| P50 | author | Moritz K Nowack | Q51772447 |
| | Matyáš Fendrych | Q57238360 |
| | Viktor Žárský | Q58212171 |
| | Tamara Pečenková | Q58237013 |
| | Juraj Sekeres | Q85831141 |
| P2093 | author name string | Riet de Rycke | |
| | Lukás Synek | |
| | Edita Janková Drdová | |
| P2860 | cites work | Rho3 of Saccharomyces cerevisiae, which regulates the actin cytoskeleton and exocytosis, is a GTPase which interacts with Myo2 and Exo70 | Q24554501 |
| | Exorcising the exocyst complex | Q26824772 |
| | Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana | Q27860555 |
| | Membrane association and functional regulation of Sec3 by phospholipids and Cdc42 | Q27930739 |
| | Cdc42 interacts with the exocyst and regulates polarized secretion. | Q27931224 |
| | Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway | Q27931724 |
| | Exo84p is an exocyst protein essential for secretion | Q27932396 |
| | Sec3p is a spatial landmark for polarized secretion in budding yeast | Q27932756 |
| | Exo70 interacts with phospholipids and mediates the targeting of the exocyst to the plasma membrane | Q27933752 |
| | Spatial regulation of the exocyst complex by Rho1 GTPase | Q27934400 |
| | The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis | Q27934654 |
| | Dimerization of the exocyst protein Sec6p and its interaction with the t-SNARE Sec9p. | Q27937433 |
| | Sec6p anchors the assembled exocyst complex at sites of secretion. | Q27937862 |
| | SNAP receptors implicated in vesicle targeting and fusion | Q28131653 |
| | Subunit composition, protein interactions, and structures of the mammalian brain sec6/8 complex and septin filaments | Q28275861 |
| | The exocyst complex associates with microtubules to mediate vesicle targeting and neurite outgrowth | Q28365291 |
| | Partitioning of lipid-modified monomeric GFPs into membrane microdomains of live cells | Q29547331 |
| | Lifeact: a versatile marker to visualize F-actin | Q29547604 |
| | GATEWAY vectors for Agrobacterium-mediated plant transformation | Q29615003 |
| | Arabidopsis dynamin-related proteins DRP2B and DRP1A participate together in clathrin-coated vesicle formation during endocytosis. | Q30494008 |
| | Syntaxin clusters assemble reversibly at sites of secretory granules in live cells | Q30497547 |
| | Visualization of regulated exocytosis with a granule-membrane probe using total internal reflection microscopy | Q30833250 |
| | Electron tomographic analysis of somatic cell plate formation in meristematic cells of Arabidopsis preserved by high-pressure freezing. | Q33339822 |
| | A Novel ROP/RAC effector links cell polarity, root-meristem maintenance, and vesicle trafficking | Q33344021 |
| | AtEXO70A1, a member of a family of putative exocyst subunits specifically expanded in land plants, is important for polar growth and plant development. | Q33835182 |
| | The mammalian exocyst, a complex required for exocytosis, inhibits tubulin polymerization | Q34327734 |
| | Fission yeast Sec3 and Exo70 are transported on actin cables and localize the exocyst complex to cell poles. | Q34328810 |
| | Centriolin anchoring of exocyst and SNARE complexes at the midbody is required for secretory-vesicle-mediated abscission | Q34457967 |
| | Actin cables and the exocyst form two independent morphogenesis pathways in the fission yeast | Q34470997 |
| | Vesicles carry most exocyst subunits to exocytic sites marked by the remaining two subunits, Sec3p and Exo70p | Q34553174 |
| | The role for the exocyst complex subunits Exo70B2 and Exo70H1 in the plant-pathogen interaction | Q34697563 |
| | Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins | Q34783580 |
| | Using intrinsically fluorescent proteins for plant cell imaging | Q36379425 |
| | Coats, tethers, Rabs, and SNAREs work together to mediate the intracellular destination of a transport vesicle | Q36815404 |
| | SNARE-ware: the role of SNARE-domain proteins in plant biology. | Q36824180 |
