Jean-Christophe Roux, Ph.D
Affiliations: | Marseille Medical Genetics | INSERM/Aix-Marseille University |
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"Jean-Christophe Roux"Mean distance: 18.58 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Jean-Marc Pequignot | grad student | Université de Lyon, CNRS 5123 | |
| Hugo Lagercrantz | post-doc | Karolinska |
Children
Sign in to add trainee| Emilie Borloz | grad student | INSERM/Aix-Marseille University | |
| Emmanuelle Dura | grad student | INSERM U910 | |
| Yann Ehinger | grad student | UCSF | |
| Rita El-Khoury | grad student | 2010- | INSERM U910 |
| Nicolas Panayotis | grad student | 2008-2011 | Aix-Marseille University |
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Publications
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| Panayotis N, Ehinger Y, Felix MS, et al. (2022) State-of-the-art therapies for Rett syndrome. Developmental Medicine and Child Neurology |
| Felix MS, Borloz E, Metwally K, et al. (2021) Ultrasound-Mediated Blood-Brain Barrier Opening Improves Whole Brain Gene Delivery in Mice. Pharmaceutics. 13 |
| Borloz E, Villard L, Roux JC. (2021) Rett syndrome: think outside the (skull) box. Faculty Reviews. 10: 59 |
| Ehinger Y, Matagne V, Cunin V, et al. (2021) Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome. International Journal of Molecular Sciences. 22 |
| Matagne V, Borloz E, Ehinger Y, et al. (2020) Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome. Neurobiology of Disease. 149: 105235 |
| Milh M, Roubertoux P, Biba N, et al. (2020) A knock-in mouse model for KCNQ2-related epileptic encephalopathy displays spontaneous generalized seizures and cognitive impairment. Epilepsia |
| Ehinger Y, Bruyère J, Panayotis N, et al. (2020) Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice. Embo Molecular Medicine. e10889 |
| Ehinger Y, Matagne V, Villard L, et al. (2018) Rett syndrome from bench to bedside: recent advances. F1000research. 7: 398 |
| Mancini J, Dubus JC, Jouve E, et al. (2018) Effect of desipramine on patients with breathing disorders in RETT syndrome. Annals of Clinical and Translational Neurology. 5: 118-127 |
| Matagne V, Ehinger Y, Saidi L, et al. (2016) A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome. Neurobiology of Disease. 99: 1-11 |