• 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

Occurrence of haemoglobin Norfolk (alpha2 57 (E6) Gly leads to Asp beta2) at the level of 33% in an Italian family from Calabria.

作者信息

Marinucci M, Mavilio F, Samoggia P, Tentori L, Spadea G, Cocone G

出版信息

Acta Haematol. 1979;61(1):39-46. doi: 10.1159/000207624.

DOI:10.1159/000207624
PMID:105539
Abstract

An abnormal, fast-moving haemoglobin was observed in 5 healthy subjects of a family from Calabria (southern Italy). In all these carriers the abnormal haemoglobin, which structural studies identified as Hb Norfolk (alpha2 57 (E6) Gly leads to Asp beta2) [4], occurs at a level averaging 33% of the total haemoglobin. Biosynthetic studies showed no evidence for unbalance of the globin chain synthetic ratio. In order to account for the observed percentages of Hb Norfolk, current concepts about the alpha-globin chain genetic system are reviewed, and different genic arrangements which would be in agreement with the experimental findings are discussed.

摘要

相似文献

1
Occurrence of haemoglobin Norfolk (alpha2 57 (E6) Gly leads to Asp beta2) at the level of 33% in an Italian family from Calabria.
Acta Haematol. 1979;61(1):39-46. doi: 10.1159/000207624.
2
Studies on a family with Hb J Calabria (alpha 2 beta 2 64 (E8) Gly replaced by Asp).关于一个患有Hb J卡拉布里亚病(α2β2 64(E8)位的甘氨酸被天冬氨酸取代)的家族的研究。
Hemoglobin. 1979;3(5):327-40. doi: 10.3109/03630267908997538.
3
Study of abnormal hemoglobin in Ehime, Japan: two structural variants of hemoglobin A (Hb I and Hb J Iran) and structural and synthetic variants of delta chain.
Jinrui Idengaku Zasshi. 1984 Sep;29(3):335-51. doi: 10.1007/BF01871249.
4
Occurrence of Hb J Paris in an Italian family and recombination studies on the free abnormal alpha-chain.
Hemoglobin. 1979;3(6):465-9. doi: 10.3109/03630267909002283.
5
Globin chain synthesis in Hb J Baltimore-beta (+)-thalassemia.血红蛋白J巴尔的摩-β(+)-地中海贫血中的珠蛋白链合成
Am J Clin Pathol. 1981 Jun;75(6):843-6. doi: 10.1093/ajcp/75.6.843.
6
The haematological puzzle of Hb J Cape Town is partly solved.血红蛋白J开普敦型的血液学谜题已部分解开。
Br J Haematol. 1986 Jun;63(2):363-7. doi: 10.1111/j.1365-2141.1986.tb05561.x.
7
Hb J-Calabria [beta 64(E8)Gly----Asp] found in a Japanese family.在一个日本家族中发现了血红蛋白J-卡拉布里亚[β64(E8)甘氨酸→天冬氨酸]。
Hemoglobin. 1989;13(2):185-8. doi: 10.3109/03630268908998070.
8
[A first case of Hb J Paris-1 alpha2[A10] Ala----Asp beta2 carrier in Bulgaria. Structural organization].[保加利亚首例Hb J巴黎-1α2[A10]丙氨酸----天冬氨酸β2携带者。结构组织]
Gematol Transfuziol. 1987 Sep;32(9):15-9.
9
Haemoglobin J Rovigo 53 alpha (E-2) aspartic acid alanin.
Rev Bras Pesqui Med Biol. 1980 Apr;13(1-3):37-9.
10
Thalassemia types in Calabria (Southern Italy).卡拉布里亚(意大利南部)的地中海贫血类型。
Birth Defects Orig Artic Ser. 1982;18(7):147-55.

引用本文的文献

1
Alpha-thalassemia and the production of different alpha chain variants in heterozygotes.α地中海贫血与杂合子中不同α链变体的产生。
Biochem Genet. 1981 Jun;19(5-6):487-98. doi: 10.1007/BF00484621.
2
Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletions.杂合子中血红蛋白G费城(α268天冬酰胺导致β2赖氨酸)的比例由α-珠蛋白基因缺失决定。
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6874-8. doi: 10.1073/pnas.77.11.6874.