Leucettines, a family of pharmacological inhibitors of DYRKs and CLKs kinases derived from the marine sponge Leucettamine B by Tahtouh, T, Fedorov, O, Lozach, O, Carreaux, F, Bazureau, J, Meunier, J, Maurice, T, Knapp, S, Meijer, L

Quantitative global phosphoproteomics of human umbilical vein endothelial cells after activation of the Rap signaling pathway. by Meijer, L, Zhou, H, Chan, O, Altelaar, A, Hennrich, M, Mohammed, S, Bos, J, Heck, A

Activation of FoxM1 during G2 requires cyclin A/Cdk-dependent relief of autorepression by the FoxM1 N-terminal domain. by Laoukili, J, Alvarez, M, Meijer, L, Stahl, M, Mohammed, S, Kleij, L, Heck, A, Medema, R

Molecular structures of cdc2-like kinases in complex with a new inhibitor chemotype by Walter, A, Chaikuad, A, Helmer, R, Loaëc, N, Preu, L, Ott, I, Knapp, S, Meijer, L, Kunick, C

Versatile selective kinase inhibitors: Chemistry and biology of indirubins by Gaboriaud-Kolar, N, Magiatis, P, Brivanlou, A, Greengard, P, Knapp, S, Nam, S, Jove, R, Meijer, L, Mikros, E, Skaltsounis, A

Discovery of pyrido[3,4-g]quinazoline derivatives as CMGC family protein kinase inhibitors: Design, synthesis, inhibitory potency and X-ray co–crystal structure by Knapp, S, Chaikuad, A, Esvan, Y, Zeinyeh, W, Boibessot, T, Nauton, L, Thery, V, Loaec, N, Meijer, L, Anizon, F, Giraud, F, Moreau, P

Discovery of pyrido[3,4-g]quinazoline derivatives as CMGC family protein kinase inhibitors: Design, synthesis, inhibitory potency and X-ray co–crystal structure by Esvan, Y, Zeinyeh, W, Boibessot, T, Nauton, L, Théry, V, Knapp, S, Chaikuad, A, Loaëc, N, Meijer, L, Anizon, F, Giraud, F, Moreau, P

Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine B. by Tahtouh, T, Elkins, J, Filippakopoulos, P, Soundararajan, M, Burgy, G, Durieu, E, Cochet, C, Schmid, R, Lo, D, Delhommel, F, Oberholzer, A, Pearl, L, Carreaux, F, Bazureau, J, Knapp, S, Meijer, L

Novel Inverse Binding Mode of Indirubin Derivatives Yields Improved Selectivity for DYRK Kinases. by Myrianthopoulos, V, Kritsanida, M, Gaboriaud-Kolar, N, Magiatis, P, Ferandin, Y, Durieu, E, Lozach, O, Cappel, D, Soundararajan, M, Filippakopoulos, P, Sherman, W, Knapp, S, Meijer, L, Mikros, E, Skaltsounis, A

Leucettines, a class of potent inhibitors of cdc2-like kinases and dual specificity, tyrosine phosphorylation regulated kinases derived from the marine sponge leucettamine B: modul... by Debdab, M, Carreaux, F, Renault, S, Soundararajan, M, Fedorov, O, Filippakopoulos, P, Lozach, O, Babault, L, Tahtouh, T, Baratte, B, Ogawa, Y, Hagiwara, M, Eisenreich, A, Rauch, U, Knapp, S, Meijer, L, Bazureau, J

Acridone alkaloids from Glycosmis chlorosperma as DYRK1A inhibitors by Beniddir, M.A.A., Le Borgne, E.A., Iorga, B.L.A., Loaëc, N.B.C., Lozach, O.B., Meijer, L.B.C., Awang, K.D., Litaudon, M.A.