• 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

Thai (delta beta)0-thalassemia and its interaction with gamma-thalassemia.

作者信息

Trent R J, Svirklys L, Jones P

机构信息

Molecular Biology Laboratory, University of Sydney, NSW, Australia.

出版信息

Hemoglobin. 1988;12(2):101-14. doi: 10.3109/03630268808998017.

DOI:10.3109/03630268808998017
PMID:2454901
Abstract

A variant of Southern Italian (delta beta)0-thalassemia is described in a women of Thai origin. The 3' breakpoint in Thai (delta beta)0-thalassemia is located about 1 kb upstream to that in Southern Italian (delta beta)0-thalassemia and produces a smaller deletion of approximately equal to 12.5 kb. Hematological phenotype, particularly Hb F output, is similar to that found in G gamma A gamma(delta beta)0-thalassemia despite the presence of a coexistent gamma-thalassemia effect.

摘要

相似文献

1
Thai (delta beta)0-thalassemia and its interaction with gamma-thalassemia.
Hemoglobin. 1988;12(2):101-14. doi: 10.3109/03630268808998017.
2
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian family.撒丁岛一个家族中缺失型δ地中海贫血与β0地中海贫血(密码子39无义突变)之间的相互作用
Prog Clin Biol Res. 1989;316B:113-21.
3
Laotian (delta beta) (0)-thalassemia: molecular characterization of a novel deletion associated with increased production of fetal hemoglobin.老挝(δβ)(0)型地中海贫血:与胎儿血红蛋白生成增加相关的新型缺失的分子特征
Blood. 1988 Sep;72(3):983-8.
4
The 18- to 23-kb deletion of the Macedonian delta beta-thalassemia includes the entire delta and beta globin genes.马其顿δβ地中海贫血的18至23kb缺失包含整个δ和β珠蛋白基因。
Blood. 1986 Oct;68(4):971-4.
5
Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area?δβ地中海贫血与胎儿血红蛋白DNA遗传性持续存在的分子比较:调控区域的证据?
Proc Natl Acad Sci U S A. 1982 Apr;79(7):2347-51. doi: 10.1073/pnas.79.7.2347.
6
A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent.在一个爱尔兰裔家族中,一个大于200 kb的缺失片段删除了整个类β珠蛋白基因簇。
Hemoglobin. 1991;15(1-2):23-41. doi: 10.3109/03630269109072482.
7
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes.具有不同数量α-珠蛋白基因的(δβ)(0)-地中海贫血杂合子中胎儿血红蛋白水平的变化。
Am J Hematol. 1990 Jul;34(3):230-1. doi: 10.1002/ajh.2830340316.
8
Different molecular defects of G gamma (A gamma delta beta)o-thalassaemia in Thailand.泰国Gγ(Aγδβ)o型地中海贫血的不同分子缺陷
Eur J Haematol. 1987 Aug;39(2):154-60.
9
Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.泰国常见高 HbF 决定因素中 HbF 的表型表达:α-地中海贫血、5'δ-球蛋白 BCL11A 结合区和 3'β-球蛋白增强子的作用。
Eur J Haematol. 2014 Jan;92(1):73-9. doi: 10.1111/ejh.12201. Epub 2013 Oct 24.
10
Thai G gamma (A gamma delta beta)zero-thalassemia and its interaction with a single gamma-globin gene on a chromosome carrying beta zero-thalassemia.
Hemoglobin. 1990;14(2):185-97. doi: 10.3109/03630269009046960.

引用本文的文献

1
Disrupting the adult globin promoter alleviates promoter competition and reactivates fetal globin gene expression.破坏成人珠蛋白启动子可减轻启动子竞争,重新激活胎儿珠蛋白基因表达。
Blood. 2022 Apr 7;139(14):2107-2118. doi: 10.1182/blood.2021014205.
2
Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization.通过阵列比较基因组杂交技术对HBA和HBB基因座缺失的特征分析
J Mol Diagn. 2016 Jan;18(1):92-9. doi: 10.1016/j.jmoldx.2015.07.011. Epub 2015 Nov 21.
3
Low fetal hemoglobin rates in patients carrying Thai (δβ)0-deletion and Turkish (δβ)0-deletion/inversion strengthen the hypothesis that the 5'δ BCL11A binding site plays a major role in its fetal hemoglobin inhibitory regulation. Response to "The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia".
携带泰国型(δβ)0-缺失和土耳其型(δβ)0-缺失/倒位的患者中胎儿血红蛋白水平较低,这强化了以下假说:5'δ BCL11A结合位点在其胎儿血红蛋白抑制调节中起主要作用。回应《β-珠蛋白基因簇中12.6 kb缺失是东南亚常见的已知泰国/越南(δβ)0-地中海贫血》
Haematologica. 2013 Sep;98(9):e119-20. doi: 10.3324/haematol.2013.093716.
4
The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia.β-珠蛋白基因簇中的12.6 kb缺失是东南亚常见的已知泰国/越南(δβ)0-地中海贫血。
Haematologica. 2013 Sep;98(9):e117-8. doi: 10.3324/haematol.2013.090613.