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