acyl-chain length links lipid composition of TGN subdomains with polar secretory trafficking of PIN2

139 ed Rab22aQ64L mutant caused fragmentation of TGN membrane domains enriched for ATP7A.

140 l microsomal spread and 2) identification of TGN and post-TGN cargo without the need for a TGN marker

141 ences the morphology and interconnections of TGN-associated secretory vesicles.

142 ing clathrin-coated vesicles, caused loss of TGN localization and somatodendritic polarity of ATP7B.

143 Thus, therapeutic monitoring of TGN and methylthioinosine derivatives has been suggested

144 ant cell division in which a large number of TGN-derived membrane vesicles fuse with one another to f

145 argo selectivity for betagamma regulation of TGN to PM transport and a novel role for betagamma in me

146 nterfering RNA (siRNA)-mediated silencing of TGN-associated adaptor proteins and a panel of dominant

147 found that Eqt-SM is enriched in a subset of TGN-derived secretory vesicles that are also enriched in

148 y, we found that ATL1 interacts with EDR1 on TGN/EE vesicles and that EDR1 suppresses ATL1-mediated c

149 Finally, we show that HCV NS2 perturbs TGN architecture, redistributing TGN membranes to closel

150 tudies showed that cleavage occurs in a post-TGN compartment and that lysosomotropic agents enhance s

151 spread and 2) identification of TGN and post-TGN cargo without the need for a TGN marker that univers

152 Golgi network (TGN) pools of PI(4)P and post-TGN traffic.

153 eir arrival at the cell surface and the post-TGN breakup of large pleomorphic membrane fragments that

154 Rab7 activity promoted TGN association, whereas Rab7(dominant negative) trapped

155 Red blood cell (RBC) TGNs and MeMPNs were measured in serial blood samples ov

156 S2 perturbs TGN architecture, redistributing TGN membranes to closely associate with HCV core protein

157 endosomal compartments, decreased retrograde TGN trafficking, and increased Abeta production in H4 ne

158 a reaction that requires Ca(2+), the soluble TGN-resident protein Cab45 is necessary for the sorting

159 and the TGN Ca(2+) pump (SPCA1) in specific TGN microdomains.

160 TGN SNAREs, and underwent Ca(2+)-stimulated TGN recruitment.

161 AC5 and RISAP is detectable at the subapical TGN compartment.

162 Here we show that TGN-localized E3/49K comprises both newly synthesized an

163 ly to the pre-Golgi, the Golgi, and also the TGN.

164 roteins to the plasma membrane, although the TGN also functions as an early endosome in plants.

165 colocalizes with secretory proteins and the TGN Ca(2+) pump (SPCA1) in specific TGN microdomains.

166 ion of proteins related to endosomes and the TGN trafficking pathway.

167 d vesicular transport between the EE and the TGN.

168 and NEV/AGD5 colocalize with clathrin at the TGN and are incorporated into CCVs.

169 irs by their degree of colocalization at the TGN and by the evolution of colocalization during their

170 s to defective MPR carrier biogenesis at the TGN and endosomes.

171 of a novel functional protein complex at the TGN and its key members: cytosolic PKD2 binds ARF-like G

172 demonstrate the sorting of native SM at the TGN and its transport to the plasma membrane by specific

173 not sialylated by a sialyltransferase at the TGN and that this enzyme and its substrate TGN46 could n

174 The primary role of PS flip at the TGN appears to be to control the oxysterol-binding prote

175 responsible for synthesis of PtdIns4P at the TGN are not well characterized.

176 tion of AP-1- and GGA-coated carriers at the TGN but may be dispensable for outward traffic en route

177 localization of YIP4 and ECH proteins at the TGN is interdependent and influences the localization of

178 to membranes, whereas GBF1 localized at the TGN mediates ARF activation that leads to the recruitmen

179 Blocking vesicle formation at the TGN revealed cis-SNARE complexes.

180 that generation of putrescine by ODC1 at the TGN stimulates release of SGLT1-containing vesicles.

181 ormation of this multiprotein complex at the TGN that controls constitutive secretion of matrix metal

182 facilitating localized actin assembly at the TGN through K33-linked ubiquitination of coronin 7.

183 mes and lysosomes is thought to occur at the TGN through recognition of sorting signals in the cytoso

184 we show that sphingomyelin production at the TGN triggers a signalling pathway leading to PtdIns(4)P

185 eractions of p14 with activated Rab11 at the TGN, resulting in p14 sorting into AP1-coated vesicles f

186 At the TGN, where PKD2 interacts with active ARF1, PKD2, and AR

187 binds to different receptor proteins at the TGN, which trigger release of vesicles with different tr

188 b11 and AP-1 both colocalize with p14 at the TGN.

