scholarly article | Q13442814 |
P356 | DOI | 10.1091/MBC.E02-01-0004 |
P8608 | Fatcat ID | release_jluoouwq4vhtzowk4oqgj4iote |
P3181 | OpenCitations bibliographic resource ID | 202938 |
P932 | PMC publication ID | 129961 |
P698 | PubMed publication ID | 12388752 |
P50 | author | David James | Q5235558 |
Sally Martin | Q50912546 | ||
P2093 | author name string | Wanjin Hong | |
Yue Xu | |||
P2860 | cites work | Localization and recycling of gp27 (hp24gamma3): complex formation with other p24 family members | Q22009946 |
The debate about transport in the Golgi--two sides of the same coin? | Q24290401 | ||
A v-SNARE implicated in intra-Golgi transport | Q24312623 | ||
Ykt6p, a Prenylated SNARE Essential for Endoplasmic Reticulum-Golgi Transport | Q24315775 | ||
A SNARE involved in protein transport through the Golgi apparatus | Q24322596 | ||
Distinct SNARE complexes mediating membrane fusion in Golgi transport based on combinatorial specificity | Q24534126 | ||
Adaptins: the final recount | Q24555129 | ||
A SNARE complex mediating fusion of late endosomes defines conserved properties of SNARE structure and function | Q24595623 | ||
Brefeldin A: insights into the control of membrane traffic and organelle structure | Q24643698 | ||
Morphological and functional association of Sec22b/ERS-24 with the pre-Golgi intermediate compartment | Q38609841 | ||
Exocytosis requires asymmetry in the central layer of the SNARE complex | Q40388114 | ||
Role of Vesicle-Associated Syntaxin 5 in the Assembly of Pre-Golgi Intermediates | Q41064399 | ||
Vesicular stomatitis virus glycoprotein is sorted and concentrated during export from the endoplasmic reticulum | Q41481250 | ||
Moving GLUT4: The Biogenesis and Trafficking of GLUT4 Storage Vesicles | Q41632292 | ||
Effects of insulin on intracellular GLUT4 vesicles in adipocytes: evidence for a secretory mode of regulation | Q42493244 | ||
A genomic perspective on membrane compartment organization. | Q44883436 | ||
Syntaxin 5 regulates endoplasmic reticulum to Golgi transport | Q46344279 | ||
A 29-Kilodalton Golgi SolubleN-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Vti1-rp2) Implicated in Protein Trafficking in the Secretory Pathway | Q47682122 | ||
Cytoplasmic coat proteins involved in endosome function | Q70787141 | ||
Differential response of resident proteins and cycling proteins of the Golgi to brefeldin A | Q70935856 | ||
Maintenance of Golgi structure and function depends on the integrity of ER export | Q24653507 | ||
Evidence that the entire Golgi apparatus cycles in interphase HeLa cells: sensitivity of Golgi matrix proteins to an ER exit block | Q24653538 | ||
Conserved structural features of the synaptic fusion complex: SNARE proteins reclassified as Q- and R-SNAREs | Q24656954 | ||
Early/recycling endosomes-to-TGN transport involves two SNARE complexes and a Rab6 isoform | Q24671033 | ||
Sequential tethering of Golgins and catalysis of SNAREpin assembly by the vesicle-tethering protein p115 | Q24673491 | ||
The Mammalian Protein (rbet1) Homologous to Yeast Bet1p Is Primarily Associated with the Pre-Golgi Intermediate Compartment and Is Involved in Vesicular Transport from the Endoplasmic Reticulum to the Golgi Apparatus | Q24677983 | ||
Rab proteins as membrane organizers | Q27860861 | ||
Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells | Q27860926 | ||
A SNARE-like protein required for traffic through the Golgi complex | Q27932115 | ||
Genetic interactions with the yeast Q-SNARE VTI1 reveal novel functions for the R-SNARE YKT6. | Q27934382 | ||
Gos1p, a Saccharomyces cerevisiae SNARE protein involved in Golgi transport. | Q27936489 | ||
The Dynamics of Golgi Protein Traffic Visualized in Living Yeast Cells | Q27938880 | ||
SNAP receptors implicated in vesicle targeting and fusion | Q28131653 | ||
Subunit structure of a mammalian ER/Golgi SNARE complex | Q28141448 | ||
ERGIC-53 and traffic in the secretory pathway | Q28143617 | ||
Ykt6 forms a SNARE complex with syntaxin 5, GS28, and Bet1 and participates in a late stage in endoplasmic reticulum-Golgi transport | Q28185724 | ||
Membrane transport: retromer to the rescue | Q28202844 | ||
Syntaxin 7 complexes with mouse Vps10p tail interactor 1b, syntaxin 6, vesicle-associated membrane protein (VAMP)8, and VAMP7 in b16 melanoma cells | Q28208262 | ||
GS15, a 15-kilodalton Golgi soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) homologous to rbet1 | Q28579141 | ||
