Lv3
238 积分 2024-09-15 加入
Novel founder variant in the S-antigen visual arrestin geneSAGis the most prevalent cause of autosomal dominant retinitis pigmentosa in Singaporean Chinese
3小时前
求助中
Functional correction of the untreatable CFTR 1717-1G>A mutation through mRNA- and sgRNA-optimized base editing
27天前
已完结
Discovery of β-Arrestin Biased Ligands of 5-HT7R
1个月前
已完结
The TBCK-PPP1R21-FERRY3/C12orf4 complex: a RAB5-GAP brake essential for endo-lysosomal homeostasis
1个月前
已完结
Single-Cell Splicing Isoform Atlas of the Adult Human Heart and Heart Failure
3个月前
已完结
In vivo base editing of Chd3 rescues behavioural abnormalities in mice
3个月前
已完结
RNA-targeting strategies as a platform for ocular gene therapy
5个月前
已完结
PHENOTYPIC VARIABILITY OF RECESSIVE RDH12-ASSOCIATED RETINAL DYSTROPHY
5个月前
已完结
GPCR activation and GRK2 assembly by a biased intracellular agonist
5个月前
已完结
Base editing correction of hypertrophic cardiomyopathy in human cardiomyocytes and humanized mice
5个月前
已完结
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