| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0092-8674(00)81723-7 |
| P698 | PubMed publication ID | 9875853 |
| P50 | author | Massimiliano Baldassarre | Q47504401 |
| Roberto Buccione | Q47504402 | ||
| Alberto Luini | Q56988538 | ||
| P2093 | author name string | A A Mironov | |
| H J Geuze | |||
| L Bonfanti | |||
| J A Martínez-Menárguez | |||
| A Fusella | |||
| O Martella | |||
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| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 993-1003 | |
| P577 | publication date | 1998-12-01 | |
| P1433 | published in | Cell | Q655814 |
| P1476 | title | Procollagen traverses the Golgi stack without leaving the lumen of cisternae: evidence for cisternal maturation | |
| P478 | volume | 95 |
| Q24291984 | A GRASP55-rab2 effector complex linking Golgi structure to membrane traffic |
| Q92860218 | A Kinetic View of Membrane Traffic Pathways Can Transcend the Classical View of Golgi Compartments |
| Q42022406 | A brief history of the cisternal progression-maturation model |
| Q98208984 | A minimal self-organisation model of the Golgi apparatus |
| Q33948272 | A novel mechanism for localizing membrane proteins to yeast trans-Golgi network requires function of synaptojanin-like protein |
| Q39959122 | A traffic-activated Golgi-based signalling circuit coordinates the secretory pathway. |
| Q37130119 | Accommodation of large cargo within Golgi cisternae |
| Q73473124 | Accumulation of properly folded human type III procollagen molecules in specific intracellular membranous compartments in the yeast Pichia pastoris |
| Q83149732 | Active and passive mechanisms drive secretory granule biogenesis during differentiation of the intestinal parasite Giardia lamblia |
| Q35570908 | Active recycling of yeast Golgi mannosyltransferase complexes through the endoplasmic reticulum |
| Q73615931 | Additional N-glycosylation and its impact on the folding of intestinal lactase-phlorizin hydrolase |
| Q33914545 | Alternative protein sorting pathways |
| Q47871584 | An Overview of Protein Secretion in Plant Cells |
| Q37244865 | Anterograde flow of cargo across the golgi stack potentially mediated via bidirectional "percolating" COPI vesicles |
| Q37866547 | Architecture of the mammalian Golgi |
| Q27932451 | Asymmetric requirements for a Rab GTPase and SNARE proteins in fusion of COPII vesicles with acceptor membranes |
| Q34729835 | AtVPS45 complex formation at the trans-Golgi network. |
| Q73314717 | Biochemical sub-fractionation of the mammalian Golgi apparatus |
| Q30476699 | Biogenesis of tubular ER-to-Golgi transport intermediates |
| Q28302982 | Building synthetic cellular organization |
| Q41285526 | COPI is essential for Golgi cisternal maturation and dynamics. |
| Q34506701 | COPI selectively drives maturation of the early Golgi |
| Q36623748 | COPI-mediated transport. |
| Q37970881 | COPII and the regulation of protein sorting in mammals |
| Q47577111 | CREB3L1-mediated functional and structural adaptation of the secretory pathway in hormone-stimulated thyroid cells |
| Q38071282 | Cell biology of the endoplasmic reticulum and the Golgi apparatus through proteomics |
| Q79767913 | Cell biology: the Golgi grows up |
| Q24296062 | Characterization of a mammalian Golgi-localized protein complex, COG, that is required for normal Golgi morphology and function |
| Q41957304 | Coalignment of plasma membrane channels and protrusions (fibripositors) specifies the parallelism of tendon |
| Q35027117 | Collagen fibril biosynthesis in tendon: a review and recent insights. |
| Q34224267 | Collagens and collagen-related diseases |
| Q34264518 | Concentrating hormones into secretory granules: layers of control |
| Q28119000 | Concentration of Sec12 at ER exit sites via interaction with cTAGE5 is required for collagen export |
| Q34475219 | Coordinated regulation of bidirectional COPI transport at the Golgi by CDC42 |
| Q44122120 | Core protein dependence of epimerization of glucuronosyl residues in galactosaminoglycans |
| Q36301626 | Correlative light-electron microscopy reveals the tubular-saccular ultrastructure of carriers operating between Golgi apparatus and plasma membrane |
| Q33803974 | Deconstructing membrane traffic |
| Q57363839 | Deconstructing membrane traffic |
| Q57364270 | Deconstructing membrane traffic |
| Q37682041 | Direct continuities between cisternae at different levels of the Golgi complex in glucose-stimulated mouse islet beta cells |
| Q28748731 | E3 Ubiquitin Ligase Synoviolin Is Involved in Liver Fibrogenesis |
