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Methods in Molecular Biology (Clifton, N.J.)|July 23, 2025
Functional Evaluation of Splice Variants Using a Minigene StrategyAngélique Nizou, Lana Mahfoud, Alexandre Janin, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|January 18, 2006
Characterization of the bovine PRKAG3 gene: structure, polymorphism, and alternative transcriptsMatthieu Roux, Angélique Nizou, Lionel Forestier, et al.Pharmaceutics|January 26, 2024
Neuroprotective Effect of Polyvalent Immunoglobulins on Mouse Models of Chemotherapy-Induced Peripheral NeuropathyMohamad Mroué, Flavien Bessaguet, Angélique Nizou, et al.Pharmaceutics|December 23, 2022
Blockade of Cholecystokinin Type 2 Receptors Prevents the Onset of Vincristine-Induced Neuropathy in MiceAmandine Bernard, Aurore Danigo, Mohamad Mroué, 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.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.Laboratory Investigation; a Journal of Technical Methods and Pathology|January 8, 2014
In vitro 3D angiogenesis assay in egg white matrix: comparison to Matrigel, compatibility to various species, and suitability for drug testingYoanne Mousseau, Séverine Mollard, Hao Qiu, et al.Biochimie|July 26, 2012
Fingolimod inhibits PDGF-B-induced migration of vascular smooth muscle cell by down-regulating the S1PR1/S1PR3 pathwayYoanne Mousseau, Séverine Mollard, Laurence Richard, et al.European Journal of Endocrinology|November 22, 2012
Two novel mutations of the calcium-sensing receptor gene affecting the same amino acid position lead to opposite phenotypes and reveal the importance of p.N802 on receptor activityAnne-Sophie Lia-Baldini, Corinne Magdelaine, Angélique Nizou, et al.Pageof 2