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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
MND
Dysferlin
Dysferlinopathy
Akt
Oculopharyngeal muscular dystrophy
Gene therapy
Myosin
Adipose tissue
Myopathy
Muscle strength
2-D PAGE
Pharyngeal muscle
Gene replacement
Neuromuscular junction NMJ
Metabolism
Aggregate
Andermann syndrome
Nuclear envelope
Calcium
Alzheimer's disease
Epigenetics
Regulatory T cells
Secreted vesicles
Antisens oligonucleotides
Transcriptomics
FAPs
Cross-bridge kinetics
Myoblast
FSHD
Functional genomics
Anti-fibrotic pharmacotherapies
OPMD
Muscle stem cells
Xenograft
Pax7
Haploinsufficiency
Mass spectrometry
Myoblasts
Muscle fibrosis
Antiserum
Agrégats de PABPN1
Triplet expansion disease
Anti-acetylcholine receptor antibodies
Satellite cell
AUTOPHAGY
Accelerometry
Amyotrophic Lateral Sclerosis
Omics
Alphavirus
Dystrophin
ARN
APOPTOSIS
DMD
Aav-U7
Inflammation
Actin
Cell therapy
Dystrophie musculaire oculopharyngée
PABPN1 agregates
DUX4
Myogenesis
ALS
Regenerative medicine
Myopathies
Geriatric assessment
Arbovirus
Ageing
Skeletal muscle
Muscle dystrophy
GENE
Annexin A2
Myositis
Neuromuscular disease
AAV
Atrophy
Satellite cells
Autoimmune diseases
DNA methylation
Muscle
Aged
Muscular dystrophy
Human
Duchenne muscular dystrophy
Differentiation
Myotube
Sporadic ALS
PABPN1
AAV vectors
Effector T cells
RNA
Thérapie génique
Sarcopenia
Biomarker
Regeneration
MUTATIONS
Lamins
AChR antibodies
Intercellular communication
Fibrosis
Exon-skipping