• 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

[乌兹别克斯坦血红蛋白病的群体遗传学研究。II. 血红蛋白病的群体动态]

[Population genetics study of hemoglobinopathies in Uzbekistan. II. Population dynamics of hemoglobinopathies].

作者信息

Asanov A Iu, Ginter E K, Bakhramov S M, Gar'kavtseva R F, Revazov A A

出版信息

Genetika. 1987 Jul;23(7):1328-33.

PMID:2958388
Abstract

It was shown that on comparing variability of selective neutral genetic marker systems with that of the beta-thalassemia system for the populations of different hierarchical level, the relative importance of selection and genetic drift could be evaluated. The genetic differentiation of the beta-thalassemia gene frequencies in elementary populations (villages) could be solely explained by genetic drift. On the other hand, the differentiation of district populations (the sizes of the populations being 10(6] for beta-thalassemia gene frequencies could be explained by selection forces. This is supported by the fact that the genetic distances and FST values are only significant for the beta-thalassemia gene and not for the neutral genetic systems, when the district populations are compared.

摘要

结果表明,在比较不同层次水平人群的选择性中性遗传标记系统和β地中海贫血系统的变异性时,可以评估选择和遗传漂变的相对重要性。基层人群(村庄)中β地中海贫血基因频率的遗传分化完全可以用遗传漂变来解释。另一方面,地区人群(人群规模为10^6)中β地中海贫血基因频率的分化可以用选择力来解释。当比较地区人群时,遗传距离和FST值仅对β地中海贫血基因有显著意义,而对中性遗传系统没有显著意义,这一事实支持了这一点。

相似文献

1
[Population genetics study of hemoglobinopathies in Uzbekistan. II. Population dynamics of hemoglobinopathies].[乌兹别克斯坦血红蛋白病的群体遗传学研究。II. 血红蛋白病的群体动态]
Genetika. 1987 Jul;23(7):1328-33.
2
[Medical genetic study of the population of Uzbekistan. V. The frequency of heterozygous beta-thalassemia in 4 kishlaks of Urgut District, Samarkand Province].
Genetika. 1978;14(12):2197-204.
3
The interactions of alpha-thalassemia with hemoglobinopathies.α地中海贫血与血红蛋白病的相互作用。
Hematol Oncol Clin North Am. 1991 Jun;5(3):453-73.
4
Large-scale population genetic analysis for hemoglobinopathies reveals different mutation spectra in central Greece compared to the rest of the country.地中海贫血的大规模群体遗传分析显示,与希腊其他地区相比,希腊中部的突变谱有所不同。
Am J Hematol. 2007 Jul;82(7):634-6. doi: 10.1002/ajh.20889.
5
[Medico-genetic study of the population of Turkmenia. IV. The population geography of hemoglobinopathies].[土库曼斯坦人群的医学遗传学研究。IV. 血红蛋白病的群体地理学]
Genetika. 1984 Sep;20(9):1536-41.
6
[Population genetics aspects of the study of hemoglobinopathies in the population of the southern regions of the Uzbek and Tadzhik Soviet Republics].[乌兹别克苏维埃社会主义共和国和塔吉克苏维埃社会主义共和国南部地区人群血红蛋白病研究的群体遗传学方面]
Probl Gematol Pereliv Krovi. 1976 Jan;21(1):37-41.
7
[Genetic traits in the area of Bodrogköz].[博德罗格科兹地区的遗传特征]
Orv Hetil. 1992 Jul 26;133(30):1869-73.
8
[Current status of the study of hemoglobinopathies in Costa Rica].[哥斯达黎加血红蛋白病的研究现状]
Sangre (Barc). 1985;30(2):168-80.
9
[Medico-genetic study of the residents of Krasnodar territory. Incidence of hemoglobinopathies].[克拉斯诺达尔地区居民的医学遗传学研究。血红蛋白病的发病率]
Genetika. 1989 Jun;25(6):1108-10.
10
Preventation of thalassemia in Australia.澳大利亚地中海贫血的预防
Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:94-6.