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Dernières publications
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Anna Underhill, Samuel Webb, Fiorella Grandi, Jing-Yi Jeng, Jacques de Monvel, et al.. MYO7A is required for the functional integrity of the mechanoelectrical transduction complex in hair cells of the adult cochlea. Proceedings of the National Academy of Sciences of the United States of America, 2025, 122 (1), pp.e2414707122. ⟨10.1073/pnas.2414707122⟩. ⟨hal-04905455⟩
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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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Chiffres clés
39
Publications avec texte intégral
Open Access
62 %
Mots clés
Maladie neuromusculaire
Brain imaging
CRISPR/SaCas9
Maternal behavior
Fetal growth restriction
MND
MUNIX
SMN
Cartilage and bone regeneration
3xTgAD Mice
Spinal muscular atrophy
ERK1/2 signaling
G-Secretase
Prematurity
Cell reprogramming
Lentiviral vectors
Bone development
MRNP assembly
Aav10
Brain development
Calcium handling
AICD
Distal myopathy
Dicer
Albumin gene targeting
Blood brain barrier
Long-term handicap
Chondrocytes
Gene therapy
GeneRide
Amyotrophic Lateral Sclerosis
Brain injury
ASOs
Brain damage
Intra-uterine growth restriction
Effector T cells
FOXO3a
Errance diagnotique
Les paramètres respiratoires
MiRNA
Amyotrophie spinale
Cell stemness
Cochlea
IPSCs
Microglia
Functional outcomes
Clinical trial
LMNA
Biological marker
Brain
Fabry disease lysosomal storage disorders adeno asociated virus-9
Longitudinal progression
Antisense oligonucleotides
Biomarker
Hair cell
Gene transfer
Bioinformatics
Modèle murin
FTD
Disease heterogeneity
Icv
IUGR
Biomarkers
Adult SMA
Genetics
Mouse model
Adenosine
Epigenetic changes
Bone involvement
Intra-CSF delivery
GABA
Brain MRI
Clinical markers
Dilated cardiomyopathy
Skeletal muscle
Diseases
DPRs
Clinical trials
Inflammation
Cofilin-1
DTI
AAV
ALS
Adult patients
IRM
FGR
Duchenne Muscular Dystrophy
Disease modifiers
Extremely preterm infants
C9orf72
Coagulation factor IX
Glucocorticosteroid
Hearing loss
ASO
Cellules souches musculaires
CNS
Early-onset sepsis
MRI
Neuromuscular disease
Genetical therapy