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Key numbers
81
Publications with fulltext
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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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⟩
Open Access
55 %
Keywords
Cytoskeleton
Cardiomyopathies
Charcot-Marie-Tooth
Dynamin 2
Nuclear envelope
Dynamine
Dynamin
Nesprin
Mechanotransduction
Dystrophie musculaire d'Emery Dreifuss
Adeno-associated virus vector
Myosin
Animal models of human disease
Myopathie
BMP signaling
Outflow tract
Adeno-associated virus
Dullard
Allele-specific silencing
Cavéoles
AFM
Autophagosome maturation
Clathrin
A-type lamins
Duchenne muscular dystrophy DMD
Cancer
Adeno-Associated virus
Duchenne muscular dystrophy
Atrial heart defects
Dynamin overexpression
Cell migration
Developmental myosin heavy chain
Centronuclear myopathy
Developmental biology
CAV-3 gene
DNM2
Cross-bridge kinetics
AD-CNM
Allele specific RNA interference
Cardiotoxin
Cross-presentation
Clathrine
AAV
Dystrophie musculaire de Duchenne
Cavins
Cellular neuroscience
Correlative microscopy
Ctdnep1
Muscular dystrophy
Autophagy cellular
Muscle
DMyHC
RNA interference
Skeletal muscle
Alpha-actinin-2
Congenital myopathy
Cell proliferation
Lamin
Disease modifiers
ACTN2
Diaphragm
Endocytosis
Myopathy
Autophagosome
Adhesion
Autophagy
Nucleus
BAF
Autosomal dominant centronuclear myopathy
Cellules de crête neurale
Biomarkers
Amphiphysin
Gene therapy
Actin nucleus
Caveolin
Adult patients
Disease heterogeneity
Biophysics
Core myopathy
Neural crest cells
CTL
Satellite cell
Coeur
Cytosquelette
Becker muscular dystrophy BMD
Cell signaling
Caveolins
Domaine LEM
Allele‐specific silencing therapy
Allele-specific silencing therapy
Dominant centronuclear myopathy
Antisense oligonucleotides
BAR proteins
AAV8
Actin
Duchenne Muscular Dystrophy
Skin
Migration
Caveolae
Atrial cardiac defects