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. 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
  5. 5. 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
  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