Articles dans des revues avec comité de lecture (7)
  1. 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
  2. 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
  3. 3. 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
  4. 4. 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
  5. 5. 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
  6. 6. Juhlen, R. G., Landgraf, D., Huebner, A., & Koehler, K. (2018). Triple A patient cells suffering from mitotic defects fail to localize PGRMC1 to mitotic kinetochore fibers. Cell Division, 13(1), 8. doi:10.1186/s13008-018-0041-5
  7. 7. Juhlen, R. G., Peitzsch, M., Gärtner, S., Landgraf, D., Eisenhofer, G., Huebner, A., & Koehler, K. (2018). Compensation for chronic oxidative stress in ALADIN null mice. Biology Open, 7(1), 030742. doi:10.1242/bio.030742