| review article | Q7318358 |
| scholarly article | Q13442814 |
| P2093 | author name string | Rainer Duden | |
| P2860 | cites work | Coupling of coat assembly and vesicle budding to packaging of putative cargo receptors | Q22008843 |
| The debate about transport in the Golgi--two sides of the same coin? | Q24290401 | ||
| β-COP, a 110 kd protein associated with non-clathrin-coated vesicles and the golgi complex, shows homology to β-adaptin | Q24319220 | ||
| Bicaudal-D regulates COPI-independent Golgi-ER transport by recruiting the dynein-dynactin motor complex | Q24321547 | ||
| The KDEL receptor, ERD2, regulates intracellular traffic by recruiting a GTPase-activating protein for ARF1 | Q24532879 | ||
| COP I domains required for coatomer integrity, and novel interactions with ARF and ARF-GAP | Q24630384 | ||
| Architecture of coatomer: molecular characterization of delta-COP and protein interactions within the complex | Q24671045 | ||
| Sorting by COP I-coated vesicles under interphase and mitotic conditions | Q24671510 | ||
| Human SEC13Rp functions in yeast and is located on transport vesicles budding from the endoplasmic reticulum | Q24672767 | ||
| ARFGAP1 promotes the formation of COPI vesicles, suggesting function as a component of the coat | Q24672898 | ||
| A single binding site for dilysine retrieval motifs and p23 within the gamma subunit of coatomer | Q24680266 | ||
| Reversible dissociation of coatomer: functional characterization of a beta/delta-coat protein subcomplex | Q24685847 | ||
| Crystal structure of Sar1-GDP at 1.7 Å resolution and the role of the NH 2 terminus in ER export | Q27636702 | ||
| Structure of the Sec23/24-Sar1 pre-budding complex of the COPII vesicle coat | Q27639671 | ||
| Role of Erv29p in collecting soluble secretory proteins into ER-derived transport vesicles | Q27929745 | ||
| COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum | Q27930804 | ||
| Yeast SEC16 gene encodes a multidomain vesicle coat protein that interacts with Sec23p | Q27931226 | ||
| Surface structure of the COPII-coated vesicle | Q27931455 | ||
| Retrograde transport from the yeast Golgi is mediated by two ARF GAP proteins with overlapping function. | Q27931738 | ||
| Order of events in the yeast secretory pathway | Q27932822 | ||
| An acidic sequence of a putative yeast Golgi membrane protein binds COPII and facilitates ER export | Q27934064 | ||
| SEC21 is a gene required for ER to Golgi protein transport that encodes a subunit of a yeast coatomer | Q27934067 | ||
| epsilon-COP is a structural component of coatomer that functions to stabilize alpha-COP | Q27935294 | ||
| Sec16p potentiates the action of COPII proteins to bud transport vesicles | Q27935297 | ||
| Concentrative sorting of secretory cargo proteins into COPII-coated vesicles | Q27935675 | ||
| Evidence for overlapping and distinct functions in protein transport of coat protein Sec24p family members | Q27936142 | ||
| SNARE-mediated retrograde traffic from the Golgi complex to the endoplasmic reticulum | Q27937494 | ||
| SEC12 encodes a guanine-nucleotide-exchange factor essential for transport vesicle budding from the ER. | Q27937857 | ||
| Coatomer is essential for retrieval of dilysine-tagged proteins to the endoplasmic reticulum | Q27938624 | ||
| Dynamics of the COPII coat with GTP and stable analogues | Q27939261 | ||
| Cargo selection into COPII vesicles is driven by the Sec24p subunit | Q27939920 | ||
| Lst1p and Sec24p cooperate in sorting of the plasma membrane ATPase into COPII vesicles in Saccharomyces cerevisiae | Q27939936 | ||
| The ADP ribosylation factor-nucleotide exchange factors Gea1p and Gea2p have overlapping, but not redundant functions in retrograde transport from the Golgi to the endoplasmic reticulum | Q27939943 | ||
| Coatomer, Arf1p, and nucleotide are required to bud coat protein complex I-coated vesicles from large synthetic liposomes | Q27940161 | ||
| Segregation of COPI-rich and anterograde-cargo-rich domains in endoplasmic-reticulum-to-Golgi transport complexes | Q28143417 | ||
| Coated vesicle assembly in the Golgi requires only coatomer and ARF proteins from the cytosol | Q28261740 | ||
| The ARF1 GTPase-activating protein: zinc finger motif and Golgi complex localization | Q28271461 | ||
| Reconstitution of SEC gene product-dependent intercompartmental protein transport | Q28295130 | ||
