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