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Derniers dépôts
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Marie Bahout, Gianmarco Severa, Emna Kamoun, Françoise Bouhour, Antoine Pegat, et al.. MYH7 -related myopathies: clinical, myopathological and genotypic spectrum in a multicentre French cohort. Journal of Neurology, Neurosurgery and Psychiatry, 2024, jnnp-2024-334263. ⟨10.1136/jnnp-2024-334263⟩. ⟨hal-04761813⟩
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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⟩
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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⟩
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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⟩
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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⟩
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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⟩
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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⟩
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CTG repeat contractions
Congenital myopathy
AAV
Cytokines
Animals
Male
Astrocyte
Rare neuromuscular diseases
Humans
Autoantibodies
Myotonic Dystrophy type 1
Heart
Errance diagnostique
Myasthenia Gravis MG
Genotype phenotype correlation
Fabry disease
Myopathy
Fibrosis
Treatment
Myotonic dystrophy type 1
Nuclear envelope
Heart failure
Neuromuscular diseases
FSHD
Myositis
Neuromuscular junction
Muscle regeneration
Alternative splicing
Lamin A/C LMNA gene
Centronuclear myopathy
LMNA
COVID-19
Transcriptomics
Myotonic Dystrophy
Thérapie génique
Myasthenia gravis
Becker muscular dystrophy
Myotonic dystrophy
Dermatomyositis
RNA interference
Satellite cell
Calcium
Skeletal muscle
Muscular dystrophy
Cell therapy
Congenital muscular dystrophy
Motoneuron
Neuromuscular disease
Muscle
MBNL
Dynamin 2
Outcome measures
Thymus
Biomarkers
Laminopathie
Laminopathy
Glutamate
Lamin A/C
Duchenne muscular dystrophy
Cytoskeleton
Autoimmunity
Mice
Myoblasts
Dilated cardiomyopathy
Therapy
Biomarker
Exercise
Regeneration
Mouse model
Inflammation
LMNA gene
Myopathies
Dystrophin
Rare diseases
Brain
Satellite cells
PABPN1
ALS
Aged
Laminopathies
Spinal muscular atrophy
Antisense oligonucleotides
Long read sequencing
Genetics
CRISPRi
Amyotrophic lateral sclerosis
CMS
Cardiomyopathy
Autoimmune diseases
Mechanotransduction
Myogenesis
DMD
Gene therapy
OPMD
Transgenic mouse model
Aging
Actin
Autophagy
RNA biology
Trinucleotide repeat expansion