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Summary Anatomy Item Literature (6354) Expression Attributions Wiki
XB-ANAT-254

Papers associated with oocyte (and nsg1)

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Inhibition of the prokaryotic pentameric ligand-gated ion channel ELIC by divalent cations., Zimmermann I., PLoS Biol. January 1, 2012; 10 (11): e1001429.              


WNK2 kinase is a novel regulator of essential neuronal cation-chloride cotransporters., Rinehart J., J Biol Chem. August 26, 2011; 286 (34): 30171-80.              


The dual-specificity kinases, TOPK and DYRK1A, are critical for oocyte maturation induced by wild-type--but not by oncogenic--ras-p21 protein., Qu Y., Front Biosci. September 1, 2007; 12 5089-97.


Two dual specificity kinases are preferentially induced by wild-type rather than by oncogenic RAS-P21 in Xenopus oocytes., Qu Y., Front Biosci. September 1, 2006; 11 2420-7.


Functional interactions of Raf and MEK with Jun-N-terminal kinase (JNK) result in a positive feedback loop on the oncogenic Ras signaling pathway., Adler V., Biochemistry. August 16, 2005; 44 (32): 10784-95.


Specificity of inhibition of ras-p21 signal transduction by peptides from GTPase activating protein (GAP) and the son-of sevenless (SOS) ras-specific guanine nucleotide exchange protein., Chie L., Protein J. May 1, 2005; 24 (4): 253-8.


Development of new anti-cancer peptides from conformational energy analysis of the oncogenic ras-p21 protein and its complexes with target proteins., Pincus MR., Front Biosci. September 1, 2004; 9 3486-509.


An effector peptide from glutathione-S-transferase-pi strongly and selectively blocks mitotic signaling by oncogenic ras-p21., Chie L., Protein J. April 1, 2004; 23 (3): 235-8.


Oncogenic and activated wild-type ras-p21 proteins induce different isoforms of protein kinase C in mitogenic signal transduction., Chie L., J Protein Chem. November 1, 2003; 22 (7-8): 625-9.


A protein methyl transferase, PRMT5, selectively blocks oncogenic ras-p21 mitogenic signal transduction., Chie L., Ann Clin Lab Sci. January 1, 2003; 33 (2): 200-7.


Identification of the site of inhibition of mitogenic signaling by oncogenic ras-p21 by a ras effector peptide., Chie L., J Protein Chem. July 1, 2002; 21 (5): 367-70.


Differences in patterns of activation of MAP kinases induced by oncogenic ras-p21 and insulin in oocytes., Ranginwale M., Exp Cell Res. September 10, 2001; 269 (1): 162-9.


The polo-like kinase Plx1 is required for activation of the phosphatase Cdc25C and cyclin B-Cdc2 in Xenopus oocytes., Qian YW., Mol Biol Cell. June 1, 2001; 12 (6): 1791-9.


Glutathione-S-Transferase as a selective inhibitor of oncogenic ras-p21-induced mitogenic signaling through blockade of activation of jun by jun-N-terminal kinase., Villafania A., Ann Clin Lab Sci. January 1, 2000; 30 (1): 57-64.


Two distinct mechanisms control the accumulation of cyclin B1 and Mos in Xenopus oocytes in response to progesterone., Frank-Vaillant M., Mol Biol Cell. October 1, 1999; 10 (10): 3279-88.


MPF amplification in Xenopus oocyte extracts depends on a two-step activation of cdc25 phosphatase., Karaïskou A., Exp Cell Res. November 1, 1998; 244 (2): 491-500.


Transcription factor E2F and cyclin E-Cdk2 complex cooperate to induce chromosomal DNA replication in Xenopus oocytes., Akamatsu E., J Biol Chem. June 26, 1998; 273 (26): 16494-500.


Selective inhibition of oncogenic ras-p21 in vivo by agents that block its interaction with jun-N-kinase (JNK) and jun proteins. Implications for the design of selective chemotherapeutic agents., Amar S., Cancer Chemother Pharmacol. January 1, 1997; 41 (1): 79-85.


Bisubstrate inhibitors of farnesyltransferase: a novel class of specific inhibitors of ras transformed cells., Manne V., Oncogene. May 4, 1995; 10 (9): 1763-79.


Activation of intracellular kinases in Xenopus oocytes by p21ras and phospholipases: a comparative study., Carnero A., Mol Cell Biol. February 1, 1995; 15 (2): 1094-101.


