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Human erythrocyte glucose 6-phosphate dehydrogenase: structure and function in normal and mutant subjects.

作者信息

Luzzatto L, Testa U

出版信息

Curr Top Hematol. 1978;1:1-70.

PMID:45418
Abstract
摘要

相似文献

1
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.
2
[Hemolytic congenital nonspherocytic anemia secondary to an erythrocyte glucose-6-phosphate dehydrogenase deficiency. Description of 2 new variants: Gd (-) Saint-Louis (Paris) and Gd (-) Hayem].[红细胞葡萄糖-6-磷酸脱氢酶缺乏继发的溶血性先天性非球形细胞贫血。两种新变异型的描述:Gd(-)圣路易型(巴黎)和Gd(-)哈耶姆型]
Nouv Rev Fr Hematol. 1974 Sep-Oct;14(5):587-600.
3
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.
4
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.
5
New developments in glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症的新进展
Isr J Med Sci. 1973 Sep-Oct;9(9):1484-98.
6
Glucose-6-phosphate dehydrogenase abnormality and hemolysis.葡萄糖-6-磷酸脱氢酶异常与溶血。
Acta Biol Med Ger. 1977;36(5-6):689-701.
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
Characteristics of a new abnormal variant of G-6-PD in human red cells.人类红细胞中葡萄糖-6-磷酸脱氢酶(G-6-PD)一种新的异常变体的特征
Acta Biol Med Ger. 1977;36(5-6):753-8.
9
Heterogeneity of red cell glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Egypt.埃及红细胞葡萄糖-6-磷酸脱氢酶(G-6-PD)缺乏症的异质性。
J Lab Clin Med. 1974 Nov;84(5):673-80.
10
[A family of new glucose 6-phosphate dehydrogenase (G 6 PD) variant associated with chronic nonspherocytic hemolytic anemia: G 6 PD Kurume (author's transl)].与慢性非球形细胞溶血性贫血相关的新型葡萄糖6-磷酸脱氢酶(G 6 PD)变异体家族:G 6 PD久留米型(作者译)
Rinsho Ketsueki. 1979 Jan;20(1):82-9.

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1
Haematology in the UK: A 60-year personal perspective.英国血液学:60年个人视角
EJHaem. 2021 May 18;2(3):569-576. doi: 10.1002/jha2.213. eCollection 2021 Aug.
2
The Changes of Leukocytes in Brain and Blood After Intracerebral Hemorrhage.脑出血后脑和血白细胞的变化。
Front Immunol. 2021 Feb 15;12:617163. doi: 10.3389/fimmu.2021.617163. eCollection 2021.
3
Molecular Characterization of G6PD Deficiency: Report of Three Novel G6PD Variants.葡萄糖-6-磷酸脱氢酶缺乏症的分子特征:三种新型葡萄糖-6-磷酸脱氢酶变体的报告
Indian J Hematol Blood Transfus. 2020 Apr;36(2):349-355. doi: 10.1007/s12288-019-01205-7. Epub 2019 Oct 16.
4
Predicting the Kinetic Properties Associated with Redox Imbalance after Oxidative Crisis in G6PD-Deficient Erythrocytes: A Simulation Study.预测葡萄糖-6-磷酸脱氢酶缺乏的红细胞氧化危机后与氧化还原失衡相关的动力学特性:一项模拟研究。
Adv Hematol. 2011;2011:398945. doi: 10.1155/2011/398945. Epub 2011 Sep 28.
5
Cooperating G6PD mutations associated with severe neonatal hyperbilirubinemia and cholestasis.与严重新生儿高胆红素血症和胆汁淤积相关的合作 G6PD 突变。
Pediatr Blood Cancer. 2011 May;56(5):840-2. doi: 10.1002/pbc.22744. Epub 2010 Oct 14.
6
Cytogenetic Analysis of an SD Chromosome from a Natural Population of DROSOPHILA MELANOGASTER.黑腹果蝇自然种群中 SD 染色体的细胞遗传学分析。
Genetics. 1980 Jun;95(2):399-412. doi: 10.1093/genetics/95.2.399.
7
Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal.母系遗传的严重葡萄糖-6-磷酸脱氢酶缺乏症是一种胚胎致死性疾病。
EMBO J. 2002 Aug 15;21(16):4229-39. doi: 10.1093/emboj/cdf426.
8
Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stress.编码葡萄糖-6-磷酸脱氢酶(G6PD)的管家基因的靶向破坏:G6PD对于戊糖合成并非必需,但对于抵御氧化应激至关重要。
EMBO J. 1995 Nov 1;14(21):5209-15. doi: 10.1002/j.1460-2075.1995.tb00205.x.
9
G6PD Ciudad de la Habana: a new slow variant with deficiency found in a Cuban family.哈瓦那市葡萄糖-6-磷酸脱氢酶:在一个古巴家庭中发现的一种新的伴有缺陷的慢变体。
Hum Genet. 1980;55(1):133-5. doi: 10.1007/BF00329141.
10
Genetic heterogeneity of glucose 6-phosphate dehydrogenase deficiency in Sardinia.撒丁岛葡萄糖-6-磷酸脱氢酶缺乏症的遗传异质性。
Hum Genet. 1980;56(1):99-105. doi: 10.1007/BF00281577.