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20 积分 2025-06-26 加入
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
2小时前
待确认
Structure-guided development of a potent human B0AT1 inhibitor effective in a mouse model of phenylketonuria
1个月前
已完结
Discovery of novel, potent and orally efficacious inhibitor of neutral amino acid transporter B0AT1 (SLC6A19)
1个月前
已完结
Wavelength-selective cleavage of photoprotecting groups: strategies and applications in dynamic systems
7个月前
已完结
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