| scholarly article | Q13442814 |
| P2093 | author name string | Roman S Polishchuk | |
| Elena V Polishchuk | |||
| Mariagrazia Capestrano | |||
| P2860 | cites work | Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis | Q24300284 |
| Molecular machinery for non-vesicular trafficking of ceramide | Q24302195 | ||
| TANGO1 facilitates cargo loading at endoplasmic reticulum exit sites | Q24318716 | ||
| Structural basis for cargo regulation of COPII coat assembly | Q24322472 | ||
| Interaction of a Golgi-associated kinesin-like protein with Rab6 | Q24322499 | ||
| Glycosphingolipid synthesis requires FAPP2 transfer of glucosylceramide | Q24337032 | ||
| FAPPs control Golgi-to-cell-surface membrane traffic by binding to ARF and PtdIns(4)P | Q24337930 | ||
| Prefission constriction of Golgi tubular carriers driven by local lipid metabolism: a theoretical model | Q24537736 | ||
| Faciogenital dysplasia protein (FGD1) regulates export of cargo proteins from the golgi complex via Cdc42 activation | Q24652358 | ||
| Maintenance of Golgi structure and function depends on the integrity of ER export | Q24653507 | ||
| In migrating fibroblasts, recycling receptors are concentrated in narrow tubules in the pericentriolar area, and then routed to the plasma membrane of the leading lamella | Q24657613 | ||
| Phagosomes fuse with late endosomes and/or lysosomes by extension of membrane protrusions along microtubules: role of Rab7 and RILP | Q24682916 | ||
| Group IV phospholipase A(2)alpha controls the formation of inter-cisternal continuities involved in intra-Golgi transport | Q27329064 | ||
| Sar1p N-terminal helix initiates membrane curvature and completes the fission of a COPII vesicle | Q27934415 | ||
| The GM130 and GRASP65 Golgi proteins cycle through and define a subdomain of the intermediate compartment | Q28214965 | ||
| Heterotypic tubular connections at the endoplasmic reticulum-Golgi complex interface | Q28565288 | ||
| Visualization of ER-to-Golgi transport in living cells reveals a sequential mode of action for COPII and COPI | Q28609158 | ||
| Rab6 coordinates a novel Golgi to ER retrograde transport pathway in live cells | Q28609753 | ||
| Mechanisms of endocytosis | Q29547609 | ||
| Endocytic recycling | Q29547737 | ||
| Rapid redistribution of Golgi proteins into the ER in cells treated with brefeldin A: evidence for membrane cycling from Golgi to ER | Q29615171 | ||
| Membrane curvature and mechanisms of dynamic cell membrane remodelling | Q29617321 | ||
| Retrograde transport from endosomes to the trans-Golgi network | Q29617826 | ||
| How proteins produce cellular membrane curvature | Q29618016 | ||
| Rab11 in recycling endosomes regulates the sorting and basolateral transport of E-cadherin | Q30475808 | ||
| Role of curvature and phase transition in lipid sorting and fission of membrane tubules | Q30475946 | ||
| Biogenesis of tubular ER-to-Golgi transport intermediates | Q30476699 | ||
| Visualization of TGN to endosome trafficking through fluorescently labeled MPR and AP-1 in living cells | Q30476964 | ||
| Morphology and dynamics of clathrin/GGA1-coated carriers budding from the trans-Golgi network | Q30477740 | ||
| Morphogenesis of post-Golgi transport carriers | Q37063364 | ||
| Imaging and imagination: understanding the endo-lysosomal system | Q37084573 | ||
| Biophysical approaches to protein-induced membrane deformations in trafficking | Q37186230 | ||
| Clathrin-independent endocytosis: a unique platform for cell signaling and PM remodeling | Q37223988 | ||
| Sorting of lysosomal proteins | Q37338623 | ||
| SNX9 - a prelude to vesicle release. | Q37353522 | ||
| Direct continuities between cisternae at different levels of the Golgi complex in glucose-stimulated mouse islet beta cells | Q37682041 | ||
| Arf family GTP loading is activated by, and generates, positive membrane curvature | Q39965840 | ||
| Modulation of nanotube formation by structural modifications of sphingolipids | Q40146046 | ||
