Role of actin cortex in the subplasmalemmal transport of secretory granules in PC-12 cells.

[1]  W. Almers,et al.  Endocytic vesicles move at the tips of actin tails in cultured mast cells , 1999, Nature Cell Biology.

[2]  W. Almers,et al.  Tracking single secretory granules in live chromaffin cells by evanescent-field fluorescence microscopy. , 1999, Biophysical journal.

[3]  M. Mooseker,et al.  Vesicle-associated brain myosin-V can be activated to catalyze actin-based transport. , 1998, Journal of cell science.

[4]  B. Imhof,et al.  Actin dynamics in living mammalian cells. , 1998, Journal of cell science.

[5]  Simon C Watkins,et al.  Neuronal Peptide Release Is Limited by Secretory Granule Mobility , 1997, Neuron.

[6]  W. Almers,et al.  Targeting of green fluorescent protein to neuroendocrine secretory granules: a new tool for real time studies of regulated protein secretion. , 1997, European journal of cell biology.

[7]  Guo-Qiang Bi,et al.  Kinesin- and Myosin-driven Steps of Vesicle Recruitment for Ca2+-regulated Exocytosis , 1997, The Journal of cell biology.

[8]  H. Horstmann,et al.  Transport, docking and exocytosis of single secretory granules in live chromaffin cells , 1997, Nature.

[9]  D. Terrian,et al.  Brain Myosin V Is a Synaptic Vesicle-associated Motor Protein: Evidence for a Ca2+-dependent Interaction with the Synaptobrevin–Synaptophysin Complex , 1997, The Journal of cell biology.

[10]  T. Yanagida,et al.  Single molecule imaging of fluorophores and enzymatic reactions achieved by objective-type total internal reflection fluorescence microscopy. , 1997, Biochemical and biophysical research communications.

[11]  Thorsten Lang,et al.  Ca2+-Triggered Peptide Secretion in Single Cells Imaged with Green Fluorescent Protein and Evanescent-Wave Microscopy , 1997, Neuron.

[12]  Navin Pokala,et al.  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 , 1997, The Journal of cell biology.

[13]  K. Nasmyth,et al.  Mother Cell–Specific HO Expression in Budding Yeast Depends on the Unconventional Myosin Myo4p and Other Cytoplasmic Proteins , 1996, Cell.

[14]  Clive R. Bagshaw,et al.  Measurement of nucleotide exchange kinetics with isolated synthetic myosin filaments using flash photolysis , 1996, FEBS letters.

[15]  T. Mitchison,et al.  Actin-Based Cell Motility and Cell Locomotion , 1996, Cell.

[16]  H. Horstmann,et al.  Docked granules, the exocytic burst, and the need for ATP hydrolysis in endocrine cells , 1995, Neuron.

[17]  T. Mitchison,et al.  Myosin is involved in postmitotic cell spreading , 1995, The Journal of cell biology.

[18]  S. Muallem,et al.  Actin filament disassembly is a sufficient final trigger for exocytosis in nonexcitable cells , 1995, The Journal of cell biology.

[19]  M. L Vitale,et al.  Chromaffin cell cortical actin network dynamics control the size of the release-ready vesicle pool and the initial rate of exocytosis , 1995, Neuron.

[20]  M. Vitale,et al.  Cytoskeleton dynamics during neurotransmitter release , 1993, Trends in Neurosciences.

[21]  A. Kusumi,et al.  Confined lateral diffusion of membrane receptors as studied by single particle tracking (nanovid microscopy). Effects of calcium-induced differentiation in cultured epithelial cells. , 1993, Biophysical journal.

[22]  Trifaró Jm,et al.  Cytoskeleton dynamics during neurotransmitter release , 1993 .

[23]  T. Stossel On the crawling of animal cells. , 1993, Science.

[24]  D. Burgess,et al.  Golgi-derived vesicles from developing epithelial cells bind actin filaments and possess myosin-I as a cytoplasmically oriented peripheral membrane protein , 1993, The Journal of cell biology.

