review article | Q7318358 |
scholarly article | Q13442814 |
P2093 | author name string | Mathew Abraham | |
Wei Guo | |||
Daniel TerBush | |||
Shu-Chan Hsu | |||
P2860 | cites work | The brain exocyst complex interacts with RalA in a GTP-dependent manner: identification of a novel mammalian Sec3 gene and a second Sec15 gene | Q24291328 |
Structural basis of the interaction between RalA and Sec5, a subunit of the sec6/8 complex | Q24306783 | ||
The syntaxin family of vesicular transport receptors | Q24310598 | ||
DelGEF, a homologue of the Ran guanine nucleotide exchange factor RanGEF, binds to the exocyst component Sec5 and modulates secretion | Q24322704 | ||
Exocyst complex subunit sec8 binds to postsynaptic density protein-95 (PSD-95): a novel interaction regulated by cypin (cytosolic PSD-95 interactor) | Q24530017 | ||
The mammalian septin MSF localizes with microtubules and is required for completion of cytokinesis | Q24537250 | ||
Rho3 of Saccharomyces cerevisiae, which regulates the actin cytoskeleton and exocytosis, is a GTPase which interacts with Myo2 and Exo70 | Q24554501 | ||
The Sec6/8 complex in mammalian cells: characterization of mammalian Sec3, subunit interactions, and expression of subunits in polarized cells | Q24555772 | ||
The Rho GTPase Rho3 has a direct role in exocytosis that is distinct from its role in actin polarity | Q24647386 | ||
Subunit structure of the mammalian exocyst complex | Q24647770 | ||
Structure of the GTPase-binding domain of Sec5 and elucidation of its Ral binding site | Q27640656 | ||
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 | ||
Compartmentalization of the cell cortex by septins is required for maintenance of cell polarity in yeast. | Q27931967 | ||
Exo84p is an exocyst protein essential for secretion | Q27932396 | ||
Sec3p is a spatial landmark for polarized secretion in budding yeast | Q27932756 | ||
Order of events in the yeast secretory pathway | Q27932822 | ||
Sec9 is a SNAP-25-like component of a yeast SNARE complex that may be the effector of Sec4 function in exocytosis | Q27933277 | ||
Vesicular transport: how many Ypt/Rab-GTPases make a eukaryotic cell? | Q27934224 | ||
Spatial regulation of the exocyst complex by Rho1 GTPase | Q27934400 | ||
Sec8p and Sec15p are components of a plasma membrane-associated 19.5S particle that may function downstream of Sec4p to control exocytosis | Q27935760 | ||
The septins: roles in cytokinesis and other processes | Q27936270 | ||
Sec6, Sec8, and Sec15 are components of a multisubunit complex which localizes to small bud tips in Saccharomyces cerevisiae | Q27936607 | ||
Sec2p mediates nucleotide exchange on Sec4p and is involved in polarized delivery of post-Golgi vesicles | Q27939177 | ||
Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules | Q28181820 | ||
The exocyst complex is required for targeting of Glut4 to the plasma membrane by insulin | Q28190100 | ||
NMDA receptor trafficking through an interaction between PDZ proteins and the exocyst complex | Q28203460 | ||
The septin protein Nedd5 associates with both the exocyst complex and microtubules and disruption of its GTPase activity promotes aberrant neurite sprouting in PC12 cells | Q28204831 | ||
PDZ domains: structural modules for protein complex assembly | Q28210680 | ||
The exocyst complex binds the small GTPase RalA to mediate filopodia formation | Q28211412 | ||
Nedd5, a mammalian septin, is a novel cytoskeletal component interacting with actin-based structures | Q28242345 | ||
Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells | Q28273946 | ||
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 | ||
Characterization of a cDNA encoding a subunit of the rat brain rsec6/8 complex | Q28571644 | ||
The secretory protein Sec8 is required for paraxial mesoderm formation in the mouse | Q28588476 | ||
