• 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

波黑人群 RH 血型系统的分子遗传学变异。

Molecular-genetic variance of RH blood group system within human population of Bosnia and Herzegovina.

机构信息

Institute for Genetic Engineering and Biotechnology Sarajevo, Zmaja od Bosne 8, 71 000 Sarajevo, Bosnia and Herzegovina.

出版信息

Bosn J Basic Med Sci. 2013 Feb;13(1):10-3. doi: 10.17305/bjbms.2013.2403.

DOI:10.17305/bjbms.2013.2403
PMID:23448604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4333926/
Abstract

There are two major theories for inheritance of Rh blood group system: Fisher - Race theory and Wiener theory. Aim of this study was identifying frequency of RHDCE alleles in Bosnian - Herzegovinian population and introduction of this method in screening for Rh phenotype in B&H since this type of analysis was not used for blood typing in B&H before. Rh blood group was typed by Polymerase Chain Reaction, using the protocols and primers previously established by other authors, then carrying out electrophoresis in 2-3% agarose gel. Percentage of Rh positive individuals in our sample is 84.48%, while the percentage of Rh negative individuals is 15.52%. Inter-rater agreement statistic showed perfect agreement (K=1) between the results of Rh blood system detection based on serological and molecular-genetics methods. In conclusion, molecular - genetic methods are suitable for prenatal genotyping and specific cases while standard serological method is suitable for high-throughput of samples.

摘要

关于 Rh 血型系统遗传有两种主要理论:Fisher-Race 理论和 Wiener 理论。本研究的目的是确定波黑人群中 RHDCE 等位基因的频率,并将这种方法引入波黑的 Rh 表型筛选中,因为在此之前,这种类型的分析并未用于波黑的血型鉴定。Rh 血型通过聚合酶链反应进行分型,使用先前由其他作者建立的方案和引物,然后在 2-3%琼脂糖凝胶中进行电泳。我们样本中 Rh 阳性个体的百分比为 84.48%,而 Rh 阴性个体的百分比为 15.52%。观察者间一致性统计显示,基于血清学和分子遗传学方法的 Rh 血型系统检测结果之间存在完全一致(K=1)。总之,分子遗传学方法适用于产前基因分型和特定情况,而标准血清学方法适用于高通量样本。

相似文献

1
Molecular-genetic variance of RH blood group system within human population of Bosnia and Herzegovina.波黑人群 RH 血型系统的分子遗传学变异。
Bosn J Basic Med Sci. 2013 Feb;13(1):10-3. doi: 10.17305/bjbms.2013.2403.
2
Molecular Variation of Rh, MN, Duffy, Kidd, Kell, and Lutheran Blood Groups in the Human Population of Bosnia and Herzegovina. Bosnia 和 Herzegovina 人群中 Rh、MN、Duffy、Kidd、Kell 和 Lutheran 血型的分子变异。
Hum Biol. 2021 Feb;92(2):81-92. doi: 10.13110/humanbiology.92.2.04.
3
RHD/CE typing by polymerase chain reaction using sequence-specific primers.使用序列特异性引物通过聚合酶链反应进行RHD/CE分型。
Transfusion. 1997 Oct;37(10):1020-6. doi: 10.1046/j.1537-2995.1997.371098016439.x.
4
Comprehensive phenotypic and molecular investigation of RhD and RhCE variants in Moroccan blood donors.对摩洛哥献血者的 RhD 和 RhCE 变异体进行全面的表型和分子研究。
Blood Transfus. 2019 Mar;17(2):151-156. doi: 10.2450/2018.0153-18. Epub 2018 Oct 24.
5
Molecular diversity of 23 Y-chromosome short tandem repeat loci in the population of Tuzla Canton, Bosnia and Herzegovina.波斯尼亚和黑塞哥维那图兹拉州人群中23个Y染色体短串联重复序列位点的分子多样性
Ann Hum Biol. 2017 Aug;44(5):419-426. doi: 10.1080/03014460.2016.1259430. Epub 2016 Nov 30.
6
Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA.通过基于聚合酶链反应的DNA扩增进行快速Rh D基因分型。
Blood. 1995 May 15;85(10):2975-80.
7
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.通过下一代测序进行RHD和RHCE基因分型是识别镰状细胞病患者分子变异的有效策略。
Blood Cells Mol Dis. 2017 Jun;65:8-15. doi: 10.1016/j.bcmd.2017.03.014. Epub 2017 Mar 31.
8
Analysis of forensic genetic parameters of 22 autosomal STR markers (PowerPlex® Fusion System) in a population sample from Bosnia and Herzegovina.波斯尼亚和黑塞哥维那人群样本中22个常染色体STR标记(PowerPlex® Fusion系统)的法医遗传学参数分析。
Ann Hum Biol. 2020 May;47(3):273-283. doi: 10.1080/03014460.2020.1740319. Epub 2020 Apr 17.
9
Gene frequencies of ABO and Rh (D) blood group alleles in a healthy infant population in Ibadan, Nigeria.尼日利亚伊巴丹健康婴儿群体中ABO和Rh(D)血型等位基因的基因频率
West Afr J Med. 1999 Oct-Dec;18(4):294-7.
10
Molecular RH blood group typing of serologically D-/CE+ donors: the use of a polymerase chain reaction-sequence-specific primer test kit with pooled samples.血清学检测为D-/CE+献血者的分子RH血型分型:使用聚合酶链反应-序列特异性引物检测试剂盒对混合样本进行检测。
Immunohematology. 2011;27(1):25-8.

