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