Articles dans des revues avec comité de lecture (9)
  1. 1. Tsimpos, P., Desiderio, S., Cabochette, P., Poelvoorde, P., Kricha, S., Vanhamme, L., Poulard, C., & Bellefroid, E. (2024). Loss of G9a does not phenocopy the requirement for Prdm12 in the development of the nociceptive neuron lineage. Neural Development, 19(1), 1. doi:10.1186/s13064-023-00179-7
  2. 2. Vermeiren, S., Cabochette, P., Dannawi, M., Desiderio, S., Sabaté San José, A., Achouri, Y., Kricha, S., Sitte, M., Salinas-Riester, G., Vanhollebeke, B., Brunet, J.-F. J., & Bellefroid, E. (2023). Prdm12 represses the expression of the visceral neuron determinants Phox2a/b in developing somatosensory ganglia. iScience, 26(12), 108364. doi:10.1016/j.isci.2023.108364
  3. 3. Martin, M., Vermeiren, S., Bostaille, N., Eubelen, M., Spitzer, D., Vermeersch, M., Profaci, C. C., Pozuelo Fernandez, E., Toussay, X., Raman-Nair, J., Tebabi, P., America, M., De Groote, A., Sanderson, L., Cabochette, P., Freitas Vale Germano, R., Torres, D., Boutry, S., de Kerchove d'Exaerde, A., Bellefroid, E., Phoenix, T. N., Devraj, K., Lacoste, B., Daneman, R., Liebner, S., & Vanhollebeke, B. (2022). Engineered Wnt ligands enable blood-brain barrier repair in neurological disorders. Science, 375(6582):eabm4459.
  4. 4. Ventéo, S., Desiderio, S., Cabochette, P., Deslys, A., Carroll, P., & Pattyn, A. P. (2019). Neurog2 Deficiency Uncovers a Critical Period of Cell Fate Plasticity and Vulnerability among Neural-Crest-Derived Somatosensory Progenitors. Cell reports, 29(10), 2953-2960.e2. doi:10.1016/j.celrep.2019.11.002
  5. 5. Campenhout, C. V., Cabochette, P., Veillard, A.-C., Laczik, M., Zelisko-Schmidt, A., Sabatel, C., Dhainaut, M., Vanhollebeke, B., Gueydan, C., & Kruys, V. (2019). Guidelines for optimized gene knockout using CRISPR/Cas9. BioTechniques, 66(6), 295-302. doi:10.2144/btn-2018-0187
  6. 6. Bonnin, E., Cabochette, P., Filosa, A., Juhlen, R. G., Komatsuzaki, S., Hezwani, M., Dickmanns, A., Martinelli, V., Vermeersch, M., Supply, L., Martins, N. N., Pirenne, L., Ravenscroft, G., Lombard, M., Port, S. S., Spillner, C., Janssens, S., Roets, E., Van Dorpe, J., Lammens, M., Kehlenbach, R. H., Ficner, R., Laing, N. N., Hoffmann, K., Vanhollebeke, B., & Fahrenkrog, B. (2018). Biallelic mutations in nucleoporin NUP88 cause lethal fetal akinesia deformation sequence. PLOS genetics, 14(12), e1007845. doi:10.1371/journal.pgen.1007845
  7. 7. Eubelen, M., Bostaille, N., Cabochette, P., Gauquier, A., Tebabi, P., Dumitru, A. C., Koehler, M., Gut, P., Alsteens, D., Stainier, D. Y. R., Garcia-Pino, A., & Vanhollebeke, B. (2018). A molecular mechanism for Wnt ligand-specific signaling. Science, 361(6403), 663. doi:10.1126/science.aat1178
  8. 8. Hübner, K., Cabochette, P., Diéguez-Hurtado, R., Wiesner, C., Wakayama, Y., Grassme, K. K., Hubert, M., Guenther, S., Belting, H.-G., Affolter, M., Adams, R. H., Vanhollebeke, B., & Herzog, W. (2018). Wnt/β-catenin signaling regulates VE-cadherin-mediated anastomosis of brain capillaries by counteracting S1pr1 signaling. Nature communications, 9(1), 4860. doi:10.1038/s41467-018-07302-x
  9. 9. Vanhollebeke, B., Stone, O. A., Bostaille, N., Cho, C., Zhou, Y., Maquet, E., Gauquier, A., Cabochette, P., Fukuhara, S., Mochizuki, N., Nathans, J., & Stainier, D. Y. R. (2015). Tip cell-specific requirement for an atypical Gpr124- and Reck-dependent Wnt/β-catenin pathway during brain angiogenesis. eLife, 4, e06489, 1-25. doi:10.7554/eLife.06489