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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
82
Publications with fulltext
Open Access
55 %
Mots clés
Amphiphysin
Caveolae
Cancer
Dynamine
Caveolins
Cytosquelette
A-type lamins
Myopathie
Autophagosome maturation
Actin nucleus
Cellules de crête neurale
Myosin
Outflow tract
Skeletal muscle
Mechanotransduction
BAR proteins
Neural crest cells
Autophagy cellular
Ctdnep1
Allele-specific silencing therapy
Skin
AFM
Duchenne Muscular Dystrophy
Muscle
Core myopathy
Cellular neuroscience
Animal models of human disease
Centronuclear myopathy
Duchenne muscular dystrophy DMD
Adeno-associated virus
Nucleus
Cardiotoxin
Cell signaling
Myopathy
RNA interference
Satellite cell
Atrial heart defects
Dystrophie musculaire d'Emery Dreifuss
Gene therapy
Caveolin
Migration
Cardiomyopathies
Clathrine
Cytoskeleton
Actin
AAV
ACTN2
BMP signaling
Developmental myosin heavy chain
Charcot-Marie-Tooth
Developmental biology
Congenital myopathy
DNM2
Adhesion
Muscular dystrophy
Correlative microscopy
Disease modifiers
Adeno-Associated virus
Allele‐specific silencing therapy
Dominant centronuclear myopathy
Endocytosis
Allele specific RNA interference
Biomarkers
Allele-specific silencing
Lamin
BAF
Domaine LEM
Cell proliferation
Cell migration
Coeur
AD-CNM
Autosomal dominant centronuclear myopathy
Atrial cardiac defects
Adeno-associated virus vector
Cavins
Becker muscular dystrophy BMD
Dynamin 2
Nuclear envelope
AAV8
Duchenne muscular dystrophy
Cavéoles
CAV-3 gene
Biophysics
Dullard
Clathrin
Nesprin
Antisense oligonucleotides
Autophagy
Alpha-actinin-2
DMyHC
Cross-bridge kinetics
Dystrophie musculaire de Duchenne
Cross-presentation
CTL
Diaphragm
Disease heterogeneity
Dynamin overexpression
Dynamin
Adult patients
Autophagosome