| | The ghost in the machine: small GTPases as spatial regulators of exocytosis | Q37244992 |
| | Exocytosis and cell polarity in plants - exocyst and recycling domains. | Q37508152 |
| | Multisubunit tethering complexes and their role in membrane fusion | Q37807806 |
| | A rab1 GTPase is required for transport between the endoplasmic reticulum and golgi apparatus and for normal golgi movement in plants | Q38306377 |
| | Development of series of gateway binary vectors, pGWBs, for realizing efficient construction of fusion genes for plant transformation. | Q40094438 |
| | Mammalian exocyst complex is required for the docking step of insulin vesicle exocytosis | Q40425782 |
| | Trafficking to the outer polar domain defines the root-soil interface | Q42471142 |
| | Pausing of Golgi bodies on microtubules regulates secretion of cellulose synthase complexes in Arabidopsis | Q43451848 |
| | Systematic analysis of SNARE molecules in Arabidopsis: dissection of the post-Golgi network in plant cells. | Q45041263 |
| | Multiple exocytotic markers accumulate at the sites of perifungal membrane biogenesis in arbuscular mycorrhizas | Q45368578 |
| | High-throughput fluorescent tagging of full-length Arabidopsis gene products in planta. | Q47610049 |
| | A mobile secretory vesicle cluster involved in mass transport from the Golgi to the plant cell exterior | Q47985227 |
| | An exocyst complex functions in plant cell growth in Arabidopsis and tobacco. | Q50459026 |
| | The Arabidopsis Exocyst Complex Is Involved in Cytokinesis and Cell Plate Maturation | Q50540459 |
| | Luminescence detection of SNARE-SNARE interaction in Arabidopsis protoplasts. | Q50574368 |
| | Differential expression control and polarized distribution of plasma membrane-resident SYP1 SNAREs in Arabidopsis thaliana. | Q50608899 |
| | Dynamics of Arabidopsis dynamin-related protein 1C and a clathrin light chain at the plasma membrane. | Q50633900 |
| | Comparison of the dynamics and functional redundancy of the Arabidopsis dynamin-related isoforms DRP1A and DRP1C during plant development. | Q50642632 |
| | Rates of exocytosis and endocytosis in Arabidopsis root hairs and pollen tubes. | Q51869736 |
| | EXPO, an exocyst-positive organelle distinct from multivesicular endosomes and autophagosomes, mediates cytosol to cell wall exocytosis in Arabidopsis and tobacco cells. | Q51892236 |
| | The Arabidopsis GNOM ARF-GEF mediates endosomal recycling, auxin transport, and auxin-dependent plant growth. | Q52109776 |
| | In-situ analysis of pectic polysaccharides in seed mucilage and at the root surface of Arabidopsis thaliana. | Q52862471 |
| | An ARF-GEF acting at the Golgi and in selective endocytosis in polarized plant cells | Q59068395 |
| | SEC8, a subunit of the putative Arabidopsis exocyst complex, facilitates pollen germination and competitive pollen tube growth | Q80925199 |
| | Variable-angle epifluorescence microscopy: a new way to look at protein dynamics in the plant cell cortex | Q81429987 |
| | Arabidopsis cortical microtubules position cellulose synthase delivery to the plasma membrane and interact with cellulose synthase trafficking compartments | Q84068679 |
| | Arabidopsis exocyst subunits SEC8 and EXO70A1 and exocyst interactor ROH1 are involved in the localized deposition of seed coat pectin | Q84553651 |
| | Exocytosis and endocytosis | Q95297219 |
| | A GFP-MAP4 reporter gene for visualizing cortical microtubule rearrangements in living epidermal cells | Q95441183 |
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 4 | |
| P921 | main subject | Arabidopsis thaliana | Q158695 |
| | visualization | Q451553 |
| P304 | page(s) | 510-520 | |
| P577 | publication date | 2013-01-02 | |
| P1433 | published in | Molecular Biology of the Cell | Q2338259 |
| P1476 | title | Visualization of the exocyst complex dynamics at the plasma membrane of Arabidopsis thaliana | |
| P478 | volume | 24 | |