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Yann Ehinger - Publications

Affiliations: 
University of California, San Francisco, San Francisco, CA 
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Moffat JJ, Sakhai SA, Hoisington ZW, Ehinger Y, Ron D. The BDNF Val68Met polymorphism causes a sex specific alcohol preference over social interaction and also acute tolerance to the anxiolytic effects of alcohol, a phenotype driven by malfunction of BDNF in the ventral hippocampus of male mice. Psychopharmacology. 240: 303-317. PMID 36622381 DOI: 10.1007/s00213-022-06305-3  0.354
2022 Panayotis N, Ehinger Y, Felix MS, Roux JC. State-of-the-art therapies for Rett syndrome. Developmental Medicine and Child Neurology. PMID 36056801 DOI: 10.1111/dmcn.15383  0.752
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  0.697
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  0.698
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  0.707
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  0.63
2018 Ehinger Y, Matagne V, Villard L, Roux JC. Rett syndrome from bench to bedside: recent advances. F1000research. 7: 398. PMID 29636907 DOI: 10.12688/F1000Research.14056.1  0.612
2016 Matagne V, Ehinger Y, Saidi L, Borges-Correia A, Barkats M, Bartoli M, Villard L, Roux JC. A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome. Neurobiology of Disease. 99: 1-11. PMID 27974239 DOI: 10.1016/J.Nbd.2016.12.009  0.743
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