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The human complement factor H: functional roles, genetic variations and disease associations.

机译:人类补体因子H:功能作用,遗传变异和疾病关联。

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摘要

Factor H is an essential regulatory protein that plays a critical role in the homeostasis of the complement system in plasma and in the protection of bystander host cells and tissues from damage by complement activation. Genetic and structural data generated during recent years have been instrumental to delineate the functional domains responsible for these regulatory activities in factor H, which is helping to understand the molecular basis underlying the different pathologies associated to factor H. This review summarises our current knowledge of the role of factor H in health and disease.
机译:因子H是必需的调节蛋白,在血浆中补体系统的体内平衡以及保护旁观者宿主细胞和组织免受补体激活的损害中起着关键作用。近年来产生的遗传和结构数据有助于描述负责H因子这些调节活性的功能域,这有助于了解与H因子相关的不同病理学的分子基础。本综述总结了我们对H因子的了解。 H因子在健康和疾病中的作用。

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