非典型溶血尿毒综合征
点突变
替代补体途径
突变
血栓性
补体系统
免疫学
补体因子I
补体因子B
医学
系数H
内科学
生物
遗传学
抗体
基因
血栓形成
作者
Yoshiyasu Ueda,Imran Mohammed,Delu Song,Damodar Gullipalli,Lin Zhou,Sayaka Sato,Yuan Wang,Shuchi Gupta,Zhongjian Cheng,Hong Wang,Jialing Bao,Yingying Mao,Lawrence F. Brass,X. Long Zheng,Takashi Miwa,Matthew Palmer,Joshua L. Dunaief,Wen‐Chao Song
出处
期刊:Blood
[Elsevier BV]
日期:2017-01-05
卷期号:129 (9): 1184-1196
被引量:56
标识
DOI:10.1182/blood-2016-07-728253
摘要
Key Points A point mutation in murine factor H (W1206R) impairs its interaction with host cells but does not affect its complement-regulating activity. W1206R mutant mice develop complement-mediated systemic thrombotic angiopathy leading to renal failure, stroke, and retinopathy.
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