Analysis of the Ras p21/mitogen-activated protein kinase signaling in vitro and in Xenopus oocytes., Fukuda M., J Biol Chem. December 30, 1994; 269 (52): 33097-101.


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.


Transient expression of the recombinant chick brain P2y1 purinoceptor and localization of the corresponding mRNA., Webb TE., Cell Mol Biol (Noisy-le-grand). May 1, 1994; 40 (3): 437-42.


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.


Farnesylation of p21 Ras proteins in Xenopus oocytes., Zhao J., Cell Mol Biol Res. January 1, 1994; 40 (4): 313-21.


Molecular dynamics of the H-ras gene-encoded p21 protein; identification of flexible regions and possible effector domains., Dykes DC., J Biomol Struct Dyn. December 1, 1993; 11 (3): 443-58.


Microinjection of acylphosphatase blocks Xenopus laevis oocytes maturation induced by ras-p21., Dolfi F., FEBS Lett. July 12, 1993; 326 (1-3): 167-70.


A nickel-binding serpin, pNiXa, induces maturation of Xenopus oocytes and shows synergism with oncogenic ras-p21 protein., Haspel J., Res Commun Chem Pathol Pharmacol. February 1, 1993; 79 (2): 131-40.


Evidence that oocyte maturation induced by an oncogenic ras-p21 protein and insulin is mediated by overlapping yet distinct mechanisms., Chung DL., Exp Cell Res. December 1, 1992; 203 (2): 329-35.


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.


Evidence that the ras oncogene-encoded p21 protein induces oocyte maturation via activation of protein kinase C., Chung DL., Proc Natl Acad Sci U S A. March 1, 1992; 89 (5): 1993-6.


Pathways for activation of the ras-oncogene-encoded p21 protein., Pincus MR., Ann Clin Lab Sci. January 1, 1992; 22 (5): 323-42.


Analysis of the p21 ras system during development of meiotic competence in Xenopus laevis oocytes., Davis D., Dev Biol. January 1, 1992; 149 (1): 1-7.


A peptide from the GAP-binding domain of the ras-p21 protein as well as azatyrosine block ras-induced maturation of Xenopus oocytes., Chung DL., Biochem Biophys Res Commun. December 31, 1991; 181 (3): 1378-84.


Expression of ras-like proteins in embryonic and adult cells of Xenopus laevis., Hanocq-Quertier J., Mol Reprod Dev. April 1, 1991; 28 (4): 325-36.


A peptide from the GAP-binding domain of the ras-p21 protein and azatyrosine block ras-induced maturation of Xenopus oocytes., Chung DL., Anticancer Res. January 1, 1991; 11 (4): 1373-8.


Transforming ras proteins accelerate hormone-induced maturation and stimulate cyclic AMP phosphodiesterase in Xenopus oocytes., Sadler SE., Mol Cell Biol. April 1, 1990; 10 (4): 1689-96.


Role of phosphatidylinositide metabolism in ras-induced Xenopus oocyte maturation., Pan BT., Mol Cell Biol. March 1, 1990; 10 (3): 923-9.


Ha-rasVal-12,Thr-59 activates S6 kinase and p34cdc2 kinase in Xenopus oocytes: evidence for c-mosxe-dependent and -independent pathways., Barrett CB., Mol Cell Biol. January 1, 1990; 10 (1): 310-5.


Functional modification of a 21-kilodalton G protein when ADP-ribosylated by exoenzyme C3 of Clostridium botulinum., Rubin EJ., Mol Cell Biol. January 1, 1988; 8 (1): 418-26.


Rapid stimulation of diacylglycerol production in Xenopus oocytes by microinjection of H-ras p21., Lacal JC., Science. October 23, 1987; 238 (4826): 533-6.


Ras p21 as a potential mediator of insulin action in Xenopus oocytes., Korn LJ., Science. May 15, 1987; 236 (4803): 840-3.


Insulin induction of Xenopus laevis oocyte maturation is inhibited by monoclonal antibody against p21 ras proteins., Deshpande AK., Mol Cell Biol. March 1, 1987; 7 (3): 1285-8.


Antibodies to the ras gene product inhibit adenylate cyclase and accelerate progesterone-induced cell division in Xenopus laevis oocytes., Sadler SE., Mol Cell Biol. February 1, 1986; 6 (2): 719-22.

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