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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⟩
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Chiffres clés
34
Publications avec texte intégral
Open Access
61 %
Mots clés
LMNA
Brain
G-Secretase
Maladie neuromusculaire
Prematurity
Epigenetic changes
Adenosine
Longitudinal progression
MND
Brain injury
MRI
Cartilage and bone regeneration
Mecp2
Intra-uterine growth restriction
Inflammation
AAV
Albumin gene targeting
Dilated cardiomyopathy
Brain MRI
ASOs
GABA
CRISPR/SaCas9
Fetal growth restriction
GeneRide
Maternal behavior
Methylosome
Adult patients
ERK1/2 signaling
Icv
Mitochondrial dysfunction
DTI
Dicer
C9orf72
Functional outcomes
AICD
Amyotrophie spinale
Clinical markers
Adult SMA
Biomarker
Biological marker
Aav10
Brain imaging
Maternal malnutrition
Coagulation factor IX
Clinical trials
3xTgAD Mice
Mitophagy
Les paramètres respiratoires
Cell reprogramming
Early-onset sepsis
Chondrocytes
Extremely preterm infants
Melatonin
Spinal muscular atrophy
Genetical therapy
Fabry disease lysosomal storage disorders adeno asociated virus-9
Microglia
Gene transfer
Biomarkers
Mouse model
Modèle murin
Effector T cells
Cell stemness
Long-term handicap
ALS
Bone development
Antisense oligonucleotides
Brain development
FGR
Lentiviral vectors
FTD
Duchenne Muscular Dystrophy
Disease heterogeneity
CNS
Metabolic disorders
MiRNA
ASO
Cellules souches musculaires
Amyotrophic Lateral Sclerosis
Blood brain barrier
FOXO3a
Bone involvement
Disease modifiers
Brain damage
Calcium handling
Distal myopathy
IUGR
MRNP assembly
IPSCs
Cofilin-1
Gene therapy
Glucocorticosteroid
MUNIX
Clinical trial
Intra-CSF delivery
DPRs
Errance diagnotique
IRM
SMN
Diseases