• 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

Characterization of glucose-6-phosphate dehydrogenase among Chinese.

作者信息

Wong P W, Shih L, Hsia D Y

出版信息

Nature. 1965 Dec 25;208(5017):1323-4. doi: 10.1038/2081323a0.

DOI:10.1038/2081323a0
PMID:5870191
Abstract
摘要

相似文献

1
Characterization of glucose-6-phosphate dehydrogenase among Chinese.中国人葡萄糖-6-磷酸脱氢酶的特征分析
Nature. 1965 Dec 25;208(5017):1323-4. doi: 10.1038/2081323a0.
2
Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a Japanese child. Clinical and metabolic studies.一名日本儿童因葡萄糖-6-磷酸脱氢酶缺乏导致的先天性非球形红细胞溶血性贫血。临床与代谢研究。
Nihon Ketsueki Gakkai Zasshi. 1972 Feb;35(1):20-31.
3
G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.G6PD 巴亚莫型。一种与先天性非球形红细胞溶血性贫血相关的葡萄糖 -6- 磷酸脱氢酶新变体。
Vox Sang. 1982;43(2):102-4. doi: 10.1111/j.1423-0410.1982.tb00533.x.
4
Glucose-6-phosphate dehydrogenase deficiency--a genetic disorder of red cell metabolism.葡萄糖-6-磷酸脱氢酶缺乏症——一种红细胞代谢的遗传性疾病。
J Postgrad Med. 1972 Apr;18(2):51-67.
5
[Glucose-6-phosphate dehydrogenase].[葡萄糖-6-磷酸脱氢酶]
Expos Annu Biochim Med. 1969;29:101-19.
6
Adaptation of the spectrophotometric methods for erythrocyte pyruvate kinase and glucose--6--phosphate dehydrogenase to use with small blood samples.将用于红细胞丙酮酸激酶和葡萄糖-6-磷酸脱氢酶的分光光度法进行调整,以便用于少量血样检测。
J Med Assoc Thai. 1977 Sep;60(9):459-63.
7
Glucose-6-phosphate dehydrogenase Beaumont: a new variant with severe enzyme deficiency and chronic nonspherocytic hemolytic anemia.葡萄糖-6-磷酸脱氢酶博蒙特型:一种伴有严重酶缺乏和慢性非球形红细胞溶血性贫血的新变体。
Enzyme. 1985;34(1):15-21. doi: 10.1159/000469354.
8
[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.
9
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.
10
[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.

引用本文的文献

1
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.对于因葡萄糖-6-磷酸脱氢酶突变导致严重酶缺乏的杂合子,体细胞选择是血细胞表型的主要决定因素。
Am J Hum Genet. 1996 Oct;59(4):887-95.
2
G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia.
Hum Genet. 1982;61(2):175-6. doi: 10.1007/BF00274214.
3
Glucose-6-phosphate dehydrogenase deficiency in Chinese.中国人中的葡萄糖-6-磷酸脱氢酶缺乏症
J Clin Pathol. 1968 Jan;21(1):44-7. doi: 10.1136/jcp.21.1.44.
4
Glucose-6-phosphate dehydrogenase deficiency and chronic haemolysis in an English family.英国家庭中的葡萄糖-6-磷酸脱氢酶缺乏症与慢性溶血
J Clin Pathol. 1970 Mar;23(2):135-9. doi: 10.1136/jcp.23.2.135.
5
Double heterozygosity for glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症的双重杂合性
J Med Genet. 1971 Jun;8(2):149-52. doi: 10.1136/jmg.8.2.149.
6
Characteristics and distribution of glucose-6-phosphate dehydrogenase-deficient variants in South China.中国南方葡萄糖-6-磷酸脱氢酶缺乏症变异体的特征与分布
Am J Hum Genet. 1972 Jul;24(4):475-84.
7
Glucose-6-phosphate dehydrogenase (G6PD) Iserlohn and G6PD Regensburg: two new severe enzyme defects in German families.葡萄糖-6-磷酸脱氢酶(G6PD)伊瑟隆型和G6PD雷根斯堡型:德国家族中的两种新的严重酶缺陷。
Blut. 1985 Aug;51(2):109-15. doi: 10.1007/BF00320119.
8
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.