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