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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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Congenital muscular dystrophy
Myositis
Mouse model
Dystrophin
Calcium
Myotonic dystrophy
Becker muscular dystrophy
Astrocyte
LMNA
Transcriptomics
Myopathies
Myoblasts
Nuclear envelope
Humans
Treatment
Myogenesis
Neuromuscular junction
Muscular dystrophy
FSHD
AAV
Inflammation
ALS
Muscle
Myotonic Dystrophy
RNA biology
Myotonic Dystrophy type 1
Cytoskeleton
Regeneration
Genotype phenotype correlation
Laminopathie
CMS
Animals
Myasthenia gravis
Cell therapy
Laminopathies
Trinucleotide repeat expansion
Lamin A/C LMNA gene
Actin
Fabry disease
Antisense oligonucleotides
Rare diseases
Exercise
Myopathy
Dermatomyositis
Dynamin 2
Rare neuromuscular diseases
Motoneuron
Laminopathy
Aging
Aged
Centronuclear myopathy
Thérapie génique
Autoantibodies
Heart failure
Heart
Autoimmunity
Amyotrophic lateral sclerosis
Spinal muscular atrophy
Therapy
Mice
Myasthenia Gravis MG
Muscle regeneration
COVID-19
Satellite cells
RNA interference
Long read sequencing
Thymus
Satellite cell
CRISPRi
Alternative splicing
Autophagy
Biomarkers
PABPN1
Dilated cardiomyopathy
Outcome measures
Skeletal muscle
Cardiomyopathy
Transgenic mouse model
Fibrosis
Genetics
Autoimmune diseases
Neuromuscular diseases
LMNA gene
Brain
Errance diagnostique
Male
Glutamate
Neuromuscular disease
DMD
Lamin A/C
Biomarker
Cytokines
Duchenne muscular dystrophy
Mechanotransduction
Gene therapy
CTG repeat contractions
OPMD
MBNL
Congenital myopathy
Myotonic dystrophy type 1