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LANGLOIS Mélanie

University of Luxembourg

Main Referenced Co-authors
CRAWFORD, Alexander Dettmar  (2)
BALLING, Rudolf  (1)
Baulac, Stephanie (1)
Becker, Felicitas (1)
Biskup, Saskia (1)
Main Referenced Keywords
Animalia (1); Article (1); Danio rerio (1);
Main Referenced Unit & Research Centers
Luxembourg Centre for Systems Biomedicine (LCSB): Chemical Biology (Crawford Group) (2)
Luxembourg Centre for Systems Biomedicine (LCSB): Bioinformatics Core (R. Schneider Group) (1)
Luxembourg Centre for Systems Biomedicine (LCSB): Experimental Neurobiology (Balling Group) (1)
Main Referenced Disciplines
Neurology (1)
Human health sciences: Multidisciplinary, general & others (1)
Genetics & genetic processes (1)

Publications (total 2)

The most downloaded
89 downloads
Zhang, Y., Kecskés, A., Copmans, D., Langlois, M., Crawford, A. D., Ceulemans, B., Lagae, L., De Witte, P. A. M., & Esguerra, C. V. (2015). Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: Inhibition of epileptic seizures by the serotonin agonist fenfluramine. PLoS ONE, 10 (5). doi:10.1371/journal.pone.0125898 https://hdl.handle.net/10993/27294

The most cited

169 citations (Scopus®)

Schubert, J., Siekierska, A., Langlois, M., May, P., Huneau, C., Becker, F., Muhle, H., Suls, A., Lemke, J. R., de Kovel, C. G. F., Thiele, H., Konrad, K., Kawalia, A., Toliat, M. R., Sander, T., Ruschendorf, F., Caliebe, A., Nagel, I., Kohl, B., ... Lerche, H. (02 November 2014). Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. Nature Genetics, 46 (12), 1327-32. doi:10.1038/ng.3130 https://hdl.handle.net/10993/18655

Zhang, Y., Kecskés, A., Copmans, D., Langlois, M., Crawford, A. D., Ceulemans, B., Lagae, L., De Witte, P. A. M., & Esguerra, C. V. (2015). Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: Inhibition of epileptic seizures by the serotonin agonist fenfluramine. PLoS ONE, 10 (5). doi:10.1371/journal.pone.0125898
Peer Reviewed verified by ORBi

Schubert, J., Siekierska, A., Langlois, M., May, P., Huneau, C., Becker, F., Muhle, H., Suls, A., Lemke, J. R., de Kovel, C. G. F., Thiele, H., Konrad, K., Kawalia, A., Toliat, M. R., Sander, T., Ruschendorf, F., Caliebe, A., Nagel, I., Kohl, B., ... Lerche, H. (02 November 2014). Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromes. Nature Genetics, 46 (12), 1327-32. doi:10.1038/ng.3130
Peer Reviewed verified by ORBi

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