• 
  Cyprien Denoeud, Guotian Luo, Joseph Paquet, Julie Boisselier, Pauline Wosinski, et al.. Enzyme-controlled, nutritive hydrogel for mesenchymal stromal cell survival and paracrine functions. Communications Biology, 2023, 6 (1), pp.1266. ⟨10.1038/s42003-023-05643-y⟩. ⟨hal-04442110⟩
• 
  Pauline Garcia, William Jarassier, Caroline Brun, Lorenzo Giordani, Fany Agostini, et al.. Setdb1 protects genome integrity in murine muscle stem cells to allow for regenerative myogenesis and inflammation. Developmental Cell, 2024, 59 (17), pp.2375-2392.e8. ⟨10.1016/j.devcel.2024.05.012⟩. ⟨hal-04747691⟩
• 
  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⟩
• 
  Fiorella Carla Grandi, Stéphanie Astord, Sonia Pezet, Elèna Gidaja, Sabrina Mazzucchi, et al.. Characterization of SMA type II skeletal muscle from treated patients shows OXPHOS deficiency and denervation. JCI Insight, 2024, 9 (20), pp.e180992. ⟨10.1172/jci.insight.180992.⟩. ⟨hal-04750849⟩
• 
  Marissa Gionet-Gonzales, Alena Casella, Daphne Diloretto, Clara Ginnell, Katherine Griffin, et al.. Sulfated Alginate Hydrogels Prolong the Therapeutic Potential of MSC Spheroids by Sequestering the Secretome. Advanced Healthcare Materials, 2021, 10 (21), pp.2101048. ⟨10.1002/adhm.202101048⟩. ⟨hal-03832652⟩
• 
  Anita Kneppers, Sabrina Ben Larbi, Marine Theret, Audrey Saugues, Carole Dabadie, et al.. AMPKα2 is a skeletal muscle stem cell intrinsic regulator of myonuclear accretion. iScience, 2023, 26 (12), pp.108343. ⟨10.1016/j.isci.2023.108343⟩. ⟨hal-04729009⟩
• 
  Antonio Farina, Cristina Birzu, Mad-Hélénie Elsensohn, Alberto Picca, Sergio Muñiz-Castrillo, et al.. Neurological outcomes in immune checkpoint inhibitor-related neurotoxicity. Brain Communications, 2023, 5 (3), pp.fcad169. ⟨10.1093/braincomms/fcad169⟩. ⟨hal-04503909⟩
• 
  Sandra Donkervoort, Carl Kutzner, Ying Hu, Xavière Lornage, John Rendu, et al.. Pathogenic Variants in the Myosin Chaperone UNC-45B Cause Progressive Myopathy with Eccentric Cores. American Journal of Human Genetics, 2020, 107 (6), pp.1078-1095. ⟨10.1016/j.ajhg.2020.11.002⟩. ⟨hal-03668017⟩
• 
  J. Theuriet, M. Masingue, A. Behin, A. Ferreiro, G. Bassez, et al.. Congenital myasthenic syndromes in adults: clinical features, diagnosis and long-term prognosis. Brain - A Journal of Neurology , 2024, Brain - A Journal of Neurology, Online ahead of print. ⟨10.1093/brain/awae124⟩. ⟨hal-04688820⟩
• 
  Maria Chatzifrangkeskou, Caroline Le Dour, Wei Wu, John Morrow, Leroy Joseph, et al.. ERK1/2 directly acts on CTGF/CCN2 expression to mediate myocardial fibrosis in cardiomyopathy caused by mutations in the lamin A/C gene. Human Molecular Genetics, 2016, 25 (11), pp.2220-2233. ⟨10.1093/hmg/ddw090⟩. ⟨hal-03862965⟩
• 
  Florian Wernert, Satish Babu Moparthi, Florence Pelletier, Jeanne Lainé, Eline Simons, et al.. The actin-spectrin submembrane scaffold restricts endocytosis along proximal axons. Science, 2024, 385 (6711), pp.eado2032. ⟨10.1126/science.ado2032⟩. ⟨hal-04678794⟩
• 
  Emmanuelle Salort-Campana, Guilhem Solé, Armelle Magot, Céline Tard, Jean-Baptiste Noury, et al.. Multidisciplinary team meetings in treatment of spinal muscular atrophy adult patients: a real-life observatory for innovative treatments. Orphanet Journal of Rare Diseases, 2024, 19 (1), pp.24. ⟨10.1186/s13023-023-03008-6⟩. ⟨hal-04667757⟩
• 
  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⟩
• 
  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⟩
• 
  Xavière Lornage, Norma B Romero, Claire A. Grosgogeat, Eduardo Malfatti, Sandra Donkervoort, et al.. ACTN2 mutations cause "Multiple structured Core Disease" (MsCD). Acta Neuropathologica, 2019, 137 (3), pp.501-519. ⟨10.1007/s00401-019-01963-8⟩. ⟨hal-03676431⟩
• 
  Corentin Meyer, Norma Romero, Teresinha Evangelista, Brunot Cadot, Jocelyn Laporte, et al.. IMPatienT: an Integrated web application to digitize, process and explore Multimodal PATIENt daTa. Journal of Neuromuscular Diseases, 2024, Online ahead of print. ⟨10.3233/JND-230085⟩. ⟨hal-03635350v3⟩
• 
  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⟩
• 
  Francesco Galli, Laricia Bragg, Maira Rossi, Daisy Proietti, Laura Perani, et al.. Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy. EMBO Molecular Medicine, 2024, 16 (4), pp.927 - 944. ⟨10.1038/s44321-024-00031-3⟩. ⟨hal-04603972⟩
• 
  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⟩
• 
  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⟩

800

1 381