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