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ECB-ANAT-94

Papers associated with cortical granule

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Oocyte differentiation in the sea urchin, Arbacia punctulata, with particular reference to the origin of cortical granules and their participation in the cortical reaction., Anderson E., J Cell Biol. May 1, 1968; 37 (2): 514-39.


Elastic-mathematical theory of cells and mitochondria in swelling process. V. Transformation of cortical granule membrane of egg cell of Strongylocentrotus pupuratus in subelastic and elastic swelling., Mela MJ., Biochim Biophys Acta. June 11, 1968; 150 (4): 541-52.


A cytological study of the relation of the cortical reaction to subsequent events of fertilization in urethane-treated eggs of the sea urchin, Arbacia punctulata., Longo FJ., J Cell Biol. December 1, 1970; 47 (3): 646-65.


Agglutination of jelly coat and cortical granule components and the block to polyspermy in the amphibian Xenopus laevis., Wyrick RE., Proc Natl Acad Sci U S A. May 1, 1974; 71 (5): 2067-71.


Concanavalin A inhibits the dispersion of the cortical granule contents of sand dollar eggs., Vacquier VD., Exp Cell Res. February 1, 1975; 90 (2): 465-8.


Cytoplasmic activation of starfish oocytes by sperm and divalent ionophore A-23187., Schuetz AW., J Cell Biol. July 1, 1975; 66 (1): 86-94.


Cortical granule proteases from sea urchin eggs., Carroll EJ., Methods Enzymol. January 1, 1976; 45 343-53.


Fertilization acid of sea urchin eggs is not a consequence of cortical granule exocytosis., Paul M., J Exp Zool. July 1, 1976; 197 (1): 127-33.


Changes in the topography of the sea urchin egg after fertilization., Eddy EM., J Cell Biol. October 1, 1976; 71 (1): 35-48.


Sequential biochemical and morphological events during assembly of the fertilization membrane of the sea urchin., Veron M., Cell. February 1, 1977; 10 (2): 321-8.


Binding of concanavalin A to the surface of sea urchin eggs and its alteration upon fertilization., Veron M., J Biol Chem. February 25, 1977; 252 (4): 1286-92.


An ultrastructural study of cross-fertilization (Arbacia female x Mytilus male)., Longo FJ., J Cell Biol. April 1, 1977; 73 (1): 14-26.


Isolation and characterization of plasma membrane-associated cortical granules from sea urchin eggs., Detering NK., J Cell Biol. December 1, 1977; 75 (3): 899-914.


Hydrogen peroxide production, chemiluminescence, and the respiratory burst of fertilization: interrelated events in early sea urchin development., Foerder CA., Proc Natl Acad Sci U S A. July 1, 1978; 75 (7): 3183-7.


Prevention of the cortical reaction in fertilized sea urchin eggs by injection of calcium-chelating ligands., Zucker RS., Biochim Biophys Acta. July 17, 1978; 541 (4): 459-66.


Hardening of the sea urchin fertilization envelope by peroxidase-catalyzed phenolic coupling of tyrosines., Hall HG., Cell. October 1, 1978; 15 (2): 343-55.


The time course of cortical vesicle fusion in sea urchin eggs observed as membrane capacitance changes., Jaffe LA., Dev Biol. November 1, 1978; 67 (1): 243-8.


Electron microscopic study of the cortical reaction of an ophiuroid echinoderm., Holland ND., Tissue Cell. January 1, 1979; 11 (3): 445-55.


Membrane fusion during secretion: cortical granule exocytosis in sex urchin eggs as studied by quick-freezing and freeze-fracture., Chandler DE., J Cell Biol. October 1, 1979; 83 (1): 91-108.


Electron microscopic study of the cortical reaction in eggs of the starfish (Patria miniata)., Holland ND., Cell Tissue Res. January 1, 1980; 205 (1): 67-76.


Isolation and partial characterization of the plasma membrane of the sea urchin egg., Kinsey WH., J Cell Biol. October 1, 1980; 87 (1): 248-54.


Morphological features of the surface of the sea urchin (Arbacia punctulata) egg: oolemma-cortical granule association., Longo FJ., Dev Biol. May 1, 1981; 84 (1): 173-82.


The effect of local anesthetics and ammonia on cortical granule-plasma membrane attachment in the sea urchin egg., Hylander BL., Dev Biol. August 1, 1981; 86 (1): 1-11.


Sea urchin fertilization envelope: uncoupling of cortical granule exocytosis from envelope assembly and isolation of an envelope intermediate from Strongylocentrotus purpuratus embryos., Carroll EJ., Dev Biol. November 1, 1982; 94 (1): 252-8.


Sea urchin embryo fertilization envelope: immunological evidence that soluble envelope proteins are derived from cortical granule secretions., Villacorta-Moeller MN., Dev Biol. December 1, 1982; 94 (2): 415-24.


