Papers associated with oocyte (and krt12.4)

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	Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm., Gaur S., Genesis. June 1, 2016; 54 (6): 334-49.
	Cytoskeleton and Cytoskeleton-Bound RNA Visualization in Frog and Insect Oocytes., Kloc M., Methods Mol Biol. January 1, 2016; 1457 179-90.
	Regulation of neurogenesis by Fgf8a requires Cdc42 signaling and a novel Cdc42 effector protein., Hulstrand AM., Dev Biol. October 15, 2013; 382 (2): 385-99.
	Par6b regulates the dynamics of apicobasal polarity during development of the stratified Xenopus epidermis., Wang S., PLoS One. October 8, 2013; 8 (10): e76854.
	Foxi2 is an animally localized maternal mRNA in Xenopus, and an activator of the zygotic ectoderm activator Foxi1e., Cha SW., PLoS One. January 1, 2012; 7 (7): e41782.
	Structural messenger RNA contains cytokeratin polymerization and depolymerization signals., Kloc M., Cell Tissue Res. November 1, 2011; 346 (2): 209-22.
	xCITED2 Induces Neural Genes in Animal Cap Explants of Xenopus Embryos., Yoon J., Exp Neurobiol. September 1, 2011; 20 (3): 123-9.
	Protein 4.1 and its interaction with other cytoskeletal proteins in Xenopus laevis oogenesis., Carotenuto R., Eur J Cell Biol. June 1, 2009; 88 (6): 343-56.
	Organization of cytokeratin cytoskeleton and germ plasm in the vegetal cortex of Xenopus laevis oocytes depends on coding and non-coding RNAs: three-dimensional and ultrastructural analysis., Kloc M., Exp Cell Res. May 1, 2007; 313 (8): 1639-51.
	Voltage clamp fluorometric measurements on a type II Na+-coupled Pi cotransporter: shedding light on substrate binding order., Virkki LV., J Gen Physiol. May 1, 2006; 127 (5): 539-55.
	Potential structural role of non-coding and coding RNAs in the organization of the cytoskeleton at the vegetal cortex of Xenopus oocytes., Kloc M., Development. August 1, 2005; 132 (15): 3445-57.
	A novel G protein-coupled receptor, related to GPR4, is required for assembly of the cortical actin skeleton in early Xenopus embryos., Tao Q, Tao Q., Development. June 1, 2005; 132 (12): 2825-36.
	Structure-function relations of the first and fourth extracellular linkers of the type IIa Na+/Pi cotransporter: II. Substrate interaction and voltage dependency of two functionally important sites., Ehnes C., J Gen Physiol. November 1, 2004; 124 (5): 489-503.
	Cytokeratin intermediate filament organisation and dynamics in the vegetal cortex of living Xenopus laevis oocytes and eggs., Clarke EJ., Cell Motil Cytoskeleton. September 1, 2003; 56 (1): 13-26.
	Regulation of nodal and BMP signaling by tomoregulin-1 (X7365) through novel mechanisms., Chang C., Dev Biol. March 1, 2003; 255 (1): 1-11.
	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.
	RNA anchoring in the vegetal cortex of the Xenopus oocyte., Alarcón VB., J Cell Sci. May 1, 2001; 114 (Pt 9): 1731-41.
	Organization and characterization of the keratin cytoskeleton in the previtellogenic ovarian follicle of the lizard Podarcis sicula raf., Maurizii MG., Mol Reprod Dev. October 1, 2000; 57 (2): 159-66.
	The Xenopus homologue of Bicaudal-C is a localized maternal mRNA that can induce endoderm formation., Wessely O., Development. May 1, 2000; 127 (10): 2053-62.
	Xenopus GDF6, a new antagonist of noggin and a partner of BMPs., Chang C., Development. August 1, 1999; 126 (15): 3347-57.
	Geminin, a neuralizing molecule that demarcates the future neural plate at the onset of gastrulation., Kroll KL., Development. August 1, 1998; 125 (16): 3247-58.
