• 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

相似文献

1
Haemoglobin D Punjab (D Los Angeles).血红蛋白D旁遮普型(D洛杉矶型)
J Med Genet. 1974 Dec;11(4):341-8. doi: 10.1136/jmg.11.4.341.
2
Haemoglobin D Punjab in a European family in Australia.
Med J Aust. 1973 Feb 17;1(7):354-6. doi: 10.5694/j.1326-5377.1973.tb200052.x.
3
The Kenya haemoglobin.肯尼亚血红蛋白。
East Afr Med J. 1974 Jun;51(6):434-43.
4
Beta-thalassaemia, glucose-6-phosphate-dehydrogenase deficiency, and haemoglobin D-Punjab in Pathans.
Lancet. 1968 Jun 15;1(7555):1284-5. doi: 10.1016/s0140-6736(68)92296-4.
5
Hemoglobin A'2 (B2) abnormality in Turkey.
New Istanbul Contrib Clin Sci. 1973 Oct;10(4):248-53.
6
Haemoglobin LeporeBoston in a Turkish family.一个土耳其家庭中的波士顿血红蛋白Lepore
J Med Genet. 1976 Oct;13(5):363-5. doi: 10.1136/jmg.13.5.363.
7
[Hemoglobin Setif (alpha 94 (G1) Asp----Tyr) in a Spanish family].
Sangre (Barc). 1990 Jun;35(3):201-4.
8
Haemoglobin Bart's and slow-moving haemoglobin x components in newborns. The homozygous state for the slow-moving X components in a Malay boy.新生儿中的血红蛋白巴特氏和慢速移动血红蛋白x成分。一名马来男孩中慢速移动X成分的纯合状态。
Acta Haematol. 1973;49(1):25-35. doi: 10.1159/000208382.
9
Beta-thalassaemia and some rare haemoglobin variants in the highlands of Scotland.β地中海贫血与苏格兰高地的一些罕见血红蛋白变异体
Scott Med J. 1973 Jan;18(1):14-20. doi: 10.1177/003693307301800104.
10
A new unstable haemoglobin: Hb Buenos Aires, beta 85 (F1) Phe leads to Ser.
Acta Haematol. 1973;50(6):357-63. doi: 10.1159/000208371.

引用本文的文献

1
Case report-unveiling a case of hemoglobin D-Punjab variant with iron deficiency anemia in Sindh (Pakistan).病例报告——揭示一例信德省(巴基斯坦)血红蛋白D-旁遮普变种合并缺铁性贫血的病例。
SAGE Open Med Case Rep. 2024 Aug 16;12:2050313X241272516. doi: 10.1177/2050313X241272516. eCollection 2024.
2
Prevalence and Regional Distribution of Beta-Hemoglobin Variants in Saudi Arabia: Insights from the National Premarital Screening Program".沙特阿拉伯β-血红蛋白变异体的流行情况和地域分布:来自全国婚前筛查计划的见解。
J Epidemiol Glob Health. 2024 Sep;14(3):1242-1248. doi: 10.1007/s44197-024-00281-x. Epub 2024 Jul 29.
3
Rare Combinational Hemoglobinopathies.罕见的复合型血红蛋白病
Cureus. 2022 Dec 8;14(12):e32327. doi: 10.7759/cureus.32327. eCollection 2022 Dec.
4
An Interesting and Rare Case of Hemoglobin D-Punjab Variant in Tamil Nadu.泰米尔纳德邦一例有趣且罕见的血红蛋白D-旁遮普变体病例
Cureus. 2022 Feb 27;14(2):e22668. doi: 10.7759/cureus.22668. eCollection 2022 Feb.
5
OCCURRENCE OF UNUSUAL HAEMOGLOBINOPATHIES IN BALOCHISTAN: HB SD AND HB SE - PRESENTATION WITH OSTEOMYELITIS.俾路支省罕见血红蛋白病的发生:HB SD 和 HB SE - 伴有骨髓炎。
Rev Paul Pediatr. 2021 Feb 3;39:e2019365. doi: 10.1590/1984-0462/2021/39/2019365. eCollection 2021.
6
HbS/D-Punjab Disease: Report of 3 Cases from Sri Lanka.血红蛋白S/δ-旁遮普病:来自斯里兰卡的3例报告。
Indian J Hematol Blood Transfus. 2018 Apr;34(2):350-352. doi: 10.1007/s12288-017-0851-7. Epub 2017 Jul 22.
7
Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis.血红蛋白D-旁遮普型:起源、分布及实验室诊断
Rev Bras Hematol Hemoter. 2015 Mar-Apr;37(2):120-6. doi: 10.1016/j.bjhh.2015.02.007. Epub 2015 Feb 23.
8
Hemoglobin variant analysis via direct surface sampling of dried blood spots coupled with high-resolution mass spectrometry.血红蛋白变异体分析:直接采集干血斑表面样本,结合高分辨质谱法。
Anal Chem. 2011 Mar 15;83(6):2265-70. doi: 10.1021/ac1030804. Epub 2011 Feb 22.
9
Hb D Los Angeles (D-Punjab) and Hb Presbyterian: analysis of the defect at the DNA level.
Hum Genet. 1990 Mar;84(4):365-7. doi: 10.1007/BF00196236.

