Papers associated with oocyte (and mapk1)

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	Progesterone but not ras requires MPF for in vivo activation of MAPK and S6 KII: MAPK is an essential conexion point of both signaling pathways., Carnero A., J Cell Biochem. August 1, 1994; 55 (4): 465-76.
	Protein kinase A acts at multiple points to inhibit Xenopus oocyte maturation., Matten W., Mol Cell Biol. July 1, 1994; 14 (7): 4419-26.
	Requirement for the MAP kinase kinase/MAP kinase cascade in Xenopus oocyte maturation., Kosako H., EMBO J. May 1, 1994; 13 (9): 2131-8.
	ras-p21 activates phospholipase D and A2, but not phospholipase C or PKC, in Xenopus laevis oocytes., Carnero A., J Cell Biochem. April 1, 1994; 54 (4): 478-86.
	Microtubule and chromatin behavior follow MAP kinase activity but not MPF activity during meiosis in mouse oocytes., Verlhac MH., Development. April 1, 1994; 120 (4): 1017-25.
	Regulation and function of the MAP kinase cascade in Xenopus oocytes., Kosako H., J Cell Sci Suppl. January 1, 1994; 18 115-9.
	At least two kinases phosphorylate the MPM-2 epitope during Xenopus oocyte maturation., Kuang J., J Cell Biol. November 1, 1993; 123 (4): 859-68.
	Reconstitution of p21ras-dependent and -independent mitogen-activated protein kinase activation in a cell-free system., VanRenterghem B., J Biol Chem. September 25, 1993; 268 (27): 19935-8.
	Requirement for Raf and MAP kinase function during the meiotic maturation of Xenopus oocytes., Fabian JR., J Cell Biol. August 1, 1993; 122 (3): 645-52.
	The human CL100 gene encodes a Tyr/Thr-protein phosphatase which potently and specifically inactivates MAP kinase and suppresses its activation by oncogenic ras in Xenopus oocyte extracts., Alessi DR., Oncogene. July 1, 1993; 8 (7): 2015-20.
	Raf-1 protein kinase is important for progesterone-induced Xenopus oocyte maturation and acts downstream of mos., Muslin AJ., Mol Cell Biol. July 1, 1993; 13 (7): 4197-202.
	The c-mos proto-oncogene protein kinase turns on and maintains the activity of MAP kinase, but not MPF, in cell-free extracts of Xenopus oocytes and eggs., Nebreda AR., EMBO J. May 1, 1993; 12 (5): 1979-86.
	The antibiotic azatyrosine suppresses progesterone or [Val12]p21 Ha-ras/insulin-like growth factor I-induced germinal vesicle breakdown and tyrosine phosphorylation of Xenopus mitogen-activated protein kinase in oocytes., Campa MJ., Proc Natl Acad Sci U S A. August 15, 1992; 89 (16): 7654-8.
	Stimulation of mitogen-activated protein kinase by oncogenic Ras p21 in Xenopus oocytes. Requirement for Ras p21-GTPase-activating protein interaction., Pomerance M., J Biol Chem. August 15, 1992; 267 (23): 16155-60.
	Xenopus MAP kinase activator is a serine/threonine/tyrosine kinase activated by threonine phosphorylation., Kosako H., EMBO J. August 1, 1992; 11 (8): 2903-8.
	Regulation of nuclear envelope precursor functions during cell division., Vigers GP., J Cell Sci. June 1, 1992; 102 ( Pt 2) 273-84.
	Erks: their fifteen minutes has arrived., Crews CM., Cell Growth Differ. February 1, 1992; 3 (2): 135-42.
	Requirements for phosphorylation of MAP kinase during meiosis in Xenopus oocytes., Posada J., Science. January 10, 1992; 255 (5041): 212-5.
	Xenopus M phase MAP kinase: isolation of its cDNA and activation by MPF., Gotoh Y., EMBO J. September 1, 1991; 10 (9): 2661-8.
	Phosphorylation of Xenopus cyclins B1 and B2 is not required for cell cycle transitions., Izumi T., Mol Cell Biol. August 1, 1991; 11 (8): 3860-7.
	Tyrosine phosphorylation and activation of homologous protein kinases during oocyte maturation and mitogenic activation of fibroblasts., Posada J., Mol Cell Biol. May 1, 1991; 11 (5): 2517-28.

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