[25]  N. Hirokawa,et al.  Organization of cortical cytoskeleton of cultured chromaffin cells and involvement in secretion as revealed by quick-freeze, deep-etching, and double-label immunoelectron microscopy , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  Julie A. Theriot,et al.  The rate of actin-based motility of intracellular Listeria monocytogenes equals the rate of actin polymerization , 1992, Nature.

[27]  Joseph A. O'Sullivan,et al.  Deblurring subject to nonnegativity constraints , 1992, IEEE Trans. Signal Process..

[28]  J. Tooze,et al.  Characterization of the immature secretory granule, an intermediate in granule biogenesis , 1991, The Journal of cell biology.

[29]  H. Qian,et al.  Single particle tracking. Analysis of diffusion and flow in two-dimensional systems. , 1991, Biophysical journal.

[30]  M. Vitale,et al.  Cortical filamentous actin disassembly and scinderin redistribution during chromaffin cell stimulation precede exocytosis, a phenomenon not exhibited by gelsolin , 1991, The Journal of cell biology.

[31]  T. Pollard,et al.  Effects of cytochalasin, phalloidin, and pH on the elongation of actin filaments. , 1991, Biochemistry.

[32]  D. Axelrod,et al.  Evanescent field excitation of fluorescence by epi-illumination microscopy. , 1989, Applied optics.

[33]  D. Eberhard,et al.  MgATP-independent and MgATP-dependent exocytosis. Evidence that MgATP primes adrenal chromaffin cells to undergo exocytosis. , 1989, The Journal of biological chemistry.

[34]  K. Morita,et al.  Effects of cytoskeleton-disrupting drugs on ouabain-stimulated catecholamine secretion from cultured adrenal chromaffin cells. , 1988, Biochemical pharmacology.

[35]  D. Aunis,et al.  Peripheral actin filaments control calcium-mediated catecholamine release from streptolysin-O-permeabilized chromaffin cells. , 1988, European journal of cell biology.

[36]  D. Taylor,et al.  Hindered diffusion of inert tracer particles in the cytoplasm of mouse 3T3 cells. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[37]  R. Burgoyne,et al.  Nicotine‐evoked disassembly of cortical actin filaments in adrenal chromaffin cells , 1986, FEBS letters.

[38]  G. Schatten,et al.  Latrunculin inhibits the microfilament-mediated processes during fertilization, cleavage and early development in sea urchins and mice. , 1986, Experimental cell research.

[39]  J. Vandekerckhove,et al.  The phalloidin binding site of F‐actin. , 1985, The EMBO journal.

[40]  L. M. Coluccio,et al.  Phalloidin enhances actin assembly by preventing monomer dissociation , 1984, The Journal of cell biology.

[41]  H. Thoenen,et al.  Relationship between NGF-mediated volume increase and "priming effect" in fast and slow reacting clones of PC12 pheochromocytoma cells. Role of cAMP. , 1983, Experimental cell research.

[42]  I. Spector,et al.  Latrunculins: novel marine toxins that disrupt microfilament organization in cultured cells. , 1983, Science.

[43]  J. Small Organization of actin in the leading edge of cultured cells: influence of osmium tetroxide and dehydration on the ultrastructure of actin meshworks , 1981, The Journal of cell biology.

[44]  J. E. Estes,et al.  Mechanism of action of phalloidin on the polymerization of muscle actin. , 1981, Biochemistry.

[45]  D. Loerke,et al.  The last few milliseconds in the life of a secretory granule , 1998, European Biophysics Journal.

[46]  M. Krendel,et al.  Disassembly of actin filaments leads to increased rate and frequency of mitochondrial movement along microtubules. , 1998, Cell motility and the cytoskeleton.

[47]  P. Forsgren,et al.  Confocal microscopy: important considerations for accurate imaging. , 1993, Methods in cell biology.

[48]  Per-Ola Forsgren,et al.  Chapter 3 Confocal Microscopy: Important Considerations for Accurate Imaging , 1993 .