| scholarly article | Q13442814 |
| P50 | author | Carolyn Coyne | Q28754337 |
| P2093 | author name string | Simon C Watkins | |
| Yasunori Yamamoto | |||
| James F Conway | |||
| Kimberly R Long | |||
| Meir Aridor | |||
| Adam L Baker | |||
| P2860 | cites work | The coxsackievirus and adenovirus receptor interacts with the multi-PDZ domain protein-1 (MUPP-1) within the tight junction | Q24303832 |
| Structural basis of membrane invagination by F-BAR domains | Q24308717 | ||
| Structural basis for cargo regulation of COPII coat assembly | Q24322472 | ||
| Molecular mechanism of membrane constriction and tubulation mediated by the F-BAR protein Pacsin/Syndapin | Q24338982 | ||
| Insights into COPII coat nucleation from the structure of Sec23.Sar1 complexed with the active fragment of Sec31 | Q24656578 | ||
| Cellular COPII proteins are involved in production of the vesicles that form the poliovirus replication complex. | Q27469873 | ||
| 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 | ||
| Structure and organization of coat proteins in the COPII cage | Q27646519 | ||
| COPII: a membrane coat formed by Sec proteins that drive vesicle budding from the endoplasmic reticulum | Q27930804 | ||
| Sar1p N-terminal helix initiates membrane curvature and completes the fission of a COPII vesicle | Q27934415 | ||
| Bi-directional protein transport between the ER and Golgi | Q29615233 | ||
| Generation of high curvature membranes mediated by direct endophilin bilayer interactions | Q29616512 | ||
| COPII-coated vesicle formation reconstituted with purified coat proteins and chemically defined liposomes | Q29616856 | ||
| Membrane curvature and mechanisms of dynamic cell membrane remodelling | Q29617321 | ||
| Modifications to the C-terminus of Arf1 alter cell functions and protein interactions | Q30432201 | ||
| Role of curvature and phase transition in lipid sorting and fission of membrane tubules | Q30475946 | ||
| Cholesterol is required for efficient endoplasmic reticulum-to-Golgi transport of secretory membrane proteins | Q30477065 | ||
| COPI coat assembly occurs on liquid-disordered domains and the associated membrane deformations are limited by membrane tension | Q30484455 | ||
| Membrane insertion of the pleckstrin homology domain variable loop 1 is critical for dynamin-catalyzed vesicle scission. | Q30491655 | ||
| Shape change and physical properties of giant phospholipid vesicles prepared in the presence of an AC electric field | Q34017319 | ||
| Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders | Q34190319 | ||
| p125 is localized in endoplasmic reticulum exit sites and involved in their organization | Q34380281 | ||
| Temperature-dependent reversible assembly of taxol-treated microtubules | Q36217145 | ||
| Quality control in the endoplasmic reticulum: folding and misfolding of vesicular stomatitis virus G protein in cells and in vitro | Q36223730 | ||
| Regulation of Sar1 NH2 terminus by GTP binding and hydrolysis promotes membrane deformation to control COPII vesicle fission | Q36320575 | ||
| The Sar1 GTPase coordinates biosynthetic cargo selection with endoplasmic reticulum export site assembly | Q36370047 | ||
| Sequential coupling between COPII and COPI vesicle coats in endoplasmic reticulum to Golgi transport | Q36382846 | ||
| The genetic basis of a craniofacial disease provides insight into COPII coat assembly. | Q36487336 | ||
| Involvement of cellular membrane traffic proteins in poliovirus replication | Q36716351 | ||
| Selective targeting of ER exit sites supports axon development | Q37389744 | ||
| GTPase cycle of dynamin is coupled to membrane squeeze and release, leading to spontaneous fission | Q37401393 | ||
| Activation of phospholipase D by the small GTPase Sar1p is required to support COPII assembly and ER export | Q39831931 | ||
| Phosphatidylinositol 4-phosphate formation at ER exit sites regulates ER export | Q40212158 | ||
| ER-to-Golgi carriers arise through direct en bloc protrusion and multistage maturation of specialized ER exit domains | Q40627644 | ||
| Mapping the lipid distribution in the membranes of BHK cells (mini-review). | Q41137717 | ||
| Sterols regulate ER-export dynamics of secretory cargo protein ts-O45-G. | Q41455784 | ||
| Differential requirements for ts-O45-G and procollagen biosynthetic transport | Q42827670 | ||
| Real-time visualization of dynamin-catalyzed membrane fission and vesicle release | Q43141309 | ||
| The polymer-supported phospholipid bilayer: tethering as a new approach to substrate-membrane stabilization | Q43897470 | ||
| Virus-induced Abl and Fyn kinase signals permit coxsackievirus entry through epithelial tight junctions | Q45420840 | ||
| Expression and purification of mammalian Sarl | Q46206529 | ||
| Secretory cargo regulates the turnover of COPII subunits at single ER exit sites | Q46907625 | ||
