Lv11
20 积分 2024-08-05 加入
FAD synthase deficiency: a severe mitochondrial myopathy involving a secondary reduction of RFVT2 expression
30分钟前
求助中
Impact of natural mutations on the riboflavin transporter 2 and their relevance to human riboflavin transporter deficiency 2
31分钟前
待确认
In silico investigation on structure–function relationship of members belonging to the human SLC52 transporter family
33分钟前
已完结
An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency
44分钟前
已完结
Functional Study of the Human Riboflavin Transporter 2 Using Proteoliposomes System
49分钟前
求助中
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B
1小时前
已完结
Identification and Functional Characterization of Rat Riboflavin Transporter 2
8小时前
已完结
Current Status of Major Mycotoxins Contamination in Food and Feed in Asia─A Review
1个月前
已完结
AGRP neurons are sufficient to orchestrate feeding behavior rapidly and without training
1个月前
已完结
Fraxetin pretreatment alleviates cisplatin‐induced kidney injury by antagonizing autophagy and apoptosis via mTORC1 activation
1个月前
已完结
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