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Biomedical Materials (Bristol, England)|January 20, 2017
Engulfment of ceramic particles by fibroblasts does not alter cell behaviorPierre-Antoine Faye, Olivier Roualdes, Fabrice Rossignol, et al.Neurobiology of Stress|February 22, 2021
Deciphering the links between psychological stress, depression, and neurocognitive decline in patients with Down syndromeFrançois Poumeaud, Clotilde Mircher, Peter J Smith, et al.Pharmaceuticals (Basel, Switzerland)|March 28, 2024
Readthrough Activators and Nonsense-Mediated mRNA Decay Inhibitor Molecules: Real Potential in Many Genetic Diseases Harboring Premature Termination CodonsNesrine Benslimane, Camille Loret, Pauline Chazelas, et al.Frontiers in Neuroscience|April 30, 2019
Focus on 1,25-Dihydroxyvitamin D3 in the Peripheral Nervous SystemPierre Antoine Faye, François Poumeaud, Federica Miressi, et al.European Journal of Cell Biology|March 28, 2025
Advances in modeling the Charcot-Marie-Tooth disease: Human induced pluripotent stem cell-derived Schwann cells harboring SH3TC2 variantsCamille Loret, Camille Scherrer, Amandine Rovini, et al.Brain Sciences|December 18, 2020
One Multilocus Genomic Variation Is Responsible for a Severe Charcot-Marie-Tooth Axonal FormFederica Miressi, Corinne Magdelaine, Pascal Cintas, et al.Journal of Tissue Engineering|March 13, 2025
From in vivo models to in vitro bioengineered neuromuscular junctions for the study of Charcot-Marie-Tooth diseaseCamille Scherrer, Camille Loret, Nicolas Védrenne, et al.Brain Research Bulletin|February 12, 2025
Addressing myelination disorders: Novel strategies using human 3D peripheral nerve modelCamille Loret, Camille Scherrer, Amandine Rovini, et al.Computational and Structural Biotechnology Journal|August 25, 2020
A mutation can hide another one: Think Structural Variants!Federica Miressi, Pierre-Antoine Faye, Ioanna Pyromali, et al.Pharmaceuticals (Basel, Switzerland)|July 29, 2023
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 GeneNesrine Benslimane, Federica Miressi, Camille Loret, et al.Pageof 3