| scholarly article | Q13442814 |
| P2093 | author name string | H Jin | |
| D C Amberg | |||
| P2860 | cites work | Bni1p, a yeast formin linking cdc42p and the actin cytoskeleton during polarized morphogenesis | Q24310527 |
| A novel Rab9 effector required for endosome-to-TGN transport | Q24318528 | ||
| Additional modules for versatile and economical PCR-based gene deletion and modification in Saccharomyces cerevisiae | Q27861085 | ||
| The Spa2-related protein, Sph1p, is important for polarized growth in yeast | Q27929770 | ||
| High rates of actin filament turnover in budding yeast and roles for actin in establishment and maintenance of cell polarity revealed using the actin inhibitor latrunculin-A. | Q27929925 | ||
| The unconventional myosin, Myo2p, is a calmodulin target at sites of cell growth in Saccharomyces cerevisiae | Q27930656 | ||
| Genetic analysis of the bipolar pattern of bud site selection in the yeast Saccharomyces cerevisiae | Q27930775 | ||
| Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway | Q27931724 | ||
| Sec3p is a spatial landmark for polarized secretion in budding yeast | Q27932756 | ||
| Order of events in the yeast secretory pathway | Q27932822 | ||
| The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles | Q27932839 | ||
| Sec9 is a SNAP-25-like component of a yeast SNARE complex that may be the effector of Sec4 function in exocytosis | Q27933277 | ||
| Immunofluorescence localization of the unconventional myosin, Myo2p, and the putative kinesin-related protein, Smy1p, to the same regions of polarized growth in Saccharomyces cerevisiae | Q27935608 | ||
| Sec8p and Sec15p are components of a plasma membrane-associated 19.5S particle that may function downstream of Sec4p to control exocytosis | Q27935760 | ||
| Tropomyosin-containing actin cables direct the Myo2p-dependent polarized delivery of secretory vesicles in budding yeast | Q27935856 | ||
| Homologs of the synaptobrevin/VAMP family of synaptic vesicle proteins function on the late secretory pathway in S. cerevisiae. | Q27936151 | ||
| Diverse essential functions revealed by complementing yeast calmodulin mutants | Q27936537 | ||
| Sec6, Sec8, and Sec15 are components of a multisubunit complex which localizes to small bud tips in Saccharomyces cerevisiae | Q27936607 | ||
| Ultrastructure of the yeast actin cytoskeleton and its association with the plasma membrane | Q27937819 | ||
| Aip3p/Bud6p, a yeast actin-interacting protein that is involved in morphogenesis and the selection of bipolar budding sites | Q27937964 | ||
| Binding and hydrolysis of guanine nucleotides by Sec4p, a yeast protein involved in the regulation of vesicular traffic. | Q27939531 | ||
| The small GTP-binding protein Rho1p is localized on the Golgi apparatus and post-Golgi vesicles in Saccharomyces cerevisiae | Q27939950 | ||
| Origins of cell polarity | Q29616587 | ||
| Vectors for the inducible overexpression of glutathione S-transferase fusion proteins in yeast | Q29618547 | ||
| A GTP-binding protein required for secretion rapidly associates with secretory vesicles and the plasma membrane in yeast | Q29620584 | ||
| Multiple functions for actin during filamentous growth of Saccharomyces cerevisiae | Q30483614 | ||
| Three-dimensional imaging of the yeast actin cytoskeleton through the budding cell cycle | Q30483921 | ||
| SEC3 mutations are synthetically lethal with profilin mutations and cause defects in diploid-specific bud-site selection | Q33968483 | ||
| PEP4 gene of Saccharomyces cerevisiae encodes proteinase A, a vacuolar enzyme required for processing of vacuolar precursors | Q34162725 | ||
| Purification and characterization of constitutive secretory vesicles from yeast | Q36217910 | ||
| The role of Myo2, a yeast class V myosin, in vesicular transport | Q36235470 | ||
| LST1 is a SEC24 homologue used for selective export of the plasma membrane ATPase from the endoplasmic reticulum | Q36256601 | ||
| The PEP4 gene encodes an aspartyl protease implicated in the posttranslational regulation of Saccharomyces cerevisiae vacuolar hydrolases | Q36463508 | ||
| The terminal tail region of a yeast myosin-V mediates its attachment to vacuole membranes and sites of polarized growth | Q36754969 | ||
| Yeast actin cytoskeleton mutants accumulate a new class of Golgi-derived secretary vesicle | Q37386905 | ||
| Movement of yeast cortical actin cytoskeleton visualized in vivo | Q37622707 | ||
| Bipartite structure of the ade3 locus of Saccharomyces cerevisiae | Q40772733 | ||
| The cycle of SEC4 function in vesicular transport | Q40810288 | ||
| Establishment of cell polarity in yeast. | Q41125267 | ||
| Precise gene disruption in Saccharomyces cerevisiae by double fusion polymerase chain reaction | Q42625677 | ||
| Structure-based systematic isolation of conditional-lethal mutations in the single yeast calmodulin gene. | Q42965170 | ||
