Loading...
Derniers dépôts
-
Anna Underhill, Samuel Webb, Fiorella Grandi, Jing-Yi Jeng, Jacques de Monvel, et al.. MYO7A is required for the functional integrity of the mechanoelectrical transduction complex in hair cells of the adult cochlea. Proceedings of the National Academy of Sciences of the United States of America, 2025, 122 (1), pp.e2414707122. ⟨10.1073/pnas.2414707122⟩. ⟨hal-04905455⟩
-
Gillian S. Butler-Browne, Fanny Roth, Negroni Elisa, Vincent Mouly, Capucine Trollet. 240th ENMC workshop: The involvement of skeletal muscle stem cells in the pathology of muscular dystrophies 25-27 January 2019, Hoofddorp, The Netherlands. 240th ENMC workshop, 2019, Amsterdam, Netherlands. pp.704-715, ⟨10.1016/j.nmd.2019.07.003⟩. ⟨hal-04011177⟩
-
Marielle Brockhoff, Nathalie Rion, Kathrin Chojnowska, Tatiana Wiktorowicz, Christopher Eickhorst, et al.. Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I. Journal of Clinical Investigation, 2017, 127 (2), pp.549-563. ⟨10.1172/JCI89616⟩. ⟨hal-03830899⟩
-
Julien Messéant, Alexandre Dobbertin, Emmanuelle Girard, Perrine Delers, Marin Manuel, et al.. MuSK frizzled-like domain is critical for mammalian neuromuscular junction formation and maintenance.. Journal of Neuroscience, 2015, 35 (12), pp.4926-4941. ⟨10.1523/JNEUROSCI.3381-14.2015⟩. ⟨hal-01165625⟩
-
Anaís Mariscal, Carmen Martínez, Lea Goethals, Elena Cortés-Vicente, Elisabeth Moltó, et al.. Modified radioimmunoassay versus ELISA to quantify anti-acetylcholine receptor antibodies in a mouse model of myasthenia gravis. Journal of Immunological Methods, 2024, 534, pp.113748. ⟨10.1016/j.jim.2024.113748⟩. ⟨hal-04774927⟩
Nombre de documents
829
Nombre de notices
1 379
widget_cloud
Aged
Exercise
Becker muscular dystrophy
Outcome measures
Cell therapy
Lamin A/C LMNA gene
LMNA
Biomarkers
Regeneration
Satellite cells
Alternative splicing
Autoantibodies
DMD
Neuromuscular junction
Astrocyte
Dynamin 2
Congenital muscular dystrophy
Motoneuron
Myositis
Mice
Muscle regeneration
CMS
Myoblasts
Glutamate
Therapy
Errance diagnostique
Dilated cardiomyopathy
Cardiomyopathy
Autoimmunity
Mouse model
Trinucleotide repeat expansion
RNA biology
Laminopathie
COVID-19
Transgenic mouse model
LMNA gene
Satellite cell
Dermatomyositis
CRISPRi
Rare neuromuscular diseases
Thérapie génique
Lamin A/C
OPMD
Calcium
Thymus
AAV
Myotonic dystrophy type 1
CTG repeat contractions
Mechanotransduction
Male
Antisense oligonucleotides
ALS
Rare diseases
Gene therapy
FSHD
Muscular dystrophy
Myotonic dystrophy
MBNL
Heart failure
Laminopathies
Fibrosis
Duchenne muscular dystrophy
Humans
Actin
Antibodies
Fabry disease
Genetics
Myasthenia gravis
Genotype phenotype correlation
Biomarker
Laminopathy
PABPN1
Neuromuscular diseases
Myotonic Dystrophy
Treatment
Cytokines
Dystrophin
Neuromuscular disease
Heart
Centronuclear myopathy
Muscle
Skeletal muscle
Nuclear envelope
Myopathies
Cytoskeleton
Transcriptomics
Spinal muscular atrophy
Myopathy
Congenital myopathy
Autophagy
Aging
Long read sequencing
Myotonic Dystrophy type 1
Myogenesis
RNA interference
Autoimmune diseases
Myasthenia Gravis MG
Animals
Amyotrophic lateral sclerosis
Inflammation