• 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

New glucose-6-phosphate dehydrogenase variants observed in Israel and their association with congenital nonspherocytic hemolytic disease.

作者信息

Ramot B, Ben-Bassat I, Shchory M

出版信息

J Lab Clin Med. 1969 Dec;74(6):895-901.

PMID:5359663
Abstract
摘要

相似文献

1
New glucose-6-phosphate dehydrogenase variants observed in Israel and their association with congenital nonspherocytic hemolytic disease.在以色列观察到的新型葡萄糖-6-磷酸脱氢酶变体及其与先天性非球形细胞溶血性贫血的关联。
J Lab Clin Med. 1969 Dec;74(6):895-901.
2
Glucose-6-phosphate dehydrogenase activity of erythrocytes in hemolytic anemia.溶血性贫血中红细胞的葡萄糖-6-磷酸脱氢酶活性
Pol Med J. 1966;5(5):975-80.
3
[Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Rumania: anthropogenetic significance].[罗马尼亚的红细胞葡萄糖-6-磷酸脱氢酶缺乏症：人类遗传学意义]
Rev Med Chir Soc Med Nat Iasi. 1977 Jul-Sep;81(3):377-82.
4
[Glucosephosphate dehydrogenase deficiency in erythrocytes and leukocytes of patients with congenital nonspherocytic hemolytic anemia and favism].[先天性非球形细胞溶血性贫血和蚕豆病患者红细胞和白细胞中的葡萄糖磷酸脱氢酶缺乏症]
Pol Tyg Lek. 1988 Feb 15;43(7):207-9.
5
Red cell glucose-6-phosphate dehydrogenase deficiency in Finland.芬兰的红细胞葡萄糖-6-磷酸脱氢酶缺乏症
Ann Clin Res. 1973 Jun;5(3):168-73.
6
Congenital nonspherocytic hemolytic disease. With erythrocyte glucose-6-phosphate dehydrogenase deficiency.先天性非球形红细胞溶血性贫血。伴红细胞葡萄糖-6-磷酸脱氢酶缺乏症。
Minn Med. 1966 Sep;49(9):1387-95.
7
[Glucose-6-phosphate dehydrogenase type Schwaben. A new enzyme variant with spontaneous hemolytic anemia].施瓦本型葡萄糖-6-磷酸脱氢酶。一种伴有自发性溶血性贫血的新型酶变体
Dtsch Med Wochenschr. 1971 Jun 11;96(24):1029-33. doi: 10.1055/s-0028-1108377.
8
[Enzymopenic hemolytic anemia in an Austrian family].[奥地利一个家族中的酶缺乏性溶血性贫血]
Wien Klin Wochenschr. 1969 Feb 21;81(8):135-7.
9
Red cell glucose-6-phosphate dehydrogenase deficiency in Finland. Further biochemical characterization of G-6-PD Helsinki.芬兰的红细胞葡萄糖-6-磷酸脱氢酶缺乏症。G-6-PD赫尔辛基型的进一步生化特征分析。
Ann Clin Res. 1974 Aug;6(4):187-97.
10
Human erythrocyte glucose 6-phosphate dehydrogenase: structure and function in normal and mutant subjects.人类红细胞葡萄糖-6-磷酸脱氢酶：正常人和突变体中的结构与功能
Curr Top Hematol. 1978;1:1-70.

引用本文的文献

1
A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum.一种独特的电泳迁移缓慢的葡萄糖6-磷酸脱氢酶变体（旭川葡萄糖6-磷酸脱氢酶），其最适pH值明显呈酸性。
Hum Genet. 1984;68(1):70-2. doi: 10.1007/BF00293876.
2
[Glucose-6-P-dehydrogenase type bodensee (a new enzyme variant)].博登湖型葡萄糖-6-磷酸脱氢酶（一种新的酶变体）
Klin Wochenschr. 1971 Oct 1;49(19):1058-62. doi: 10.1007/BF01732914.
3
A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family.
在一个黑人家庭中发现一种与慢性非球形红细胞溶血性贫血相关的新型葡萄糖-6-磷酸脱氢酶（G-6-PD）变异体。
J Med Genet. 1972 Jun;9(2):160-4. doi: 10.1136/jmg.9.2.160.
4
Glucose-6-phosphate dehydrogenase Boston. A new variant associated with congenital nonspherocytic hemolytic disease.葡萄糖-6-磷酸脱氢酶波士顿型。一种与先天性非球形细胞溶血性疾病相关的新变异型。
Humangenetik. 1971;13(3):218-21. doi: 10.1007/BF00326945.
5
G-6-PD Poznań, variant with severe enzyme deficiency.
Humangenetik. 1975 Jun 19;28(2):163-5. doi: 10.1007/BF00735750.
6
Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita.在日本发现三种与先天性非球形红细胞溶血性贫血相关的新的电泳正常的葡萄糖-6-磷酸脱氢酶变异体：G6PD 荻洼型、横滨型和秋田型。
Hum Genet. 1978 Nov 24;45(1):11-7. doi: 10.1007/BF00277568.
7
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variants.
Hum Genet. 1978 Jan 19;40(2):177-84. doi: 10.1007/BF00272298.