GS28, a 28-kilodalton Golgi SNARE that participates in ER-Golgi transport | Q28580207 | ||
Membrane fusion and exocytosis | Q29614426 | ||
SNARE-mediated membrane fusion | Q29619234 | ||
Protein sorting by transport vesicles | Q29619990 | ||
Protein sorting by directed maturation of Golgi compartments | Q33676844 | ||
Transport-vesicle targeting: tethers before SNAREs | Q33772639 | ||
Coat proteins regulating membrane traffic. | Q33798205 | ||
BET1, BOS1, and SEC22 are members of a group of interacting yeast genes required for transport from the endoplasmic reticulum to the Golgi complex | Q34020613 | ||
ER export: public transportation by the COPII coach | Q34309052 | ||
The endocytic pathway: a mosaic of domains | Q34389525 | ||
The curious status of the Golgi apparatus | Q34485921 | ||
Molecular cloning, characterization, subcellular localization and dynamics of p23, the mammalian KDEL receptor | Q36232312 | ||
Differential regulation of secretory compartments containing the insulin-responsive glucose transporter 4 in 3T3-L1 adipocytes | Q36933224 | ||
Anterograde flow of cargo across the golgi stack potentially mediated via bidirectional "percolating" COPI vesicles | Q37244865 | ||
Matrix proteins can generate the higher order architecture of the Golgi apparatus | Q38306901 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | cell biology | Q7141 |
Golgi apparatus | Q83181 | ||
P304 | page(s) | 3493-3507 | |
P577 | publication date | 2002-10-01 | |
P1433 | published in | Molecular Biology of the Cell | Q2338259 |
P1476 | title | GS15 forms a SNARE complex with syntaxin 5, GS28, and Ykt6 and is implicated in traffic in the early cisternae of the Golgi apparatus | |
P478 | volume | 13 |
Q40536380 | 25-hydroxycholesterol acts in the Golgi compartment to induce degradation of tyrosinase |
Q36469712 | A Conserved Structural Motif Mediates Retrograde Trafficking of Shiga Toxin Types 1 and 2 |
Q90021381 | A SNARE geranylgeranyltransferase essential for the organization of the Golgi apparatus |
Q28943556 | A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids |
Q34845032 | A model for the self-organization of vesicular flux and protein distributions in the Golgi apparatus |
Q46990070 | A multigene family encoding R-SNAREs in the ciliate Paramecium tetraurelia. |
Q39118163 | A trs20 Mutation That Mimics an SEDT‐Causing Mutation Blocks Selective and Non‐Selective Autophagy: A Model for TRAPP III Organization |
Q36321109 | ARFGAP1 plays a central role in coupling COPI cargo sorting with vesicle formation. |
Q36095697 | Analysis of de novo Golgi complex formation after enzyme-based inactivation |
Q57021023 | Another longin SNARE for autophagosome-lysosome fusion-how does Ykt6 work? |
Q30379553 | COG lobe B sub-complex engages v-SNARE GS15 and functions via regulated interaction with lobe A sub-complex. |
Q24306195 | COG-7-deficient Human Fibroblasts Exhibit Altered Recycling of Golgi Proteins |
Q36623748 | COPI-mediated transport. |
Q37947559 | COPII and COPI Traffic at the ER-Golgi Interface |
Q38121411 | Cargo trafficking between endosomes and the trans-Golgi network. |
Q90413818 | Characterisation of GLUT4 trafficking in HeLa cells: comparable kinetics and orthologous trafficking mechanisms to 3T3-L1 adipocytes |
Q39630964 | Coat-tether interaction in Golgi organization |
Q36321499 | Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells. |
Q30448470 | Complex formation among murine cytomegalovirus US22 proteins encoded by genes M139, M140, and M141. |
Q37884609 | Control of Organelle Size: The Golgi Complex |
Q37220226 | Countercurrent distribution of two distinct SNARE complexes mediating transport within the Golgi stack |
Q36208803 | Defects in the COG complex and COG-related trafficking regulators affect neuronal Golgi function |
Q33854507 | Deficiency of the Cog8 subunit in normal and CDG-derived cells impairs the assembly of the COG and Golgi SNARE complexes |
Q30499465 | Dependence of Golgi apparatus integrity on nitric oxide in vascular cells: implications in pulmonary arterial hypertension |
Q24317338 | Disruption of the integrin alphaLbeta2 transmembrane domain interface by beta2 Thr-686 mutation activates alphaLbeta2 and promotes micro-clustering of the alphaL subunits |
Q34078604 | Dynamic transport of SNARE proteins in the Golgi apparatus |
Q40163297 | Dysfunction of Golgi tethers, SNAREs, and SNAPs in monocrotaline-induced pulmonary hypertension. |
Q89812491 | Functional dissection of the retrograde Shiga toxin trafficking inhibitor Retro-2 |