| Sorting and retrieval between the endoplasmic reticulum and Golgi apparatus | Q40380591 | ||
| Possible role of deep tubular invaginations of the plasma membrane in MHC-I trafficking | Q40426114 | ||
| Secretory traffic triggers the formation of tubular continuities across Golgi sub-compartments. | Q40500388 | ||
| Delivery of raft-associated, GPI-anchored proteins to the apical surface of polarized MDCK cells by a transcytotic pathway | Q40572614 | ||
| ER-to-Golgi carriers arise through direct en bloc protrusion and multistage maturation of specialized ER exit domains | Q40627644 | ||
| Three-dimensional analysis of post-Golgi carrier exocytosis in epithelial cells | Q40675232 | ||
| Dissection of COPI and Arf1 dynamics in vivo and role in Golgi membrane transport | Q40733038 | ||
| Fusion of constitutive membrane traffic with the cell surface observed by evanescent wave microscopy | Q40889721 | ||
| Membrane Dynamics at the Endoplasmic Reticulum–Golgi Interface | Q41523777 | ||
| COPII and secretory cargo capture into transport vesicles | Q41566685 | ||
| Arf1-GTP-induced tubule formation suggests a function of Arf family proteins in curvature acquisition at sites of vesicle budding | Q41914282 | ||
| Coalignment of plasma membrane channels and protrusions (fibripositors) specifies the parallelism of tendon | Q41957304 | ||
| Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells | Q42132231 | ||
| Opinion: The maturing role of COPI vesicles in intra-Golgi transport | Q43697078 | ||
| Migrating fibroblasts perform polarized, microtubule-dependent exocytosis towards the leading edge | Q44630460 | ||
| Vesicular tubular clusters between the ER and Golgi mediate concentration of soluble secretory proteins by exclusion from COPI-coated vesicles | Q45345737 | ||
| Live imaging of bidirectional traffic from the ERGIC. | Q45345739 | ||
| Evolutionary biology. Pelvic problems for mammals | Q47778685 | ||
| Generation of coated intermediates of clathrin-mediated endocytosis on protein-free liposomes | Q47802787 | ||
| Ultrastructure of long-range transport carriers moving from the trans Golgi network to peripheral endosomes | Q50726204 | ||
| Endocytic delivery to lysosomes mediated by concurrent fusion and kissing events in living cells | Q50777337 | ||
| Clathrin adaptor GGA1 polymerizes clathrin into tubules. | Q55043516 | ||
| Endosomal sorting and signalling: an emerging role for sorting nexins. | Q55050015 | ||
| Procollagen Traverses the Golgi Stack without Leaving the Lumen of Cisternae | Q57705543 | ||
| Role of microtubules in fusion of post-Golgi vesicles to the plasma membrane | Q30477742 | ||
| The closure of Pak1-dependent macropinosomes requires the phosphorylation of CtBP1/BARS. | Q30481720 | ||
| Mechanism of constitutive export from the golgi: bulk flow via the formation, protrusion, and en bloc cleavage of large trans-golgi network tubular domains. | Q30486978 | ||
| The calcium binding loops of the cytosolic phospholipase A2 C2 domain specify targeting to Golgi and ER in live cells | Q30499501 | ||
| Dynamics of secretory membrane trafficking | Q33214161 | ||
| Transport through the Golgi apparatus by rapid partitioning within a two-phase membrane system | Q33343854 | ||
| The dynamin family of mechanoenzymes: pinching in new places | Q33850036 | ||
| Secretory protein trafficking and organelle dynamics in living cells | Q33921421 | ||
| Tubulovesicular processes emerge from trans-Golgi cisternae, extend along microtubules, and interlink adjacent trans-golgi elements into a reticulum | Q33976972 | ||
| A minimal system allowing tubulation with molecular motors pulling on giant liposomes | Q34024836 | ||
| Cooperation of GGAs and AP-1 in packaging MPRs at the trans-Golgi network | Q34148158 | ||
| Gut thoughts on the Golgi complex | Q34156731 | ||
| Trans-Golgi network (TGN) of different cell types: three-dimensional structural characteristics and variability | Q34296683 | ||
