Jean-Christophe Roux, Ph.D

Affiliations: 
Marseille Medical Genetics INSERM/Aix-Marseille University 
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"Jean-Christophe Roux"
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Publications

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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
Roux JC, Villard L. (2015) Neurobehavioral testing of mouse models of Rett syndrome Neuromethods. 100: 399-430
El-Khoury R, Panayotis N, Matagne V, et al. (2014) GABA and glutamate pathways are spatially and developmentally affected in the brain of Mecp2-deficient mice. Plos One. 9: e92169
Kaddoum L, Panayotis N, Mazarguil H, et al. (2013) Isoform-specific anti-MeCP2 antibodies confirm that expression of the e1 isoform strongly predominates in the brain. F1000research. 2: 204
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