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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
78
Publications avec texte intégral
Open Access
55 %
Mots clés
AD-CNM
Cavins
Myopathie
Dullard
Endocytosis
Cross-bridge kinetics
Allele‐specific silencing therapy
Allele-specific silencing therapy
Myosin
Biomarkers
Satellite cell
Biophysics
Dystrophin
ACTN2
Developmental myosin heavy chain
Migration
Dominant centronuclear myopathy
Skeletal muscle
BAR proteins
AAV
Cross-presentation
Allele specific RNA interference
Dynamin 2
Congenital myopathy
Diaphragm
BMP signaling
Duchenne muscular dystrophy DMD
Coeur
Charcot-Marie-Tooth
DMyHC
AAV8
Developmental biology
BAF
Dynamin overexpression
Clathrin
Amphiphysin
AFM
Dystrophie musculaire de Duchenne
Cell migration
Cellules de crête neurale
Cell proliferation
Autosomal dominant centronuclear myopathy
Cytosquelette
Disease modifiers
Antisense oligonucleotides
Ctdnep1
Correlative microscopy
Cardiotoxin
Duchenne muscular dystrophy
A-type lamins
Adeno-associated virus vector
Muscle
DNM2
Mechanotransduction
Disease heterogeneity
Duchenne Muscular Dystrophy
Nuclear envelope
Autophagosome
Skin
Adult patients
Caveolae
Centronuclear myopathy
Cancer
Muscular dystrophy
Allele-specific silencing
Lamin
Caveolin
Animal models of human disease
Core myopathy
Clathrine
Autophagosome maturation
Domaine LEM
Gene therapy
Adeno-Associated virus
Myopathy
Adhesion
Nucleus
Cytoskeleton
Neural crest cells
CTL
Outflow tract
Cellular neuroscience
Caveolins
Dynamine
Adeno-associated virus
Cavéoles
Dynamin
Alpha-actinin-2
Nesprin
CAV-3 gene
Atrial cardiac defects
RNA interference
Atrial heart defects
Actin nucleus
Actin
Cell signaling
Cardiomyopathies
Autophagy
Dystrophie musculaire d'Emery Dreifuss
Becker muscular dystrophy BMD