Skeletal muscle-specific PRMT1 deletion causes muscle atrophy via deregulation of PRMT6/FOXO3 axis.

被引：0
|
作者：
Choi, S. [1 ]
Jeong, H. [2 ]
Kim, H. [2 ]
Choi, D. [1 ]
Koo, S. [1 ]
Kang, J. [2 ]
机构：
[1] Korea Univ, Div Life Sci, Seoul, South Korea
[2] Sungkyunkwan Univ, Dept Mol Cell Biol, Sch Med, Suwon, South Korea
来源：
MOLECULAR BIOLOGY OF THE CELL | 2018年 / 29卷 / 26期
关键词：
D O I：
暂无
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
P2487
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页数：1
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