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Key numbers

Last submissions
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Caroline Le Dour, Maria Chatzifrangkeskou, Coline Macquart, Maria M Magiera, Cécile Peccate, et al.. Actin-microtubule cytoskeletal interplay mediated by MRTF-A/SRF signaling promotes dilated cardiomyopathy caused by LMNA mutations. Nature Communications, 2022, 13 (1), pp.7886. ⟨10.1038/s41467-022-35639-x⟩. ⟨hal-03921784⟩
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Mark R Viggars, Daniel Owens, Claire Stewart, Catherine Coirault, Abigail L Mackey, et al.. PCM1 labelling reveals myonuclear and nuclear dynamics in skeletal muscle across species. American Journal of Physiology - Cell Physiology, 2022, Online ahead of print. ⟨10.1152/ajpcell.00285.2022⟩. ⟨inserm-03852473⟩
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Valentin Jacquier, Manon Prévot, Thierry Gostan, Rémy Bordonné, Sofia Benkhelifa-Ziyyat, et al.. Splicing efficiency of minor introns in a mouse model of SMA predominantly depends on their branchpoint sequence and can involve the contribution of major spliceosome components. RNA, 2022, 28 (3), pp.303-319. ⟨10.1261/rna.078329.120⟩. ⟨hal-03687098⟩
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Open Access
52 %
Keywords
Myopathie
AD-CNM
Satellite cell
Dystrophin
Antisense oligonucleotides
Cell proliferation
Clathrine
Dynamin 2
Cancer
AFM
Muscular dystrophy
Allele-specific silencing
BMP signaling
Caveolin
Endocytosis
ACTN2
Lamin
AAV
Biomarkers
BAF
Cross-bridge kinetics
AAV8
Clathrin
Cell signaling
Adeno-associated virus vector
Autophagosome
Cell migration
Autophagy
Actin nucleus
Correlative microscopy
Core myopathy
Cardiotoxin
Ctdnep1
Atrial cardiac defects
Adhesion
Adult patients
Skin
Migration
Amphiphysin
DNM2
Cavéoles
Neural crest cells
CTL
Becker muscular dystrophy BMD
Domaine LEM
Dynamine
Caveolins
Gene therapy
Allele specific RNA interference
Allele-specific silencing therapy
EHD2
Mechanotransduction
Alpha-actinin-2
Developmental myosin heavy chain
RNA interference
Dominant centronuclear myopathy
Disease heterogeneity
CAV-3 gene
Cavins
Dystrophie musculaire d'Emery Dreifuss
Congenital myopathy
Myopathy
Cellular neuroscience
Cytosquelette
Caveolae
Actin
Biophysics
Animal models of human disease
Cross-presentation
Muscle
Disease modifiers
Duchenne Muscular Dystrophy
Myosin
Nucleus
Developmental biology
BAR proteins
Centronuclear myopathy
Dynamin
Défauts cardiaques auriculaires
Skeletal muscle
Dystrophine
DMyHC
Autophagosome maturation
Atrial heart defects
Dynamin overexpression
Cytoskeleton
Adeno-associated virus
Coeur
Duchenne muscular dystrophy DMD
Nuclear envelope
Charcot-Marie-Tooth
Outflow tract
Dystrophie musculaire de Duchenne
Adeno-Associated virus
Dullard
Diaphragm
Nesprin
Autosomal dominant centronuclear myopathy
Cellules de crête neurale
Duchenne muscular dystrophy