| P2093 | author name string | Gero Steinberg | |
| P2860 | cites work | Myosin-V is a processive actin-based motor | Q22003739 |
| | Myosin VI is an actin-based motor that moves backwards | Q22010643 |
| | Bni1p, a yeast formin linking cdc42p and the actin cytoskeleton during polarized morphogenesis | Q24310527 |
| | Animals and fungi are each other's closest relatives: congruent evidence from multiple proteins | Q24563729 |
| | EB1 proteins regulate microtubule dynamics, cell polarity, and chromosome stability | Q24670199 |
| | Cellular motility driven by assembly and disassembly of actin filaments | Q27860676 |
| | Rho1p-Bni1p-Spa2p interactions: implication in localization of Bni1p at the bud site and regulation of the actin cytoskeleton in Saccharomyces cerevisiae | Q27931452 |
| | Lipid rafts function in biosynthetic delivery of proteins to the cell surface in yeast | Q27932650 |
| | The Saccharomyces cerevisiae MYO2 gene encodes an essential myosin for vectorial transport of vesicles | Q27932839 |
| | Role of formins in actin assembly: nucleation and barbed-end association | Q27934072 |
| | Role of type I myosins in receptor-mediated endocytosis in yeast | Q27934380 |
| | Cell surface polarization during yeast mating | Q27934709 |
| | The yeast class V myosins, Myo2p and Myo4p, are nonprocessive actin-based motors | Q27935400 |
| | MSS4, a phosphatidylinositol-4-phosphate 5-kinase required for organization of the actin cytoskeleton in Saccharomyces cerevisiae. | Q27939032 |
| | A new vital stain for visualizing vacuolar membrane dynamics and endocytosis in yeast | Q28131611 |
| | The dynamic behavior of the APC-binding protein EB1 on the distal ends of microtubules | Q28140999 |
| | The molecular motor toolbox for intracellular transport | Q28211349 |
| | Cell wall deficiency in "slime" strains of Neurospora crassa: osmotic inhibition of cell wall synthesis and beta-D-glucan synthase activity | Q71720391 |
| | Fungal Morphogenesis: Cell Wall Construction in Mucor rouxii | Q72395535 |
| | Organelle movements in the wild type and wall-less fz;sg;os-1 mutants of Neurospora crassa are mediated by cytoplasmic microtubules | Q72711434 |
| | A kinesin-like mechanoenzyme from the zygomycete Syncephalastrum racemosum shares biochemical similarities with conventional kinesin from Neurospora crassa | Q73478366 |
| | Endocytosis and membrane turnover in the germ tube of uromyces fabae | Q77315436 |
| | MYO2 is not essential for viability, but is required for polarized growth and dimorphic switches in Candida albicans | Q44313140 |
| | Slow diffusion of proteins in the yeast plasma membrane allows polarity to be maintained by endocytic cycling | Q44587849 |
| | Disturbance of sphingolipid biosynthesis abrogates the signaling of Mss4, phosphatidylinositol-4-phosphate 5-kinase, in yeast | Q45291359 |
| | Cytoplasmic contractions in growing fungal hyphae and their morphogenetic consequences. | Q46561792 |
| | The kinesin Klp2 mediates polarization of interphase microtubules in fission yeast | Q46588800 |
| | Role of fission yeast myosin I in organization of sterol-rich membrane domains | Q46623979 |
| | Yeast lipid rafts?--an emerging view | Q46842383 |
| | Cloning and functional expression of a 'fast' fungal kinesin | Q48012235 |
| | Constitutive activation of endocytosis by mutation of myoA, the myosin I gene of Aspergillus nidulans | Q48034331 |
| | Endocytosis is essential for pathogenic development in the corn smut fungus Ustilago maydis | Q48086500 |
| | A Class-V Myosin Required for Mating, Hyphal Growth, and Pathogenicity in the Dimorphic Plant PathogenUstilago maydis [W] | Q48220397 |
| | Two type V myosins with non-overlapping functions in the fission yeast Schizosaccharomyces pombe: Myo52 is concerned with growth polarity and cytokinesis, Myo51 is a component of the cytokinetic actin ring | Q50106639 |
| | A critical role for the type V myosin, Myo52, in septum deposition and cell fission during cytokinesis in Schizosaccharomyces pombe. | Q53640078 |
| | Candida albicans hyphae have a Spitzenkörper that is distinct from the polarisome found in yeast and pseudohyphae. | Q53669257 |
| | Hyphal tips of wild-type and spreading colonial mutants of Neurospora crassa. | Q54655766 |
| | The RNA-binding protein Rrm4 is essential for polarity in Ustilago maydis and shuttles along microtubules | Q57683047 |
| | Preparing the way: fungal motors in microtubule organization | Q57942121 |
