Emilie Borloz - Publications
Affiliations: | INSERM/Aix-Marseille University |
Year | Citation | Score | |||
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2021 | Felix MS, Borloz E, Metwally K, Dauba A, Larrat B, Matagne V, Ehinger Y, Villard L, Novell A, Mensah S, Roux JC. Ultrasound-Mediated Blood-Brain Barrier Opening Improves Whole Brain Gene Delivery in Mice. Pharmaceutics. 13. PMID 34452206 DOI: 10.3390/pharmaceutics13081245 | 0.683 | |||
2021 | Borloz E, Villard L, Roux JC. Rett syndrome: think outside the (skull) box. Faculty Reviews. 10: 59. PMID 34308425 DOI: 10.12703/r/10-59 | 0.565 | |||
2021 | Ehinger Y, Matagne V, Cunin V, Borloz E, Seve M, Bourgoin-Voillard S, Borges-Correia A, Villard L, Roux JC. Analysis of Astroglial Secretomic Profile in the Mecp2-Deficient Male Mouse Model of Rett Syndrome. International Journal of Molecular Sciences. 22. PMID 33919253 DOI: 10.3390/ijms22094316 | 0.679 | |||
2020 | Matagne V, Borloz E, Ehinger Y, Saidi L, Villard L, Roux JC. Severe offtarget effects following intravenous delivery of AAV9-MECP2 in a female mouse model of Rett syndrome. Neurobiology of Disease. 149: 105235. PMID 33383186 DOI: 10.1016/j.nbd.2020.105235 | 0.693 | |||
2020 | Ehinger Y, Bruyère J, Panayotis N, Abada YS, Borloz E, Matagne V, Scaramuzzino C, Vitet H, Delatour B, Saidi L, Villard L, Saudou F, Roux JC. Huntingtin phosphorylation governs BDNF homeostasis and improves the phenotype of Mecp2 knockout mice. Embo Molecular Medicine. e10889. PMID 31913581 DOI: 10.15252/Emmm.201910889 | 0.56 | |||
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