Parties d'ouvrages collectifs (3)
  1. 1. Lussi, Y. C., & Fahrenkrog, B. (2009). Nuclear pore complex organization and nucleoporin functions. In R. H. Kehlenbach (Ed.), Nuclear Transport (pp. 19-37). Landes Bioscience.
  2. 2. Paulillo, S. M., & Fahrenkrog, B. (2008). The nuclear pore complex: from higher eukaryotes to plants. In Plant cell compartments: selected topics (pp. 1-17).
  3. 3. Fahrenkrog, B., & Aebi, U. (2006). The Nuclear Pore Complex. In D. Ganten & K. Ruckpaul (Eds.), Encyclopedic Reference of Genomics and Proteomics in Molecular Medicine. Springer.
    4.   Articles dans des revues avec comité de lecture (73)
  4. 1. Juhlen, R. G., Grauer, L., Martinelli, V., Rencurel, C., & Fahrenkrog, B. (2024). Alteration of actin cytoskeletal organisation in fetal akinesia deformation sequence. Scientific reports, 14(1), 1742. doi:10.1038/s41598-023-50615-1
  5. 2. Ravindran, E., Juhlen, R. G., Vieira-Vieira, C. C., Ha, T., Salzberg, Y., Fichtman, B., Luise-Becker, L., Martins, N. N., Picker-Minh, S., Bessa, P., Arts, P., Jackson, M. M., Taranath, A., Kamien, B., Barnett, C., Li, N., Tarabykin, V., Stoltenburg-Didinger, G., Harel, A., Selbach, M., Dickmanns, A., Fahrenkrog, B., Hu, H., Scott, H., & Kaindl, A. A. (2021). Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders. Human molecular genetics, 30(22), 2068-2081. doi:10.1093/hmg/ddab160
  6. 3. Ait-Ammar, A., Bellefroid, M., Daouad, F., Martinelli, V., Van Assche, J., Wallet, C., Rodari, A., De Rovere, M., Fahrenkrog, B., Schwartz, C., Van Lint, C., Gautier, V., & Rohr, O. (2021). Inhibition of HIV-1 gene transcription by KAP1 in myeloid lineage (C. Van Lint, V. Gautier and O. Rohr are co-last authors). Scientific reports, 11(1), 2692. doi:10.1038/s41598-021-82164-w
  7. 4. Mendes, A., Juhlen, R. G., Bousbata, S., & Fahrenkrog, B. (2020). Disclosing the Interactome of Leukemogenic NUP98-HOXA9 and SET-NUP214 Fusion Proteins Using a Proteomic Approach. Cells, 9(7). doi:10.3390/cells9071666
  8. 5. Jühlen, R., Martinelli, V., Vinci, C., Breckpot, J., & Fahrenkrog, B. (2020). Centrosome and ciliary abnormalities in fetal akinesia deformation sequence human fibroblasts. Scientific reports, 10(1), 19301. doi:10.1038/s41598-020-76192-1
  9. 6. Rodrigues Mendes, M. A., & Fahrenkrog, B. (2019). NUP214 in Leukemia: It's More than Transport. Cells, 8(1), pii: E76. doi:10.3390/cells8010076
  10. 7. Juhlen, R. G., & Fahrenkrog, B. (2018). Moonlighting nuclear pore proteins: tissue-specific nucleoporin function in health and disease. Histochemistry and cell biology, 150(6), 593-605. doi:10.1007/s00418-018-1748-8
  11. 8. 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
  12. 9. Shoaib, M., Walter, D., Gillespie, P. P., Izard, F., Fahrenkrog, B., Llères, D., Lerdrup, M., Johansen, J. V., Hansen, K., Julien, E., Blow, J. J., & Sørensen, C. S. (2018). Histone H4K20 methylation mediated chromatin compaction threshold ensures genome integrity by limiting DNA replication licensing. Nature communications, 9(1), 3704. doi:10.1038/s41467-018-06066-8
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