| | Confocal microscopy of FM4-64 as a tool for analysing endocytosis and vesicle trafficking in living fungal hyphae | Q58487399 |
| | Filipin as a fluorescent probe for the location of cholesterol in the membranes of fragmented sarcoplasmic reticulum | Q68503391 |
| | Ultrastructural analysis of hyphal tip cell growth in fungi: Spitzenkörper, cytoskeleton and endomembranes after freeze-substitution | Q70667560 |
| | Microtubule polymerization dynamics | Q28259930 |
| | Model systems, lipid rafts, and cell membranes | Q28261365 |
| | Polarisome meets spitzenkörper: microscopy, genetics, and genomics converge | Q28306629 |
| | Nonfilamentous C. albicans mutants are avirulent | Q29617839 |
| | Morphogenesis in the yeast cell cycle: regulation by Cdc28 and cyclins | Q29620238 |
| | Harnessing actin dynamics for clathrin-mediated endocytosis | Q29620544 |
| | Functional characterization of myosin I tail regions in Candida albicans | Q30163789 |
| | An intact SH3 domain is required for myosin I-induced actin polymerization. | Q30168825 |
| | Localization of wild type and mutant class I myosin proteins in Aspergillus nidulans using GFP-fusion proteins | Q30175256 |
| | Structural requirements for in vivo myosin I function in Aspergillus nidulans | Q30176036 |
| | The UNC-104/KIF1 family of kinesins | Q30306751 |
| | A dynein loading zone for retrograde endosome motility at microtubule plus-ends | Q30477422 |
| | Dynein-dependent motility of microtubules and nucleation sites supports polarization of the tubulin array in the fungus Ustilago maydis | Q30477466 |
| | Microtubule organization requires cell cycle-dependent nucleation at dispersed cytoplasmic sites: polar and perinuclear microtubule organizing centers in the plant pathogen Ustilago maydis | Q30477560 |
| | Maximal polar growth potential depends on the polarisome component AgSpa2 in the filamentous fungus Ashbya gossypii | Q30480607 |
| | Role of Unc104/KIF1-related motor proteins in mitochondrial transport in Neurospora crassa | Q30845378 |
| | The role of microtubules in rapid hyphal tip growth of Aspergillus nidulans | Q30854680 |
| | Functional characterization and localization of the Aspergillus nidulans formin SEPA | Q30857097 |
| | Dynein supports motility of endoplasmic reticulum in the fungus Ustilago maydis | Q30857136 |
| | Fungal morphogenesis and virulence | Q32004798 |
| | Kinesin and dynein superfamily proteins in organelle transport and cell division. | Q32107692 |
| | Protoplasmic organization of hyphal tips among fungi: vesicles and Spitzenkörper | Q33774207 |
| | Mechanisms of hyphal tip growth: tube dwelling amebae revisited | Q33787852 |
| | Kinesin is essential for cell morphogenesis and polarized secretion in Neurospora crassa | Q33886733 |
| | Myosin I is required for hypha formation in Candida albicans | Q33904587 |
| | A myosin family tree. | Q33917616 |
| | Myosin I mutants with only 1% of wild-type actin-activated MgATPase activity retain essential in vivo function(s) | Q33929915 |
| | The cytoskeleton in plant and fungal cell tip growth | Q33940456 |
| | Lipid rafts and membrane dynamics | Q33985713 |
| | Molecular requirements for the internalisation step of endocytosis: insights from yeast | Q34201680 |
| | Lipid raft polarization contributes to hyphal growth in Candida albicans | Q34361022 |
| | Monophyletic origins of the metazoa: an evolutionary link with fungi | Q34363076 |
| | The molecular biology of appressorium turgor generation by the rice blast fungus Magnaporthe grisea | Q34405853 |
| | The Neurospora organelle motor: a distant relative of conventional kinesin with unconventional properties | Q34453294 |
| | Force and compliance: rethinking morphogenesis in walled cells | Q34996839 |
| | A complete inventory of fungal kinesins in representative filamentous ascomycetes | Q35125571 |
| | Yeast-to-hyphal transition triggers formin-dependent Golgi localization to the growing tip in Candida albicans | Q35128293 |
| | Taking the A-train: actin-based force generators and organelle targeting | Q35208574 |
| | Seeing is believing: imaging actin dynamics at single sites of endocytosis. | Q35832636 |
| | Mechanisms of polarized growth and organelle segregation in yeast | Q35912839 |
| | Where sterols are required for endocytosis | Q35935378 |
| | Spoilage of vegetable crops by bacteria and fungi and related health hazards | Q36102153 |
| | Cytoplasmic microtubules and fungal morphogenesis: ultrastructural effects of methyl benzimidazole-2-ylcarbamate determined by freeze-substitution of hyphal tip cells | Q36201758 |