本文引用的文献

1
PowerMarker: an integrated analysis environment for genetic marker analysis.PowerMarker:用于遗传标记分析的集成分析环境。
Bioinformatics. 2005 May 1;21(9):2128-9. doi: 10.1093/bioinformatics/bti282. Epub 2005 Feb 10.
2
The Rh blood group system: a review.Rh血型系统综述
Blood. 2000 Jan 15;95(2):375-87.
3
Antenatal genotyping of the blood groups of the fetus.胎儿血型的产前基因分型。
Vox Sang. 1998;74 Suppl 2:365-74. doi: 10.1111/j.1423-0410.1998.tb05444.x.
4
Molecular genetic basis of the human Rhesus blood group system.人类恒河猴血型系统的分子遗传基础。
Nat Genet. 1993 Sep;5(1):62-5. doi: 10.1038/ng0993-62.
5
Rh E/e genotyping by allele-specific primer amplification.通过等位基因特异性引物扩增进行Rh E/e基因分型。
Blood. 1995 Feb 1;85(3):829-32.
6
Sequence analysis of cDNA derived from reticulocyte mRNAs coding for Rh polypeptides and demonstration of E/e and C/c polymorphisms.对编码Rh多肽的网织红细胞mRNA衍生的cDNA进行序列分析,并证实E/e和C/c多态性。
Vox Sang. 1994;67(2):203-9. doi: 10.1111/j.1423-0410.1994.tb01661.x.
7
Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA.通过基于聚合酶链反应的DNA扩增进行快速Rh D基因分型。
Blood. 1995 May 15;85(10):2975-80.
8
Construction of a genetic linkage map in man using restriction fragment length polymorphisms.利用限制性片段长度多态性构建人类遗传连锁图谱。
Am J Hum Genet. 1980 May;32(3):314-31.
9
A simple salting out procedure for extracting DNA from human nucleated cells.一种从人有核细胞中提取DNA的简单盐析方法。
Nucleic Acids Res. 1988 Feb 11;16(3):1215. doi: 10.1093/nar/16.3.1215.
10
Molecular cloning and protein structure of a human blood group Rh polypeptide.一种人类血型Rh多肽的分子克隆与蛋白质结构
Proc Natl Acad Sci U S A. 1990 Aug;87(16):6243-7. doi: 10.1073/pnas.87.16.6243.