• 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

中国瑶族群体中MHCⅢ类基因和GLO基因的遗传多态性

Genetic polymorphism of MHC class III and GLO in Chinese Yao nationality.

作者信息

Wang C, Tian Y W, Wu X W, Zhao X Z

机构信息

Department of Pathophysiology, Tongji Medical University, Wuhan.

出版信息

J Tongji Med Univ. 1990;10(1):37-42. doi: 10.1007/BF02909120.

DOI:10.1007/BF02909120
PMID:2348487
Abstract

Yao nationality is one of the minority nationalities living mainly in South China (Guangxi Province). The purpose of this study was to provide data of MHC class III and GLO in Chinese Yao nationality and the different genetic background of Yao and Han nationality, the latter representing the major nationality in China. The genetic polymorphism of MHC class III and GLO in Chinese Yao nationality was determined. Previously the Japanese were considered to have the lowest C2C frequencies (0.9386), but now we ascertained that the Yao have the lowest C2C frequencies (0.9336). The data concerning gene frequencies of Yao are presented. They were also compared with the available data of Han.

摘要

瑶族是主要居住在中国南方(广西省)的少数民族之一。本研究的目的是提供中国瑶族主要组织相容性复合体(MHC)Ⅲ类基因和6-磷酸葡萄糖酸脱氢酶(GLO)的数据,以及瑶族与代表中国主要民族的汉族不同的遗传背景。测定了中国瑶族MHCⅢ类基因和GLO的遗传多态性。以前认为日本人的C2C频率最低(0.9386),但现在我们确定瑶族的C2C频率最低(0.9336)。列出了瑶族的基因频率数据,并与汉族的现有数据进行了比较。

相似文献

1
Genetic polymorphism of MHC class III and GLO in Chinese Yao nationality.中国瑶族群体中MHCⅢ类基因和GLO基因的遗传多态性
J Tongji Med Univ. 1990;10(1):37-42. doi: 10.1007/BF02909120.
2
Genetic polymorphisms of HLA class III and GLO1 in Chinese Yao nationality.中国瑶族人群中HLAⅢ类基因和GLO1基因的遗传多态性
Gene Geogr. 1990 Apr;4(1):29-34.
3
Human MHC class III (Bf, C2, C4) genes and GLO: their association with other HLA antigens and extended haplotypes in the Spanish population.人类MHCⅢ类(Bf、C2、C4)基因与GLO:它们在西班牙人群中与其他HLA抗原及扩展单倍型的关联。
Tissue Antigens. 1988 Jan;31(1):14-25. doi: 10.1111/j.1399-0039.1988.tb02060.x.
4
Polymorphism of BF, C2, and GLO in Japanese patients with insulin-dependent diabetes mellitus: confirmation of an increase of BF*FT.日本胰岛素依赖型糖尿病患者中BF、C2和GLO的多态性:BF*FT增加的确认
Hum Genet. 1982;62(1):86-8. doi: 10.1007/BF00295609.
5
HLA, complement C2, C4, properdin factor B and glyoxalase types in South Indian diabetics.南印度糖尿病患者的人类白细胞抗原、补体C2、C4、备解素因子B和乙二醛酶类型
Diabetes Res Clin Pract. 1985 Mar;1(1):41-7. doi: 10.1016/s0168-8227(85)80027-9.
6
Genetic variability of the MHC class III complement proteins C2, BF, C4A and C4B in southern Brazil.巴西南部MHC III类补体蛋白C2、BF、C4A和C4B的基因变异性
Exp Clin Immunogenet. 1994;11(4):192-6.
7
Human C4 polymorphism: pedigree analysis of qualitative, quantitative, and functional parameters as a basis for phenotype interpretations.人类C4多态性:定性、定量和功能参数的系谱分析作为表型解释的基础。
Hum Genet. 1984;65(4):362-72. doi: 10.1007/BF00291561.
8
Complotype SC30 is associated with susceptibility to develop ulcerative colitis in Mexicans.复合体型SC30与墨西哥人患溃疡性结肠炎的易感性相关。
J Clin Gastroenterol. 1998 Sep;27(2):178-9. doi: 10.1097/00004836-199809000-00020.
9
Multiple sclerosis: immunogenetic analyses of sib-pair double case families. II. Studies on the association of multiple sclerosis with C2, C4, BF, C3, C6, and GLO polymorphisms.
Immunobiology. 1983 Mar;164(2):160-70. doi: 10.1016/S0171-2985(83)80007-2.
10
Complotypes in pemphigus vulgaris: differences between Jewish and non-Jewish patients.寻常型天疱疮的复合单倍型:犹太患者与非犹太患者之间的差异。
Hum Immunol. 1990 Apr;27(4):298-304. doi: 10.1016/0198-8859(90)90081-y.

本文引用的文献

1
Genetics of HLA disease association.HLA疾病关联的遗传学
Annu Rev Genet. 1981;15:169-87. doi: 10.1146/annurev.ge.15.120181.001125.
2
Inherited structural polymorphism of the fourth component of human complement.人类补体第四成分的遗传性结构多态性。
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3576-80. doi: 10.1073/pnas.77.6.3576.
3
Disease associations with complotypes, supratypes and haplotypes.疾病与补体复合体型、超型和单倍型的关联。
Immunol Rev. 1983;70:5-22. doi: 10.1111/j.1600-065x.1983.tb00707.x.
4
Genetic polymorphism in human glycine-rich beta-glycoprotein.人类富含甘氨酸的β-糖蛋白中的基因多态性。
J Exp Med. 1972 Jan;135(1):68-80. doi: 10.1084/jem.135.1.68.
5
Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.人类补体C2的遗传性结构多态性:C2与Bf之间存在基因连锁的证据。
J Exp Med. 1976 Oct 1;144(4):1111-5. doi: 10.1084/jem.144.4.1111.
6
Two HLA-linked loci controlling the fourth component of human complement.控制人类补体第四成分的两个与HLA连锁的基因座。
Proc Natl Acad Sci U S A. 1978 Oct;75(10):5165-9. doi: 10.1073/pnas.75.10.5165.