| | Cytoplasmic dynein and actin-related protein Arp1 are required for normal nuclear distribution in filamentous fungi | Q36234661 |
| | The role of Myo2, a yeast class V myosin, in vesicular transport | Q36235470 |
| | Identification of two type V myosins in fission yeast, one of which functions in polarized cell growth and moves rapidly in the cell | Q36281735 |
| | Fission yeast myosin-I, Myo1p, stimulates actin assembly by Arp2/3 complex and shares functions with WASp | Q36316569 |
| | Secretory vesicle transport velocity in living cells depends on the myosin-V lever arm length | Q36324635 |
| | Molecular details of formin-mediated actin assembly | Q36346689 |
| | myoA of Aspergillus nidulans encodes an essential myosin I required for secretion and polarized growth | Q36382420 |
| | Analysis of the role of the Spitzenkörper in fungal morphogenesis by computer simulation of apical branching in Aspergillus niger. | Q36550918 |
| | Evidence that Spitzenkörper behavior determines the shape of a fungal hypha: a test of the hyphoid model | Q36687691 |
| | A fungal kinesin required for organelle motility, hyphal growth, and morphogenesis | Q36848846 |
| | Specific sterols required for the internalization step of endocytosis in yeast | Q36940667 |
| | Extension growth of the water mold Achlya: interplay of turgor and wall strength | Q36999200 |
| | PAK kinases Ste20 and Pak1 govern cell polarity at different stages of mating in Cryptococcus neoformans | Q37537946 |
| | The STE20/germinal center kinase POD6 interacts with the NDR kinase COT1 and is involved in polar tip extension in Neurospora crassa | Q38420200 |
| | Cell cycle progression and cell polarity require sphingolipid biosynthesis in Aspergillus nidulans | Q39460989 |
| | A balance of KIF1A-like kinesin and dynein organizes early endosomes in the fungus Ustilago maydis | Q39647423 |
| | Plasma membrane polarization during mating in yeast cells | Q39730581 |
| | The phosphoinositol sphingolipids of Saccharomyces cerevisiae are highly localized in the plasma membrane | Q39941568 |
| | Autoradiographic Study of Mannan Incorporation into the Growing Cell Walls of Saccharomyces cerevisiae | Q40094293 |
| | A putative endosomal t-SNARE links exo- and endocytosis in the phytopathogenic fungus Ustilago maydis | Q40387504 |
| | Protein secretion in filamentous fungi--trying to understand a highly productive black box. | Q40534258 |
| | Apical branching in a temperature sensitive mutant of Aspergillus niger. | Q40860000 |
| | Role for RNA-binding proteins implicated in pathogenic development of Ustilago maydis | Q40895371 |
| | The role of the kinesin motor KipA in microtubule organization and polarized growth of Aspergillus nidulans | Q40952367 |
| | Hyphal tip cell ultrastructure of the fungus Fusarium: Improved preservation by freeze-substitution | Q41037039 |
| | Lipid raft-based membrane compartmentation of a plant transport protein expressed in Saccharomyces cerevisiae | Q41488116 |
| | Dynein and dynactin deficiencies affect the formation and function of the Spitzenkörper and distort hyphal morphogenesis of Neurospora crassa | Q41744827 |
| | Microtubules are dispensable for the initial pathogenic development but required for long-distance hyphal growth in the corn smut fungus Ustilago maydis | Q41950056 |
| | Distinct ceramide synthases regulate polarized growth in the filamentous fungus Aspergillus nidulans | Q41952166 |
| | Identification of a motor protein required for filamentous growth in Ustilago maydis | Q42152048 |
| | Kinesin from the plant pathogenic fungus Ustilago maydis is involved in vacuole formation and cytoplasmic migration | Q42458156 |
| | The role of the cytoskeleton in the polarized growth of the germ tube in Candida albicans | Q42500799 |
| | Myosin-V, Kinesin-1, and Kinesin-3 cooperate in hyphal growth of the fungus Ustilago maydis | Q42590891 |
| | Identification of genes in the bW/bE regulatory cascade in Ustilago maydis | Q43818289 |
| | Sterol-rich plasma membrane domains in the fission yeast Schizosaccharomyces pombe | Q44180322 |
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | lipid | Q11367 |
| P304 | page(s) | 351-360 | |
| P577 | publication date | 2007-01-26 | |
| P1433 | published in | Eukaryotic Cell | Q5408685 |
| P1476 | title | Hyphal growth: a tale of motors, lipids, and the Spitzenkörper. | |
| P478 | volume | 6 | |