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Dernières publications
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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⟩
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Elena Marchesi, Matteo Bovolenta, Lorenzo Preti, Massimo L Capobianco, Kamel Mamchaoui, et al.. Synthesis and Exon-Skipping Properties of a 3′-Ursodeoxycholic Acid-Conjugated Oligonucleotide Targeting DMD Pre-mRNA: Pre-Synthetic versus Post-Synthetic Approach. Molecules, 2021, 26 (24), pp.7662. ⟨10.3390/molecules26247662⟩. ⟨hal-03510261⟩
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Manuel Schmidt, Anja Weidemann, Christine Poser, Anne Bigot, Julia von Maltzahn. Stimulation of Non-canonical NF-κB Through Lymphotoxin-β-Receptor Impairs Myogenic Differentiation and Regeneration of Skeletal Muscle. Frontiers in Cell and Developmental Biology, 2021, 9, ⟨10.3389/fcell.2021.721543⟩. ⟨hal-03405959⟩
Chiffres clés
47
Publications avec texte intégral
Open Access
86 %
Mots clés
CDNA synthesis
MT RNA/DNA Editing
Myotube
Mitochondrial ROS
Exon skipping
Skeletal muscle
Mdx52 mice
Flavonoid
Glucocorticoid-induced muscle atrophy
Canine X-linked muscular dystrophy in Japan CXMD J
CXCR4
Adeno-associated viral vector
Alternative splicing
CFTR correctors
FSHD
Microarray
Developmental biology
DM1 myoblasts
Conjugation
KLF15
CLS
Myotonic dystrophy
Motor neuron
Becker muscular dystrophy
Lamin A/C nuclei
Computer software
Gene therapy
Fibroblast
DNM2
Exon-skipping
Gel electrophoresis
Mdx
Expanded repeats
Insulin
Duchenne muscular dystrophy
CTG⋅CAGn repeat
DMD
Migration
Dominant centronuclear myopathy
HDMD/Dmd-null mice
Dystrophin
Antisense morpholino
Acetylcholine receptor subunit epsilon
Bile acid
Myogenesis
BMD
Mechanisms of disease
Cell biology
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
LRP4
Allele-specific silencing
Immortalized dystrophic canine myoblast
Autophagosome
Actin
Human artificial chromosomes
Chromatin
Endocytosis
Folding-defective proteins
Eteplirsen
Lamina-associated domain
Autophagy
RNA interference
Coculture
Fibrosis
Atrial cardiac defects
Muscle
LTβR
FoxO
Human muscle stem/progenitor cells
Dynamin 2
Gene network analysis
Glucose
Neuromuscular junction
CXCL12
Adhesion
Machine learning
Clinical trial candidate screening
MSCs
Emerin
Laminographie
Drisapersen
Gut microbiota
ITSN1
3D co-culture
Mechano-transduction
Differentiation
CRISPR/Cas9
Centronuclear myopathy
DsDNA break repair
Immortalisation
Human
Allele-specific silencing therapy
Antisense oligonucleotide
Cell-penetrating peptide
Lymphotoxin-β-receptor
CMS
Fear response
Exondys 51
ICU-acquired weakness
BAF