| 'Coatomer': a cytosolic protein complex containing subunits of non-clathrin-coated Golgi transport vesicles | Q28300053 | ||
| Localization of large ADP-ribosylation factor-guanine nucleotide exchange factors to different Golgi compartments: evidence for distinct functions in protein traffic | Q28573549 | ||
| Visualization of ER-to-Golgi transport in living cells reveals a sequential mode of action for COPII and COPI | Q28609158 | ||
| Coatomer interaction with di-lysine endoplasmic reticulum retention motifs | Q28609806 | ||
| Direct and GTP-dependent interaction of ADP ribosylation factor 1 with coatomer subunit beta | Q28609830 | ||
| gp25L/emp24/p24 protein family members of the cis-Golgi network bind both COP I and II coatomer | Q28631479 | ||
| Dynamics of transitional endoplasmic reticulum sites in vertebrate cells | Q28645796 | ||
| Coat proteins and vesicle budding | Q28645867 | ||
| Intracellular Aspects of the Process of Protein Synthesis | Q29615237 | ||
| Distinct sets of SEC genes govern transport vesicle formation and fusion early in the secretory pathway | Q29618501 | ||
| Protein sorting by transport vesicles | Q29619990 | ||
| Structure of the Sec23p/24p and Sec13p/31p complexes of COPII | Q30856900 | ||
| A primer on vesicle budding | Q33603151 | ||
| Bulk flow redux? | Q33700560 | ||
| The lectin ERGIC-53 is a cargo transport receptor for glycoproteins | Q33880105 | ||
| New COP1-binding motifs involved in ER retrieval | Q33890112 | ||
| Three ways to make a vesicle | Q33938411 | ||
| Regulators and effectors of the ARF GTPases. | Q33954573 | ||
| Breaking the COPI monopoly on Golgi recycling | Q33994991 | ||
| Cisternal maturation and vesicle transport: join the band wagon! (Review). | Q35189830 | ||
| Signal-mediated retrieval of a membrane protein from the Golgi to the ER in yeast | Q36234823 | ||
| Cargo selection by the COPII budding machinery during export from the ER | Q36255308 | ||
| LST1 is a SEC24 homologue used for selective export of the plasma membrane ATPase from the endoplasmic reticulum | Q36256601 | ||
| Retrieval of transmembrane proteins to the endoplasmic reticulum | Q36383169 | ||
| Specific interaction of the yeast cis-Golgi syntaxin Sed5p and the coat protein complex II component Sec24p of endoplasmic reticulum-derived transport vesicles | Q36450547 | ||
| Disruptions in Golgi structure and membrane traffic in a conditional lethal mammalian cell mutant are corrected by epsilon-COP. | Q36534885 | ||
| Dissection of COPI and Arf1 dynamics in vivo and role in Golgi membrane transport | Q40733038 | ||
| COPI in ER/Golgi and intra-Golgi transport: do yeast COPI mutants point the way? | Q40845661 | ||
| A role for ADP ribosylation factor in the control of cargo uptake during COPI-coated vesicle biogenesis | Q40908409 | ||
| A di-acidic signal required for selective export from the endoplasmic reticulum | Q41098719 | ||
| Localization of a yeast early Golgi mannosyltransferase, Och1p, involves retrograde transport | Q41982832 | ||
| GTP hydrolysis by arf-1 mediates sorting and concentration of Golgi resident enzymes into functional COP I vesicles | Q42680908 | ||
| Beta-COP localizes mainly to the cis-Golgi side in exocrine pancreas | Q42770080 | ||
| Isolation of functional Golgi-derived vesicles with a possible role in retrograde transport | Q42837749 | ||
| KDEL receptor (Erd2p)-mediated retrograde transport of the cholera toxin A subunit from the Golgi involves COPI, p23, and the COOH terminus of Erd2p | Q42855070 | ||
| ARF-GAP-mediated interaction between the ER-Golgi v-SNAREs and the COPI coat | Q42917503 | ||
| Sorting of Golgi resident proteins into different subpopulations of COPI vesicles: a role for ArfGAP1. | Q42952095 | ||
| Coat assembly directs v-SNARE concentration into synthetic COPII vesicles | Q43821870 | ||
| Beta-COP is essential for biosynthetic membrane transport from the endoplasmic reticulum to the Golgi complex in vivo | Q45345741 | ||
| Evidence for a COP-I-independent transport route from the Golgi complex to the endoplasmic reticulum | Q45345946 | ||
| A coat subunit of Golgi-derived non-clathrin-coated vesicles with homology to the clathrin-coated vesicle coat protein beta-adaptin. | Q46034973 | ||
| COPII-cargo interactions direct protein sorting into ER-derived transport vesicles | Q46046050 | ||
| Nucleation of COPII vesicular coat complex by endoplasmic reticulum to Golgi vesicle SNAREs | Q46137704 | ||
