Lv11
79 积分 2025-07-21 加入
Hyperactive microtubule binding of RP1L1 R45W underlies retinal degeneration and is suppressed by glycerol
53分钟前
求助中
Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes
5个月前
已完结
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
5个月前
已完结
Hyperactive microtubule binding of RP1L1 (R45W) underlies retinal degeneration and is suppressed by glycerol
5个月前
已关闭
AAVLINK: A potent DNA-recombination method for large cargo delivery in gene therapy
5个月前
已完结
Genetic landscape of hereditary cardiomyopathies and arrhythmias in China
6个月前
已完结
Clinical and Molecular Characterization ofPROM1-Related Retinal Degeneration
11个月前
已完结
Deep phenotyping of PROM1-associated retinal degeneration
11个月前
已完结
Stem cell-based therapies for retinal diseases: focus on clinical trials and future prospects
11个月前
已完结
Post-transplant cyclophosphamide, abatacept, and vedolizumab to prevent GVHD after hematopoietic stem cells transplantation in children with acute leukemia: results of a prospective trial
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