Promoter traps in embryonic stem cells: a genetic screen to identify and mutate developmental genes in mice | Q29616222 | ||
Self- and actin-templated assembly of Mammalian septins | Q29618509 | ||
Yeast syntaxins Sso1p and Sso2p belong to a family of related membrane proteins that function in vesicular transport | Q29619583 | ||
The diversity of Rab proteins in vesicle transport | Q29620216 | ||
A ras-like protein is required for a post-Golgi event in yeast secretion | Q29620275 | ||
Targeting vesicles to specific sites on the plasma membrane: the role of the sec6/8 complex | Q33594269 | ||
Septins: cytoskeletal polymers or signalling GTPases? | Q33730378 | ||
Transport-vesicle targeting: tethers before SNAREs | Q33772639 | ||
Functional cooperation between the microtubule and actin cytoskeletons | Q33840293 | ||
rSec6 and rSec8, mammalian homologs of yeast proteins essential for secretion | Q33857254 | ||
Protein complexes in transport vesicle targeting | Q33913418 | ||
Sec1/Munc18 proteins: mediators of membrane fusion moving to center stage | Q34031651 | ||
Membrane tethering and fusion in the secretory and endocytic pathways | Q34156712 | ||
Mutations in the exocyst component Sec5 disrupt neuronal membrane traffic, but neurotransmitter release persists | Q34176051 | ||
Immunological characterization of exocyst complex subunits in cell differentiation | Q34227607 | ||
Insulin signaling pathways in time and space. | Q34534983 | ||
Exocytosis: the many masters of the exocyst | Q34574356 | ||
Secretion and cell-surface growth are blocked in a temperature-sensitive mutant of Saccharomyces cerevisiae | Q34692247 | ||
Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins | Q34783580 | ||
Cytoskeleton: what does GTP do for septins? | Q35006060 | ||
Signaling complex organization by PDZ domain proteins | Q35059536 | ||
Conservation and specialization. The role of the exocyst in neuronal exocytosis | Q35063154 | ||
A rat brain Sec1 homologue related to Rop and UNC18 interacts with syntaxin | Q35087004 | ||
The molecular machinery for secretion is conserved from yeast to neurons | Q36184412 | ||
The Sec15 protein responds to the function of the GTP binding protein, Sec4, to control vesicular traffic in yeast | Q36221387 | ||
Compromised cytoarchitecture and polarized trafficking in autosomal dominant polycystic kidney disease cells | Q36328246 | ||
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 | ||
Sec15 protein, an essential component of the exocytotic apparatus, is associated with the plasma membrane and with a soluble 19.5S particle | Q36529409 | ||
cdc42 regulates the exit of apical and basolateral proteins from the trans-Golgi network | Q39645140 | ||
The Rho family of small GTPases is involved in epithelial cystogenesis and tubulogenesis. | Q40658466 | ||
The exocyst affects protein synthesis by acting on the translocation machinery of the endoplasmic reticulum | Q40660360 | ||
Three-dimensional analysis of post-Golgi carrier exocytosis in epithelial cells | Q40675232 | ||
Cdc42 controls secretory and endocytic transport to the basolateral plasma membrane of MDCK cells | Q40918582 | ||
Drosophila sec10 is required for hormone secretion but not general exocytosis or neurotransmission | Q44230260 | ||
ADPKD: a human disease altering Golgi function and basolateral exocytosis in renal epithelia. | Q52542310 | ||
The C. elegans unc-18 gene encodes a protein expressed in motor neurons | Q70478386 | ||
Association of Ral GTP-binding protein with human platelet dense granules | Q71433548 | ||
The beta subunit of the Sec61p endoplasmic reticulum translocon interacts with the exocyst complex in Saccharomyces cerevisiae | Q73193182 | ||
Purification and characterization of yeast exocyst complex | Q73517566 | ||
Ras family therapy: Rab, Rho and Ral talk to the exocyst | Q74327244 | ||