	Modified mRNA rescue of maternal CK1/8 mRNA depletion in Xenopus oocytes., Raats JM., Antisense Nucleic Acid Drug Dev. August 1, 1997; 7 (4): 263-77.
	The organization and animal-vegetal asymmetry of cytokeratin filaments in stage VI Xenopus oocytes is dependent upon F-actin and microtubules., Gard DL., Dev Biol. April 1, 1997; 184 (1): 95-114.
	Microinjection of anti-alpha-tubulin antibody (DM1A) inhibits progesterone-induced meiotic maturation and deranges the microtubule array in follicle-enclosed oocytes of the frog, Rana pipiens., Lessman CA., Zygote. February 1, 1997; 5 (1): 83-95.
	Patterns of localization and cytoskeletal association of two vegetally localized RNAs, Vg1 and Xcat-2., Forristall C., Development. January 1, 1995; 121 (1): 201-8.
	Isolated vegetal cortex from Xenopus oocytes selectively retains localized mRNAs., Elinson RP., Dev Biol. December 1, 1993; 160 (2): 554-62.
	XLPOU-60, a Xenopus POU-domain mRNA, is oocyte-specific from very early stages of oogenesis, and localised to presumptive mesoderm and ectoderm in the blastula., Whitfield T., Dev Biol. February 1, 1993; 155 (2): 361-70.
	[A morphological study of the keratin cytoskeleton of the oocyte from the clawed toad using heterologous monoclonal antibodies]., Riabova LV., Ontogenez. January 1, 1993; 24 (6): 22-32.
	Function of maternal cytokeratin in Xenopus development., Torpey N., Nature. June 4, 1992; 357 (6377): 413-5.
	Distinct distribution of vimentin and cytokeratin in Xenopus oocytes and early embryos., Torpey NP., J Cell Sci. January 1, 1992; 101 ( Pt 1) 151-60.
	The role of intermediate filaments in early Xenopus development studied by antisense depletion of maternal mRNA., Heasman J., Dev Suppl. January 1, 1992; 119-25.
	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.
	Cytokeratin phosphorylation, cytokeratin filament severing and the solubilization of the maternal mRNA Vg1., Klymkowsky MW., J Cell Biol. August 1, 1991; 114 (4): 787-97.
	MPF-induced breakdown of cytokeratin filament organization in the maturing Xenopus oocyte depends upon the translation of maternal mRNAs., Klymkowsky MW., Dev Biol. August 1, 1989; 134 (2): 479-85.
	Expression of intermediate filament proteins during development of Xenopus laevis. I. cDNA clones encoding different forms of vimentin., Herrmann H., Development. February 1, 1989; 105 (2): 279-98.
	Xenopus endo B is a keratin preferentially expressed in the embryonic notochord., LaFlamme SE., Genes Dev. July 1, 1988; 2 (7): 853-62.
	Polar asymmetry in the organization of the cortical cytokeratin system of Xenopus laevis oocytes and embryos., Klymkowsky MW., Development. July 1, 1987; 100 (3): 543-57.
	Cloning of cDNA and amino acid sequence of a cytokeratin expressed in oocytes of Xenopus laevis., Franz JK., Proc Natl Acad Sci U S A. September 1, 1986; 83 (17): 6475-9.
	The cytoskeleton of Xenopus oocytes and its role in development., Wylie CC., J Embryol Exp Morphol. November 1, 1985; 89 Suppl 1-15.
	Cell type-specific expression of nuclear lamina proteins during development of Xenopus laevis., Benavente R., Cell. May 1, 1985; 41 (1): 177-90.
	Oocytes and early embryos of Xenopus laevis contain intermediate filaments which react with anti-mammalian vimentin antibodies., Godsave SF., J Embryol Exp Morphol. October 1, 1984; 83 169-87.
	Intermediate filaments in the Xenopus oocyte: the appearance and distribution of cytokeratin-containing filaments., Godsave SF., J Embryol Exp Morphol. October 1, 1984; 83 157-67.

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