Increasing evidence that genetic variation in Complement factor H ...
2012年6月28日 · The most frequent mutations are in CFH, which encodes complement factor H, a protein that accelerates decay of the active C3 convertase complex, and also acts as a …
Journal of Human Genetics - Nature
2013年3月8日 · An international journal publishing articles on human genetics, including medical genetics and human genome analysis. Check out the latest issue! Find previous Special …
Like CFH, CFHR5 is a gene in the Reg-ulator of Complement Activity cluster on chromosome 1. It encodes a protein homo-logous to CFH, which is able to regulate components of the alternative...
jhg cfh - ceo - GTR | LinkedIn
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北京大学基础医学院 - bjmu.edu.cn
2023年1月18日 · 补体因子 h （ cfh ）是补体系统中丰度最高的 负 调控因子 ，其存在防止补体的过度活化 。 cfh 的功能缺失是补体介导的相关 组织 损伤（如：狼疮肾炎、缺血再灌注急性肾 …
补体因子H（CFH）基因家族的周期性结构变异，选择的聚集点和 …
补体因子H（CFH）基因家族的结构变异和单核苷酸变异是几种复杂的遗传疾病的基础，包括年龄相关性黄斑变性（AMD）和非典型溶血性尿毒症综合征（AHUS）。为了了解其多样性和进 …
JOURNAL OF HUMAN GENETICS_影响因子(IF)_中科院分区_SCI期 …
JOURNAL OF HUMAN GENETICS杂志网站提供J HUM GENET期刊影响因子、JCR和中科院分区查询，SCI期刊投稿经验，Impact Factor（IF），官方投稿网址，审稿周期/时间，研究方 …
Human Complement Factor H/CFH Standard (人补体因子H (CFH)
补体因子H，又称H因子1和CFH，是一种含唾液酸的糖蛋白，在调节补体介导的免疫系统中起着不可或缺的作用，该免疫系统参与微生物防御、免疫复合物处理和细胞程序性死亡。 CFH作为 …
CFH and CFHR structural variants in atypical Hemolytic Uremic …
2023年1月30日 · Methods: In this study, we report the results of CFH-CFHR Copy Number Variation (CNV) analysis and the characterization of resulting structural variants (SVs) in a …
Polypoidal choroidal vasculopathy (PCV), a subtype of age-related macular degeneration (AMD) more frequently seen in East Asians, has both common and distinct clinical manifestations …