Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy
出版年份 2014 全文链接
标题
Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 23, Issue 16, Pages 4249-4259
出版商
Oxford University Press (OUP)
发表日期
2014-04-02
DOI
10.1093/hmg/ddu142
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- More than a bystander: the contributions of intrinsic skeletal muscle defects in motor neuron diseases
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- (2010) Dina Shafey et al. JOURNAL OF PROTEOME RESEARCH
- Hearts of Dystonia musculorum Mice Display Normal Morphological and Histological Features but Show Signs of Cardiac Stress
- (2010) Justin G. Boyer et al. PLoS One
- Mouse Survival Motor Neuron Alleles That Mimic SMN2 Splicing and Are Inducible Rescue Embryonic Lethality Early in Development but Not Late
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- Impaired Synaptic Vesicle Release and Immaturity of Neuromuscular Junctions in Spinal Muscular Atrophy Mice
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- Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?
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- Neuronal SMN expression corrects spinal muscular atrophy in severe SMA mice while muscle-specific SMN expression has no phenotypic effect
- (2008) T. O. Gavrilina et al. HUMAN MOLECULAR GENETICS
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