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