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King, Oliver
One or more keywords matched the following items that are connected to King, Oliver
Item TypeName
Academic Article Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis.
Academic Article Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers.
Academic Article Telomere position effect regulates DUX4 in human facioscapulohumeral muscular dystrophy.
Academic Article Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS.
Concept Muscular Dystrophy, Facioscapulohumeral
Concept Muscular Dystrophies, Limb-Girdle
Academic Article Human skeletal muscle xenograft as a new preclinical model for muscle disorders.
Academic Article Facioscapulohumeral muscular dystrophy: Are telomeres the end of the story?
Academic Article Identifying diagnostic DNA methylation profiles for facioscapulohumeral muscular dystrophy in blood and saliva using bisulfite sequencing.
Academic Article Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy.
Academic Article Morpholino-mediated Knockdown of DUX4 Toward Facioscapulohumeral Muscular Dystrophy Therapeutics.
Academic Article Precise therapeutic gene correction by a simple nuclease-induced double-stranded break.
Academic Article Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy.
Academic Article iMyoblasts for ex vivo and in vivo investigations of human myogenesis and disease modeling.
Academic Article A Targeted Approach for Evaluating DUX4-Regulated Proteins as Potential Serum Biomarkers for Facioscapulohumeral Muscular Dystrophy Using Immunoassay Proteomics.
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  • Muscular Dystrophies