| Q40627644 | ER-to-Golgi carriers arise through direct en bloc protrusion and multistage maturation of specialized ER exit domains |
| Q40909584 | ER/Golgi intermediates acquire Golgi enzymes by brefeldin A-sensitive retrograde transport in vitro |
| Q36746956 | Electron tomography of immunolabeled cryosections |
| Q34144676 | Enhancement of procollagen biosynthesis by p180 through augmented ribosome association on the endoplasmic reticulum in response to stimulated secretion |
| Q24653564 | Evidence that Golgi structure depends on a p115 activity that is independent of the vesicle tether components giantin and GM130 |
| Q36293742 | Exclusion of golgi residents from transport vesicles budding from Golgi cisternae in intact cells |
| Q39771902 | Expansion of the trans-Golgi network following activated collagen secretion is supported by a coiled-coil microtubule-bundling protein, p180, on the ER. |
| Q37886778 | Faithful chaperones |
| Q64911099 | Fatty-acid binding protein 5 modulates the SAR1 GTPase cycle and enhances budding of large COPII cargoes. |
| Q34016461 | Following the fate in vivo of COPI vesicles generated in vitro. |
| Q28217025 | Functional linkage between the endoplasmic reticulum protein Hsp47 and procollagen expression in human vascular smooth muscle cells |
| Q36256637 | Fusogenic domains of golgi membranes are sequestered into specialized regions of the stack that can be released by mechanical fragmentation. |
| Q24651935 | GBF1: A novel Golgi-associated BFA-resistant guanine nucleotide exchange factor that displays specificity for ADP-ribosylation factor 5 |
| Q40826396 | GMx33: a novel family of trans-Golgi proteins identified by proteomics |
| Q38010009 | Glycosylation disorders of membrane trafficking |
| Q34630434 | Golgi biogenesis |
| Q34036999 | Golgi compartmentation and identity |
| Q37538065 | Golgi enzymes are enriched in perforated zones of golgi cisternae but are depleted in COPI vesicles. |
| Q37295069 | Golgi function and dysfunction in the first COG4-deficient CDG type II patient |
| Q59058669 | Golgi maturation visualized in living yeast |
| Q27931787 | Golgi structure correlates with transitional endoplasmic reticulum organization in Pichia pastoris and Saccharomyces cerevisiae |
| Q36293363 | Golgi structure in three dimensions: functional insights from the normal rat kidney cell |
| Q38118081 | Golgi tubules: their structure, formation and role in intra-Golgi transport |
| Q38143688 | Golgi's way: a long path toward the new paradigm of the intra-Golgi transport |
| Q27329064 | Group IV phospholipase A(2)alpha controls the formation of inter-cisternal continuities involved in intra-Golgi transport |
| Q34156731 | Gut thoughts on the Golgi complex |
| Q73828749 | HSP47 binds cooperatively to triple helical type I collagen but has little effect on the thermal stability or rate of refolding |
| Q47602229 | Heritable Skeletal Disorders Arising from Defects in Processing and Transport of Type I Procollagen from the ER: Perspectives on Possible Therapeutic Approaches |
| Q37813005 | How Golgi glycosylation meets and needs trafficking: the case of the COG complex |
| Q34358823 | How the Golgi works: a cisternal progenitor model |
| Q24594137 | Hsp47: a molecular chaperone that interacts with and stabilizes correctly-folded procollagen |
| Q35756927 | In situ structural analysis of Golgi intracisternal protein arrays. |
| Q51842205 | In vitro transport on cis and trans sides of the Golgi involves two distinct types of coatomer and ADP-ribosylation factor-independent transport intermediates. |
| Q40697983 | Intact Golgi synthesize complex branched O-linked chains on glycoside primers: evidence for the functional continuity of seven glycosyltransferases and three sugar nucleotide transporters |
| Q58991836 | Intra-Golgi Transport: Roles for Vesicles, Tubules, and Cisternae |
| Q30008858 | Intracellular mechanisms of molecular recognition and sorting for transport of large extracellular matrix molecules |
| Q33767582 | Intracellular protein traffic in lymphocytes: "how do I get THERE from HERE"? |
| Q35131675 | Intracellular sorting and transport of proteins |
| Q30511983 | Irradiation-induced protein inactivation reveals Golgi enzyme cycling to cell periphery |
| Q35015163 | Journeys through the Golgi--taking stock in a new era. |
| Q26752223 | LARP6 Meets Collagen mRNA: Specific Regulation of Type I Collagen Expression |
| Q41621223 | Land-locked mammalian Golgi reveals cargo transport between stable cisternae. |
