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Dernières publications
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Julia Pereira Lemos, Liliane Patrícia Gonçalves Tenório, Vincent Mouly, Gillian Butler-Browne, Daniella Arêas Mendes-Da-Cruz, et al.. T cell biology in neuromuscular disorders: a focus on Duchenne Muscular Dystrophy and Amyotrophic Lateral Sclerosis. Frontiers in Immunology, 2023, 14, pp.120283. ⟨10.3389/fimmu.2023.1202834⟩. ⟨hal-04603915⟩
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Fanny Roth, Jamila Dhiab, Alexis Boulinguiez, Hadidja-Rose Mouigni, Saskia Lassche, et al.. Assessment of PABPN1 nuclear inclusions on a large cohort of patients and in a human xenograft model of oculopharyngeal muscular dystrophy. Acta Neuropathologica, 2022, ⟨10.1007/s00401-022-02503-7⟩. ⟨hal-03832636⟩
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Elisa Negroni, Maria Kondili, Laura Muraine, Mona Bensalah, Gillian Sandra Butler-Browne, et al.. Muscle fibro-adipogenic progenitors from a single-cell perspective: Focus on their “virtual” secretome. Frontiers in Cell and Developmental Biology, 2022, 10, ⟨10.3389/fcell.2022.952041⟩. ⟨hal-03830589⟩
Chiffres clés
105
Publications avec texte intégral
Open Access
61 %
Mots clés
Muscular dystrophy
Skeletal muscle
DUX4
Agrégats de PABPN1
Atrophy
Myosin
AAV vectors
Gene therapy
Myotube
Geriatric assessment
Pax7
Haploinsufficiency
Regenerative medicine
Muscle
Arbovirus
Biomarker
Alzheimer's disease
Alphavirus
Fibrosis
Mass spectrometry
AChR antibodies
Dysferlin
2-D PAGE
Myoblasts
Actin
MND
Myogenesis
Muscle stem cells
Omics
AUTOPHAGY
Aged
Oculopharyngeal muscular dystrophy
Regulatory T cells
PABPN1 agregates
Annexin A2
Muscle fibrosis
Anti-fibrotic pharmacotherapies
Cross-bridge kinetics
Epigenetics
OPMD
Myoblast
Autoimmune diseases
Differentiation
Satellite cells
Sporadic ALS
Amyotrophic Lateral Sclerosis
Andermann syndrome
Duchenne muscular dystrophy
Aav-U7
Inflammation
Myopathy
APOPTOSIS
RNA
Sarcopenia
Triplet expansion disease
Exon-skipping
Dysferlinopathy
Transcriptomics
DMD
Cell therapy
Metabolism
Gene replacement
Satellite cell
Xenograft
Functional genomics
Human
Neuromuscular junction NMJ
ALS
Secreted vesicles
Akt
Myositis
Muscle strength
Regeneration
GENE
Antisens oligonucleotides
Muscle dystrophy
MUTATIONS
Aggregate
FAPs
Thérapie génique
Dystrophin
PABPN1
Adipose tissue
Accelerometry
Dystrophie musculaire oculopharyngée
Antiserum
Neuromuscular disease
Lamins
Effector T cells
Calcium
Nuclear envelope
FSHD
AAV
Intercellular communication
DNA methylation
Pharyngeal muscle
Anti-acetylcholine receptor antibodies
Ageing
Myopathies
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