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Derniers dépôts
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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, ⟨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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Medhi Hassani, Dylan Moutachi, Mégane Lemaitre, Alexis Boulinguiez, Denis Furling, et al.. Beneficial effects of resistance training on both mild and severe mouse dystrophic muscle function as a preclinical option for Duchenne muscular dystrophy. PLoS ONE, 2024, 19, ⟨10.1371/journal.pone.0295700⟩. ⟨hal-04501283⟩
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Pierre Joanne, Yeranuhi Hovhannisyan, Alexandre Simon, Gaëlle Revet, Romain Diot, et al.. Generation of human induced pluripotent stem cell lines from five patients with Myofibrillar myopathy carrying different heterozygous mutations in the DES gene. Stem Cell Research, 2024, 76, pp.103338. ⟨10.1016/j.scr.2024.103338⟩. ⟨hal-04466294⟩
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Heart failure
Neuromuscular junction
Becker muscular dystrophy
Alternative splicing
COVID-19
CRISPRi
LMNA
LMNA gene
Satellite cell
Myogenesis
Transcriptomics
Motoneuron
Myotonic dystrophy type 1
Mouse model
Autoimmune diseases
Myasthenia Gravis MG
Myotonic Dystrophy
Dynamin 2
Autoimmunity
Muscle
Errance diagnostique
Heart
Gene therapy
RNA biology
CMS
Therapy
Aged
Cancer
Brain
Satellite cells
Dilated cardiomyopathy
RNA interference
Fibrosis
Muscle regeneration
Muscular dystrophy
Cytoskeleton
Regeneration
Cytokines
Thérapie génique
Trinucleotide repeat expansion
Myotonic Dystrophy type 1
Dermatomyositis
Long read sequencing
DMD
Aging
Laminopathy
Astrocyte
Lamin A/C LMNA gene
Inflammation
Clinical trials
Centronuclear myopathy
Mechanotransduction
Laminopathie
Genotype phenotype correlation
Laminopathies
OPMD
Fabry disease
Biomarker
Thymus
Myasthenia gravis
Outcome measures
Humans
PABPN1
Autoantibodies
Congenital myopathy
Rare neuromuscular diseases
Cardiomyopathy
Myoblasts
Calcium
Myopathy
Skeletal muscle
Antisense oligonucleotides
Duchenne muscular dystrophy
Congenital muscular dystrophy
Cell therapy
CTG repeat contractions
Exercise
Myopathies
Animals
ALS
Rare diseases
Actin
Amyotrophic lateral sclerosis
AAV
Male
Neuromuscular disease
Myotonic dystrophy
FSHD
Autophagy
Neuromuscular diseases
MBNL
Transgenic mouse model
Treatment
Dystrophin
Nuclear envelope
Oxidative stress
Glutamate
Myositis
Biomarkers
Lamin A/C