| Q37155106 | Loss of SEC-23 inCaenorhabditis elegansCauses Defects in Oogenesis, Morphogenesis, and Extracellular Matrix Secretion |
| Q33948258 | Lumenal endosomal and Golgi-retrieval determinants involved in pH-sensitive targeting of an early Golgi protein |
| Q24653507 | Maintenance of Golgi structure and function depends on the integrity of ER export |
| Q92282189 | Maturation-driven transport and AP-1-dependent recycling of a secretory cargo in the Golgi |
| Q38529922 | Mechanisms for exporting large-sized cargoes from the endoplasmic reticulum. |
| Q47241756 | Medial Golgi but not late Golgi glycosyltransferases exist as high molecular weight complexes. Role of luminal domain in complex formation and localization |
| Q74278666 | Megavesicles implicated in the rapid transport of intracisternal aggregates across the Golgi stack |
| Q28203221 | Membrane traffic fuses with cartilage development |
| Q37540106 | Membrane traffic within the Golgi apparatus |
| Q98771690 | Modeling Normal and Pathological Ear Cartilage in vitro Using Somatic Stem Cells in Three-Dimensional Culture |
| Q34211660 | Models for Golgi traffic: a critical assessment |
| Q92802210 | Models of Intracellular Transport: Pros and Cons |
| Q34968950 | Models of intracellular transport and evolution of the Golgi complex |
| Q24616550 | Molecular basis for the action of the collagen-specific chaperone Hsp47/SERPINH1 and its structure-specific client recognition |
| Q36722139 | Morpho-functional architecture of the Golgi complex of neuroendocrine cells |
| Q35983662 | Morphodynamics of the secretory pathway. |
| Q31869432 | Morphogenesis and dynamics of the yeast Golgi apparatus |
| Q37063364 | Morphogenesis of post-Golgi transport carriers |
| Q27939138 | Mutations in a highly conserved region of the Arf1p activator GEA2 block anterograde Golgi transport but not COPI recruitment to membranes |
| Q34804045 | Nanoscale architecture of endoplasmic reticulum export sites and of Golgi membranes as determined by electron tomography. |
| Q36845704 | New insights into membrane trafficking and protein sorting. |
| Q28817008 | Nonequilibrium description of de novo biogenesis and transport through Golgi-like cisternae |
| Q30559090 | Nonmuscle myosin II powered transport of newly formed collagen fibrils at the plasma membrane. |
| Q24305239 | Novel isotypic gamma/zeta subunits reveal three coatomer complexes in mammals |
| Q43697078 | Opinion: The maturing role of COPI vesicles in intra-Golgi transport |
| Q33779916 | Organization of the ER-Golgi interface for membrane traffic control |
| Q33954550 | Organization of the Golgi apparatus |
| Q36381406 | Peri-Golgi vesicles contain retrograde but not anterograde proteins consistent with the cisternal progression model of intra-Golgi transport |
| Q34532226 | Photohighlighting approaches to access membrane dynamics of the Golgi apparatus |
| Q28611911 | Processing and targeting of granule proteins in human neutrophils |
| Q33302124 | Procollagen triple helix assembly: an unconventional chaperone-assisted folding paradigm |
| Q57374577 | Prohormone transport through the secretory pathway of neuroendocrine cells |
| Q34720541 | Proinsulin endoproteolysis confers enhanced targeting of processed insulin to the regulated secretory pathway |
| Q35953865 | Protein kinase C δ regulates the release of collagen type I from vascular smooth muscle cells via regulation of Cdc42. |
| Q73275998 | Protein sorting in the Golgi apparatus: a consequence of maturation and triggered sorting |
| Q34117427 | Protein-specific chaperones: the role of hsp47 begins to gel. |
| Q39749967 | Qualitative and quantitative ultrastructural analysis of the membrane rearrangements induced by coronavirus |
| Q37204055 | Quantitative analysis of intra-Golgi transport shows intercisternal exchange for all cargo |
| Q34438696 | Rab GTPase mediated procollagen trafficking in ascorbic acid stimulated osteoblasts |
| Q29619989 | Rabs and their effectors: achieving specificity in membrane traffic |
| Q33964517 | Recent advances in understanding Golgi biogenesis |
| Q77591339 | Reevaluation of the effects of brefeldin A on plant cells using tobacco Bright Yellow 2 cells expressing Golgi-targeted green fluorescent protein and COPI antisera |
| Q28314912 | Regulation of post-Golgi LH3 trafficking is essential for collagen homeostasis |
| Q27932804 | Retrograde transport of the mannosyltransferase Och1p to the early Golgi requires a component of the COG transport complex |
| Q92763147 | Role of Intracellular Transport in the Centriole-Dependent Formation of Golgi Ribbon |
