Personalized gene and cell therapy for Duchenne Muscular Dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
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1. Mechanisms of Chimeric Cell Therapy in Duchenne Muscular Dystrophy;Biomedicines;2024-09-02
2. Leucyl-tRNA Synthetase Contributes to Muscle Weakness through Mammalian Target of Rapamycin Complex 1 Activation and Autophagy Suppression in a Mouse Model of Duchenne Muscular Dystrophy;The American Journal of Pathology;2024-08
3. The complex landscape of DMD mutations: moving towards personalized medicine;Frontiers in Genetics;2024-03-26
4. Amelioration of Morphological Pathology in Cardiac, Respiratory, and Skeletal Muscles Following Intraosseous Administration of Human Dystrophin Expressing Chimeric (DEC) Cells in Duchenne Muscular Dystrophy Model;Biomedicines;2024-03-06
5. Biomarkers in Duchenne Muscular Dystrophy: Current Status and Future Directions;Journal of Neuromuscular Diseases;2023-11-07
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