| scholarly article | Q13442814 |
| P50 | author | Derek McCusker | Q64678867 |
| P2093 | author name string | Douglas R Kellogg | |
| P2860 | cites work | Rab11-FIP3 and FIP4 interact with Arf6 and the exocyst to control membrane traffic in cytokinesis | Q24321408 |
| The Sec6/8 complex in mammalian cells: characterization of mammalian Sec3, subunit interactions, and expression of subunits in polarized cells | Q24555772 | ||
| The Exocyst is a multiprotein complex required for exocytosis in Saccharomyces cerevisiae | Q24561799 | ||
| A comprehensive analysis of protein-protein interactions in Saccharomyces cerevisiae | Q27860755 | ||
| Membrane association and functional regulation of Sec3 by phospholipids and Cdc42 | Q27930739 | ||
| The arrest of secretion response in yeast: signaling from the secretory path to the nucleus via Wsc proteins and Pkc1p | Q27931302 | ||
| Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway | Q27931724 | ||
| Growth site localization of Rho1 small GTP-binding protein and its involvement in bud formation in Saccharomyces cerevisiae. | Q27931888 | ||
| Sec3p is a spatial landmark for polarized secretion in budding yeast | Q27932756 | ||
| Cdk1-dependent regulation of the mitotic inhibitor Wee1. | Q27933013 | ||
| Cdk1-dependent control of membrane-trafficking dynamics. | Q27933503 | ||
| Exo70 interacts with phospholipids and mediates the targeting of the exocyst to the plasma membrane | Q27933752 | ||
| Zds2p regulates Swe1p-dependent polarized cell growth in Saccharomyces cerevisiae via a novel Cdc55p interaction domain | Q27934282 | ||
| Phenotypic analysis of temperature-sensitive yeast actin mutants | Q27934481 | ||
| A protein interaction map for cell polarity development. | Q27934870 | ||
| Dynamic, Rho1p-dependent localization of Pkc1p to sites of polarized growth | Q27935380 | ||
| Late-G1 cyclin-CDK activity is essential for control of cell morphogenesis in budding yeast | Q27935703 | ||
| Cdk1 coordinates cell-surface growth with the cell cycle. | Q27937136 | ||
| Activation of yeast protein kinase C by Rho1 GTPase. | Q27937669 | ||
| Exomer: A coat complex for transport of select membrane proteins from the trans-Golgi network to the plasma membrane in yeast | Q27938814 | ||
| Spatial regulation of Cdc55-PP2A by Zds1/Zds2 controls mitotic entry and mitotic exit in budding yeast | Q27939362 | ||
| The Exo70 subunit of the exocyst is an effector for both Cdc42 and Rho3 function in polarized exocytosis | Q27939800 | ||
| Exo70p mediates the secretion of specific exocytic vesicles at early stages of the cell cycle for polarized cell growth | Q27940157 | ||
| Relationship of actin and tubulin distribution to bud growth in wild-type and morphogenetic-mutant Saccharomyces cerevisiae | Q28131615 | ||
| Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells | Q28273946 | ||
| Global analysis of Cdk1 substrate phosphorylation sites provides insights into evolution | Q29616847 | ||
| Morphogenesis in the yeast cell cycle: regulation by Cdc28 and cyclins | Q29620238 | ||
| Endocytosis optimizes the dynamic localization of membrane proteins that regulate cortical polarity | Q30480167 | ||
| The yeast GRASP Grh1 colocalizes with COPII and is dispensable for organizing the secretory pathway. | Q30495976 | ||
| Modeling vesicle traffic reveals unexpected consequences for Cdc42p-mediated polarity establishment | Q30498426 | ||
| Cell cycle arrest caused by CLN gene deficiency in Saccharomyces cerevisiae resembles START-I arrest and is independent of the mating-pheromone signalling pathway | Q30663148 | ||
| Sec5, a member of the exocyst complex, mediates Drosophila embryo cellularization. | Q34021555 | ||
| Membrane traffic: a driving force in cytokinesis | Q34391536 | ||
| Centriolin anchoring of exocyst and SNARE complexes at the midbody is required for secretory-vesicle-mediated abscission | Q34457967 | ||
| The Zds proteins control entry into mitosis and target protein phosphatase 2A to the Cdc25 phosphatase | Q34470987 | ||
| Vesicles carry most exocyst subunits to exocytic sites marked by the remaining two subunits, Sec3p and Exo70p | Q34553174 | ||
| Endosomal recycling controls plasma membrane area during mitosis | Q35808824 | ||
| A link between mitotic entry and membrane growth suggests a novel model for cell size control | Q35866189 | ||
| Mechanism of recruiting Sec6/8 (exocyst) complex to the apical junctional complex during polarization of epithelial cells | Q36012274 | ||
| Coordinated protein sorting, targeting and distribution in polarized cells | Q36015653 | ||
| Cell polarization and cytokinesis in budding yeast | Q36028928 | ||
| Iqg1p, a yeast homologue of the mammalian IQGAPs, mediates cdc42p effects on the actin cytoskeleton | Q36256321 | ||
| Correlative light-electron microscopy reveals the tubular-saccular ultrastructure of carriers operating between Golgi apparatus and plasma membrane | Q36301626 | ||
| Lava lamp, a novel peripheral golgi protein, is required for Drosophila melanogaster cellularization | Q36316531 | ||
