Parties d'ouvrages collectifs (2)
  1. 1. Nierhaus, K. K., & Lafontaine, D. (2004). Ribosome assembly. In K. K. Nierhaus & D. D. Wilson (Eds.), Protein Synthesis and Ribosome Structure: Translating the Genome (pp. 85-143). Weinheim: Wiley. doi:10.1002/3527603433.ch3
  2. 2. Lafontaine, D., & Tollervey, D. (1998). Regulatory aspects of rRNA modifications and pre-rRNA processing. In H. Grosjean & R. Benne (Eds.), Modification and editing of RNA (pp. 281-288). Washington: ASM Press.
    3.   Articles dans des revues avec comité de lecture (100)
  3. 1. Zorbas, C., Soenmez, A., Léger, J., De Vleeschouwer, C., & Lafontaine, D. (2024). Detecting material state changes in the nucleolus by label-free digital holographic microscopy. EMBO reports. doi:10.1038/s44319-024-00134-5
  4. 2. Issa, A., Schlotter, F., Flayac, J., Chen, J., Wacheul, L., Philippe, M., Sardini, L., Mostefa, L., Vandermoere, F., Bertrand, E., Verheggen, C., Lafontaine, D., & Massenet, S. (2024). The nucleolar phase of signal recognition particle assembly. Life science alliance, 7(8), e202402614. doi:10.26508/lsa.202402614
  5. 3. Giménez, Y., Palacios, M., Sánchez-Domínguez, R., Zorbas, C., Peral, J., Puzik, A., Ugalde, L., Alberquilla, O., Villanueva, M., Río, P., Gálvez, E., Da Costa, L. L., Strullu, M., Catala, A., Ruiz-Llobet, A., Segovia, J. C., Sevilla, J., Strahm, B., Niemeyer, C. M., Belendez, C., Leblanc, T., Lafontaine, D., Bueren, J., & Navarro, S. (2024). Lentivirus-mediated gene therapy corrects ribosomal biogenesis and shows promise for Diamond Blackfan anemia. JCI insight, 9(10), e171650. doi:10.1172/jci.insight.171650
  6. 4. Wlodarski, M., Lafontaine, D., et al. (2024). Diagnosis, treatment, and surveillance of Diamond-Blackfan anaemia syndrome: international consensus statement. The Lancet Haematology, 11, 368-382. doi:10.1016/S2352-3026(24)00063-2
  7. 5. Calì, E., Quirin, M. A. C. T., Lafontaine, D., Maroofian, R., et al. (2024). Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders. Genetics in medicine., doi.org/10.1016/j.gim.2024.101251.
  8. 6. Leeman-Neill, R., Song, D., Bizarro, J., Wacheul, L., Rothschild, G., Singh, S., Yang, Y., Sarode, A., Gollapalli, K., Wu, L., Zhang, W., Chen Y, Y., Lauring, M., Whisenant, E., Bhavsar, S., Lim, J., Swerdlow, S., Bhagat, G., Zhao, Q., Berchowitz, L., Lafontaine, D., Wang, J., & Basu, U. (2023). Noncoding mutations cause super-enhancer retargeting resulting in protein synthesis dysregulation during B cell lymphoma progression. Nature genetics, 55(12), 2160-2174. doi:10.1038/s41588-023-01561-1
  9. 7. Naarmann-de Vries, I., Zorbas, C., Lemsara, A., Piechotta, M., Ernst, F. G., Wacheul, L., Lafontaine, D., & Dieterich, C. (2023). Comprehensive identification of diverse ribosomal RNA modifications by targeted nanopore direct RNA sequencing and JACUSA2. RNA biology, 20(1), 652-665. doi:10.1080/15476286.2023.2248752
  10. 8. Cappe, B., Vadi, M., Sack, E., Wacheul, L., Verstraeten, B., Dufour, S., Franck, J., Xie, W., Impens, F., Hendrix, A., Lafontaine, D., Vandenabeele, P., & Riquet, F. (2023). Systematic compositional analysis of exosomal extracellular vesicles produced by cells undergoing apoptosis, necroptosis and ferroptosis. Journal of Extracellular Vesicles, 12(10). doi:10.1002/jev2.12365
  11. 9. Liberman, N., Rothi, H., Gerashchenko, M., Zorbas, C., Boulias, K., MacWhinnie, F., Ying, A. K., Flood Taylor, A., Al Haddad, J., Shibuya, H., Roach, L., Dong, A., Dellacona, S., Lafontaine, D., Gladyshev, V. N., & Greer, E. L. (2023). 18S rRNA methyltransferases DIMT1 and BUD23 drive intergenerational hormesis. Molecular cell, 83(18), 3268-3282.e7. doi:10.1016/j.molcel.2023.08.014
  12. 10. Lafontaine, D. (2023). When two became three: Shaping the nucleolus with Treacle. Cell reports, 42(9), 113060. doi:10.1016/j.celrep.2023.113060
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