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Results: 1-16 |
Results: 16
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
B cell co-receptors regulating T cell-dependent antibody production in common variable immunodeficiency: CD27 pathway defects identify subsets of severely immuno-compromised patients.
Authors: Jacquot, S Macon-Lemaitre, L Paris, E Kobata, T Tanaka, Y Morimoto, C Schlossman, SF Tron, F
Citation: S. Jacquot et al., B cell co-receptors regulating T cell-dependent antibody production in common variable immunodeficiency: CD27 pathway defects identify subsets of severely immuno-compromised patients., INT IMMUNOL, 13(7), 2001, pp. 871-876
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
Nucleophilic additions of sodium alkoxides to 4,4-dichloro-1,1-diphenyl-2-azabuta-1,3-diene
Authors: Jacquot, S Schmitt, G Laude, B Kubicki, MM Blacque, O
Citation: S. Jacquot et al., Nucleophilic additions of sodium alkoxides to 4,4-dichloro-1,1-diphenyl-2-azabuta-1,3-diene, EUR J ORG C, (7), 2000, pp. 1235-1239
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
CD27/CD70 interactions regulate T dependent B cell differentiation
Authors: Jacquot, S
Citation: S. Jacquot, CD27/CD70 interactions regulate T dependent B cell differentiation, IMMUNOL RES, 21(1), 2000, pp. 23-30
CD134L engagement enhances human B cell Ig production: CD154/CD40, CD70/CD27, and CD134/CD134L interactions coordinately regulate T cell-dependent B cell responses
Authors: Morimoto, S Kanno, Y Tanaka, Y Tokano, Y Hashimoto, H Jacquot, S Morimoto, C Schlossman, SF Yagita, H Okumura, K Kobata, T
Citation: S. Morimoto et al., CD134L engagement enhances human B cell Ig production: CD154/CD40, CD70/CD27, and CD134/CD134L interactions coordinately regulate T cell-dependent B cell responses, J IMMUNOL, 164(8), 2000, pp. 4097-4104
Reaction of diphenyldiazomethane with N-methyloxy- and N-ethyloxycarbonyl-N-(2,2,2-trichloroethylidene)amines
Authors: Jacquot, S Belaissaoui, A Schmitt, G Laude, B Kubicki, MM Blacque, O
Citation: S. Jacquot et al., Reaction of diphenyldiazomethane with N-methyloxy- and N-ethyloxycarbonyl-N-(2,2,2-trichloroethylidene)amines, EUR J ORG C, (7), 1999, pp. 1541-1544
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
Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS)
Authors: Abidi, F Jacquot, S Lassiter, C Trivier, E Hanauer, A Schwartz, CE
Citation: F. Abidi et al., Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS), EUR J HUM G, 7(1), 1999, pp. 20-26
Cardiac involvement in Coffin-Lowry syndrome
Authors: Massin, MM Radermecker, MA Verloes, A Jacquot, S Grenade, T
Citation: Mm. Massin et al., Cardiac involvement in Coffin-Lowry syndrome, ACT PAEDIAT, 88(4), 1999, pp. 468-470
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
Requirement of Rsk-2 for epidermal growth factor-activated phosphorylationof histone H3
Authors: Sassone-Corsi, P Mizzen, CA Cheung, P Crosio, C Monaco, L Jacquot, S Hanauer, A Allis, CD
Citation: P. Sassone-corsi et al., Requirement of Rsk-2 for epidermal growth factor-activated phosphorylationof histone H3, SCIENCE, 285(5429), 1999, pp. 886-891
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: 1-16 |