Jehasse, K., Jouhanneau, J.-S., Wetz, S., Schwedt, A., Poulet, J. F. A., Neumann-Raizel, P., & Kampa, B. M. (18 January 2024). Immediate reuse of patch-clamp pipettes after ultrasonic cleaning. Scientific Reports, 14 (1), 1660. doi:10.1038/s41598-024-51837-7 |
Halfmann, C., Rüland, T., Müller, F., Jehasse, K., & Kampa, B. M. (15 September 2023). Electrophysiological properties of layer 2/3 pyramidal neurons in the primary visual cortex of a retinitis pigmentosa mouse model (rd10). Frontiers in Cellular Neuroscience, 17, 1258773. doi:10.3389/fncel.2023.1258773 |
Ciganok-Hückels, N., Jehasse, K., Kricsfalussy-Hrabár, L., Ritter, M., Rüland, T., & Kampa, B. M. (09 May 2023). Postnatal development of electrophysiological and morphological properties in layer 2/3 and layer 5 pyramidal neurons in the mouse primary visual cortex. Cerebral Cortex, 33 (10), 5875 - 5884. doi:10.1093/cercor/bhac467 |
Porquet, F., Weidong, L., Jehasse, K., Gazon, H., Kondili, M., Blacher, S., Massotte, L., Di Valentin, E., Furling, D., Gillet, N., Klein, A. F., Seutin, V., & Willems, L. (2023). Specific DMPK-promoter targeting by CRISPRi reverses myotonic dystrophy type 1-associated defects in patient muscle cells. Molecular Therapy: Nucleic Acids, 32, 857 - 871. doi:10.1016/j.omtn.2023.05.007 |
Jehasse, K., Jacquerie, K., de Froidmont, A., Lemoine, C., Grisar, T., Stouffs, K., Lakaye, B., & Seutin, V. (2021). Functional analysis of the F337C mutation in the CLCN1 gene associated with dominant myotonia congenita reveals an alteration of the macroscopic conductance and voltage dependence. Molecular Genetics and Genomic Medicine, 1588. doi:10.1002/mgg3.1588 |