Publications
Hypoxia enhances human B19 erythrovirus gene expression in primary erythroid cells
Sylvie Pillet, Nathalie Le Guyader, Thomas Hofer, Florence Nguyenkhac, Marcel Koken, et al.. Hypoxia enhances human B19 erythrovirus gene expression in primary erythroid cells. Virology, 2004, 327 (1), pp.1-7. ⟨10.1016/j.virol.2004.06.020⟩. ⟨hal-04901504⟩
Effects of high light on transcripts of stress-associated genes for the cyanobacteria Synechocystis sp. PCC 6803 and Prochlorococcus MED4 and MIT9313.
Isabelle Mary, Chao-Jung Tu, Arthur Grossman, Daniel Vaulot. Effects of high light on transcripts of stress-associated genes for the cyanobacteria Synechocystis sp. PCC 6803 and Prochlorococcus MED4 and MIT9313.. Microbiology, 2004, 150 (Pt 5), pp.1271-81. ⟨hal-00528888⟩
Cyclin-dependent kinase inhibitor indirubin-3'-oxime selectively inhibits human papillomavirus type 16 E7-induced numerical centrosome anomalies
S. Duensing, A. Duensing, Lee D. C., Edwards K. M., Piboonniyom S. O., et al.. Cyclin-dependent kinase inhibitor indirubin-3'-oxime selectively inhibits human papillomavirus type 16 E7-induced numerical centrosome anomalies. Oncogene, 2004, 23, pp.8206-8215. ⟨hal-00018940⟩
Cyclin-dependent kinase inhibitor indirubin-3'-oxime selectively inhibits human papillomavirus type 16 E7-induced numerical centrosome anomalies
T. Pies, Schaper K. J., M. Leost, Zaharevitz D. W., R. Gussio, et al.. Cyclin-dependent kinase inhibitor indirubin-3'-oxime selectively inhibits human papillomavirus type 16 E7-induced numerical centrosome anomalies. Oncogene, 2004, 23, pp.8206-8215. ⟨hal-00018945⟩
Pharmacological inhibitors of glycogen synthase kinase 3
T. Pies, Schaper K. J., M. Leost, Zaharevitz D. W., R. Gussio, et al.. Pharmacological inhibitors of glycogen synthase kinase 3. Trends in pharmacological sciences., 2004, 25, pp.471-480. ⟨hal-00018947⟩
Anti-inflammatory, analgesic and kinase inhibition activities of some acridine derivatives
Sondhi S.M, G. Bhattacharjee, Jameel R.K., R. Shukla, R. Raghubir, et al.. Anti-inflammatory, analgesic and kinase inhibition activities of some acridine derivatives. Central Eur. J. Chem, 2004, 2, pp.1-15. ⟨hal-00018950⟩
Inhibitors of Leishmania mexicana CRK3 cyclin-dependent kinase: chemical library screen and antileishmanial activity
Grant K. M., Dunion M. H., V. Yardley, A. L. Skaltsounis, D. Marko, et al.. Inhibitors of Leishmania mexicana CRK3 cyclin-dependent kinase: chemical library screen and antileishmanial activity. Antimicrobial Agents and Chemotherapy, 2004, 48, pp.3033-3042. ⟨hal-00018952⟩
La pourpre de Méditerranée, une source inattendue d'inhibiteurs de GSK3
L. Meijer. La pourpre de Méditerranée, une source inattendue d'inhibiteurs de GSK3. Médecine/Sciences, 2004, 20, pp.516-518. ⟨hal-00018953⟩
Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis
Guengerich F. P., Sorrells J. L., S. Schmitt, Krauser J. A., P. Aryal, et al.. Generation of new protein kinase inhibitors utilizing cytochrome p450 mutant enzymes for indigoid synthesis. Journal of Medicinal Chemistry, 2004, 47, pp.3236-3241. ⟨hal-00018956⟩
Expression and activity of cyclin-dependent kinases and glycogen synthase kinase-3 during NT2 neuronal differentiation
M. Gompel, C. Soulie, I. Ceballos-Picot, L. Meijer. Expression and activity of cyclin-dependent kinases and glycogen synthase kinase-3 during NT2 neuronal differentiation. Neurosignals, 2004, 13, pp.134-143. ⟨hal-00020117⟩
Meridianins, a new family of protein kinase inhibitors isolated from the ascidian Aplidium meridianum
M. Gompel, M. Leost, De Kier Joffe E. B., L. Puricelli, Franco L. H., et al.. Meridianins, a new family of protein kinase inhibitors isolated from the ascidian Aplidium meridianum. Bioorganic and Medicinal Chemistry Letters, 2004, 14, pp.1703-1707. ⟨hal-00020119⟩
Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediate the antiproliferative effects of indirubins
M. Knockaert, M. Blondel, S. Bach, M. Leost, C. Elbi, et al.. Independent actions on cyclin-dependent kinases and aryl hydrocarbon receptor mediate the antiproliferative effects of indirubins. Oncogene, 2004, 23, pp.4400-4412. ⟨hal-00020122⟩