Release of granule contents from sea urchin egg cortices. New assay procedures and inhibition by sulfhydryl-modifying reagents., Haggerty JG., J Biol Chem. February 10, 1983; 258 (3): 1819-25.


Characterization of cortical secretory vesicles from the sea urchin egg., Decker SJ., Dev Biol. March 1, 1983; 96 (1): 37-45.


High hydrostatic pressure and the dissection of fertilization responses. I. The relationship between cortical granule exocytosis and proton efflux during fertilization of the sea urchin egg., Schmidt T., Exp Cell Res. July 1, 1983; 146 (2): 235-48.


Calcium-dependent exocytosis in an in vitro secretory granule plasma membrane preparation from sea urchin eggs and the effects of some inhibitors of cytoskeletal function., Whitaker MJ., Proc R Soc Lond B Biol Sci. July 22, 1983; 218 (1213): 397-413.


Monoclonal antibodies to the sea urchin egg vitelline layer inhibit fertilization by blocking sperm adhesion., Gache C., Exp Cell Res. August 1, 1983; 147 (1): 75-84.


Cortical vesicle exocytosis in isolated cortices of sea urchin eggs: description of a turbidometric assay and its utilization in studying effects of different media on discharge., Sasaki H., Dev Biol. August 1, 1983; 98 (2): 327-37.


Sea urchin egg cortical granule exocytosis is followed by a burst of membrane retrieval via uptake into coated vesicles., Fisher GW., Dev Biol. October 1, 1983; 99 (2): 456-72.


Filipin/sterol complexes in fertilized and unfertilized sea urchin egg membranes., Carron CP., Dev Biol. October 1, 1983; 99 (2): 482-8.


Induction of calcium-dependent, localized cortical granule breakdown in sea-urchin eggs by voltage pulsation., Rossignol DP., Biochim Biophys Acta. December 19, 1983; 763 (4): 346-55.


Modulation of calcium sensitivity by a specific cortical protein during sea urchin egg cortical vesicle exocytosis., Sasaki H., Dev Biol. January 1, 1984; 101 (1): 125-35.


Alteration of lipid organization following fertilization of sea urchin eggs., Freidus DJ., Biochim Biophys Acta. March 23, 1984; 803 (3): 191-6.


Purification and characterization of trypsin-like enzyme from sea urchin eggs: substrate specificity and physiological role., Sawada H., Biochem Biophys Res Commun. June 15, 1984; 121 (2): 598-604.


Fertilization increases the polyphosphoinositide content of sea urchin eggs., Turner PR., Nature. August 1, 1984; 310 (5976): 414-5.


Temporal sequence and spatial distribution of early events of fertilization in single sea urchin eggs., Eisen A., J Cell Biol. November 1, 1984; 99 (5): 1647-54.


Exocytosis in vitro: ultrastructure of the isolated sea urchin egg cortex as seen in platinum replicas., Chandler DE., J Ultrastruct Res. November 1, 1984; 89 (2): 198-211.


Purification and properties of ovoperoxidase, the enzyme responsible for hardening the fertilization membrane of the sea urchin egg., Deits T., J Biol Chem. November 10, 1984; 259 (21): 13525-33.


Comparison of quick-frozen and chemically fixed sea-urchin eggs: structural evidence that cortical granule exocytosis is preceded by a local increase in membrane mobility., Chandler DE., J Cell Sci. December 1, 1984; 72 23-36.


Inositol 1,4,5-triphosphate microinjection triggers activation, but not meiotic maturation in amphibian and starfish oocytes., Picard A., FEBS Lett. March 25, 1985; 182 (2): 446-50.


Cortical granule exocytosis in sea urchin eggs is inhibited by drugs that alter intracellular calcium stores., Stapleton CL., J Exp Zool. May 1, 1985; 234 (2): 289-99.


Irreversible swelling of secretory granules during exocytosis caused by calcium., Zimmerberg J., Nature. June 1, 1985; 315 (6020): 581-4.


Analysis of sea urchin egg cortical transformation in the absence of cortical granule exocytosis., Fisher GW., Dev Biol. June 1, 1985; 109 (2): 489-503.


Mild proteolytic digestion restores exocytotic activity to N-ethylmaleimide-inactivated cell surface complex from sea urchin eggs., Jackson RC., J Cell Biol. July 1, 1985; 101 (1): 6-11.


A marker of animal-vegetal polarity in the egg of the sea urchin Paracentrotus lividus. The pigment band., Sardet C., Exp Cell Res. September 1, 1985; 160 (1): 73-82.


Regulation of cortical vesicle exocytosis in sea urchin eggs by inositol 1,4,5-trisphosphate and GTP-binding protein., Turner PR., J Cell Biol. January 1, 1986; 102 (1): 70-6.


Structure, assembly and function of the surface envelope (fertilization envelope) from eggs of the sea urchin, Strongylocentrotus purpuratus., Carroll EJ., Adv Exp Med Biol. January 1, 1986; 207 261-91.

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