| Lasker Basic Medical Research Award. SEC mutants and the secretory apparatus | Q46655482 | ||
| Lasker Basic Medical Research Award. The machinery and principles of vesicle transport in the cell | Q48361351 | ||
| Protein Sorting upon Exit from the Endoplasmic Reticulum | Q57179707 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 197-207 | |
| P577 | publication date | 2003-07-01 | |
| P1433 | published in | Molecular Membrane Biology | Q6895964 |
| P1476 | title | ER-to-Golgi transport: COP I and COP II function (Review). | |
| P478 | volume | 20 |
| Q61804753 | A genome-wide analysis of coatomer protein (COP) subunits of apicomplexan parasites and their evolutionary relationships |
| Q28567584 | A novel multiprotein complex is required to generate the prechylomicron transport vesicle from intestinal ER |
| Q37332280 | A role for endoplasmic reticulum exit sites in foot-and-mouth disease virus infection |
| Q39972438 | A selective autophagy pathway that degrades gluconeogenic enzymes during catabolite inactivation |
| Q64964440 | Acylation - A New Means to Control Traffic Through the Golgi. |
| Q33881671 | Arf3 is activated uniquely at the trans-Golgi network by brefeldin A-inhibited guanine nucleotide exchange factors |
| Q36597945 | Cell biology of membrane trafficking in human disease |
| Q35189830 | Cisternal maturation and vesicle transport: join the band wagon! (Review). |
| Q36321499 | Cog3p depletion blocks vesicle-mediated Golgi retrograde trafficking in HeLa cells. |
| Q50602548 | Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene. |
| Q28312166 | Coordinated activation of the secretory pathway during notochord formation in the Xenopus embryo |
| Q51618036 | Coupling between vesicle shape and the non-homogeneous lateral distribution of membrane constituents in Golgi bodies. |
| Q34566704 | Cranio-lenticulo-sutural dysplasia is caused by a SEC23A mutation leading to abnormal endoplasmic-reticulum-to-Golgi trafficking |
| Q40153875 | Cystic fibrosis transmembrane conductance regulator (CFTR) functionality is dependent on coatomer protein I (COPI). |
| Q40526994 | Differential compartmentalization of the calpain/calpastatin network with the endoplasmic reticulum and Golgi apparatus |
| Q41943225 | Distinct functions for Arf guanine nucleotide exchange factors at the Golgi complex: GBF1 and BIGs are required for assembly and maintenance of the Golgi stack and trans-Golgi network, respectively |
| Q33213541 | Dynamics of COPII vesicles and the Golgi apparatus in cultured Nicotiana tabacum BY-2 cells provides evidence for transient association of Golgi stacks with endoplasmic reticulum exit sites. |
| Q36591563 | Dysfunction of Wntless triggers the retrograde Golgi-to-ER transport of Wingless and induces ER stress |
| Q37619765 | ER exit sites--localization and control of COPII vesicle formation |
| Q41917839 | Endoplasmic reticulum involvement in yeast cell death. |
| Q36642389 | Evolution of insect proteomes: insights into synapse organization and synaptic vesicle life cycle |
| Q33877872 | Expression variability of co-regulated genes differentiates Saccharomyces cerevisiae strains |
| Q28594953 | Expression, Localization, and Biochemical Characterization of Nicotinamide Mononucleotide Adenylyltransferase 2 |
| Q24600792 | Folding-competent and folding-defective forms of ricin A chain have different fates after retrotranslocation from the endoplasmic reticulum |
| Q34450749 | Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor |
| Q27642838 | Gamma-COP appendage domain - structure and function |
| Q47872931 | Generation of wavy structure on lipid membrane by peripheral proteins: a linear elastic analysis |
| Q41962920 | Glucose induces rapid changes in the secretome of Saccharomyces cerevisiae |
| Q27940008 | Growth control of Golgi phosphoinositides by reciprocal localization of sac1 lipid phosphatase and pik1 4-kinase |
| Q52431178 | High-throughput Cos-Seq screen with intracellular Leishmania infantum for the discovery of novel drug-resistance mechanisms. |
| Q36003749 | Hsp70 promotes epithelial sodium channel functional expression by increasing its association with coat complex II and its exit from endoplasmic reticulum. |
| Q38758968 | Hypoxia Modulates the Response of Mast Cells to Staphylococcus aureus Infection |
| Q24297434 | Identification and characterization of GIV, a novel Galpha i/s-interacting protein found on COPI, endoplasmic reticulum-Golgi transport vesicles |
