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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⟩
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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
52
Publications avec texte intégral
Open Access
75 %
Mots clés
Activin Receptors
CaV subunits
Dystrophie musculaire de Becker
LncRNA
Genomic
Gene modifiers
Multi resolution modeling
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Muscle hypertrophy
Exon skipping
Becker Muscular Dystrophy
Morphogenesis
Humans
CaVβs
Duchenne muscular dystrophy
Mice
Muscle development
Dynamin 2
Connexins
Becker muscular dystrophy
DHPR α1S
CTNNB1
Multi exon skipping
Animal/physiopathology
Ex-vivo
Dystrophine
Dystrophin
Long noncoding RNA
Human Umbilical Vein Endothelial Cells
Adult muscle stem cells
Duchenne DMD dystrophy
Cell Line
Drp1
Metabolism
Cultured
Homeostasis
Dystrophin central domain
Calcium
Inhibitors
Energy Metabolism/drug effects
Inbred C57BL
Dilated Cardiomyopathy
Skeletal muscle
Mdx mouse
Multiresolution modeling
Dystrophie Musculaire de Becker BMD
MES
Becker BMD muscular dystrophy
Cells
Modificateurs de gènes
LKB1
Base Sequence
MiARN
Knockout
Muscle Biology
Muscle
Delivery
Invivo
Molecular Sequence Data
Dystrophy
Diseases
Dystrophin-EGFP
Becker muscular dystrophy BMD
Centronuclear myopathy
Calcium Channels
L-Type
CD38
Liver
Cell homeostasis
Hear
Duchenne muscular dystrophy DMD
Cardiomyopathy
Heart Failure
Autophagy
Allele‐specific silencing therapy
Cachexia
Molecular docking
Génomique
Muscle Strength
BMD
Mitochondrial fission
Long QT
Dystrophie Musculaire de Duchenne DMD
Antisense oligonucleotides
Epigenetics
Cell Biology
Muscle damage
Cardiomyopathie
Muscle cell fusion
Immunoglobulin Fc Fragments/pharmacology
Animals
Male
DMD
Inbred mdx
Gene expression
LncARN
Clinical trials
Gene Expression Regulation/drug effects
DMO
Hepatocellular carcinoma