Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction.
about
From phenologs to silent suppressors: Identifying potential therapeutic targets for human disease.Novel interactors of the Drosophila Survival Motor Neuron (SMN) Complex suggest its full conservation.Plant snRNP Biogenesis: A Perspective from the Nucleolus and Cajal Bodies.Genetic screen identifies a requirement for SMN in mRNA localisation within the Drosophila oocyte.
P2860
Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction.
description
2017 nî lūn-bûn
@nan
2017 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@ast
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@en
type
label
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@ast
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@en
prefLabel
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@ast
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@en
P2093
P2860
P356
P1476
Spinal Muscular Atrophy: From ...... to Neuromuscular Dysfunction.
@en
P2093
Maia Lanfranco
Neville Vassallo
Ruben J Cauchi
P2860
P356
10.3389/FMOLB.2017.00041
P577
2017-06-08T00:00:00Z