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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⟩
Nombre de documents
791
Nombre de notices
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Rare diseases
Satellite cells
Fibrosis
Cytoskeleton
Myoblasts
Male
Biomarkers
Becker muscular dystrophy
Aging
Dynamin 2
LMNA gene
Mouse model
Errance diagnostique
Amyotrophic lateral sclerosis
Neuromuscular diseases
Congenital muscular dystrophy
Antisense oligonucleotides
Regeneration
Long read sequencing
Glutamate
MBNL
ALS
RNA biology
Inflammation
Laminopathy
PABPN1
Laminopathie
Heart failure
Muscle
Fabry disease
COVID-19
Dystrophin
Motoneuron
Cytokines
Cell therapy
Thérapie génique
Humans
Transgenic mouse model
Dilated cardiomyopathy
Gene therapy
Neuromuscular disease
Myotonic Dystrophy
Laminopathies
Neuromuscular junction
Myogenesis
Dermatomyositis
Thymus
Brain
CMS
Autophagy
Satellite cell
Lamin A/C
CRISPRi
Myasthenia gravis
Clinical trials
OPMD
Biomarker
Duchenne muscular dystrophy
Skeletal muscle
Muscular dystrophy
Actin
Calcium
Myopathy
Centronuclear myopathy
Cancer
Astrocyte
Myopathies
Myotonic dystrophy
DMD
Rare neuromuscular diseases
RNA interference
Autoantibodies
Therapy
Trinucleotide repeat expansion
Animals
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Myotonic Dystrophy type 1
Mechanotransduction
Myositis
Treatment
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AAV
FSHD
Myotonic dystrophy type 1
Heart
Autoimmune diseases
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Muscle regeneration
LMNA
Alternative splicing
Exercise
Myasthenia Gravis MG
Congenital myopathy
Genotype phenotype correlation
Outcome measures
CTG repeat contractions
Cardiomyopathy
Nuclear envelope
Lamin A/C LMNA gene
Transcriptomics