Lv11
30 积分 2024-10-31 加入
Molecular and clinical features of inherited neuropathies due to PMP22 duplication
1小时前
待确认
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
9天前
已完结
Rare mutations associating with serum creatinine and chronic kidney disease
12天前
已完结
Retinol binding protein 4 antagonists and protein synthesis inhibitors: Potential for therapeutic development
24天前
已完结
Avacincaptad Pegol for Geographic Atrophy Secondary to Age-Related Macular Degeneration: Two-Year Efficacy and Safety Results from the GATHER2 Phase 3 Trial
27天前
已完结
Efficacy and safety of avacincaptad pegol in patients with geographic atrophy (GATHER2): 12-month results from a randomised, double-masked, phase 3 trial
27天前
已完结
Emerging therapies for inherited retinal degeneration
30天前
已完结
Discovery of NP3-253, a Potent Brain Penetrant Inhibitor of the NLRP3 Inflammasome
1个月前
已完结
Discovery of NP3-253, a Potent Brain Penetrant Inhibitor of the NLRP3 Inflammasome
1个月前
已完结
Ofirnoflast: a first-in-class NEK7-targeted inhibitor of the NLRP3 inflammasome
2个月前
已完结
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