| Yeast Cdc42 functions at a late step in exocytosis, specifically during polarized growth of the emerging bud | Q36380043 | ||
| Sec6/8 complexes on trans-Golgi network and plasma membrane regulate late stages of exocytosis in mammalian cells | Q36380060 | ||
| A subset of yeast vacuolar protein sorting mutants is blocked in one branch of the exocytic pathway | Q36381155 | ||
| Parallel secretory pathways to the cell surface in yeast | Q36382718 | ||
| Regulation of Mih1/Cdc25 by protein phosphatase 2A and casein kinase 1 | Q36491745 | ||
| Exiting the Golgi complex | Q37114569 | ||
| The exomer coat complex transports Fus1p to the plasma membrane via a novel plasma membrane sorting signal in yeast | Q37448310 | ||
| Exit from the trans-Golgi network: from molecules to mechanisms | Q37873171 | ||
| Repression of ribosome and tRNA synthesis in secretion-defective cells is signaled by a novel branch of the cell integrity pathway. | Q39453180 | ||
| Dynamin and clathrin are required for the biogenesis of a distinct class of secretory vesicles in yeast | Q39646586 | ||
| Internalization efficiency of the transferrin receptor | Q41635998 | ||
| Lack of GTP-bound Rho1p in secretory vesicles of Saccharomyces cerevisiae | Q41807504 | ||
| Polarized insertion of new membrane from a cytoplasmic reservoir during cleavage of the Drosophila embryo | Q41861295 | ||
| Cell growth and size homeostasis in proliferating animal cells | Q41893651 | ||
| Phosphatidic acid is a pH biosensor that links membrane biogenesis to metabolism. | Q42924633 | ||
| Wall replication in saccharomyces species: use of fluorescein-conjugated concanavalin A to reveal the site of mannan insertion | Q43897794 | ||
| Conservation of mechanisms controlling entry into mitosis: budding yeast wee1 delays entry into mitosis and is required for cell size control | Q44124467 | ||
| The critical size is set at a single-cell level by growth rate to attain homeostasis and adaptation | Q47238312 | ||
| Synchronization of secretory protein traffic in populations of cells. | Q50501044 | ||
| Spatial coordination of cytokinetic events by compartmentalization of the cell cortex. | Q50798677 | ||
| Mechanisms that help the yeast cell cycle clock tick: G2 cyclins transcriptionally activate G2 cyclins and repress G1 cyclins | Q56951163 | ||
| Genetic control of the cell division cycle in yeast. 3. Seven genes controlling nuclear division | Q70542031 | ||
| G proteins mediate changes in cell shape by stabilizing the axis of polarity | Q73958558 | ||
| P433 | issue | 6 | |
| P304 | page(s) | 845-851 | |
| P577 | publication date | 2012-11-07 | |
| P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
| P1476 | title | Plasma membrane growth during the cell cycle: unsolved mysteries and recent progress | |
| P478 | volume | 24 |
| Q33819289 | A CULLINary ride across the secretory pathway: more than just secretion |
| Q49362084 | A Lipid Transfer Protein Signaling Axis Exerts Dual Control of Cell-Cycle and Membrane Trafficking Systems. |
| Q45950081 | A conserved signaling network monitors delivery of sphingolipids to the plasma membrane in budding yeast. |
| Q90310175 | A heat-sensitive Osh protein controls PI4P polarity |
| Q90028620 | Abundances of transcripts, proteins, and metabolites in the cell cycle of budding yeast reveal coordinate control of lipid metabolism |
| Q53107729 | Determination of cell cycle phases in live B16 melanoma cells using IRMS. |
| Q47559592 | Generalized fractional diffusion equations for subdiffusion in arbitrarily growing domains |
| Q37267971 | Golgi-associated RhoBTB3 targets cyclin E for ubiquitylation and promotes cell cycle progression |
| Q52717095 | Isoprenoids increase bovine endometrial stromal cell tolerance to the cholesterol-dependent cytolysin from Trueperella pyogenes. |
| Q36992966 | Mitotic phosphorylation of Exo84 disrupts exocyst assembly and arrests cell growth |
| Q38744702 | Modeling the Mechanics of Cell Division: Influence of Spontaneous Membrane Curvature, Surface Tension, and Osmotic Pressure |
| Q64911556 | Molecular mechanisms of contractile-ring constriction and membrane trafficking in cytokinesis. |
| Q35190036 | Morphogenesis checkpoint kinase Swe1 is the executor of lipolysis-dependent cell-cycle progression |
| Q47953286 | Nine unanswered questions about cytokinesis. |
| Q27343045 | Roles of the TRAPP-II Complex and the Exocyst in Membrane Deposition during Fission Yeast Cytokinesis |
| Q37745637 | Scaffold-mediated gating of Cdc42 signalling flux |
| Q64897967 | Spatial and Translational Regulation of Exocyst Subunits by Cell Cycle in Budding Yeast. |
| Q39037306 | Translational control of lipogenic enzymes in the cell cycle of synchronous, growing yeast cells |
| Q27304958 | Unique spatiotemporal activation pattern of Cdc42 by Gef1 and Scd1 promotes different events during cytokinesis. |
| Q92482156 | Uptake and subcellular distribution of radiolabeled polymersomes for radiotherapy |
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