| Interactions of three domains distinguishing the Ras-related GTP-binding proteins Ypt1 and Sec4. | Q54310462 | ||
| P4510 | describes a project that uses | ImageQuant | Q112270642 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 647-661 | |
| P577 | publication date | 2000-02-01 | |
| P1433 | published in | Molecular Biology of the Cell | Q2338259 |
| P1476 | title | The secretory pathway mediates localization of the cell polarity regulator Aip3p/Bud6p | |
| P478 | volume | 11 |
| Q28472248 | A biochemical genomics screen for substrates of Ste20p kinase enables the in silico prediction of novel substrates |
| Q33565316 | A sphingolipid-dependent diffusion barrier confines ER stress to the yeast mother cell |
| Q27932526 | Actin recovery and bud emergence in osmotically stressed cells requires the conserved actin interacting mitogen-activated protein kinase kinase kinase Ssk2p/MTK1 and the scaffold protein Spa2p |
| Q27930218 | Actin-mediated delivery of astral microtubules instructs Kar9p asymmetric loading to the bud-ward spindle pole. |
| Q33636115 | Array comparative genomic hybridization analysis of Trichoderma reesei strains with enhanced cellulase production properties |
| Q27938337 | Cdc50p, a conserved endosomal membrane protein, controls polarized growth in Saccharomyces cerevisiae |
| Q27935929 | Cdc50p, a protein required for polarized growth, associates with the Drs2p P-type ATPase implicated in phospholipid translocation in Saccharomyces cerevisiae |
| Q34049702 | Cell polarity protein Spa2P associates with proteins involved in actin function in Saccharomyces cerevisiae |
| Q34343368 | Cell polarity: a tale of two Ts. |
| Q30557768 | Cell-cycle regulation of formin-mediated actin cable assembly |
| Q33914537 | Cyclical regulation of the exocyst and cell polarity determinants for polarized cell growth |
| Q27937400 | Differential activities and regulation of Saccharomyces cerevisiae formin proteins Bni1 and Bnr1 by Bud6. |
| Q30477608 | Dynamic positioning of mitotic spindles in yeast: role of microtubule motors and cortical determinants |
| Q36279745 | Fission yeast Aip3p (spAip3p) is required for an alternative actin-directed polarity program |
| Q34718516 | Functional characterization of Aspergillus nidulans homologues of Saccharomyces cerevisiae Spa2 and Bud6. |
| Q33965134 | Gic2p may link activated Cdc42p to components involved in actin polarization, including Bni1p and Bud6p (Aip3p). |
| Q90746482 | Integrated control of formin-mediated actin assembly by a stationary inhibitor and a mobile activator |
| Q73897163 | It's a kar9ochore to capture microtubules |
| Q36320849 | Lethal giant larvae proteins interact with the exocyst complex and are involved in polarized exocytosis |
| Q27938894 | Ligand-induced activation of a formin-NPF pair leads to collaborative actin nucleation |
| Q35474950 | Mechanism and cellular function of Bud6 as an actin nucleation-promoting factor. |
| Q27935161 | Mlc1p promotes septum closure during cytokinesis via the IQ motifs of the vesicle motor Myo2p |
| Q35605736 | Polarized distribution of intracellular components by class V myosins in Saccharomyces cerevisiae |
| Q37066693 | Ras regulates the polarity of the yeast actin cytoskeleton through the stress response pathway |
| Q36322447 | Regulation of a formin complex by the microtubule plus end protein tea1p |
| Q52962426 | Role of bud6p and tea1p in the interaction between actin and microtubules for the establishment of cell polarity in fission yeast. |
| Q30513976 | Secretory pathway-dependent localization of the Saccharomyces cerevisiae Rho GTPase-activating protein Rgd1p at growth sites |
| Q36321221 | Septin-dependent compartmentalization of the endoplasmic reticulum during yeast polarized growth |
| Q27935764 | Stable and dynamic axes of polarity use distinct formin isoforms in budding yeast |
| Q27929827 | Stable preanaphase spindle positioning requires Bud6p and an apparent interaction between the spindle pole bodies and the neck |
| Q27675162 | Structure of the formin-interaction domain of the actin nucleation-promoting factor Bud6 |
| Q27939278 | The GAP activity of Msb3p and Msb4p for the Rab GTPase Sec4p is required for efficient exocytosis and actin organization |
| Q27934723 | The PXL1 gene of Saccharomyces cerevisiae encodes a paxillin-like protein functioning in polarized cell growth |
| Q58486711 | The role of the proteins Kar9 and Myo2 in orienting the mitotic spindle of budding yeast |
| Q92294756 | YFR016c/Aip5 is part of an actin nucleation complex in yeast |
| Q30479323 | Yeast formins Bni1 and Bnr1 utilize different modes of cortical interaction during the assembly of actin cables |
| Q35096252 | Yeasts make their mark |
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