Articles dans des revues avec comité de lecture (149)
69.
Vandurm, P., Guiguen, A., Cauvin, C., Georges, B., Le Van, K., Michaux, C., Cardona, C., Mbemba, G., Mouscadet, J.-F., Hevesi, L., Van Lint, C., & Wouters, J. (2011). Synthesis, biological evaluation and molecular modeling studies of quinolonyl diketo acid derivatives: new structural insight into the HIV-1 integrase inhibition. European journal of medicinal chemistry, 46(5), 1749-1756. doi:10.1016/j.ejmech.2011.02.02870.
Colin, L., Vandenhoudt, N., De Walque, S., Van Driessche, B., Bergamaschi, A., Martinelli, V., Cherrier, T., Vanhulle, C., Guiguen, A., David, A., Burny, A., Herbein, G., Pancino, G., Rohr, O., & Van Lint, C. (2011). The AP-1 binding sites located in the pol gene intragenic regulatory region of HIV-1 are important for viral replication. PloS one, 6(4), e19084. doi:10.1371/journal.pone.001908471.
Redel, L., Le Douce, V., Cherrier, T., Marban, C., Janossy, A., Aunis, D., Van Lint, C., Rohr, O., & Schwartz, C. (2010). HIV-1 regulation of latency in the monocyte-macrophage lineage and in CD4+ T lymphocytes. Journal of leukocyte biology, 87, 575-588. doi:10.1189/jlb.040926472.
Pierard, V., Guiguen, A., Colin, L., Wijmeersch, G., Vanhulle, C., Van Driessche, B., Dekoninck, A., Blazkova, J., Cardona, C., Merimi, M., Vierendeel, V., Calomme, C., Nguyen, T. L.-A., Nuttinck, M., Twizere, J.-C., Kettmann, R., Portetelle, D., Burny, A., Hirsch, I., Rohr, O., & Van Lint, C. (2010). DNA cytosine methylation in the bovine leukemia virus promoter is associated with latency in a lymphoma-derived B-cell line: Potential involvement of direct inhibition of CREB/CREM/ATF transcription factor binding. The Journal of biological chemistry. doi:10.1074/jbc.M110.10760773.
Lens, Z., Dewitte, F., Monte, D., Baert, J.-L., Bompard, C., Sénéchal, M., Van Lint, C., De Launoit, Y., Villeret, V., & Verger, A. (2010). Solution structure of the N-terminal transactivation domain of ERM modified by SUMO-1. Biochemical and biophysical research communications, 399(1), 104-110. doi:10.1016/j.bbrc.2010.07.04974.
Trono, D., Van Lint, C., Rouzioux, C., Verdin, E., Barré-Sinoussi, F., Chun, T.-W., & Chomont, N. (2010). HIV persistence and the prospect of long-term drug-free remissions for HIV-infected individuals. Science, 329(5988), 174-180. doi:10.1126/science.119104776.
Vandurm, P., Cauvin, C., Guiguen, A., Georges, B., Le Van, K., Martinelli, V., Cardona, C., Mbemba, G., Mouscadet, J.-F., Hevesi, L., Van Lint, C., & Wouters, J. (2009). Structural and theoretical studies of [6-bromo-1-(4-fluorophenylmethyl)-4(1H)-quinolinon-3-yl)]-4-hydroxy-2-oxo-3-butenoïc acid as HIV-1 integrase inhibitor. Bioorganic & medicinal chemistry letters, 19(16), 4806-4809. doi:10.1016/j.bmcl.2009.06.04477.
Vire, B., De Walque, S., Restouin, A., Olive, D., Van Lint, C., & Collette, Y. (2009). Anti-leukemia activity of MS-275 histone deacetylase inhibitor implicates 4-1BBL/4-1BB immunomodulatory functions. PloS one, 4(9), e7085. doi:10.1371/journal.pone.000708578.
Reuse, S., Calao, M., Kabeya, K., Guiguen, A., Gatot, J.-S., Quivy, V., Vanhulle, C., Lamine, A., Vaira, D., Demonte, D., Martinelli, V., Veithen, E., Cherrier, T., Avettand, V., Poutrel, S., Piette, J., De Launoit, Y., Moutschen, M., Burny, A., Rouzioux, C., De Wit, S., Herbein, G., Rohr, O., Collette, Y., Lambotte, O., Clumeck, N., & Van Lint, C. (2009). Synergistic activation of HIV-1 expression by deacetylase inhibitors and prostratin: implications for treatment of latent infection. PloS one, 4(6), e6093. doi:10.1371/journal.pone.000609379.
Le Van, K., Cauvin, C., De Walque, S., Georges, B., Boland, S., Martinelli, V., Demonte, D., Durant, F., Hevesi, L., & Van Lint, C. (2009). New pyridinone derivatives as potent HIV-1 nonnucleoside reverse transcriptase inhibitors. Journal of medicinal chemistry, 52(12), 3636-3643. doi:10.1021/jm801438e80.
Cherrier, T., Suzanne, S., Redel, L., Calao, M., Marban, C., Samah, B., Mukerjee, R., Schwartz, C., Gras, G., Sawaya, B. E., Zeichner, S. L., Aunis, D., Van Lint, C., & Rohr, O. (2009). p21(WAF1) gene promoter is epigenetically silenced by CTIP2 and SUV39H1. Oncogene, 28(38), 3380-3389. doi:10.1038/onc.2009.193