Papers associated with cell cortex

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	Evolutionary modification of AGS protein contributes to formation of micromeres in sea urchins., Poon J., Nat Commun. August 22, 2019; 10 (1): 3779.
	Asymmetric division through a reduction of microtubule centering forces., Sallé J., J Cell Biol. March 4, 2019; 218 (3): 771-782.
	Resistance is futile: Centering forces yield for asymmetric cell division., Alper J., J Cell Biol. March 4, 2019; 218 (3): 727-728.
	Meis transcription factor maintains the neurogenic ectoderm and regulates the anterior-posterior patterning in embryos of a sea urchin, Hemicentrotus pulcherrimus., Yaguchi J., Dev Biol. December 1, 2018; 444 (1): 1-8.
	Centralspindlin in Rappaport''s cleavage signaling., Mishima M., Semin Cell Dev Biol. May 1, 2016; 53 45-56.
	Activator-inhibitor coupling between Rho signalling and actin assembly makes the cell cortex an excitable medium., Bement WM., Nat Cell Biol. November 1, 2015; 17 (11): 1471-83.
	Development and juvenile anatomy of the nemertodermatid Meara stichopi (Bock) Westblad 1949 (Acoelomorpha)., Børve A., Front Zool. May 9, 2014; 11 50.
	Differential regulation of disheveled in a novel vegetal cortical domain in sea urchin eggs and embryos: implications for the localized activation of canonical Wnt signaling., Peng CJ., PLoS One. January 1, 2013; 8 (11): e80693.
	The effect of taxol microinjection on the microtubular structure in polar body formation of starfish oocytes., Kikuchi Y., Cytoskeleton (Hoboken). February 1, 2012; 69 (2): 125-32.
	Wnt6 activates endoderm in the sea urchin gene regulatory network., Croce J., Development. August 1, 2011; 138 (15): 3297-306.
	Intracellular transport by an anchored homogeneously contracting F-actin meshwork., Mori M., Curr Biol. April 12, 2011; 21 (7): 606-11.
	Concordance and interaction of guanine nucleotide dissociation inhibitor (RhoGDI) with RhoA in oogenesis and early development of the sea urchin., Zazueta-Novoa V., Dev Growth Differ. April 1, 2011; 53 (3): 427-39.
	Stable and dynamic microtubules coordinately shape the myosin activation zone during cytokinetic furrow formation., Foe VE., J Cell Biol. November 3, 2008; 183 (3): 457-70.
	An agent-based model contrasts opposite effects of dynamic and stable microtubules on cleavage furrow positioning., Odell GM., J Cell Biol. November 3, 2008; 183 (3): 471-83.
	Actin cytoskeleton modulates calcium signaling during maturation of starfish oocytes., Kyozuka K., Dev Biol. August 15, 2008; 320 (2): 426-35.
	Cortical Isolation from Xenopus laevis Oocytes and Eggs., Sive HL., CSH Protoc. June 1, 2007; 2007 pdb.prot4753.
	Activator of G-protein signaling in asymmetric cell divisions of the sea urchin embryo., Voronina E., Dev Growth Differ. December 1, 2006; 48 (9): 549-57.
	The emergence of pattern in embryogenesis: regulation of beta-catenin localization during early sea urchin development., Ettensohn CA., Sci STKE. November 14, 2006; 2006 (361): pe48.
	Temporal change in local forces and total force all over the surface of the sea urchin egg during cytokinesis., Miyoshi H., Cell Motil Cytoskeleton. April 1, 2006; 63 (4): 208-21.
	Interaction between EB1 and p150glued is required for anaphase astral microtubule elongation and stimulation of cytokinesis., Strickland LI., Curr Biol. December 20, 2005; 15 (24): 2249-55.
	Differential stability of beta-catenin along the animal-vegetal axis of the sea urchin embryo mediated by dishevelled., Weitzel HE., Development. June 1, 2004; 131 (12): 2947-56.
	Transitions regulating the timing of cytokinesis in embryonic cells., Shuster CB., Curr Biol. May 14, 2002; 12 (10): 854-8.
	Repairing a torn cell surface: make way, lysosomes to the rescue., McNeil PL., J Cell Sci. March 1, 2002; 115 (Pt 5): 873-9.
	A rab3 homolog in sea urchin functions in cell division., Conner SD., FASEB J. August 1, 2000; 14 (11): 1559-66.
	Syntaxin is required for cell division., Conner SD., Mol Biol Cell. August 1, 1999; 10 (8): 2735-43.
	Identification and characterization of a constitutive HSP75 in sea urchin embryos., Sconzo G., Biochem Biophys Res Commun. May 8, 1997; 234 (1): 24-9.
	Cleavage furrow: timing of emergence of contractile ring actin filaments and establishment of the contractile ring by filament bundling in sea urchin eggs., Mabuchi I., J Cell Sci. July 1, 1994; 107 ( Pt 7) 1853-62.
	Selective inhibition of cytokinesis in sea urchin embryos by the marine natural product pseudopterolide., Grace KJ., Mol Pharmacol. April 1, 1992; 41 (4): 631-8.
	Nuclear migration and spindle formation in the fourth cleavage of sea urchin eggs under the influence of inhibitors., Czihak G., Cell Struct Funct. April 1, 1992; 17 (2): 145-50.
	Evidence for the involvement of microtubules, ER, and kinesin in the cortical rotation of fertilized frog eggs., Houliston E., J Cell Biol. September 1, 1991; 114 (5): 1017-28.
	Differential behavior of centrosomes in unequally dividing blastomeres during fourth cleavage of sea urchin embryos., Holy J., J Cell Sci. March 1, 1991; 98 ( Pt 3) 423-31.
	Deformation analyses in cell and developmental biology. Part II--Mechanical experiments on cells., Cheng LY., J Biomech Eng. February 1, 1987; 109 (1): 18-24.
	Alpha-actinin from sea urchin eggs: biochemical properties, interaction with actin, and distribution in the cell during fertilization and cleavage., Mabuchi I., J Cell Biol. February 1, 1985; 100 (2): 375-83.

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