| Q38732515 | Importance of organellar proteins, protein translocation and vesicle transport routes for pollen development and function. |
| Q27940121 | Involvement of specific COPI subunits in protein sorting from the late endosome to the vacuole in yeast |
| Q24302095 | JAGN1 deficiency causes aberrant myeloid cell homeostasis and congenital neutropenia |
| Q34334493 | KIAA1199 interacts with glycogen phosphorylase kinase β-subunit (PHKB) to promote glycogen breakdown and cancer cell survival. |
| Q41947119 | Limiting transport steps and novel interactions of Connexin-43 along the secretory pathway. |
| Q92413717 | Maintaining order: COG complex controls Golgi trafficking, processing, and sorting |
| Q37026524 | Manipulation of rab GTPase function by intracellular bacterial pathogens |
| Q36639032 | Membrane-anchored growth factor, HB-EGF, on the cell surface targeted to the inner nuclear membrane |
| Q27675211 | Molecular Basis for Recognition of Dilysine Trafficking Motifs by COPI |
| Q37627813 | Multipronged interaction of the COG complex with intracellular membranes |
| Q33315718 | Mutational analysis of betaCOP (Sec26p) identifies an appendage domain critical for function |
| Q27939138 | Mutations in a highly conserved region of the Arf1p activator GEA2 block anterograde Golgi transport but not COPI recruitment to membranes |
| Q36138163 | Parotid secretory granules: crossroads of secretory pathways and protein storage. |
| Q35143088 | Polybasic trafficking signal mediates golgi export, ER retention or ER export and retrieval based on membrane-proximity |
| Q33522513 | Quantitative proteomics analysis of cell cycle-regulated Golgi disassembly and reassembly |
| Q96813589 | Rab1b-GBF1-ARFs mediated intracellular trafficking is required for classical swine fever virus replication in swine umbilical vein endothelial cells |
| Q38219637 | Rewiring of cellular membrane homeostasis by picornaviruses |
| Q34763238 | Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation |
| Q42810228 | Sampling the cell with anomalous diffusion - the discovery of slowness |
| Q38896670 | Sigma 1 Receptor and Ion Channel Dynamics in Cancer |
| Q24305411 | Specific functions of BIG1 and BIG2 in endomembrane organization |
| Q24321239 | Stress-induced ER to Golgi translocation of ceramide synthase 1 is dependent on proteasomal processing |
| Q24301490 | Syntaxin 17 cycles between the ER and ERGIC and is required to maintain the architecture of ERGIC and Golgi |
| Q37563486 | Synthetic biology of minimal systems |
| Q24564894 | The COG and COPI complexes interact to control the abundance of GEARs, a subset of Golgi integral membrane proteins |
| Q33574322 | The TOR complex 1 is distributed in endosomes and in retrograde vesicles that form from the vacuole membrane and plays an important role in the vacuole import and degradation pathway |
| Q40319158 | The cytoplasmic tail of heparin-binding EGF-like growth factor regulates bidirectional intracellular trafficking between the plasma membrane and ER. |
| Q48045527 | The ecological and genetic basis of convergent thick-lipped phenotypes in cichlid fishes |
| Q28741996 | The human metapneumovirus matrix protein stimulates the inflammatory immune response in vitro |
| Q38088350 | The secretory pathway: exploring yeast diversity |
| Q36739888 | The subcellular distribution of calnexin is mediated by PACS-2 |
| Q41842747 | The vacuolar import and degradation pathway merges with the endocytic pathway to deliver fructose-1,6-bisphosphatase to the vacuole for degradation |
| Q33569799 | The vacuole import and degradation pathway utilizes early steps of endocytosis and actin polymerization to deliver cargo proteins to the vacuole for degradation |
| Q46975738 | Tumour cells can employ extracellular Ins(1,2,3,4,5,6)P(6) and multiple inositol-polyphosphate phosphatase 1 (MINPP1) dephosphorylation to improve their proliferation. |
| Q36320232 | Two human ARFGAPs associated with COP-I-coated vesicles. |
| Q35575193 | Vacuole import and degradation pathway: Insights into a specialized autophagy pathway |
| Q40261959 | Yeast Reporter Assay to Identify Cellular Components of Ricin Toxin A Chain Trafficking |
| Q28580019 | rSac3, a novel Sac domain phosphoinositide phosphatase, promotes neurite outgrowth in PC12 cells |
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