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