189 hosphatidylinositol 4-kinase function at the TGN.

190 e sorting of specific cargo molecules at the TGN.

191 regation of protein and lipid domains at the TGN.

192 f the ART/Rsp5 ubiquitylation complex at the TGN.

193 Arl3-based ciliary trafficking module at the TGN.

194 ins into functional enzymatic domains at the TGN.

195 n by controlling dense core formation at the TGN.

196 for the sorting of secretory cargoes at the TGN.

197 R1 negatively regulates ATL1 activity at the TGN/EE and thus controls stress responses initiated by A

198 rf-binding protein)-coated structures at the TGN/endosomal interface, resulting in the peripheral dis

199 ll surface regulates membrane traffic at the TGN/endosomal interface.

200 DISLL, which controls transport between the TGN and endosomes via interaction with GGA proteins.

201 sis, ATP7A constitutively cycles between the TGN and plasma membrane (PM).

202 e found that TGN46, which cycles between the TGN and the plasma membrane, was not sialylated by a sia

203 thrin/AP-mediated cycling of ANK between the TGN, endosomes, and the cell surface regulates membrane

204 ergo progressive sorting after they exit the TGN toward the cell surface.

205 ld be required for the viral DNA to exit the TGN.

206 , yet renders the protein unable to exit the TGN.

207 ar sites and reveals a critical role for the TGN in GPCR signaling.Recent investigations suggest that

208 e incoming viral genome dissociates from the TGN and associates with microtubules after the onset of

209 d auxin carriers to plasma membrane from the TGN and reveal how trafficking of auxin influx carriers

210 een implicated in polar trafficking from the TGN but the underlying mechanisms linking lipid composit

211 flux carrier to the plasma membrane from the TGN during hook development and defects in BIG or ARF1 r

212 that timely exit of these proteins from the TGN is critical for effective pre-invasive immune respon

213 key regulators of protein transport from the TGN so far is elusive.

214 pathway lead to relocation of PIST from the TGN to an endosome-like compartment.

215 ither protein causes ANK dispersion from the TGN to cytoplasmic endosome-like puncta.

216 nsport of specific carriers, CARTS, from the TGN to the cell surface.

217 copper out of cells by trafficking from the TGN to the plasma membrane.

218 that CTL1 regulates protein sorting from the TGN to the PM through its function in lipid homeostasis.

219 RK2ct-KERE inhibits cargo transport from the TGN to the PM.

220 ed trafficking of vacuolar proteins from the TGN to the PVC in plants.

221 roteins Pma1 and Can1 are missorted from the TGN to the vacuole in drs2 cells.

222 of SORLA in endosomes and depletion from the TGN, and in an overall enhanced APP processing.

223 PV-harboring transport vesicles bud from the TGN, followed by association with mitotic chromosomes.

224 mation of tubular membrane carriers from the TGN, perinuclear accumulation of early endosomes and imp

225 generic ACT7-dependent trafficking from the TGN, the EXOCYST84b (EXO84b) tethering factor mediates P

226 ain contacts initiate exit of ATP7B from the TGN, whereas increased phosphorylation may be needed to

227 equired for receptor sorting to and from the TGN.

228 bation of secretory vesicle genesis from the TGN.

229 ) are required for Vangl2 transport from the TGN.

230 distribution of CCV cargo exported from the TGN.

231 ot obligatory for ATP7B trafficking from the TGN.

232 eptors can be released from retention in the TGN by coexpression of the plasma membrane-associated sc

233 y synthesized proteins are segregated in the TGN for eventual apical delivery.

234 e studies demonstrate that clustering in the TGN is required for normal biosynthetic apical sorting o

235 d reaches a steady-state distribution in the TGN within 2 h.

236 In alp3, PEN3 accumulates in the TGN, causing delays in recruitment to the host-pathogen

237 at levels of both GM1 and cholesterol in the TGN-endosomal compartment are upregulated in some inheri

238 ell wall polysaccharide epitopes seen in the TGN.

239 ssumes a transmembranous conformation in the TGN.

240 The receptors were arrested in the TGN.

241 hermore, HPV16 capsid proteins arrive in the TGN/Golgi in a retromer-dependent fashion during entry,

242 d to efficiently traffic retrograde into the TGN and endoplasmic reticulum and into the recycling end

243 ng site also affected Ca(2+) import into the TGN and secretory cargo sorting.

244 HeLa cells, inhibited Ca(2+) entry into the TGN and secretory cargo sorting.

245 lin-rich domains of the plasma membrane, the TGN and recycling endosomes.