The exocyst is a Ral effector complex | Q77342588 | ||
Membrane traffic: exocyst III--makes a family | Q77486378 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | exocytosis | Q323426 |
P304 | page(s) | 243-65 | |
P577 | publication date | 2004-01-01 | |
P1433 | published in | International Review of Cytology | Q2687019 |
P1476 | title | The exocyst complex in polarized exocytosis | |
P478 | volume | 233 |
Q28000096 | A Rab8 guanine nucleotide exchange factor-effector interaction network regulates primary ciliogenesis |
Q37511751 | A functional interplay between the small GTPase Rab11a and mitochondria-shaping proteins regulates mitochondrial positioning and polarization of the actin cytoskeleton downstream of Src family kinases |
Q39634814 | A novel role for TNFAIP2: its correlation with invasion and metastasis in nasopharyngeal carcinoma. |
Q27934432 | A phosphatidylinositol-transfer protein and phosphatidylinositol-4-phosphate 5-kinase control Cdc42 to regulate the actin cytoskeleton and secretory pathway in yeast |
Q50460637 | A pollen coat-inducible autoinhibited Ca2+-ATPase expressed in stigmatic papilla cells is required for compatible pollination in the Brassicaceae. |
Q24536241 | AS160, the Akt substrate regulating GLUT4 translocation, has a functional Rab GTPase-activating protein domain |
Q35845730 | Activity-dependent synaptic GRIP1 accumulation drives synaptic scaling up in response to action potential blockade |
Q84286071 | An emerging role for IQGAP1 in regulating protein traffic |
Q50459026 | An exocyst complex functions in plant cell growth in Arabidopsis and tobacco. |
Q38620790 | Arabidopsis EXO70A1 recruits Patellin3 to the cell membrane independent of its role as exocyst subunit. |
Q92422856 | Arabidopsis Trichome Contains Two Plasma Membrane Domains with Different Lipid Compositions Which Attract Distinct EXO70 Subunits |
Q33835182 | AtEXO70A1, a member of a family of putative exocyst subunits specifically expanded in land plants, is important for polar growth and plant development. |
Q48239208 | Calcium signalling mediates self-incompatibility response in the Brassicaceae. |
Q37505642 | Cell and molecular biology of invadopodia |
Q36580830 | Cell polarity in filamentous fungi: shaping the mold |
Q52722874 | Cell polarity protein Spa2 coordinates Chs2 incorporation at the division site in budding yeast. |
Q48067705 | Cellular pathways regulating responses to compatible and self-incompatible pollen in Brassica and Arabidopsis stigmas intersect at Exo70A1, a putative component of the exocyst complex. |
Q30501053 | Characterization of Mug33 reveals complementary roles for actin cable-dependent transport and exocyst regulators in fission yeast exocytosis |
Q57936684 | Characterization of the Arabidopsis thaliana exocyst complex gene families by phylogenetic, expression profiling, and subcellular localization studies |
Q38485826 | Chromium stress response effect on signal transduction and expression of signaling genes in rice |
Q40046042 | Collaboration between Distinct Rab Small GTPase Trafficking Circuits Mediates Bacterial Clearance from the Bladder Epithelium |
Q34559663 | Compartmentalization of the exocyst complex in lipid rafts controls Glut4 vesicle tethering |
Q30447603 | Compartmentalizing the neuronal plasma membrane from axon initial segments to synapses |
Q34891306 | Cortactin: a multifunctional regulator of cellular invasiveness |
Q28000129 | Crosstalk of Arf and Rab GTPases en route to cilia |
Q33914537 | Cyclical regulation of the exocyst and cell polarity determinants for polarized cell growth |
Q46457149 | Decreased proteinase A excretion by strengthening its vacuolar sorting and weakening its constitutive secretion in Saccharomyces cerevisiae. |
Q28512125 | Dlg1, Sec8, and Mtmr2 regulate membrane homeostasis in Schwann cell myelination |
