1702 documents
- Gisèle Bonne. Insights in the pathophysiological mechanisms of striated muscle Laminopathies. European Meeting on Intermediate Filaments, Elly Hol, Jun 2023, Noorwijkerhout, Netherlands. ⟨hal-04189581⟩
- Florent Porquet, Lin Weidong, Kévin Jehasse, Hélène Gazon, Maria Kondili, et al.. Specific DMPK-promoter targeting by CRISPRi reverses myotonic dystrophy type 1-associated defects in patient muscle cells. Molecular Therapy - Nucleic Acids, 2023, 32, pp.857 - 871. ⟨10.1016/j.omtn.2023.05.007⟩. ⟨hal-04287597⟩
- Cedric Happi Mbakam, Jeanne Roustant, Joel Rousseau, Pouire Yameogo, Yaoyao Lu, et al.. Prime editing strategies to mediate exon skipping in DMD gene. Frontiers in Medicine, 2023, 10, ⟨10.3389/fmed.2023.1128557⟩. ⟨hal-04253826⟩
- Alex Corscadden, Louison Lallemant, Hélène Benyamine, Jean-Christophe Comte, Aline Huguet-Lachon, et al.. Defects in mouse cortical glutamate uptake can be unveiled in vivo by a two-in-one quantitative microdialysis.. NeuroFrance, May 2023, Lyon, France. ⟨hal-04005564⟩
- Paul Magneron, Louison Lallemant, Luis Guillermo Correa Parra, Mário Gomes-Pereira, Geneviève Gourdon. Cytoskeleton abnormalities triggered by toxic CUG RNA repeats in DM1 astrocytes.. NeuroFrance, May 2023, Lyon20, France. ⟨hal-04005541⟩
- B Potier, Louison Lallemant, Sandrine Parrot, Aline Huguet-Lachon, Geneviève Gourdon, et al.. DM1 transgenic mice exhibit abnormal neurotransmitter homeostasis and synaptic plasticity in association with RNA mis-splicing in the hippocampus.. NeuroFrance, May 2023, Lyon, France. ⟨hal-04005556⟩
- Paul Magneron, Louison Lallemant, Luis Guillermo Correa Parra, Geneviève Gourdon, Mário Gomes-Pereira. Cytoskeleton abnormalities triggered by toxic CUG RNA repeats in DM1 astrocytes.. French Glial Cell Club, May 2023, Lyon, France. ⟨hal-04005531⟩
- Gisèle Bonne. Le Treatabolome : une base de donnée des traitements existant pour les maladies rares à l’échelle du gène/variant. Webinaire de la Filière en Santé Filnemus, May 2023, Paris, France. ⟨hal-04189577⟩
- Caroline Le Guiner, T Larcher, A Lafoux, G Toumaniantz, S Webb, et al.. Characterization of the muscular and cardiac diseases of the DMSXL mouse model, a transgenic mouse model for Myotonic Dystrophy type 1. American Society of Gene & Cell Therapy, May 2023, LOS ANGELES, United States. ⟨hal-04096181⟩
- Louise Benarroch, Julia Madsen-Østerbye, Mohamed Abdelhalim, Kamel Mamchaoui, Jessica Ohana, et al.. Validation of Myo-converted fi broblasts as a relevant model to study chromatin organization defects in striated muscle laminopathies. 4th International Meeting on Laminopathies, May 2023, Madrid, Spain. ⟨10.3233/JND-239001⟩. ⟨hal-04189720⟩
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