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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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Valentin Jacquier, Manon Prévot, Thierry Gostan, Rémy Bordonné, Sofia Benkhelifa-Ziyyat, et al.. Splicing efficiency of minor introns in a mouse model of SMA predominantly depends on their branchpoint sequence and can involve the contribution of major spliceosome components. RNA, 2022, 28 (3), pp.303-319. ⟨10.1261/rna.078329.120⟩. ⟨hal-03687098⟩
Chiffres clés
38
Publications avec texte intégral
Open Access
62 %
Mots clés
Bone development
Bioinformatics
Diseases
Cell reprogramming
MRI
ERK1/2 signaling
Genetical therapy
CNS
Neuromuscular disease
DPRs
ASO
Skeletal muscle
Gene transfer
Disease heterogeneity
GeneRide
Chondrocytes
Long-term handicap
Brain MRI
3xTgAD Mice
Clinical trials
Cofilin-1
Maternal malnutrition
G-Secretase
Glucocorticosteroid
AICD
Cellules souches musculaires
Albumin gene targeting
Bone involvement
FTD
IUGR
C9orf72
Fabry disease lysosomal storage disorders adeno asociated virus-9
Mouse model
Early-onset sepsis
Adult patients
Dicer
Calcium handling
GABA
Adult SMA
IRM
SMN
Brain imaging
Dilated cardiomyopathy
Cartilage and bone regeneration
Extremely preterm infants
MND
Functional outcomes
Modèle murin
FGR
Antisense oligonucleotides
Blood brain barrier
CRISPR/SaCas9
Distal myopathy
Les paramètres respiratoires
Biological marker
Lentiviral vectors
Intra-CSF delivery
Disease modifiers
Gene therapy
Duchenne Muscular Dystrophy
MiRNA
Amyotrophic Lateral Sclerosis
Melatonin
Errance diagnotique
Prematurity
IPSCs
Clinical markers
DTI
AAV
Mecp2
Amyotrophie spinale
Brain damage
Inflammation
Longitudinal progression
MUNIX
Icv
Brain injury
MRNP assembly
Clinical trial
Biomarkers
Effector T cells
Adenosine
ASOs
FOXO3a
Brain
Brain development
Epigenetic changes
Biomarker
Spinal muscular atrophy
Microglia
Genetics
Maternal behavior
Coagulation factor IX
ALS
Aav10
Fetal growth restriction
Maladie neuromusculaire
Intra-uterine growth restriction
LMNA
Cell stemness