AAAAAA
Results:
1-13
|
Results: 13
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
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
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
Authors:
Fryns, JP
Borghgraef, M
Brown, TW
Chelly, J
Fisch, GS
Hamel, B
Hanauer, A
Lacombe, D
Luo, L
MacPherson, JN
Mandel, JL
Moraine, C
Mulley, J
Nelson, D
Oostra, B
Partington, M
Ramakers, GJA
Ropers, HH
Rousseau, F
Schwartz, C
Steinbach, P
Stoll, C
Tranebjaerg, L
Turner, G
Van Bokhoven, H
Vianna-Morgante, A
Villard, L
Warren, ST
Citation: Jp. Fryns et al., 9th international workshop on fragile X syndrome and X-linked mental retardation, AM J MED G, 94(5), 2000, pp. 345-360
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
Authors:
Filisetti, D
Ostermann, G
von Bredow, M
Strom, T
Filler, G
Ehrich, J
Pannetier, S
Garnier, JM
Rowe, P
Francis, F
Julienne, A
Hanauer, A
Econs, MJ
Oudet, C
Citation: D. Filisetti et al., Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues, EUR J HUM G, 7(5), 1999, pp. 615-619
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
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
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
Authors:
Villard, L
Bonino, MC
Abidi, F
Ragusa, A
Belougne, J
Lossi, AM
Seaver, L
Bonnefont, JP
Romano, C
Fichera, M
Lacombe, D
Hanauer, A
Philip, N
Schwartz, C
Fontes, M
Citation: L. Villard et al., Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome, J MED GENET, 36(3), 1999, pp. 183-186
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
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
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:
1-13
|