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Plateforme d’immortalisation MyoLine – CRM collection
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Last submissions
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⟩
Eline Lemerle, Jeanne Lainé, Marion Benoist, Gilles Moulay, Anne Bigot, et al.. Caveolae and Bin1 form ring-shaped platforms for T-tubule initiation.
eLife
, 2023, 12,
⟨10.7554/eLife.84139⟩
.
⟨hal-04094370⟩
Dzhangar Dzhumashev, Andrea Timpanaro, Safa Ali, Andrea de Micheli, Kamel Mamchaoui, et al.. Quantum Dot-Based Screening Identifies F3 Peptide and Reveals Cell Surface Nucleolin as a Therapeutic Target for Rhabdomyosarcoma.
Cancers
, 2022, 14 (20), pp.5048.
⟨10.3390/cancers14205048⟩
.
⟨hal-03832696⟩
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⟩
Sebastián Montealegre, Élise Lebigot, Hugo Debruge, Norma Beatriz Romero, Bénédicte Héron, et al.. FDX2 and ISCU Gene Variations Lead to Rhabdomyolysis with Distinct Severity and Iron Regulation.
Neurology Genetics
, 2022, 8 (1),
⟨10.1212/NXG.0000000000000648⟩
.
⟨hal-03604086⟩
Christopher J Walsh, Carlos Escudero King, Muskan Gupta, Pamela J Plant, Margaret J Herridge, et al.. MicroRNA regulatory networks associated with abnormal muscle repair in survivors of critical illness.
Journal of Cachexia, Sarcopenia and Muscle
, 2022,
⟨10.1002/jcsm.12903⟩
.
⟨hal-03549744⟩
Swati Dudhal, Lylia Mekzine, Bernard Prudhon, Karishma Soocheta, Bruno Cadot, et al.. Development of versatile allele-specific siRNAs able to silence all the dominant dynamin 2 mutations.
Molecular Therapy - Nucleic Acids
, 2022, 29, pp.733-748.
⟨10.1016/j.omtn.2022.08.016⟩
.
⟨hal-03778880⟩
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⟩
Key numbers
48
Publications with fulltext
Open Access
87 %
Keywords
CMS
Gene therapy
Actin
FoxO
Expanded repeats
Antisense morpholino
Atrial cardiac defects
Becker muscular dystrophy BMD Duchenne muscular dystrophy DMD miRNA nNOS
Eteplirsen
DM1 myoblasts
Folding-defective proteins
ITSN1
Emerin
Alternative splicing
Lamina-associated domain
CFTR correctors
Cell Therapy
Fibroblast
Human muscle stem/progenitor cells
Immortalized dystrophic canine myoblast
Cell-penetrating peptide
CXCL12
Adeno-associated viral vector
DsDNA break repair
Allele-specific silencing
CTG⋅CAGn repeat
Dynamin 2
RNA interference
Drisapersen
CDNA synthesis
Skeletal muscle
Motor neuron
Dystrophin
Exondys 51
CRISPR/Cas9
Dominant centronuclear myopathy
3D co-culture
Endocytosis
Exon-skipping
Glucose
HDMD/Dmd-null mice
Autophagy
Conjugation
Insulin
Muscle
Becker muscular dystrophy
Gene network analysis
Laminographie
DNM2
LTβR
Acetylcholine receptor subunit epsilon
BMD
Mdx52 mice
KLF15
Antisense oligonucleotide
LRP4
ICU-acquired weakness
MT RNA/DNA Editing
Migration
DMD
Bile acid
BAF
Centronuclear myopathy
Differentiation
Gene Therapy
Exon skipping
FSHD
Allele-specific silencing therapy
Computer software
Myogenesis
Duchenne Muscular Dystrophy
Fear response
Coculture
Exon Skipping
Mdx
Lymphotoxin-β-receptor
Gel electrophoresis
Chromatin
Developmental biology
Cell biology
Immortalisation
CXCR4
Fibrosis
Canine X-linked muscular dystrophy in Japan CXMD J
Myotube
Neuromuscular junction
Flavonoid
MSCs
Gut microbiota
CLS
Lamin A/C nuclei
Adhesion
Myotonic dystrophy
Glucocorticoid-induced muscle atrophy
Clinical trial candidate screening
Duchenne muscular dystrophy
Human
Human artificial chromosomes
Autophagosome
Machine learning