Lv2
150 积分 2023-01-04 加入
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity
18天前
已完结
Restoration of dystrophin expression in mice by suppressing a nonsense mutation through the incorporation of unnatural amino acids
1个月前
已完结
Unnatural Amino Acid‐Based Ionic Liquid Enables Oral Treatment of Nonsense Mutation Disease in Mice
1个月前
已完结
Programmable deaminase-free base editors for G-to-Y conversion by engineered glycosylase
7个月前
已完结
Revisiting the critical roles of reactive astrocytes in neurodegeneration
8个月前
已完结
Eteplirsen: First Global Approval
8个月前
已完结
Therapeutic approaches for Duchenne muscular dystrophy
8个月前
已完结
enOsCas12f1-mediated exon skipping for Duchenne muscular dystrophy therapy in humanized mouse model
8个月前
已完结
Enhanced C‐To‐T and A‐To‐G Base Editing in Mitochondrial DNA with Engineered DdCBE and TALED (Adv. Sci. 3/2024)
9个月前
已完结
Base editing correction of hypertrophic cardiomyopathy in human cardiomyocytes and humanized mice
9个月前
已完结
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