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Dernières publications
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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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Nicolas Vignier, Maria Chatzifrangkeskou, Luca Pinton, Hugo Wioland, Thibaut Marais, et al.. The non-muscle ADF/cofilin-1 controls sarcomeric actin filament integrity and force production in striated muscle laminopathies. Cell Reports, 2021, 36 (8), pp.109601. ⟨10.1016/j.celrep.2021.109601⟩. ⟨hal-03350074⟩
Chiffres clés
32
Publications avec texte intégral
Open Access
60 %
Mots clés
Mecp2
Fetal growth restriction
Dilated cardiomyopathy
CNS
Functional outcomes
Brain injury
Biomarker
Icv
Disease heterogeneity
Adult patients
Blood brain barrier
Lentiviral vectors
CRISPR/SaCas9
DPRs
ALS
Longitudinal progression
Bone involvement
Spinal muscular atrophy
AAV
Bone development
ASO
FOXO3a
MRI
Brain development
GeneRide
IRM
Brain damage
Motoneurone
Gene transfer
Distal myopathy
Cellules souches musculaires
LMNA
Calcium handling
MRNP assembly
AICD
ASOs
Cell stemness
Coagulation factor IX
Diseases
Brain imaging
Early-onset sepsis
3xTgAD Mice
Biomarkers
Clinical trials
Murine model
Aav10
Epigenetic changes
Intra-uterine growth restriction
Intra-CSF delivery
Motor neurons
Albumin gene targeting
Cartilage and bone regeneration
Mitochondrial dysfunction
Brain
Cofilin-1
Biological marker
FTD
Maternal behavior
Antisense oligonucleotides
MND
SMN
Metabolic disorders
Inflammation
MUNIX
Clinical trial
GABA
Maladie neuromusculaire
Genetical therapy
Modèle murin
DTI
Chondrocytes
MiRNA
FGR
Maternal malnutrition
Disease modifiers
Fabry disease lysosomal storage disorders adeno asociated virus-9
Les paramètres respiratoires
Brain MRI
IPSCs
G-Secretase
ERK1/2 signaling
Prematurity
Melatonin
Mitophagy
Errance diagnotique
Glucocorticosteroid
Mouse model
Adult SMA
C9orf72
Long-term handicap
Microglia
Gene therapy
Clinical markers
Dicer
Adenosine
Amyotrophie spinale
IUGR
Extremely preterm infants
Methylosome
Cell reprogramming