帕金森氏症的分子研究。

F1000 medicine reports Pub Date : 2011-01-01 Epub Date: 2011-04-01 DOI:10.3410/M3-7
Bobby Thomas, M Flint Beal
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引用次数: 88

摘要

帕金森病是一种神经退行性运动障碍,其特征是中脑多巴胺能神经元的丧失,导致运动异常和自主神经功能障碍。尽管进行了深入的研究,但帕金森病的病因仍然知之甚少,这使我们没有有效的治疗选择。然而,最近与帕金森病遗传形式相关的基因的鉴定已经彻底改变了该领域的研究,并开始为疾病发病机制提供新的线索。在这里,我们讨论了这些最新的遗传进展,并强调了它们在我们寻求更好地理解常见潜在疾病机制方面的重要性,这将有助于我们确定帕金森病的创新神经保护疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular insights into Parkinson's disease.

Molecular insights into Parkinson's disease.

Molecular insights into Parkinson's disease.

Parkinson's disease is a neurodegenerative movement disorder characterized by loss of midbrain dopaminergic neurons leading to motor abnormalities and autonomic dysfunctions. Despite intensive research, the etiology of Parkinson's disease remains poorly understood leaving us with no effective therapeutic options. However, the recent identification of genes linked to heritable forms of Parkinson's disease has revolutionized research in the field and has begun to provide new clues to disease pathogenesis. Here we discuss these recent genetic advances and highlight their significance in our quest to better understand common underlying disease mechanisms that will help us identify innovative neuroprotective therapies for Parkinson's disease.

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