肌萎缩侧索硬化
运动神经元
神经科学
核糖核酸
生物
麻痹
神经退行性变
变性(医学)
RNA结合蛋白
基因
医学
疾病
遗传学
脊髓
病理
精神科
作者
Fadia Ibrahim,Tadashi Nakaya,Zissimos P. Mourelatos
出处
期刊:Annual Review of Pathology-mechanisms of Disease
[Annual Reviews]
日期:2011-03-02
卷期号:7 (1): 323-352
被引量:20
标识
DOI:10.1146/annurev-pathol-011110-130307
摘要
Motor neuron diseases (MNDs) are neurodegenerative disorders that lead to paralysis and typically carry a dismal prognosis. In children, inherited spinal muscular atrophies are the predominant diseases that affect motor neurons, whereas in adults, amyotrophic lateral sclerosis, which is inherited but mostly sporadic, is the most common MND. In recent years, we have witnessed a revolution in this field, sparked by the discovery of the genes that cause MNDs. Remarkably, at least 10 genes, whose products are either RNA-binding proteins or proteins that function in RNA processing and regulation, cause MNDs and place the dysregulation of RNA pathways at the center of motor neuron degeneration pathogenesis.
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