Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis
about
SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.Downregulation of sorting nexin 10 is associated with overexpression of miR-30d during liver cancer progression in rats.Structure of the PX domain of SNX25 reveals a novel phospholipid recognition model by dimerization in the PX domain.
P2860
Structure of human SNX10 reveals insights into its role in human autosomal recessive osteopetrosis
description
2014 nî lūn-bûn
@nan
2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@ast
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@en
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@nl
type
label
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@ast
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@en
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@nl
prefLabel
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@ast
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@en
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@nl
P2093
P2860
P356
P1433
P1476
Structure of human SNX10 revea ...... osomal recessive osteopetrosis
@en
P2093
Duanqing Pei
Jinsong Liu
Tingting Xu
Xiaodong Shu
Yinghua Ye
P2860
P304
P356
10.1002/PROT.24689
P407
P577
2014-12-01T00:00:00Z