scholarly article | Q13442814 |
P2093 | author name string | Jian Zhang | |
Wei Guo | |||
Xiaoyu Zhang | |||
Daniel TerBush | |||
Puyue Wang | |||
Patrick Brennwald | |||
Akanksha Gangar | |||
P2860 | cites work | Rho3 of Saccharomyces cerevisiae, which regulates the actin cytoskeleton and exocytosis, is a GTPase which interacts with Myo2 and Exo70 | Q24554501 |
The yeast par-1 homologs kin1 and kin2 show genetic and physical interactions with components of the exocytic machinery | Q24557447 | ||
The Rho GTPase Rho3 has a direct role in exocytosis that is distinct from its role in actin polarity | Q24647386 | ||
The critical role of Exo84p in the organization and polarized localization of the exocyst complex | Q27930273 | ||
Cdc42 interacts with the exocyst and regulates polarized secretion. | Q27931224 | ||
Sec3p is needed for the spatial regulation of secretion and for the inheritance of the cortical endoplasmic reticulum | Q27931819 | ||
The COOH-terminal domain of Myo2p, a yeast myosin V, has a direct role in secretory vesicle targeting | Q27932330 | ||
Exo84p is an exocyst protein essential for secretion | Q27932396 | ||
Sec3p is a spatial landmark for polarized secretion in budding yeast | Q27932756 | ||
Sec9 is a SNAP-25-like component of a yeast SNARE complex that may be the effector of Sec4 function in exocytosis | Q27933277 | ||
Polarized growth controls cell shape and bipolar bud site selection in Saccharomyces cerevisiae | Q27933604 | ||
The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis | Q27934654 | ||
Yeast homologues of tomosyn and lethal giant larvae function in exocytosis and are associated with the plasma membrane SNARE, Sec9 | Q27935690 | ||
Tropomyosin-containing actin cables direct the Myo2p-dependent polarized delivery of secretory vesicles in budding yeast | Q27935856 | ||
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 | ||
Functional specialization within a vesicle tethering complex: bypass of a subset of exocyst deletion mutants by Sec1p or Sec4p | Q27939279 | ||
Tomosyn interacts with the t-SNAREs syntaxin4 and SNAP23 and plays a role in insulin-stimulated GLUT4 translocation | Q28183008 | ||
Vesicle tethering complexes in membrane traffic | Q28206189 | ||
The exocyst complex in polarized exocytosis | Q28252102 | ||
Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells | Q28273946 | ||
Mammalian homolog of Drosophila tumor suppressor lethal (2) giant larvae interacts with basolateral exocytic machinery in Madin-Darby canine kidney cells | Q33953411 | ||
Establishing cell polarity in development | Q34522245 | ||
Exocytosis: the many masters of the exocyst | Q34574356 | ||
The secretory pathway mediates localization of the cell polarity regulator Aip3p/Bud6p | Q34685181 | ||
A lethal giant kinase in cell polarity. | Q35096233 | ||
Polarized epithelial membrane traffic: conservation and plasticity | Q35096249 | ||
Adaptation of core mechanisms to generate cell polarity | Q35109711 | ||
The role of Myo2, a yeast class V myosin, in vesicular transport | Q36235470 | ||
The AP-1A and AP-1B clathrin adaptor complexes define biochemically and functionally distinct membrane domains | Q36324568 | ||
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 | ||
Apical membrane aminopeptidase appears at site of cell-cell contact in cultured kidney epithelial cells | Q36398123 | ||
Sro7p, a Saccharomyces cerevisiae counterpart of the tumor suppressor l(2)gl protein, is related to myosins in function | Q38334814 | ||
Malignant Neoplasms of Genetic Origin in Drosophila melanogaster | Q39603384 | ||
The Par complex directs asymmetric cell division by phosphorylating the cytoskeletal protein Lgl. | Q40664929 | ||
Three-dimensional analysis of post-Golgi carrier exocytosis in epithelial cells | Q40675232 | ||
Role of cortical tumour-suppressor proteins in asymmetric division of Drosophila neuroblast | Q42497214 | ||
The tumour-suppressor genes lgl and dlg regulate basal protein targeting in Drosophila neuroblasts | Q42497218 | ||
The Saccharomyces cerevisiae SOP1 and SOP2 genes, which act in cation homeostasis, can be functionally substituted by the Drosophila lethal(2)giant larvae tumor suppressor gene | Q42687279 | ||
The Drosophila lethal(2)giant larvae tumor suppressor protein forms homo-oligomers and is associated with nonmuscle myosin II heavy chain | Q42771059 | ||
A polarity complex of mPar-6 and atypical PKC binds, phosphorylates and regulates mammalian Lgl. | Q44357555 | ||
Cooperative regulation of cell polarity and growth by Drosophila tumor suppressors | Q47070295 | ||
The tumor suppressor gene, lethal(2)giant larvae (1(2)g1), is required for cell shape change of epithelial cells during Drosophila development. | Q52548490 | ||
Interactions between the crumbs, lethal giant larvae and bazooka pathways in epithelial polarization. | Q52602094 | ||
Ras family therapy: Rab, Rho and Ral talk to the exocyst | Q74327244 | ||
P4510 | describes a project that uses | ImageQuant | Q112270642 |
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | exocytosis | Q323426 |
P304 | page(s) | 273-283 | |
P577 | publication date | 2005-07-01 | |
P1433 | published in | Journal of Cell Biology | Q1524550 |
P1476 | title | Lethal giant larvae proteins interact with the exocyst complex and are involved in polarized exocytosis | |
P478 | volume | 170 |