Papers associated with vitelline membrane

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	[Characterization of vitelline membrane DNA of Xenopus laevis oocytes]., Hanocq-Quertier J., Arch Int Physiol Biochim. December 1, 1970; 78 (5): 998-1000.
	A freeze-fracture and concanavalin A-binding study of the membrane of cleaving Xenopus embryos., Sanders EJ., Differentiation. November 2, 1976; 7 (1): 13-21.
	Steroid and peptide control mechanisms in membrane of Xenopus laevis oocytes resuming meiotic division., Baulieu EE., Ciba Found Symp. January 1, 1983; 98 137-58.
	Steroidal and peptidic control mechanisms in membrane of Xenopus laevis oocytes resuming meiotic division., Baulieu EE., J Steroid Biochem. July 1, 1983; 19 (1A): 139-45.
	Induction of germinal vesicle breakdown in Xenopus laevis oocytes: response of denuded oocytes to progesterone and insulin., Hirai S., Dev Biol. November 1, 1983; 100 (1): 214-21.
	Patch clamp measurements on Xenopus laevis oocytes: currents through endogenous channels and implanted acetylcholine receptor and sodium channels., Methfessel C., Pflugers Arch. December 1, 1986; 407 (6): 577-88.
	Water and urea permeability properties of Xenopus oocytes: expression of mRNA from toad urinary bladder., Zhang RB., Am J Physiol. January 1, 1991; 260 (1 Pt 1): C26-34.
	Insulin receptors on Xenopus laevis oocytes: effects of injection of ob/ob mouse liver mRNA., Diss DA., J Cell Sci. September 1, 1991; 100 ( Pt 1) 167-71.
	Competence prepattern in the animal hemisphere of the 8-cell-stage Xenopus embryo., Kinoshita K., Dev Biol. November 1, 1993; 160 (1): 276-84.
	A functional test for maternally inherited cadherin in Xenopus shows its importance in cell adhesion at the blastula stage., Heasman J., Development. January 1, 1994; 120 (1): 49-57.
	H2O2-induced chloride currents are indicative of an endogenous Na(+)-Ca2+ exchange mechanism in Xenopus oocytes., Schlief T., J Physiol. July 1, 1995; 486 ( Pt 1) 123-30.
	Tight junctions in early amphibian development: detection of junctional cingulin from the 2-cell stage and its localization at the boundary of distinct membrane domains in dividing blastomeres in low calcium., Cardellini P., Dev Dyn. September 1, 1996; 207 (1): 104-13.
	Enzymatic removal of vitelline membrane and other protocol modifications for whole mount in situ hybridization of Xenopus embryos., Islam N., Trends Genet. November 1, 1996; 12 (11): 459.
	A new technique for evaluating volume sensitivity of ion channels., Schütt W., Pflugers Arch. January 1, 1997; 433 (3): 368-75.
	Improved preparation of Xenopus oocytes for patch-clamp recording., Choe H., Pflugers Arch. March 1, 1997; 433 (5): 648-52.
	Formation of new plasma membrane during the first cleavage cycle in the egg of Xenopus laevis: an immunocytological study., Aimar C., Dev Growth Differ. December 1, 1997; 39 (6): 693-704.
	Leucine transport in Xenopus laevis oocytes: functional and morphological analysis of different defolliculation procedures., Marciani P., Comp Biochem Physiol A Mol Integr Physiol. April 1, 1998; 119 (4): 1009-17.
	A constitutively activated mutant of galphaq down-regulates EP-cadherin expression and decreases adhesion between ectodermal cells at gastrulation., Rizzoti K., Mech Dev. August 1, 1998; 76 (1-2): 19-31.
	Plasma membrane plasticity of Xenopus laevis oocyte imaged with atomic force microscopy., Schillers H., Cell Physiol Biochem. January 1, 2000; 10 (1-2): 99-107.
	On the discrepancy between whole-cell and membrane patch mechanosensitivity in Xenopus oocytes., Zhang Y., J Physiol. February 15, 2000; 523 Pt 1 101-15.
	Expression of connexin 30 in Xenopus embryos and its involvement in hatching gland function., Levin M., Dev Dyn. September 1, 2000; 219 (1): 96-101.
	Paraquat embryotoxicity in the Xenopus laevis cleavage phase., Vismara C., Aquat Toxicol. November 1, 2001; 55 (1-2): 85-93.
	Plakoglobin is required for maintenance of the cortical actin skeleton in early Xenopus embryos and for cdc42-mediated wound healing., Kofron M., J Cell Biol. August 19, 2002; 158 (4): 695-708.
	K(ATP) channel activity is required for hatching in Xenopus embryos., Cheng SM., Dev Dyn. December 1, 2002; 225 (4): 588-91.
