肌萎缩侧索硬化
RNA干扰
SOD1
小发夹RNA
核糖核酸
生物
基因
小干扰RNA
基因表达
信使核糖核酸
小RNA
遗传学
细胞生物学
医学
疾病
病理
作者
Albert A. Rizvanov,Şükrü Güllüoğlu,Mehmet E. Yalvaç,András Palotás,Р. Р. Исламов
出处
期刊:Current Drug Metabolism
[Bentham Science]
日期:2011-07-25
卷期号:12 (7): 679-683
被引量:2
标识
DOI:10.2174/138920011796504464
摘要
Amyotrophic lateral sclerosis (ALS) is a debilitating neuro-degenerative disorder characterized by progressive loss of motor neurons. The etiology and molecular pathogenesis of cell death in most sub-types of the disease are largely unknown. The best documented cause of moto-neuron degeneration is the mutation in the superoxide dismutase-1 (SOD1) gene, which occurs in 10% of the familial forms of ALS. Discovery of RNA interference (RNAi), which plays an important role in the regulation of gene expression, has proven to be a powerful tool to study the pathogenesis and to develop innovative treatment options for hereditary diseases, including familial variants of ALS. This review summarizes current research advances in RNAi in relation to ALS. Keywords: Amyotrophic lateral sclerosis (ALS), gene expression, messenger RNA (mRNA), micro RNA (miRNA), RNA interference (RNAi), short (or small) hair-pin RNAs (shRNA), short (or small) interfering RNA (siRNA), superoxide dismutase (SOD), Thomas Tuschl's group, silencer RNAs
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