Q35973878 | ERK1/2 regulate exocytosis through direct phosphorylation of the exocyst component Exo70 |
Q39638312 | EXO70 protein influences dengue virus secretion |
Q51892236 | EXPO, an exocyst-positive organelle distinct from multivesicular endosomes and autophagosomes, mediates cytosol to cell wall exocytosis in Arabidopsis and tobacco cells. |
Q40045728 | Early Arabidopsis root hair growth stimulation by pathogenic strains of Pseudomonas syringae |
Q37537921 | Endocytosis and spatial restriction of cell signaling |
Q36321307 | Essential function of Drosophila Sec6 in apical exocytosis of epithelial photoreceptor cells |
Q37146947 | Exo70 generates membrane curvature for morphogenesis and cell migration |
Q27933752 | Exo70 interacts with phospholipids and mediates the targeting of the exocyst to the plasma membrane |
Q42833931 | Exo70 interacts with the Arp2/3 complex and regulates cell migration |
Q36962536 | Exo70 is transcriptionally up-regulated by hepatic nuclear factor 4α and contributes to cell cycle control in hepatoma cells |
Q37537855 | Exo70 isoform switching upon epithelial-mesenchymal transition mediates cancer cell invasion |
Q27940157 | Exo70p mediates the secretion of specific exocytic vesicles at early stages of the cell cycle for polarized cell growth |
Q24598553 | Exocyst complex component 3-like 2 (EXOC3L2) associates with the exocyst complex and mediates directional migration of endothelial cells |
Q45904711 | Exocyst complex component Sec8: a presumed component in the progression of human oral squamous-cell carcinoma by secretion of matrix metalloproteinases. |
Q99418402 | Exocyst components promote an incompatible interaction between Glycine max (soybean) and Heterodera glycines (the soybean cyst nematode) |
Q41862913 | Exocyst function is regulated by effector phosphorylation. |
Q37256934 | Exocyst is involved in polarized cell migration and cerebral cortical development |
Q27308745 | Exocyst subunits Exo70 and Exo84 cooperate with small GTPases to regulate behavior and endocytic trafficking in C. elegans |
Q37508152 | Exocytosis and cell polarity in plants - exocyst and recycling domains. |
Q35518837 | Functional test of Brassica self-incompatibility modifiers in Arabidopsis thaliana |
Q24336708 | GOLPH3 bridges phosphatidylinositol-4- phosphate and actomyosin to stretch and shape the Golgi to promote budding |
Q35119229 | Germ cell intercellular bridges |
Q27938690 | Homologues of oxysterol-binding proteins affect Cdc42p- and Rho1p-mediated cell polarization in Saccharomyces cerevisiae |
Q37060680 | How peptide hormone vesicles are transported to the secretion site for exocytosis |
Q38702072 | How to bake a brain: yeast as a model neuron. |
Q40179194 | Identification of Interacting Motifs Between Armadillo Repeat Containing 1 (ARC1) and Exocyst 70 A1 (Exo70A1) Proteins in Brassica oleracea |
Q25256672 | Increased synaptic microtubules and altered synapse development in Drosophila sec8 mutants |
Q24294708 | Interaction of BIG2, a brefeldin A-inhibited guanine nucleotide-exchange protein, with exocyst protein Exo70 |
Q35989025 | Intracellular trafficking in Drosophila visual system development: a basis for pattern formation through simple mechanisms. |
Q39332459 | Invadosomes are coming: new insights into function and disease relevance |
Q38387100 | Lethal (2) giant larvae: an indispensable regulator of cell polarity and cancer development |
Q36320849 | Lethal giant larvae proteins interact with the exocyst complex and are involved in polarized exocytosis |
Q39771216 | M-Sec promotes membrane nanotube formation by interacting with Ral and the exocyst complex |
Q53232953 | M-sec regulates polarized secretion of inflammatory endothelial chemokines and facilitates CCL2-mediated lymphocyte transendothelial migration. |
Q34778354 | Mechanisms and function of dendritic exocytosis |
