Loading...
Dernières publications
-
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⟩
-
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⟩
-
Ingo Riederer, Daniella Arêas Mendes-Da-Cruz, Guilherme Cordenonsi da Fonseca, Mariela Natacha González, Otavio Brustolini, et al.. Zika virus disrupts gene expression in human myoblasts and myotubes: Relationship with susceptibility to infection. PLoS Neglected Tropical Diseases, 2022, 16 (2), pp.e0010166. ⟨10.1371/journal.pntd.0010166⟩. ⟨hal-03832616⟩
Chiffres clés
98
Publications avec texte intégral
Open Access
60 %
Mots clés
MUTATIONS
AAV vectors
Myopathies
Biopsies humaines
Bile salt hydrolases
Neuromuscular junction NMJ
Bioinformatique
Atrophy
Muscle dystrophy
Cell therapy
Dysferlinopathy
Cross-bridge kinetics
Inflammation
Alphavirus
DNA methylation
GENE
Skeletal muscle
Arbovirus
PABPN1
Geriatric assessment
Botulinum neurotoxin
Bioinformatics
ALS
APOPTOSIS
Akt
Agrégats de PABPN1
Regeneration
Muscle stem cells
Duchenne muscular dystrophy
Differentiation
PABPN1 agregates
Biomarker
Dystrophie musculaire oculopharyngée
Pax7
Triplet expansion disease
Antisens oligonucleotides
Oculopharyngeal muscular dystrophy
Muscle
AChR antibodies
Aggregate
Dystrophin
Pharyngeal muscle
Satellite cell
Human
Myositis
C2 domains
Myoblast
CNOT6L
Fibrosis
DUX4
Intercellular communication
Sarcopenia
Adipose tissue
Satellite cells
Nuclear envelope
ARN
Muscle strength
RNA
2-D PAGE
Autoimmune diseases
Antiserum
Calcium
Xenograft
Myotube
Aav-U7
Gene therapy
CS
C2C12 cells
Anti-acetylcholine receptor antibodies
AUTOPHAGY
Myogenesis
Functional genomics
Dysferlin
Myoblasts
Alzheimer's disease
Accelerometry
Gene replacement
Metabolism
Myosin
Andermann syndrome
BINDING SPECIFICITY
AAV
CD49d
DMD
Muscle fibrosis
Ageing
Aged
Haploinsufficiency
Exon-skipping
Autologous
FAPs
Myopathy
Transcriptomics
OPMD
Annexin A2
Lamins
FSHD
Anti-fibrotic pharmacotherapies
Thérapie génique
Actin