Loading...
Dernières publications
-
Valentina Taglietti, Kaouthar Kefi, Lea Rivera, Oriane Bergiers, Nastasia Cardone, et al.. Thyroid-stimulating hormone receptor signaling restores skeletal muscle stem cell regeneration in rats with muscular dystrophy. Science Translational Medicine, 2023, 15 (685), ⟨10.1126/scitranslmed.add5275⟩. ⟨hal-04150315⟩
-
A. Morin, Amalia Stantzou, Olga N. Petrova, John C.W. Hildyard, T. Tensorer, et al.. Dystrophin myonuclear domain restoration governs treatment efficacy in dystrophic muscle. Proceedings of the National Academy of Sciences of the United States of America, 2023, 120 (2), ⟨10.1073/pnas.2206324120⟩. ⟨hal-04122777⟩
-
Valentina Taglietti, Kaouthar Kefi, Iwona Bronisz-Budzyńska, Busra Mirciloglu, Mathilde Rodrigues, et al.. Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis. Acta Neuropathologica Communications, 2022, 10 (1), ⟨10.1186/s40478-022-01355-2⟩. ⟨hal-03828280⟩
Chiffres clés
48
Publications avec texte intégral
Open Access
67 %
Mots clés
Muscular Dystrophy
Cardiomyopathie
MES
Invivo
Cell Biology
NAD+
Liver
L-Type
Muscle Biology
Mdx mouse
Animal/physiopathology
Multi exon skipping
Cell homeostasis
Dystrophin
Muscle development
Duchenne muscular dystrophy
Inhibitors
Centronuclear myopathy
Exon skipping
CaV subunits
Activin Receptors
Cardiomyopathy
Cultured
Gene expression
Dystrophie musculaire de Becker
Homeostasis
Gene modifiers
Cells
Hepatocellular carcinoma
Antisense oligonucleotides
Clinical trials
Muscle Strength
Muscles/physiopathology
Diseases
MiARN
Dystrophin central domain
DMO
Duchenne DMD dystrophy
Mice
Energy Metabolism/drug effects
Skeletal muscle
Dystrophie Musculaire de Duchenne DMD
Dystrophy
Inbred C57BL
DMD
Muscular dystrophy
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Dystrophin-EGFP
Cell Line
Male
CTNNB1
LncARN
Muscle
BMD
Calcium
Dystrophine
Animals
Mitochondrial fission
Long noncoding RNA
CaVβs
Drp1
Molecular Sequence Data
Humans
Morphogenesis
Immunoglobulin Fc Fragments/pharmacology
Delivery
Gene Expression Regulation/drug effects
Human Umbilical Vein Endothelial Cells
Cachexia
Metabolism
Becker BMD muscular dystrophy
Multi resolution modeling
Genomic
Becker muscular dystrophy BMD
Autophagy
NNOS
Epigenetics
Dynamin 2
Modificateurs de gènes
Génomique
LKB1
Long QT
Muscular Atrophy
Becker muscular dystrophy
Myotendinous junction
Myogenesis
Molecular docking
Base Sequence
Ex-vivo
Knockout
DHPR α1S
Calcium Channels
LncRNA
Hear
Inbred mdx
Duchenne muscular dystrophy DMD
Multiresolution modeling
Dystrophie Musculaire de Becker BMD
CD38
Allele‐specific silencing therapy