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Dernières publications
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Francesco Galli, Laricia Bragg, Maira Rossi, Daisy Proietti, Laura Perani, et al.. Cell-mediated exon skipping normalizes dystrophin expression and muscle function in a new mouse model of Duchenne Muscular Dystrophy. EMBO Molecular Medicine, 2024, 16 (4), pp.927 - 944. ⟨10.1038/s44321-024-00031-3⟩. ⟨hal-04603972⟩
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Ekaterina Kiseleva, Olesya Serbina, Anna Karpukhina, Vincent Mouly, Yegor S Vassetzky. Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype. Journal of Cellular Physiology, 2022, 237 (8), pp.3328-3337. ⟨10.1002/jcp.30789⟩. ⟨hal-03796151⟩
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Muhammad Haseeb Iqbal, Jeanne Rosine Faratiana, Emeline Pradel, Varvara Gribova, Kamel Mamchaoui, et al.. Brush-Induced Orientation of Collagen Fibers in Layer-by-Layer Nanofilms: A Simple Method for the Development of Human Muscle Fibers. ACS Nano, In press, ⟨10.1021/acsnano.2c06329⟩. ⟨hal-03832239⟩
Chiffres clés
51
Publications avec texte intégral
Open Access
87 %
Mots clés
CFTR correctors
ICU-acquired weakness
Cell Therapy
CDNA synthesis
Expanded repeats
Immortalisation
Lamin A/C nuclei
Exon skipping
Autophagy
Myotube
Myogenesis
CXCR4
Cell-penetrating peptide
Human artificial chromosomes
Coculture
CMS
Conjugation
Antisense morpholino
CRISPR/Cas9
Muscle
CTG⋅CAGn repeat
DiPRO1
Exon Skipping
DM1 myoblasts
DMD
Centronuclear myopathy
Bile acid
Exondys 51
Autophagosome
Gene network analysis
Fear response
Glucose
Myotonic dystrophy
Clinical trial candidate screening
Emerin
Folding-defective proteins
Dystrophin
Motor neuron
Lymphotoxin-β-receptor
Laminographie
Cell biology
Adhesion
Adeno-associated viral vector
Skeletal muscle
Human
Gene therapy
Fibroblast
Machine learning
Becker muscular dystrophy
Exon-skipping
HDMD/Dmd-null mice
Developmental biology
RNA interference
Gut microbiota
Lamina-associated domain
Alternative splicing
Differentiation
Fibrosis
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Canine X-linked muscular dystrophy in Japan CXMD J
Dynamin 2
LRP4
Immortalized dystrophic canine myoblast
Antisense oligonucleotide
Migration
Human muscle stem/progenitor cells
Actin
3D co-culture
Glucocorticoid-induced muscle atrophy
Gene Therapy
Eteplirsen
KLF15
Duchenne muscular dystrophy
DsDNA break repair
DNM2
BMD
Chromatin
Atrial cardiac defects
Drisapersen
Flavonoid
MSCs
Computer software
Mdx
Gel electrophoresis
ITSN1
Allele-specific silencing
BAF
FSHD
FoxO
Duchenne Muscular Dystrophy
Acetylcholine receptor subunit epsilon
Endocytosis
MT RNA/DNA Editing
Dominant centronuclear myopathy
CXCL12
CLS
Allele-specific silencing therapy
LTβR
Insulin
Neuromuscular junction