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Derniers dépôts
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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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Julia Pereira Lemos, Liliane Patrícia Gonçalves Tenório, Vincent Mouly, Gillian Butler-Browne, Daniella Arêas Mendes-Da-Cruz, et al.. T cell biology in neuromuscular disorders: a focus on Duchenne Muscular Dystrophy and Amyotrophic Lateral Sclerosis. Frontiers in Immunology, 2023, 14, pp.120283. ⟨10.3389/fimmu.2023.1202834⟩. ⟨hal-04603915⟩
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Alternative splicing
Biomarkers
Spinal muscular atrophy
Myogenesis
Cardiomyopathy
Neuromuscular junction
Myasthenia Gravis MG
Rare neuromuscular diseases
AAV
Mice
Fibrosis
Calcium
Myotonic dystrophy type 1
Congenital myopathy
Satellite cell
Satellite cells
CRISPRi
Autoantibodies
Dilated cardiomyopathy
Laminopathies
Brain
Glutamate
Heart
Transgenic mouse model
Mouse model
Laminopathie
Therapy
CMS
Thymus
Laminopathy
Aging
Myotonic Dystrophy
Mechanotransduction
Thérapie génique
MBNL
Duchenne muscular dystrophy
Cancer
DMD
Gene therapy
RNA interference
Outcome measures
Skeletal muscle
Myopathies
FSHD
Myositis
Autoimmunity
Transcriptomics
ALS
Fabry disease
Dermatomyositis
Myotonic dystrophy
Neuromuscular diseases
Long read sequencing
Aged
Becker muscular dystrophy
Actin
Nuclear envelope
Genotype phenotype correlation
Astrocyte
Muscle
Muscular dystrophy
Biomarker
Inflammation
Motoneuron
Lamin A/C LMNA gene
Exercise
Myoblasts
Humans
Cytoskeleton
Treatment
Congenital muscular dystrophy
PABPN1
CTG repeat contractions
COVID-19
Male
Myopathy
Neuromuscular disease
Amyotrophic lateral sclerosis
Myotonic Dystrophy type 1
Centronuclear myopathy
Muscle regeneration
Errance diagnostique
Dynamin 2
Trinucleotide repeat expansion
LMNA
Animals
OPMD
Cytokines
Cell therapy
Myasthenia gravis
Lamin A/C
Autoimmune diseases
RNA biology
Rare diseases
LMNA gene
Heart failure
Regeneration
Dystrophin
Antisense oligonucleotides
Autophagy