• 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

Factor B reference typing report.

作者信息

Geserick G, Abbal M, Brenden M, Braun-Stilwell M, Mauff G, Schröder H, Siemens I

机构信息

Institut für Gerichtliche Medizin, Humboldt-Universität, Berlin, FRG.

出版信息

Complement Inflamm. 1990;7(4-6):183-9. doi: 10.1159/000463146.

DOI:10.1159/000463146
PMID:1708321
Abstract

In a factor B (BF) Reference Typing of the VIth Complement Genetics Workshop and Conference, Mainz, FRG, 1989, 99 samples from 13 laboratories, including 18 families, were investigated with the majority of presently known typing procedures. Among the major ('standard') allotypes BF SO4 was found to be new. For the group of common BF F subtypes samples from 11 laboratories including complete family data from 5 laboratories were compared. The subtypes BF FA and FB were recognized and confirmed to be identical in the samples from all groups. Within a third group rare subtype variants of F and S were compared and characterized. In samples submitted from individuals with assumed non-expressed (BF*QO) alleles unexpected and hypomorphic gene products were seen. The investigation of DNA samples for restriction fragment length polymorphisms from the same set of individuals revealed a correlation of the Msp I 0.7-kb fragment with BF F, and confirmed the correlation of a Taq I 6.6-kb fragment with BF FA.

摘要

相似文献

1
Factor B reference typing report.
Complement Inflamm. 1990;7(4-6):183-9. doi: 10.1159/000463146.
2
BF DNA reference typing.BF DNA参考分型
Complement Inflamm. 1990;7(4-6):190-2. doi: 10.1159/000463147.
3
Factor B (BF) nomenclature statement.补体B因子(BF)命名声明。
Complement Inflamm. 1990;7(4-6):255-60. doi: 10.1159/000463158.
4
Reference typing report for complement factor B.
Exp Clin Immunogenet. 1998;15(4):261-3. doi: 10.1159/000019080.
5
Apparently non-expressed alleles of factor B (BF) code for hypomorphic proteins.补体因子B(BF)的明显未表达等位基因编码亚效蛋白。
Immunogenetics. 1992;37(1):24-8. doi: 10.1007/BF00223541.
6
A DNA restriction fragment length polymorphism in the complement region of the human MHC shows an absolute correlation with polymorphism of complement factor B(Bf) defined by isoelectric focusing.人类主要组织相容性复合体(MHC)补体区域的DNA限制性片段长度多态性与通过等电聚焦定义的补体因子B(Bf)多态性呈现出绝对相关性。
J Immunogenet. 1985 Dec;12(6):321-6.
7
Genomic analysis of the F subtypes of human complement factor B.
Eur J Immunogenet. 1994 Dec;21(6):415-23. doi: 10.1111/j.1744-313x.1994.tb00214.x.
8
The BF F subtypes are detectable in the Ba fragment of factor B.B因子F亚型可在B因子的Ba片段中检测到。
Forensic Sci Int. 1989 Aug;42(3):279-86. doi: 10.1016/0379-0738(89)90096-0.
9
C4 DNA RFLP reference typing report.C4 DNA限制性片段长度多态性参考分型报告。
Complement Inflamm. 1990;7(4-6):218-24. doi: 10.1159/000463150.
10
Another family with a silent allele of properdin factor B polymorphism (BF QO).另一个具有备解素因子B多态性沉默等位基因(BF QO)的家族。
Hum Genet. 1985;70(4):321-3. doi: 10.1007/BF00295369.

引用本文的文献

1
Complement and glomerulonephritis--an update.补体与肾小球肾炎——最新进展
Pediatr Nephrol. 1993 Apr;7(2):226-32. doi: 10.1007/BF00864413.
2
HLA complement gene polymorphisms in multiple sclerosis. A study on 80 Italian patients.多发性硬化症中的HLA补体基因多态性。对80名意大利患者的研究。
J Neurol. 1995 Jan;242(2):64-8. doi: 10.1007/BF00887817.
3
Apparently non-expressed alleles of factor B (BF) code for hypomorphic proteins.补体因子B(BF)的明显未表达等位基因编码亚效蛋白。
Immunogenetics. 1992;37(1):24-8. doi: 10.1007/BF00223541.