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Derniers dépôts
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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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Angelos Gerassimopoulos, Céline Michaud, Mélanie Gaillet, Cyril Rousseau, Adriana Gonzalez, et al.. Santé et recours aux soins et à la prévention des travailleuses du sexe dominicaines vivant le long du fleuve Maroni. 6e journées des travaux scientifiques des soignant.e.s de Guyane, May 2023, Cayenne, Guyane française. ⟨hal-04585175⟩
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Joe-Elie Salem, Marie Bretagne, Baptiste Abbar, Sarah Leonard-Louis, Stéphane Ederhy, et al.. Abatacept/Ruxolitinib and Screening for Concomitant Respiratory Muscle Failure to Mitigate Fatality of Immune-Checkpoint Inhibitor Myocarditis. Cancer Discovery, 2023, 13 (5), pp.1100-1115. ⟨10.1158/2159-8290.CD-22-1180⟩. ⟨hal-04578810⟩
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Antonio Atalaia, Dagmar Wandrei, Nawel Lalout, Rachel Thompson, Adrian Tassoni, et al.. EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disorders. Orphanet Journal of Rare Diseases, 2024, 19 (1), pp.66. ⟨10.1186/s13023-024-03059-3⟩. ⟨hal-04460667⟩
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Vanessa Ueberschlag-Pitiot, Amalia Stantzou, Julien Messéant, Megane Lemaitre, Daniel Owens, et al.. Gonad-related factors promote muscle performance gain during postnatal development in male and female mice. AJP - Endocrinology and Metabolism, 2017, 313 (1), pp.E12-E25. ⟨10.1152/ajpendo.00446.2016⟩. ⟨hal-03677800⟩
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Hubert Smeets, Bram Verbrugge, Xavier Bulbena, Liliya Hristova, Julia Vogt, et al.. European Joint Programme on Rare Diseases workshop: LAMA2-muscular dystrophy: paving the road to therapy March 17–19, 2023, Barcelona, Spain. LAMA2-muscular dystrophy: paving the road to therapy, Neuromuscular Disorders, 36, pp.16 - 22, 2024, ⟨10.1016/j.nmd.2024.01.001⟩. ⟨hal-04546346⟩
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Fibrosis
Neuromuscular diseases
Laminopathie
OPMD
Congenital muscular dystrophy
Thymus
Nuclear envelope
Neuromuscular disease
Transcriptomics
Therapy
Satellite cell
Aged
Myotonic Dystrophy
ALS
Mice
Centronuclear myopathy
Skeletal muscle
MBNL
Autoantibodies
Myoblasts
Myopathies
Long read sequencing
Neuromuscular junction
Heart failure
FSHD
Laminopathies
Satellite cells
Amyotrophic lateral sclerosis
Calcium
Lamin A/C
Errance diagnostique
CTG repeat contractions
Cardiomyopathy
RNA biology
Inflammation
LMNA
DMD
Actin
Becker muscular dystrophy
Myopathy
Cancer
Duchenne muscular dystrophy
Dystrophin
Male
Autoimmune diseases
Regeneration
CMS
Brain
PABPN1
Glutamate
Exercise
RNA interference
Myasthenia Gravis MG
Myositis
Antisense oligonucleotides
Heart
Autophagy
Lamin A/C LMNA gene
Congenital myopathy
Mechanotransduction
Genotype phenotype correlation
CRISPRi
Fabry disease
Astrocyte
Dermatomyositis
Laminopathy
Gene therapy
Muscle
Treatment
Transgenic mouse model
Humans
Myotonic dystrophy type 1
Rare diseases
Biomarker
LMNA gene
Outcome measures
Animals
COVID-19
Cell therapy
Cytoskeleton
Myotonic dystrophy
Dilated cardiomyopathy
Myotonic Dystrophy type 1
Alternative splicing
Autoimmunity
Cytokines
AAV
Dynamin 2
Biomarkers
Mouse model
Rare neuromuscular diseases
Trinucleotide repeat expansion
Muscular dystrophy
Muscle regeneration
Thérapie génique
Myasthenia gravis
Clinical trials
Aging
Myogenesis
Motoneuron