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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
37
Publications avec texte intégral
Open Access
61 %
Mots clés
FOXO3a
AICD
Aav10
Maternal behavior
Cofilin-1
Cartilage and bone regeneration
Bone development
Adult SMA
Intra-CSF delivery
Adenosine
Clinical markers
Amyotrophic Lateral Sclerosis
Extremely preterm infants
Cell reprogramming
Icv
Spinal muscular atrophy
CNS
IPSCs
Fetal growth restriction
Fabry disease lysosomal storage disorders adeno asociated virus-9
Dicer
ASO
Coagulation factor IX
Mouse model
SMN
Intra-uterine growth restriction
MRNP assembly
Inflammation
Cell stemness
LMNA
Bone involvement
Brain
3xTgAD Mice
Biomarker
ALS
Brain development
G-Secretase
Calcium handling
GeneRide
MUNIX
FTD
Early-onset sepsis
ASOs
Genetics
Adult patients
Disease heterogeneity
Brain injury
Skeletal muscle
Gene transfer
Clinical trials
Glucocorticosteroid
Dilated cardiomyopathy
Gene therapy
Duchenne Muscular Dystrophy
Blood brain barrier
Brain imaging
Brain MRI
Biomarkers
Maternal malnutrition
Maladie neuromusculaire
Modèle murin
Functional outcomes
IUGR
Long-term handicap
Melatonin
DPRs
MND
Diseases
Brain damage
Mecp2
Cellules souches musculaires
Biological marker
Les paramètres respiratoires
Microglia
MiRNA
Genetical therapy
Distal myopathy
Effector T cells
Clinical trial
ERK1/2 signaling
Albumin gene targeting
MRI
Antisense oligonucleotides
Prematurity
Errance diagnotique
Neuromuscular disease
FGR
Longitudinal progression
IRM
Amyotrophie spinale
Epigenetic changes
CRISPR/SaCas9
DTI
C9orf72
GABA
Chondrocytes
Disease modifiers
AAV
Bioinformatics
Lentiviral vectors