Publications



1719 documents

  • Dylan Moutachi, Janek Hyzewicz, Pauline Roy, Mégane Lemaitre, Damien Bachasson, et al.. Treadmill running and mechanical overloading improved the strength of the plantaris muscle in the dystrophin‐desmin double knockout (DKO) mouse. The Journal of Physiology, In press, ⟨10.1113/JP286425⟩. ⟨hal-04643936⟩
  • Henry Kaminski, Linda Kusner, Gary Cutter, Rozen Le Panse, Cameron Wright, et al.. Does Surgical Removal of the Thymus Have Deleterious Consequences?. Neurology, 2024, 102 (12), ⟨10.1212/WNL.0000000000209482⟩. ⟨hal-04617840⟩
  • Frédérique Truffault, Ludivine Auger, Nadine Dragin, Jean-Thomas Vilquin, Elie Fadel, et al.. Comparison of juvenile and adult myasthenia gravis in a French cohort with focus on thymic histology. Scientific Reports, 2024, 14 (1), pp.13955. ⟨10.1038/s41598-024-63162-0⟩. ⟨hal-04617835⟩
  • Savine Vicart, Yann Péréon, K. Ghorab, A. Pegat, R. Dufresne, et al.. Self-reported outcomes and quality of life of patients with non-dystrophic myotonia: The French IMPACT 2022 survey.. Revue Neurologique, 2024, Revue Neurologique, Online ahead of print. ⟨10.1016/j.neurol.2024.04.007⟩. ⟨hal-04613788⟩
  • Jagan Mohan, Satish B Moparthi, Christine Girard-Blanc, Daniele Campisi, Stéphane Blanchard, et al.. ATG16L1 induces the formation of phagophore-like membrane cups. Nature Structural and Molecular Biology, In press, ⟨10.1038/s41594-024-01300-y⟩. ⟨hal-04611251⟩
  • Eden Engal, Aveksha Sharma, Uria Aviel, Nadeen Taqatqa, Sarah Juster, et al.. DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis. Science Advances , 2024, 10 (22), pp.eadn7732. ⟨10.1126/sciadv.adn7732⟩. ⟨hal-04603956⟩
  • Paul Dowling, Capucine Trollet, Laura Muraine, Elisa Negroni, Dieter Swandulla, et al.. The potential of proteomics for in-depth bioanalytical investigations of satellite cell function in applied myology. Expert Review of Proteomics, 2024, pp.1-7. ⟨10.1080/14789450.2024.2356578⟩. ⟨inserm-04603178⟩
  • Judit Núñez-Manchón, Júlia Capó, Alicia Martínez-Piñeiro, Eduard Juanola, Jovan Pesovic, et al.. Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity. iScience, 2024, 27 (6), pp.109930. ⟨10.1016/j.isci.2024.109930⟩. ⟨hal-04603947⟩
  • Alice Granados, Maeva Zamperoni, Roberta Rapone, Maryline Moulin, Ekaterina Boyarchuk, et al.. SETDB1 modulates the TGFβ response in Duchenne muscular dystrophy myotubes. Science Advances , 2024, 10 (18), pp.eadj8042. ⟨10.1126/sciadv.adj8042⟩. ⟨hal-04601015⟩
  • Paloma Navas-Navarro, Hélène Benyamine, Lucie Vezzana, Aline Huguet-Lachon, Geneviève Gourdon, et al.. Treatment of myotonic dystrophy type 1 with CRISPR/Cas9. Myology 2024, Apr 2024, Paris, France. ⟨hal-04567285⟩

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