Julien Couthouis researcher
Couthouis, Julien, 1982-....
VIAF ID: 212135586 (Personal)
Permalink: http://viaf.org/viaf/212135586
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Works
Title | Sources |
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Age-related loss of neural stem cell O-GlcNAc promotes a glial fate switch through STAT3 activation | |
Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations | |
CRISPR-Cas9 screens in human cells and primary neurons identify modifiers of C9ORF72 dipeptide-repeat-protein toxicity. | |
Déterminisme de la toxicité d’amyloïdes dans la levure Saccharomyces cerevisiae | |
ERAD defects and the HFE-H63D variant are associated with increased risk of liver damages in Alpha 1-Antitrypsin Deficiency | |
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy | |
Exome sequencing to identify de novo mutations in sporadic ALS trios | |
Genome-wide synthetic lethal CRISPR screen identifies FIS1 as a genetic interactor of ALS-linked C9ORF72 | |
Knockout of reactive astrocyte activating factors slows disease progression in an ALS mouse model | |
LRRK2 modifies α-syn pathology and spread in mouse models and human neurons. | |
PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista Junctions. | |
Spt4 selectively regulates the expression of C9orf72 sense and antisense mutant transcripts. | |
Targeted exon capture and sequencing in sporadic amyotrophic lateral sclerosis | |
These violent repeats have violent extends | |
The toxicity of an "artificial" amyloid is related to how it interacts with membranes. | |
Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly | |
A yeast functional screen predicts new candidate ALS disease genes |