	Cell-autonomous and signal-dependent expression of liver and intestine marker genes in pluripotent precursor cells from Xenopus embryos., Chen Y, Chen Y., Mech Dev. March 1, 2003; 120 (3): 277-88.
	Oriented cell divisions asymmetrically segregate aPKC and generate cell fate diversity in the early Xenopus embryo., Chalmers AD., Development. June 1, 2003; 130 (12): 2657-68.
	A technical consideration concerning the removal of oocyte vitelline membranes for patch clamp recording., Wang MH., Biochem Biophys Res Commun. November 19, 2004; 324 (3): 971-2.
	Lysophosphatidic acid signaling controls cortical actin assembly and cytoarchitecture in Xenopus embryos., Lloyd B., Development. February 1, 2005; 132 (4): 805-16.
	Distinct effectors of platelet-derived growth factor receptor-alpha signaling are required for cell survival during embryogenesis., Van Stry M., Proc Natl Acad Sci U S A. June 7, 2005; 102 (23): 8233-8.
	Identification of asymmetrically localized transcripts along the animal-vegetal axis of the Xenopus egg., Kataoka K., Dev Growth Differ. October 1, 2005; 47 (8): 511-21.
	Oocyte isolation and enucleation., Liu XS., Methods Mol Biol. January 1, 2006; 322 31-41.
	Elaboration of a novel technique for purification of plasma membranes from Xenopus laevis oocytes., Leduc-Nadeau A., Am J Physiol Cell Physiol. March 1, 2007; 292 (3): C1132-6.
	Removing the Vitelline Membrane from Xenopus laevis Embryos., Sive HL., CSH Protoc. May 1, 2007; 2007 pdb.prot4732.
	Integrated microsystem for non-invasive electrophysiological measurements on Xenopus oocytes., Dahan E., Biosens Bioelectron. June 15, 2007; 22 (12): 3196-202.
	Hairy2 functions through both DNA-binding and non DNA-binding mechanisms at the neural plate border in Xenopus., Nichane M., Dev Biol. October 15, 2008; 322 (2): 368-80.
	Hatching mechanism of the Chinese soft-shelled turtle Pelodiscus sinensis., Yasumasu S., Comp Biochem Physiol B Biochem Mol Biol. April 1, 2010; 155 (4): 435-41.
	Xenopus Kazrin interacts with ARVCF-catenin, spectrin and p190B RhoGAP, and modulates RhoA activity and epithelial integrity., Cho K., J Cell Sci. December 1, 2010; 123 (Pt 23): 4128-44.
	Progesterone-induced changes in the phosphoryl potential during the meiotic divisions in amphibian oocytes: role of Na/K-ATPase., Morrill GA., BMC Dev Biol. January 26, 2011; 11 67.
	XMeis3 is necessary for mesodermal Hox gene expression and function., In der Rieden PM., PLoS One. March 9, 2011; 6 (3): e18010.
	Plakophilin-3 is required for late embryonic amphibian development, exhibiting roles in ectodermal and neural tissues., Munoz WA., PLoS One. January 1, 2012; 7 (4): e34342.
	An integrated field-effect microdevice for monitoring membrane transport in Xenopus laevis oocytes via lateral proton diffusion., Schaffhauser DF., PLoS One. January 1, 2012; 7 (7): e39238.
	Purines as potential morphogens during embryonic development., Massé K., Purinergic Signal. September 1, 2012; 8 (3): 503-21.
	Plasma membrane events associated with the meiotic divisions in the amphibian oocyte: insights into the evolution of insulin transduction systems and cell signaling., Morrill GA., BMC Dev Biol. January 23, 2013; 13 3.
	Evidence from mathematical modeling that carbonic anhydrase II and IV enhance CO2 fluxes across Xenopus oocyte plasma membranes., Occhipinti R., Am J Physiol Cell Physiol. November 1, 2014; 307 (9): C841-58.
	Xhe2 is a member of the astacin family of metalloproteases that promotes Xenopus hatching., Hong CS., Genesis. December 1, 2014; 52 (12): 946-51.
	Methylmercury exposure during early Xenopus laevis development affects cell proliferation and death but not neural progenitor specification., Huyck RW., Neurotoxicol Teratol. January 1, 2015; 47 102-13.
	Xenopus borealis as an alternative source of oocytes for biophysical and pharmacological studies of neuronal ion channels., Cristofori-Armstrong B., Sci Rep. January 12, 2015; 5 14763.
	On the embryonic cell division beyond the contractile ring mechanism: experimental and computational investigation of effects of vitelline confinement, temperature and egg size., Gladilin E., PeerJ. December 10, 2015; 3 e1490.

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