| Phospholipase A2 (PLA2) enzymes in membrane trafficking: mediators of membrane shape and function | Q35106869 | ||
| Structural aspects of Golgi function | Q35639793 | ||
| Regulatory mechanisms of dynamin-dependent endocytosis | Q36088968 | ||
| COPII-coated vesicles: flexible enough for large cargo? | Q36173514 | ||
| Large pleiomorphic traffic intermediates in the secretory pathway. | Q36182126 | ||
| Kinetic analysis of secretory protein traffic and characterization of golgi to plasma membrane transport intermediates in living cells | Q36256009 | ||
| Golgi Tubule Traffic and the Effects of Brefeldin A Visualized in Living Cells | Q36275025 | ||
| Variations on the Intracellular Transport Theme: Maturing Cisternae and Trafficking Tubules | Q36276382 | ||
| Correlative light-electron microscopy reveals the tubular-saccular ultrastructure of carriers operating between Golgi apparatus and plasma membrane | Q36301626 | ||
| Discs-Large and Strabismus are functionally linked to plasma membrane formation | Q36318576 | ||
| Recycling endosomes can serve as intermediates during transport from the Golgi to the plasma membrane of MDCK cells | Q36322619 | ||
| Reconstitution of COPII vesicle fusion to generate a pre-Golgi intermediate compartment | Q36322819 | ||
| Neural cell adhesion molecule promotes accumulation of TGN organelles at sites of neuron-to-neuron contacts | Q36323783 | ||
| Imaging constitutive exocytosis with total internal reflection fluorescence microscopy. | Q36328242 | ||
| The Sar1 GTPase coordinates biosynthetic cargo selection with endoplasmic reticulum export site assembly | Q36370047 | ||
| The multiple activities of CtBP/BARS proteins: the Golgi view | Q36398905 | ||
| A trans-Golgi network golgin is required for the regulated secretion of TNF in activated macrophages in vivo | Q36491396 | ||
| Membrane deformation by protein coats | Q36510403 | ||
| The formation of TGN-to-plasma-membrane transport carriers | Q36528788 | ||
| Connections between the various elements of the cis- and mid-compartments of the Golgi apparatus of early rat spermatids | Q36718467 | ||
| P433 | issue | 23 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3847-3856 | |
| P577 | publication date | 2009-10-17 | |
| P13046 | publication type of scholarly work | review article | Q7318358 |
| P1433 | published in | FEBS Letters | Q1388051 |
| P1476 | title | Shaping tubular carriers for intracellular membrane transport | |
| P478 | volume | 583 |
| Q48673647 | A systems biology approach reveals new endoplasmic reticulum-associated targets for the correction of the ATP7B mutant causing Wilson disease. |
| Q89360998 | Dynamic L-type CaV1.2 channel trafficking facilitates CaV1.2 clustering and cooperative gating |
| Q83502912 | ERES (ER exit sites) and the “Secretory Unit Concept” |
| Q92555145 | Efficacy of targeted liposomes and nanocochleates containing imatinib plus dexketoprofen against fibrosarcoma |
| Q38118081 | Golgi tubules: their structure, formation and role in intra-Golgi transport |
| Q28475825 | Inhibition of Cellular Protein Secretion by Norwalk Virus Nonstructural Protein p22 Requires a Mimic of an Endoplasmic Reticulum Export Signal |
| Q41621223 | Land-locked mammalian Golgi reveals cargo transport between stable cisternae. |
| Q40312285 | Methods for analyzing the role of phospholipase A₂ enzymes in endosome membrane tubule formation |
| Q30503263 | Mobility in geometrically confined membranes |
| Q35374933 | Phospholipase D2 is involved in the formation of Golgi tubules and ArfGAP1 recruitment |
| Q26995761 | Regulation of the Golgi complex by phospholipid remodeling enzymes |
| Q36289077 | Structural insights into WHAMM-mediated cytoskeletal coordination during membrane remodeling |
| Q37821046 | The Golgi apparatus: an organelle with multiple complex functions |
| Q38170871 | Trafficking mechanisms of extracellular matrix macromolecules: insights from vertebrate development and human diseases |
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