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Focus on 1,25-Dihydroxyvitamin D3 in the Peripheral Nervous System.
Faye PA, Poumeaud F, Miressi F, Lia AS, Demiot C, Magy L, Favreau F, Sturtz FG. Faye PA, et al. Among authors: miressi f. Front Neurosci. 2019 Apr 12;13:348. doi: 10.3389/fnins.2019.00348. eCollection 2019. Front Neurosci. 2019. PMID: 31031586 Free PMC article. Review.
Focus on cell therapy to treat corneal endothelial diseases.
Faye PA, Poumeaud F, Chazelas P, Duchesne M, Rassat M, Miressi F, Lia AS, Sturtz F, Robert PY, Favreau F, Benayoun Y. Faye PA, et al. Among authors: miressi f. Exp Eye Res. 2021 Mar;204:108462. doi: 10.1016/j.exer.2021.108462. Epub 2021 Jan 23. Exp Eye Res. 2021. PMID: 33493477 Free article. Review.
Amlexanox: Readthrough Induction and Nonsense-Mediated mRNA Decay Inhibition in a Charcot-Marie-Tooth Model of hiPSCs-Derived Neuronal Cells Harboring a Nonsense Mutation in GDAP1 Gene.
Benslimane N, Miressi F, Loret C, Richard L, Nizou A, Pyromali I, Faye PA, Favreau F, Lejeune F, Lia AS. Benslimane N, et al. Among authors: miressi f. Pharmaceuticals (Basel). 2023 Jul 21;16(7):1034. doi: 10.3390/ph16071034. Pharmaceuticals (Basel). 2023. PMID: 37513945 Free PMC article.
A mutation can hide another one: Think Structural Variants!
Miressi F, Faye PA, Pyromali I, Bourthoumieux S, Derouault P, Husson M, Favreau F, Sturtz F, Magdelaine C, Lia AS. Miressi F, et al. Comput Struct Biotechnol J. 2020 Aug 2;18:2095-2099. doi: 10.1016/j.csbj.2020.07.021. eCollection 2020. Comput Struct Biotechnol J. 2020. PMID: 32832037 Free PMC article.
CovCopCan: An efficient tool to detect Copy Number Variation from amplicon sequencing data in inherited diseases and cancer.
Derouault P, Chauzeix J, Rizzo D, Miressi F, Magdelaine C, Bourthoumieu S, Durand K, Dzugan H, Feuillard J, Sturtz F, Mérillou S, Lia AS. Derouault P, et al. Among authors: miressi f. PLoS Comput Biol. 2020 Feb 12;16(2):e1007503. doi: 10.1371/journal.pcbi.1007503. eCollection 2020 Feb. PLoS Comput Biol. 2020. PMID: 32049956 Free PMC article.