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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
Open Access
87 %
Mots clés
Bile acid
Genetics
Bioinformatics
FoxO
Muscle
DNM2
Differentiation
Allele-specific silencing therapy
Fibrosis
Fibroblast
Flavonoid
Human
Myotonic dystrophy
Laminographie
Canine X-linked muscular dystrophy in Japan CXMD J
CXCR4
Antisense morpholino
Dynamin 2
Folding-defective proteins
Conjugation
CTG⋅CAGn repeat
Glucocorticoid-induced muscle atrophy
Autophagy
Human muscle stem/progenitor cells
LRP4
Adhesion
CLS
Exondys 51
Myogenesis
Dominant centronuclear myopathy
Lamina-associated domain
Migration
Clinical trial candidate screening
Fear response
DiPRO1
BMD
DM1 myoblasts
Dystrophin
Gene Therapy
Gene network analysis
Immortalisation
Centronuclear myopathy
Gel electrophoresis
FSHD
Actin
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
LTβR
Duchenne muscular dystrophy
DMD
CFTR correctors
RNA interference
CRISPR/Cas9
Cell biology
Expanded repeats
HDMD/Dmd-null mice
Exon Skipping
3D co-culture
Neuromuscular disease
Myotube
Endocytosis
Drisapersen
Motor neuron
Glucose
Exon-skipping
Duchenne Muscular Dystrophy
Developmental biology
CMS
Biomimetism
BAF
ITSN1
CXCL12
Atrial cardiac defects
Adeno-associated viral vector
Human artificial chromosomes
Immortalized dystrophic canine myoblast
Autophagosome
ICU-acquired weakness
Insulin
Gut microbiota
KLF15
Neuromuscular junction
Lamin A/C nuclei
Alternative splicing
Gene therapy
DsDNA break repair
Antisense oligonucleotide
Chromatin
CDNA synthesis
Computer software
Allele-specific silencing
Becker muscular dystrophy
Culture platform
Skeletal muscle
Cell-penetrating peptide
Emerin
Acetylcholine receptor subunit epsilon
Exon skipping
Eteplirsen
Cell Therapy
Coculture