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