Loading...
Dernières publications
-
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⟩
-
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⟩
-
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⟩
-
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
Allele-specific silencing
Glucose
Fibrosis
Coculture
Human
Dominant centronuclear myopathy
Developmental biology
Duchenne muscular dystrophy
DNM2
ICU-acquired weakness
FSHD
DM1 myoblasts
Lamina-associated domain
Dystrophin
Conjugation
Myogenesis
LRP4
FoxO
Gene network analysis
CXCR4
MSCs
3D co-culture
Bile acid
Eteplirsen
Neuromuscular junction
Antisense oligonucleotide
Chromatin
Exon skipping
Endocytosis
Mdx52 mice
Fear response
Cell-penetrating peptide
Expanded repeats
Allele-specific silencing therapy
CFTR correctors
Human artificial chromosomes
Fibroblast
RNA interference
Autophagosome
MT RNA/DNA Editing
Adhesion
Folding-defective proteins
Gut microbiota
Drisapersen
Immortalisation
Mitochondrial ROS
KLF15
Exon-skipping
BAF
Flavonoid
Skeletal muscle
Myotonic dystrophy
Exondys 51
Computer software
CTG⋅CAGn repeat
Emerin
Clinical trial candidate screening
Alternative splicing
Becker muscular dystrophy
Glucocorticoid-induced muscle atrophy
Antisense morpholino
CDNA synthesis
Gel electrophoresis
DMD
Immortalized dystrophic canine myoblast
Adeno-associated viral vector
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Gene therapy
CLS
Mechanisms of disease
Actin
Lymphotoxin-β-receptor
Motor neuron
CXCL12
DsDNA break repair
Muscle
Acetylcholine receptor subunit epsilon
HDMD/Dmd-null mice
Differentiation
Cell biology
Lamin A/C nuclei
BMD
CRISPR/Cas9
Atrial cardiac defects
Laminographie
Insulin
Human muscle stem/progenitor cells
Canine X-linked muscular dystrophy in Japan CXMD J
LTβR
Myotube
Machine learning
ITSN1
Dynamin 2
Centronuclear myopathy
Mdx
Mechano-transduction
Microarray
Migration
Autophagy
CMS