Q47412206 | Mediterranean views on epithelial polarity |
Q39429237 | Membrane Trafficking in Plant Immunity |
Q27930739 | Membrane association and functional regulation of Sec3 by phospholipids and Cdc42 |
Q37412692 | Membrane organization and dynamics in cell polarity |
Q36994689 | Membrane trafficking in osteoblasts and osteoclasts: new avenues for understanding and treating skeletal diseases |
Q36992966 | Mitotic phosphorylation of Exo84 disrupts exocyst assembly and arrests cell growth |
Q92922438 | Modulation of Cell-Cell Interactions in Drosophila Oocyte Development |
Q35649197 | Modulation of neurotransmitter release by the second messenger-activated protein kinases: implications for presynaptic plasticity |
Q26860718 | Molecular complexes that direct rhodopsin transport to primary cilia |
Q38245882 | Molecular mechanisms of de novo lumen formation |
Q52653945 | Mosaic deletion of EXOC6B: further evidence for an important role of the exocyst complex in the pathogenesis of intellectual disability. |
Q36957578 | Oncogenic BRAF-Mediated Melanoma Cell Invasion |
Q35809213 | Organelles and trafficking machinery for postsynaptic plasticity |
Q33432360 | POINeT: protein interactome with sub-network analysis and hub prioritization |
Q30494269 | Phosphatidylinositol 4,5-bisphosphate directs spermatid cell polarity and exocyst localization in Drosophila. |
Q36095751 | Phosphatidylinositol 4,5-bisphosphate mediates the targeting of the exocyst to the plasma membrane for exocytosis in mammalian cells |
Q42481907 | Phytophthora infestans RXLR Effector AVR1 Interacts with Exocyst Component Sec5 to Manipulate Plant Immunity. |
Q27935373 | Purification of active HOPS complex reveals its affinities for phosphoinositides and the SNARE Vam7p |
Q41959519 | Quantitative proteomics of yeast post-Golgi vesicles reveals a discriminating role for Sro7p in protein secretion |
Q35191801 | Rab11 function in Trypanosoma brucei: identification of conserved and novel interaction partners |
Q33918372 | Rab11 is required for epithelial cell viability, terminal differentiation, and suppression of tumor-like growth in the Drosophila egg chamber. |
Q30480761 | Rab11 is required for membrane trafficking and actomyosin ring constriction in meiotic cytokinesis of Drosophila males |
Q37064855 | Ral GTPases and cancer: linchpin support of the tumorigenic platform |
Q33557696 | RalA promotes a direct exocyst-Par6 interaction to regulate polarity in neuronal development |
Q39791607 | RalA suppresses early stages of Ras-induced squamous cell carcinoma progression |
Q22001510 | RalA-exocyst complex regulates integrin-dependent membrane raft exocytosis and growth signaling |
Q40124894 | Receptor-mediated regulation of tomosyn-syntaxin 1A interactions in bovine adrenal chromaffin cells |
Q37930060 | Revisiting the regulated secretory pathway: from frogs to human |
Q30431874 | RhoGDI3 and RhoG: Vesicular trafficking and interactions with the Sec3 Exocyst subunit |
Q33897855 | Role of Rab11 in planar cell polarity and apical constriction during vertebrate neural tube closure |
Q28769316 | Role of septins and the exocyst complex in the function of hydrolytic enzymes responsible for fission yeast cell separation |
Q33815352 | Role of the Small GTPase Rho3 in Golgi/Endosome trafficking through functional interaction with adaptin in Fission Yeast |
Q34763238 | Role of the conserved oligomeric Golgi (COG) complex in protein glycosylation |
Q80925199 | SEC8, a subunit of the putative Arabidopsis exocyst complex, facilitates pollen germination and competitive pollen tube growth |
Q34338417 | Sec15 is an effector for the Rab11 GTPase in mammalian cells |
Q34021555 | Sec5, a member of the exocyst complex, mediates Drosophila embryo cellularization. |
Q33410396 | Sec61beta, a subunit of the Sec61 protein translocation channel at the endoplasmic reticulum, is involved in the transport of Gurken to the plasma membrane |