246 iched in secretory vesicle subdomains of the TGN and are critical for de novo polar secretory sorting

247 accompanied by apparent fragmentation of the TGN and redistribution of K15P to a dispersed peripheral

248 retory granule formation at the level of the TGN are still elusive.

249 icellulose and distinguishes the role of the TGN in secretion from its roles in endocytic and vacuola

250 Disruption of the TGN significantly reduced nuclear translocation of viral

251 leavage from gp160 and trafficked out of the TGN.

252 1 and SYP61, which are key components of the TGN.

253 x with actin to modulate the function of the TGN/EE at the intersection of the exocytic and endocytic

254 or-ligand pair is largely independent of the TGN/EE.

255 LISA and coimmunoprecipitation show that the TGN/endosomal small GTPase Rab14 and PKCiota interact di

256 ense proteins continuously cycle through the TGN and that timely exit of these proteins from the TGN

257 Indeed, transporter trafficking to the TGN after internalization is required for their degradat

258 nvolved in trafficking from endosomes to the TGN and the cell surface.

259 The syntaxin TlgB(Tlg2) localizing to the TGN appears to mediate retrograde traffic connecting pos

260 Transport from recycling endosomes to the TGN has also been reported, but much less is understood

261 proteins from the recycling endosome to the TGN in Caenorhabditis elegans.

262 de transport of CI-MPR from endosomes to the TGN independently of the core retromer trimer.

263 s suggest that retrograde trafficking to the TGN induces local Gs-protein activation and cAMP/PKA sig

264 possibility that compartments distal to the TGN mediate or contribute to biosynthetic sorting.

265 and UL37 are known to be transported to the TGN sites of virus envelopment and to function in virion

266 constitutive internalization of LGR5 to the TGN suggests the existence of novel biochemical roles fo

267 of internalized Shiga toxin B subunit to the TGN, as well as recycling of internalized transferrin to

268 raction mediates localization of Sec7 to the TGN, because deletion of the HDS1 domain or mutation of

269 adation in lysosomes and retrieves it to the TGN, where insulin--responsive vesicles are formed.

270 uitment of the PI3K C2A kinase domain to the TGN-induced deltaR export downstream of NGF.

271 red for efficient recruitment of GARP to the TGN.

272 -like GTPase (ARL1) and shuttles ARL1 to the TGN.

273 h AP-4, and for recruitment of tepsin to the TGN.

274 for trafficking of ATP7A from the PM to the TGN.

275 facilitate BIG1 and BIG2 recruitment to the TGN.

276 s to the recruitment of BIG1 and BIG2 to the TGN.

277 pathway bypasses retrograde transport to the TGN.

278 n of PtdIns4P and recruitment of AP-1 to the TGN.

279 r-coated compartment that brings them to the TGN.

280 ARL1, in turn, localizes Arfaptin2 to the TGN.

281 e early or late endosome and traffics to the TGN/Golgi via the retrograde pathway during cell entry.

282 fusion of endosome-derived carriers with the TGN and recycling endosomes, respectively.

283 n TGN, showing only partial overlap with the TGN marker golgin-97.

284 ting post-Golgi (sorting) endosomes with the TGN.

285 the evolution of colocalization during their TGN-to-surface transport.

286 In this TGN compartment, apical secretion and endocytic membrane

287 Enforced targeting of Crn7 to TGN bypasses the requirement of K33-ubiquitination for T

288 ing sensor (+ALPS) motif for localization to TGN/EE membranes.

289 UB13 fusion protein (YFP-PUB13) localizes to TGN and Golgi compartments and that PUB13, PI4Kbeta1, an

290 (Crn7), which facilitates Crn7 targeting to TGN through a ubiquitin-dependent interaction with Eps15

291 gh recognition of a specific WLM endosome-to-TGN sorting motif.

292 620N) there is a perturbation in endosome-to-TGN transport but not endosome-to-plasma membrane recycl

293 nal effects on retromer-mediated endosome-to-TGN transport, provide new insight into retromer deregul

294 to a pronounced defect in CI-MPR endosome-to-TGN transport.

295 of tubular profiles required for endosome-to-TGN transport.

296 n-regulated pathways, but also blocked PM-to-TGN internalization of ATP7A.

297 Furthermore, adherers with varying TGN levels had varying 6MP dose intensity (odds ratio [O

298 lasma membrane only in border cells, whereas TGN-LVs containing the XG and PGA/RG-I epitopes fuse wit

299 They also colocalize to similar extents with TGN and recycling endosome markers, as well as with baso

300 xhibited Ca(2+)-stimulated interactions with TGN SNAREs, and underwent Ca(2+)-stimulated TGN recruitm