本文引用的文献

1
A Third Abnormal Hemoglobin Associated with Hereditary Hemolytic Anemia.一种与遗传性溶血性贫血相关的第三种异常血红蛋白。
Proc Natl Acad Sci U S A. 1951 Dec;37(12):775-84. doi: 10.1073/pnas.37.12.775.
2
Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.异常血红蛋白的研究。I. 通过碱变性法在镰状细胞贫血和其他血液系统疾病中的显示
Blood. 1951 May;6(5):413-28.
3
Alpha, beta and gamma hemoglobin polypeptide chains during the neonatal period with description of a fetal form of hemoglobin Da-St. Louis.新生儿期的α、β和γ血红蛋白多肽链以及一种胎儿型血红蛋白Da - 圣路易斯的描述。
Blood. 1962 Feb;19:137-67.
4
[Hemoglobin D in a Frankfurt family].
Folia Haematol (Frankf). 1960 Apr;4:233-41.
5
Clinical manifestations of inherited abnormal hemoglobins. I. The interaction of hemoglobin-S with hemoglobin-D.遗传性异常血红蛋白的临床表现。I. 血红蛋白S与血红蛋白D的相互作用。
Blood. 1955 May;10(5):389-404.
6
A NEW HAEMOGLOBIN, D IBADAN (BETA-87 THREONINE -- LYSINE), PRODUCING NO SICKLE-CELL HAEMOGLOBIN D DISEASE WITH HAEMOGLOBIN S.一种新的血红蛋白,伊巴丹D型(β-87苏氨酸——赖氨酸),与血红蛋白S不会产生镰状细胞血红蛋白D病。
Nature. 1965 Mar 27;205:1273-6. doi: 10.1038/2051273a0.
7
SICKLE CELL HEMOGLOBIN D DISEASE IN A NEGRO COLOMBIAN PATIENT.一名哥伦比亚黑人患者的镰状细胞血红蛋白D病
Ann Intern Med. 1965 Jun;62:1301-6. doi: 10.7326/0003-4819-62-6-1301.
8
THE AMINO ACID COMPOSITION OF HEMOGLOBIN. VI. SEPARATION OF THE TRYPTIC PEPTIDES OF HEMOGLOBIN KNOXVILLE NO. I ON DOWEX-I X-2 AND SEPHADEX.血红蛋白的氨基酸组成。VI. 血红蛋白诺克斯维尔1号胰蛋白酶解肽段在Dowex - I X - 2和葡聚糖凝胶上的分离
Biochim Biophys Acta. 1965 Jan 4;97:47-60. doi: 10.1016/0304-4165(65)90268-0.
9
HAEMOGLOBINOPATHIES IN THAILAND. II. INCIDENCE AND DISTRIBUTION OF ELEVATIONS OF HAEMOGLOBIN A2 AND HAEMOGLOBIN F; A SURVEY OF 2790 PEOPLE.泰国的血红蛋白病。II. 血红蛋白A2和血红蛋白F升高的发病率及分布;对2790人的调查
Br J Haematol. 1965 Mar;11:227-36. doi: 10.1111/j.1365-2141.1965.tb06582.x.
10
A NEW HAEMOGLOBIN-JA OXFORD FOUND DURING A SURVEY OF AN ENGLISH POPULATION.
Nature. 1964 Oct 17;204:269-70. doi: 10.1038/204269a0.

血红蛋白D旁遮普型(D洛杉矶型)

Haemoglobin D Punjab (D Los Angeles).

作者信息

Vella F, Lehmann H

出版信息

J Med Genet. 1974 Dec;11(4):341-8. doi: 10.1136/jmg.11.4.341.

DOI:10.1136/jmg.11.4.341
PMID:4613830
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1013202/
Abstract

A search for haemoglobin variants undertaken in Canada revealed 21 unrelated instances of Hb D Punjab amongst 207,300 specimens tested. Of these, eight came from East Indian immigrants and the rest from Canadians of United Kingdom origin. No instances of Hb D Punjab were found in 14,500 specimens from Canadian Indians that were tested. The geographical origins of 27 instances of Hb D Punjab characterized at the MRC Abnormal Haemoglobin Unit, Cambridge are presented. Of these five were natives of the British Isles. The results of surveys undertaken in the United Kingdom are summarized. The global distribution of Hb D Punjab is discussed.

摘要

在加拿大开展的一项血红蛋白变体研究发现,在检测的207,300份样本中有21例不相关的血红蛋白D旁遮普变体。其中,8例来自东印度移民,其余来自祖籍英国的加拿大人。在检测的14,500份加拿大印第安人样本中未发现血红蛋白D旁遮普变体。本文介绍了在剑桥医学研究委员会异常血红蛋白研究室鉴定的27例血红蛋白D旁遮普变体的地理来源。其中5例来自不列颠群岛。总结了在英国开展的调查结果。并讨论了血红蛋白D旁遮普变体在全球的分布情况。