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Dernières publications
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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⟩
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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⟩
Chiffres clés
54
Publications avec texte intégral
Open Access
76 %
Mots clés
Duchenne muscular dystrophy
Dystrophie Musculaire de Becker BMD
Génomique
Genomic
Dystrophie myotonique de type 1 DM1
LncARN
Cultured
Long noncoding RNA
Delivery
Dystrophie musculaire de Becker
Becker muscular dystrophy BMD
Becker Muscular Dystrophy
Mice
Ex-vivo
DMO
Autophagy
Human Umbilical Vein Endothelial Cells
Dystrophie Musculaire de Duchenne DMD
Cardiomyopathie
Skeletal muscle
Drp1
MES
Gene Expression Regulation/drug effects
Heart Failure
CaVβ1
Exon skipping
Knockout
DMD
Humans
Male
LncRNA
Inbred C57BL
Modificateurs de gènes
Dystrophin
Animals
Animal/physiopathology
Adult muscle stem cells
CaVβs
Clinical trials
Gene expression
Epigenetics
Multiresolution modeling
Muscle Biology
Activin Receptors
Inbred mdx
Dynamin 2
Diseases
Antisense oligonucleotides
Multi resolution modeling
DHPR α1S
Duchenne DMD dystrophy
Cardiomyopathy
Molecular docking
Multi exon skipping
Metabolism
Molecular Sequence Data
Mitochondrial fission
Liver
BMD
Immunoglobulin Fc Fragments/pharmacology
Cell Line
LKB1
Dystrophine
Invivo
Calcium
Cell homeostasis
Long QT
Energy Metabolism/drug effects
Duchenne muscular dystrophy DMD
CD38
Homeostasis
L-Type
Base Sequence
Becker muscular dystrophy
Dystrophy
Cell Biology
CaV subunits
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Hear
Dystrophin central domain
Isoforms
Connexins
Centronuclear myopathy
Cachexia
Gene modifiers
Morphogenesis
Isoformes
Mdx mouse
Dilated Cardiomyopathy
Dystrophin-EGFP
Becker BMD muscular dystrophy
Inhibitors
Allele‐specific silencing therapy
CTNNB1
MiARN
Jonction neuromusculaire JNM
Hepatocellular carcinoma
Calcium Channels
Cells
Muscle