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G6PD Toronto.

作者信息

Crookston J H, Yoshida A, Lin M, Booser D J

出版信息

Biochem Genet. 1973 Mar;8(3):259-65. doi: 10.1007/BF00486178.

DOI:10.1007/BF00486178
PMID:4701992
Abstract
摘要

相似文献

1
G6PD Toronto.葡萄糖-6-磷酸脱氢酶多伦多型
Biochem Genet. 1973 Mar;8(3):259-65. doi: 10.1007/BF00486178.
2
Glucose-6-phosphate dehydrogenase Jackson. A new variant associated with hemolytic anemia.葡萄糖-6-磷酸脱氢酶杰克逊。一种与溶血性贫血相关的新变体。
Acta Haematol. 1974;51(5):310-4. doi: 10.1159/000208311.
3
Combined erythrocyte glucosephosphate isomerase (GPI) and glucose-6-phosphate dehydrogenase (G6PD) deficiency in an Italian family.意大利一个家族中红细胞磷酸葡萄糖异构酶(GPI)和葡萄糖-6-磷酸脱氢酶(G6PD)联合缺乏症
Hum Genet. 1981;57(2):226-9. doi: 10.1007/BF00282031.
4
Equine glucose-6-phosphate dehydrogenase deficiency.
Vet Pathol. 1994 Sep;31(5):518-27. doi: 10.1177/030098589403100503.
5
[II. Chronic hemolytic anemia caused by erythrocytic deficiency of glucose-6-phosphate dehydrogenase (G6PD)].[二、葡萄糖-6-磷酸脱氢酶(G6PD)红细胞缺乏引起的慢性溶血性贫血]
Pediatria (Napoli). 1979 Dec 31;87(4):V-VI.
6
Intraerythrocytic distribution of glucose-6-phosphate dehydrogenase (G-6-PD) in haemolytic anaemias.葡萄糖-6-磷酸脱氢酶(G-6-PD)在溶血性贫血患者红细胞内的分布
Bull Calcutta Sch Trop Med. 1971 Apr;19(2):33-5.
7
[Clinico-genetic significance of glucose-6-phosphate dehydrogenase deficiency of erythrocytes].[红细胞葡萄糖-6-磷酸脱氢酶缺乏症的临床遗传学意义]
Pediatriia. 1982 Jun(6):33-6.
8
Clinical and biochemical studies on mutant red cell enzymes mainly associated with hemolytic anemia.主要与溶血性贫血相关的突变红细胞酶的临床和生化研究。
Jinrui Idengaku Zasshi. 1980 Jun;25(2):83-92. doi: 10.1007/BF01873607.
9
[New anomalous variant of "Kremenchug" glucose-6-phosphate dehydrogenase linked to acute drug-induced hemolytic anemia].["与急性药物性溶血性贫血相关的“克雷门丘格”葡萄糖-6-磷酸脱氢酶新异常变体]
Probl Gematol Pereliv Krovi. 1977 Nov(11):47-50.
10
Discussion on pharmacogenetic interaction in G6PD deficiency and methods to identify potential hemolytic drugs.葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症的药物遗传学相互作用及潜在溶血药物识别方法的探讨
Cardiovasc Hematol Disord Drug Targets. 2010 Jun;10(2):143-50. doi: 10.2174/187152910791292547.

引用本文的文献

1
Further evidence for heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Papua New Guinea.巴布亚新几内亚葡萄糖-6-磷酸脱氢酶缺乏症异质性的进一步证据。
Hum Genet. 1980;56(2):209-12. doi: 10.1007/BF00295696.
2
Gd(-) Muret and gd(-) Colomiers, two new variants of glucose-6-phosphate dehydrogenase associated with favism.Gd(-) 米雷和gd(-) 科洛米耶,两种与蚕豆病相关的葡萄糖-6-磷酸脱氢酶新变体。
Hum Genet. 1981;57(3):332-4. doi: 10.1007/BF00278958.
3
Molecular mechanism of glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症的分子机制。

本文引用的文献

1
Methaemoglobin reduction test: a new, simple, in vitro test for identifying primaquine-sensitivity.高铁血红蛋白还原试验:一种用于鉴定伯氨喹敏感性的新型、简便的体外试验。
Bull World Health Organ. 1960;22(6):633-40.
2
Negro variant of glucose-6-phosphate dehydrogenase deficiency (A-) in man.人类葡萄糖-6-磷酸脱氢酶缺乏症(A-型)的黑人变异型
Science. 1967 Jan 6;155(3758):97-9. doi: 10.1126/science.155.3758.97.
3
Tissue enzyme levels in erythrocyte glucose-6-phosphate dehydrogenase deficiency.
Humangenetik. 1974;25(2):101-9. doi: 10.1007/BF00283310.
4
Glucose-6-phosphate dehydrogenase (G6PD) Guantánamo and G6PD Caujerí: two new glucose-6-phosphate dehydrogenase-deficient variants found in Cuba.
Biochem Genet. 1987 Apr;25(3-4):231-8. doi: 10.1007/BF00499316.
5
G6PD Lozere and Trinacria-like. Segregation of two non hemolytic variants in a French family.
Hum Genet. 1976 Dec 15;34(3):293-8. doi: 10.1007/BF00295293.
J Lab Clin Med. 1965 Dec;66(6):937-42.
4
Further studies on glucose-6-phosphate dehydrogenase deficiency in Chinese subjects.关于中国人群葡萄糖-6-磷酸脱氢酶缺乏症的进一步研究。
J Lab Clin Med. 1970 May;75(5):788-97.
5
Human glucose-6-phosphate dehydrogenase variants.人类葡萄糖-6-磷酸脱氢酶变体
Bull World Health Organ. 1971;45(2):243-53.
6
A Philippino glucose-6-phosphate dehydrogenase variant (G6PD Union) with enzyme deficiency and altered substrate specificity.一种具有酶缺乏和底物特异性改变的菲律宾葡萄糖-6-磷酸脱氢酶变体(G6PD 联盟)
Blood. 1970 Apr;35(4):506-13.
7
Glucose 6-phosphate dehydrogenase of human erythrocytes. I. Purification and characterization of normal (B+) enzyme.人红细胞葡萄糖-6-磷酸脱氢酶。I. 正常(B+)酶的纯化与特性分析
J Biol Chem. 1966 Nov 10;241(21):4966-76.