| Q42952040 | Role of disulfide bridges formed in the luminal domain of ATF6 in sensing endoplasmic reticulum stress |
| Q90437359 | Roles of the endoplasmic reticulum-resident, collagen-specific molecular chaperone Hsp47 in vertebrate cells and human disease |
| Q47073812 | Sec13 safeguards the integrity of the endoplasmic reticulum and organogenesis of the digestive system in zebrafish |
| Q47073852 | Secretory COPII coat component Sec23a is essential for craniofacial chondrocyte maturation |
| Q40500388 | Secretory traffic triggers the formation of tubular continuities across Golgi sub-compartments. |
| Q44061975 | Sequence-specific recognition of collagen triple helices by the collagen-specific molecular chaperone HSP47. |
| Q37617712 | Shaping tubular carriers for intracellular membrane transport |
| Q39038778 | Sialylation of N-glycans: mechanism, cellular compartmentalization and function. |
| Q46427017 | Silencing of mammalian Sar1 isoforms reveals COPII-independent protein sorting and transport |
| Q24652373 | Small cargo proteins and large aggregates can traverse the Golgi by a common mechanism without leaving the lumen of cisternae |
| Q30778000 | Small cargoes pass through synthetically glued Golgi stacks. |
| Q24794775 | Spatial partitioning of secretory cargo from Golgi resident proteins in live cells. |
| Q28576941 | Src kinase regulates the integrity and function of the Golgi apparatus via activation of dynamin 2 |
| Q37235221 | Stacking the odds for Golgi cisternal maturation |
| Q34350039 | Stapled Golgi cisternae remain in place as cargo passes through the stack. |
| Q28345195 | Steady-state localization of a medial-Golgi glycosyltransferase involves transit through the trans-Golgi network |
| Q28000068 | Stepwise proteolytic activation of type I procollagen to collagen within the secretory pathway of tendon fibroblasts in situ |
| Q87910204 | Stochastic Model of Maturation and Vesicular Exchange in Cellular Organelles |
| Q51838071 | Structural integrity of the Golgi is temperature sensitive in conditional-lethal mutants with no detectable GM130. |
| Q33903020 | Structure of the Golgi and distribution of reporter molecules at 20 degrees C reveals the complexity of the exit compartments |
| Q34588434 | The C terminus of collagen SQT-3 has complex and essential functions in nematode collagen assembly |
| Q37821046 | The Golgi apparatus: an organelle with multiple complex functions |
| Q77671372 | The Golgi apparatus: going round in circles? |
| Q39735151 | The KDEL receptor mediates a retrieval mechanism that contributes to quality control at the endoplasmic reticulum |
| Q51763360 | The KDEL receptor signalling cascade targets focal adhesion kinase on focal adhesions and invadopodia. |
| Q48168375 | The Prenylated Rab GTPase Receptor PRA1.F4 Contributes to Protein Exit from the Golgi Apparatus |
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| Q36370047 | The Sar1 GTPase coordinates biosynthetic cargo selection with endoplasmic reticulum export site assembly |
| Q36117665 | The V0-ATPase mediates apical secretion of exosomes containing Hedgehog-related proteins in Caenorhabditis elegans |
| Q35880048 | The [corrected] SEC23-SEC31 [corrected] interface plays critical role for export of procollagen from the endoplasmic reticulum |
| Q36846125 | The bone morphogenetic protein 1/Tolloid-like metalloproteinases |
| Q38010442 | The coronavirus E protein: assembly and beyond |
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| Q28214582 | The cytoplasmic tail of alpha 1,3-galactosyltransferase inhibits Golgi localization of the full-length enzyme |
| Q24290401 | The debate about transport in the Golgi--two sides of the same coin? |
| Q39138387 | The dynamics of engineered resident proteins in the mammalian Golgi complex relies on cisternal maturation |
| Q34313550 | The future of Golgi research |
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| Q28191029 | The molecular interactions of heat shock protein 47 (Hsp47) and their implications for collagen biosynthesis |
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| Q38780940 | The plant secretory pathway seen through the lens of the cell wall |
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| Q37625133 | The yeast Golgi apparatus: insights and mysteries |
| Q53001273 | Three-dimensional and immune electron microscopic analysis of the secretory pathway in Saccharomyces cerevisiae. |
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