Q22337345 | Self/non-self recognition mechanisms in sexual reproduction: New insight into the self-incompatibility system shared by flowering plants and hermaphroditic animals |
Q64897967 | Spatial and Translational Regulation of Exocyst Subunits by Cell Cycle in Budding Yeast. |
Q34450386 | Spatial restriction of receptor tyrosine kinase activity through a polarized endocytic cycle controls border cell migration |
Q91642416 | Sphingolipids are required for exocyst polarity and exocytic secretion in Saccharomyces cerevisiae |
Q27659629 | Structure-function study of the N-terminal domain of exocyst subunit Sec3 |
Q27967650 | Syntaxin 3 and SNAP-25 pairing, regulated by omega-3 docosahexaenoic acid, controls the delivery of rhodopsin for the biogenesis of cilia-derived sensory organelles, the rod outer segments |
Q44474951 | The Arabidopsis exocyst subunit SEC3A is essential for embryo development and accumulates in transient puncta at the plasma membrane. |
Q35102641 | The Caenorhabditis elegans GARP complex contains the conserved Vps51 subunit and is required to maintain lysosomal morphology |
Q27939800 | The Exo70 subunit of the exocyst is an effector for both Cdc42 and Rho3 function in polarized exocytosis |
Q33515025 | The GTPase RalA regulates different steps of the secretory process in pancreatic beta-cells |
Q39446377 | The N-Terminal UND Motif of the Arabidopsis U-Box E3 Ligase PUB18 Is Critical for the Negative Regulation of ABA-Mediated Stomatal Movement and Determines Its Ubiquitination Specificity for Exocyst Subunit Exo70B1. |
Q37696883 | The Neurospora crassa exocyst complex tethers Spitzenkörper vesicles to the apical plasma membrane during polarized growth. |
Q52911172 | The ROP2-RIC7 pathway negatively regulates light-induced stomatal opening by inhibiting exocyst subunit Exo70B1 in Arabidopsis. |
Q34960668 | The Rho-GEF Gef3 interacts with the septin complex and activates the GTPase Rho4 during fission yeast cytokinesis. |
Q39013611 | The Role of the Cytoskeleton and Myosin-Vc in the Targeting of KCa3.1 to the Basolateral Membrane of Polarized Epithelial Cells |
Q27323982 | The bud tip is the cellular hot spot of protein secretion in yeasts |
Q27930273 | The critical role of Exo84p in the organization and polarized localization of the exocyst complex |
Q26772111 | The exocyst in Candida albicans polarized secretion and filamentation |
Q34803211 | The exocyst is required for trypanosome invasion and the repair of mechanical plasma membrane wounds. |
Q36718374 | The interaction of IQGAP1 with the exocyst complex is required for tumor cell invasion downstream of Cdc42 and RhoA. |
Q37222227 | The known unknowns of antigen processing and presentation. |
Q28585208 | The neural cell adhesion molecule promotes FGFR-dependent phosphorylation and membrane targeting of the exocyst complex to induce exocytosis in growth cones |
Q34697563 | The role for the exocyst complex subunits Exo70B2 and Exo70H1 in the plant-pathogen interaction |
Q38702463 | The role of Exo70 in vascular smooth muscle cell migration |
Q37422550 | The role of the exocyst in matrix metalloproteinase secretion and actin dynamics during tumor cell invadopodia formation |
Q36992940 | The yeast LATS/Ndr kinase Cbk1 regulates growth via Golgi-dependent glycosylation and secretion |
Q24669945 | The yeast actin cytoskeleton: from cellular function to biochemical mechanism |
Q33346255 | Tip growth: signaling in the apical dome |
Q36628114 | Unilateral nephrectomy elongates primary cilia in the remaining kidney via reactive oxygen species. |
Q37460702 | par-1, atypical pkc, and PP2A/B55 sur-6 are implicated in the regulation of exocyst-mediated membrane trafficking in Caenorhabditis elegans |
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