Q37858330 | Golgi Bypass: Skirting Around the Heart of Classical Secretion |
Q50004856 | Highly conserved motifs within the large Sec7 ARF guanine nucleotide exchange factor GBF1 target it to the Golgi and are critical for GBF1 activity. |
Q34358823 | How the Golgi works: a cisternal progenitor model |
Q24297405 | Human Sin1 contains Ras-binding and pleckstrin homology domains and suppresses Ras signalling |
Q42727146 | Identification of functionally interacting SNAREs by using complementary substitutions in the conserved '0' layer |
Q41811577 | Inhibition of Rab prenylation by statins induces cellular glycosphingolipid remodeling |
Q39984867 | Intracellular trafficking of LRP9 is dependent on two acidic cluster/dileucine motifs |
Q33653677 | Lamellipodium extension and membrane ruffling require different SNARE-mediated trafficking pathways |
Q90099934 | MT1-MMP recruits the ER-Golgi SNARE Bet1 for efficient MT1-MMP transport to the plasma membrane |
Q42618291 | Molecular mechanism of mitotic Golgi disassembly and reassembly revealed by a defined reconstitution assay. |
Q37089621 | Monoubiquitination of Syntaxin 5 Regulates Golgi Membrane Dynamics during the Cell Cycle |
Q34201603 | Organization of SNAREs within the Golgi Stack |
Q38959357 | Oxidized phagosomal NOX2 complex is replenished from lysosomes. |
Q37306202 | Oxysterol-binding protein (OSBP) is required for the perinuclear localization of intra-Golgi v-SNAREs |
Q24300115 | PRA1 promotes the intracellular trafficking and NF-kappaB signaling of EBV latent membrane protein 1 |
Q24297647 | Participation of the syntaxin 5/Ykt6/GS28/GS15 SNARE complex in transport from the early/recycling endosome to the trans-Golgi network |
Q24313021 | RNA interference-mediated silencing of the syntaxin 5 gene induces Golgi fragmentation but capable of transporting vesicles |
Q36458562 | Rab GTPase localization and Rab cascades in Golgi transport |
Q35071524 | Rab9-dependent retrograde transport and endosomal sorting of the endopeptidase furin. |
Q37857950 | Rabs, SNAREs and α-synuclein — Membrane trafficking defects in synucleinopathies |
Q37171510 | Retrograde trafficking of AB5 toxins: mechanisms to therapeutics |
Q36336697 | Role of tethering factors in secretory membrane traffic. |
Q28580997 | R‐SNARE ykt6 resides in membrane‐associated protease‐resistant protein particles and modulates cell cycle progression when over‐expressed |
Q50499539 | SNARE proteins are not excessive for the formation of post-Golgi SNARE complexes in HeLa cells |
Q36632649 | SNAREs in neurons--beyond synaptic vesicle exocytosis (Review). |
Q38930726 | Soluble NSF attachment protein receptor molecular mimicry by a Legionella pneumophila Dot/Icm effector. |
Q92257375 | Stx5-Mediated ER-Golgi Transport in Mammals and Yeast |
Q24301008 | Syntaxin 16 and syntaxin 5 are required for efficient retrograde transport of several exogenous and endogenous cargo proteins |
Q41493300 | Tethering factor P115: a new model for tether-SNARE interactions |
Q30047640 | The COG Complex, Rab6 and COPI Define a Novel Golgi Retrograde Trafficking Pathway that is Exploited by SubAB Toxin |
Q24564894 | The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins |
Q38631626 | The Golgin protein Coy1 functions in intra-Golgi retrograde transport and interacts with the COG complex and Golgi SNAREs |
Q34552505 | The Gos28 SNARE protein mediates intra-Golgi transport of rhodopsin and is required for photoreceptor survival |
Q46456087 | The Small GTPase Ral orchestrates MVB biogenesis and exosome secretion |
Q28509101 | The cytoplasmic domain of Vamp4 and Vamp5 is responsible for their correct subcellular targeting: the N-terminal extenSion of VAMP4 contains a dominant autonomous targeting signal for the trans-Golgi network |
Q36173925 | The golgin GCC88 is required for efficient retrograde transport of cargo from the early endosomes to the trans-Golgi network |
Q37863216 | The regulation of endosome-to-Golgi retrograde transport by tethers and scaffolds. |
Q24293051 | The ubiquitin ligase HACE1 regulates Golgi membrane dynamics during the cell cycle |
Q24322253 | Trans-Golgi network syntaxin 10 functions distinctly from syntaxins 6 and 16 |
Q34147309 | Unraveling the Golgi ribbon |
Q24292933 | VAMP4 is required to maintain the ribbon structure of the Golgi apparatus |
Q98292736 | Vesicle transport through interaction with t-SNAREs 1a (Vti1a)'s roles in neurons |
Q50296322 | cis-Golgi t-SNAREs bind YKT6 on tethered vesicle |
Search more.