| Efficient coupling of Sec23-Sec24 to Sec13-Sec31 drives COPII-dependent collagen secretion and is essential for normal craniofacial development. | Q47073719 | ||
| Aggregation and vesiculation of membrane proteins by curvature-mediated interactions | Q59063394 | ||
| Vesicle fission of giant unilamellar vesicles of liquid-ordered-phase membranes induced by amphiphiles with a single long hydrocarbon chain | Q79514520 | ||
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 14 | |
| P304 | page(s) | 115-128 | |
| P577 | publication date | 2010-07-01 | |
| P1433 | published in | Journal of Cell Biology | Q1524550 |
| P1476 | title | Sar1 assembly regulates membrane constriction and ER export | |
| P478 | volume | 190 |
| Q37702698 | A cascade of ER exit site assembly that is regulated by p125A and lipid signals |
| Q34202987 | A genome-wide RNAi screen identifies regulators of cholesterol-modified hedgehog secretion in Drosophila |
| Q90250961 | A simple supported tubulated bilayer system for evaluating protein-mediated membrane remodeling |
| Q30540013 | Altering membrane topology with Sar1 does not impair spindle assembly in Xenopus egg extracts. |
| Q27021670 | COPI budding within the Golgi stack |
| Q41881232 | COPII machinery cooperates with ER-localized Hsp40 to sequester misfolded membrane proteins into ER-associated compartments |
| Q35208451 | Coatomer and dimeric ADP ribosylation factor 1 promote distinct steps in membrane scission |
| Q37233992 | Differential roles of C-terminal Eps15 homology domain proteins as vesiculators and tubulators of recycling endosomes |
| Q37807408 | Emergent properties of proteostasis-COPII coupled systems in human health and disease |
| Q42184327 | Epithelial organization and cyst lumen expansion require efficient Sec13-Sec31-driven secretion |
| Q34426263 | GRAF1 forms a complex with MICAL-L1 and EHD1 to cooperate in tubular recycling endosome vesiculation |
| Q47602229 | Heritable Skeletal Disorders Arising from Defects in Processing and Transport of Type I Procollagen from the ER: Perspectives on Possible Therapeutic Approaches |
| Q28743560 | Human embryonic stem cells derived from embryos at different stages of development share similar transcription profiles |
| Q34622829 | Insights into the mechanisms of membrane curvature and vesicle scission by the small GTPase Sar1 in the early secretory pathway |
| Q38529922 | Mechanisms for exporting large-sized cargoes from the endoplasmic reticulum. |
| Q39637109 | Mechanisms of membrane curvature generation in membrane traffic. |
| Q39119129 | Multibudded tubules formed by COPII on artificial liposomes |
| Q51751501 | Mutant SOD1 inhibits ER-Golgi transport in amyotrophic lateral sclerosis. |
| Q37808481 | Physical aspects of COPI vesicle formation. |
| Q27023633 | Protein export at the ER: loading big collagens into COPII carriers |
| Q27330124 | Quantification of Protein-Induced Membrane Remodeling Kinetics In Vitro with Lipid Multilayer Gratings. |
| Q41526609 | Regulation of the Sar1 GTPase Cycle Is Necessary for Large Cargo Secretion from the Endoplasmic Reticulum |
| Q34421232 | Reticulon Short Hairpin Transmembrane Domains Are Used to Shape ER Tubules |
| Q90864188 | Ribosomal mistranslation leads to silencing of the unfolded protein response and increased mitochondrial biogenesis |
| Q97636476 | STEEP mediates STING ER exit and activation of signaling |
| Q36466099 | Sar1 GTPase Activity Is Regulated by Membrane Curvature. |
| Q45844500 | Sar1 bends membranes into shape |
| Q41285549 | Sar1 localizes at the rims of COPII-coated membranes in vivo. |
| Q27939376 | Sar1, a Novel Regulator of ER-Mitochondrial Contact Sites |
| Q35759972 | Sec24p and Sec16p cooperate to regulate the GTP cycle of the COPII coat |
| Q39269881 | Sedlin controls the ER export of procollagen by regulating the Sar1 cycle |
| Q36972153 | Small GTPase Sar1 is crucial for proglutelin and α-globulin export from the endoplasmic reticulum in rice endosperm |
| Q91716745 | Small GTPases SAR1A and SAR1B regulate the trafficking of the cardiac sodium channel Nav1.5. |
| Q35880048 | The [corrected] SEC23-SEC31 [corrected] interface plays critical role for export of procollagen from the endoplasmic reticulum |
| Q37583530 | The endoplasmic reticulum coat protein II transport machinery coordinates cellular lipid secretion and cholesterol biosynthesis |
| Q47297367 | The plant membrane surrounding powdery mildew haustoria shares properties with the endoplasmic reticulum membrane |
| Q36040933 | The structure of the Sec13/31 COPII cage bound to Sec23 |
| Q37827119 | Thermodynamics and mechanics of membrane curvature generation and sensing by proteins and lipids |
| Q26821930 | Vesicle-mediated export from the ER: COPII coat function and regulation |
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