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Dernières publications
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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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Clémence Labasse, Guy Brochier, Ana-Lia Taratuto, Bruno Cadot, John Rendu, et al.. Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies. Acta Neuropathologica Communications, 2022, 10 (1), pp.101. ⟨10.1186/s40478-022-01400-0⟩. ⟨hal-03820052⟩
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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⟩
Chiffres clés
Open Access
55 %
Mots clés
Amphiphysin
Developmental myosin heavy chain
Biophysics
Core myopathy
Allele‐specific silencing therapy
Dystrophie musculaire d'Emery Dreifuss
Dynamin overexpression
Becker muscular dystrophy BMD
RNA interference
Biomarkers
Charcot-Marie-Tooth
Diaphragm
Myosin
Dominant centronuclear myopathy
Adult patients
Centronuclear myopathy
Dullard
Congenital myopathy
Cell migration
Duchenne muscular dystrophy
Disease modifiers
Lamin
Developmental biology
Autophagosome
Clathrine
BAF
DNM2
Actin
Cross-presentation
AAV8
Ctdnep1
Cellular neuroscience
Disease heterogeneity
Satellite cell
Mechanotransduction
Cross-bridge kinetics
Duchenne Muscular Dystrophy
Allele specific RNA interference
Dystrophie musculaire de Duchenne
ACTN2
Nesprin
Adeno-associated virus vector
Cell signaling
Cytoskeleton
Muscular dystrophy
Cavéoles
Skin
Cardiomyopathies
Myopathy
Nuclear envelope
Correlative microscopy
Domaine LEM
Duchenne muscular dystrophy DMD
Cancer
AAV
AD-CNM
Cardiotoxin
Dynamin
BMP signaling
AFM
Animal models of human disease
Antisense oligonucleotides
Cavins
Dynamin 2
Caveolin
Neural crest cells
CTL
Allele-specific silencing
Caveolae
Coeur
Gene therapy
A-type lamins
Autophagy
Nucleus
Dynamine
Atrial heart defects
Caveolins
Actin nucleus
Muscle
Autosomal dominant centronuclear myopathy
Allele-specific silencing therapy
Atrial cardiac defects
Alpha-actinin-2
BAR proteins
Cellules de crête neurale
Outflow tract
Myopathie
CAV-3 gene
Autophagosome maturation
Cytosquelette
Endocytosis
Autophagy cellular
Adhesion
Adeno-associated virus
DMyHC
Adeno-Associated virus
Cell proliferation
Skeletal muscle
Migration
Clathrin