Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy
about
On-chip, multisite extracellular and intracellular recordings from primary cultured skeletal myotubes.Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-IIIAdvances in understanding the role of disease-associated proteins in spinal muscular atrophy.Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation.A-44G transition in SMN2 intron 6 protects patients with spinal muscular atrophy.
P2860
Commonality amid diversity: Multi-study proteomic identification of conserved disease mechanisms in spinal muscular atrophy
description
2016 nî lūn-bûn
@nan
2016 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@ast
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@en
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@nl
type
label
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@ast
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@en
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@nl
prefLabel
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@ast
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@en
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@nl
P50
P3181
P1476
Commonality amid diversity: Mu ...... sms in spinal muscular atrophy
@en
P304
P3181
P356
10.1016/J.NMD.2016.06.004
P577
2016-06-07T00:00:00Z