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:
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
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:
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:
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