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Results: 1-11 |
Results: 11
Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome
Authors: Delaunoy, JP Abidi, F Zeniou, M Jacquot, S Merienne, K Pannetier, S Schmitt, M Schwartz, CE Hanauer, A
Citation: Jp. Delaunoy et al., Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome, HUM MUTAT, 17(2), 2001, pp. 103-116
Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylaseactivities
Authors: Merienne, K Pannetier, S Harel-Bellan, A Sassone-Corsi, P
Citation: K. Merienne et al., Mitogen-regulated RSK2-CBP interaction controls their kinase and acetylaseactivities, MOL CELL B, 21(20), 2001, pp. 7089-7096
The ribosomal S6 kinases, cAMP-responsive element-binding, and STAT3 proteins are regulated by different leukemia inhibitory factor signaling pathways in mouse embryonic stem cells
Authors: Boeuf, H Merienne, K Jacquot, S Duval, D Zeniou, M Hauss, C Reinhardt, B Huss-Garcia, Y Dierich, A Frank, DA Hanauer, A Kedinger, C
Citation: H. Boeuf et al., The ribosomal S6 kinases, cAMP-responsive element-binding, and STAT3 proteins are regulated by different leukemia inhibitory factor signaling pathways in mouse embryonic stem cells, J BIOL CHEM, 276(49), 2001, pp. 46204-46211
Activation of RSK by UV-light: phosphorylation dynamics and involvement ofthe MAPK pathway
Authors: Merienne, K Jacquot, S Zeniou, M Pannetier, S Sassone-Corsi, P Hanauer, A
Citation: K. Merienne et al., Activation of RSK by UV-light: phosphorylation dynamics and involvement ofthe MAPK pathway, ONCOGENE, 19(37), 2000, pp. 4221-4229
A phosphoserine-regulated docking site in the protein kinase RSK2 that recruits and activates PDK1
Authors: Frodin, M Jensen, CJ Merienne, K Gammeltoft, S
Citation: M. Frodin et al., A phosphoserine-regulated docking site in the protein kinase RSK2 that recruits and activates PDK1, EMBO J, 19(12), 2000, pp. 2924-2934
Molecular and structural basis of the specificity of a neutralizing acetylcholine receptor-mimicking antibody, using combined mutational and molecular modeling analyses
Authors: Germain, N Merienne, K Zinn-Justin, S Boulain, JC Ducancel, F Menez, A
Citation: N. Germain et al., Molecular and structural basis of the specificity of a neutralizing acetylcholine receptor-mimicking antibody, using combined mutational and molecular modeling analyses, J BIOL CHEM, 275(28), 2000, pp. 21578-21586
A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation
Authors: Merienne, K Jacquot, S Pannetier, S Zeniou, M Bankier, A Gecz, J Mandel, JL Mulley, J Sassone-Corsi, P Hanauer, A
Citation: K. Merienne et al., A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation, NAT GENET, 22(1), 1999, pp. 13-14
Coffin-Lowry syndrome: Current, status
Authors: Jacquot, S Merienne, K Trivier, E Zeniou, M Pannetier, S Hanauer, A
Citation: S. Jacquot et al., Coffin-Lowry syndrome: Current, status, AM J MED G, 85(3), 1999, pp. 214-215
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome
Authors: Manouvrier-Hanu, S Amiel, J Jacquot, S Merienne, K Moerman, A Coeslier, A Labarriere, F Vallee, L Croquette, MF Hanauer, A
Citation: S. Manouvrier-hanu et al., Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome, J MED GENET, 36(10), 1999, pp. 775-778
Germline mosaicism in Coffin-Lowry syndrome
Authors: Jacquot, S Merienne, K Pannetier, S Blumenfeld, S Schinzel, A Hanauer, A
Citation: S. Jacquot et al., Germline mosaicism in Coffin-Lowry syndrome, EUR J HUM G, 6(6), 1998, pp. 578-582
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: Extensive allelic heterogeneity and a high rate of de novo mutations
Authors: Jacquot, S Merienne, K De Cesare, D Pannetier, S Mandel, JL Sassone-Corsi, P Hanauer, A
Citation: S. Jacquot et al., Mutation analysis of the RSK2 gene in Coffin-Lowry patients: Extensive allelic heterogeneity and a high rate of de novo mutations, AM J HU GEN, 63(6), 1998, pp. 1631-1640
Risultati: 1-11 |