• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Glomerulonephritis associated with deficiencies and polymorphisms of complement components encoded in the class III region of the MHC.

作者信息

Welch T R, Frenzke M

机构信息

Division of Nephrology and Hypertension, Children's Hospital Research Foundation, Cincinnati, Ohio, USA.

出版信息

Front Biosci. 2001 Aug 1;6:D898-903. doi: 10.2741/welch.

DOI:10.2741/welch
PMID:11487500
Abstract

An association between the complement system and immune complex glomerular disease in humans has long been recognized. In fact, much of our early understanding of the immunochemistry of complement activation developed with the study of acute and chronic glomerulonephritis (1). This manuscript will examine associations between glomerulonephritis and the three complement components encoded within the major histocompatibility complex: C4, C2, and factor B (B). The mechanisms by which deficiencies or polymorphisms in these components can mediate disease will be examined.

摘要

相似文献

1
Glomerulonephritis associated with deficiencies and polymorphisms of complement components encoded in the class III region of the MHC.
Front Biosci. 2001 Aug 1;6:D898-903. doi: 10.2741/welch.
2
Genetics of complement.补体的遗传学
Curr Top Hematol. 1980;3:111-74.
3
[B, C2 and C4 complement factors, the HLA system and diseases. Genetic relation].[B、C2和C4补体因子、HLA系统与疾病。遗传关系]
Pathol Biol (Paris). 1983 Sep;31(7):622-30.
4
Genetic polymorphism of human complement proteins.人类补体蛋白的基因多态性。
Rev Fr Transfus Immunohematol. 1979 Dec;22(5):587-614.
5
Serum concentrations of C4 isotypes and factor B in type I C2 deficiency suggest haplotype-dependent quantitative expression of MHC class III complement genes.I型C2缺乏症患者血清中C4同种型和B因子的浓度表明MHC III类补体基因存在单倍型依赖性定量表达。
Exp Clin Immunogenet. 1995;12(2):66-73.
6
Inherited complement component abnormalities.遗传性补体成分异常。
Annu Rev Med. 1986;37:333-46. doi: 10.1146/annurev.me.37.020186.002001.
7
The molecular genetics of components of complement.补体成分的分子遗传学
Adv Immunol. 1986;38:203-44. doi: 10.1016/s0065-2776(08)60007-3.
8
Are major histocompatibility system class III products independent markers for susceptibility to rheumatoid arthritis?主要组织相容性系统III类产物是类风湿关节炎易感性的独立标志物吗?
Dis Markers. 1986 Jun;4(1-2):151-5.
9
Major-histocompatibility-complex extended haplotypes in membranoproliferative glomerulonephritis.膜增生性肾小球肾炎中的主要组织相容性复合体扩展单倍型
N Engl J Med. 1986 Jun 5;314(23):1476-81. doi: 10.1056/NEJM198606053142303.
10
Genetic aspects of complement and glomerulonephritis.补体与肾小球肾炎的遗传学方面
Adv Nephrol Necker Hosp. 1984;13:271-96.

引用本文的文献

1
Crystal structure of C5b-6 suggests structural basis for priming assembly of the membrane attack complex.C5b-6 的晶体结构提示了膜攻击复合物组装的启动的结构基础。
J Biol Chem. 2012 Jun 1;287(23):19642-52. doi: 10.1074/jbc.M112.361121. Epub 2012 Apr 12.