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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
36
Publications avec texte intégral
Open Access
61 %
Mots clés
MUNIX
Brain injury
Bone involvement
Mecp2
Glucocorticosteroid
ASOs
Clinical trials
Albumin gene targeting
Duchenne Muscular Dystrophy
Mitophagy
MiRNA
GABA
Intra-uterine growth restriction
Brain development
ASO
CNS
Brain damage
Modèle murin
Lentiviral vectors
FOXO3a
Cartilage and bone regeneration
Antisense oligonucleotides
Adenosine
Epigenetic changes
Clinical markers
Maternal behavior
Cell stemness
ALS
Brain imaging
Biomarker
IPSCs
Intra-CSF delivery
Calcium handling
Genetical therapy
Fabry disease lysosomal storage disorders adeno asociated virus-9
AICD
Coagulation factor IX
IUGR
Clinical trial
Bone development
LMNA
FTD
Icv
Errance diagnotique
FGR
Microglia
Longitudinal progression
Amyotrophic Lateral Sclerosis
CRISPR/SaCas9
GeneRide
Chondrocytes
DPRs
Melatonin
Disease modifiers
Maternal malnutrition
Fetal growth restriction
Gene transfer
G-Secretase
Early-onset sepsis
Brain
ERK1/2 signaling
Metabolic disorders
Cofilin-1
Adult patients
Cellules souches musculaires
Biomarkers
Amyotrophie spinale
Dicer
IRM
3xTgAD Mice
SMN
Methylosome
Mouse model
Cell reprogramming
Functional outcomes
Effector T cells
Disease heterogeneity
MND
Diseases
Blood brain barrier
Adult SMA
Les paramètres respiratoires
Gene therapy
Distal myopathy
MRI
MRNP assembly
Long-term handicap
Aav10
Extremely preterm infants
Maladie neuromusculaire
DTI
Spinal muscular atrophy
Biological marker
Prematurity
AAV
Brain MRI
Mitochondrial dysfunction
Inflammation
C9orf72
Dilated cardiomyopathy