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Genetic heterogeneity and pathophysiology of G6PD deficiency.

作者信息

Luzzatto L

出版信息

Br J Haematol. 1974 Oct;28(2):151-5. doi: 10.1111/j.1365-2141.1974.tb06649.x.

DOI:10.1111/j.1365-2141.1974.tb06649.x
PMID:4154774
Abstract
摘要

相似文献

1
Genetic heterogeneity and pathophysiology of G6PD deficiency.
Br J Haematol. 1974 Oct;28(2):151-5. doi: 10.1111/j.1365-2141.1974.tb06649.x.
2
Hemolysis due to inherited erythrocyte enzyme deficiencies.由于遗传性红细胞酶缺乏引起的溶血。
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[Hereditary hemolytic erythocyte enzymopathies].[遗传性溶血性红细胞酶病]
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Biochemical genetics in medicine.医学中的生化遗传学
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Molecular Epidemiological Survey of Glucose-6-Phosphate Dehydrogenase Deficiency and Thalassemia in Uygur and Kazak Ethnic Groups in Xinjiang, Northwest China.中国西北新疆维吾尔族和哈萨克族葡萄糖-6-磷酸脱氢酶缺乏症和地中海贫血的分子流行病学调查
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New stable mutant (Gd(-) variants: G6PD Tashkent and G6PD Nucus. Molecular basis of hereditary enzyme deficiency.新的稳定突变体(Gd(-)变体:G6PD塔什干型和G6PD努库斯型。遗传性酶缺乏的分子基础。
Acta Biol Med Ger. 1981;40(4-5):559-62.
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Red cell enzymopathies as a model of inborn errors of metabolism.红细胞酶病作为先天性代谢缺陷的一个模型。
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Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of both.葡萄糖-6-磷酸脱氢酶缺乏症、杂合子β地中海贫血以及两者合并情况下红细胞的氧化还原和能量状态
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Genetic variation in the quantitative levels of an NADP (H)-binding protein (FX) in human erythrocytes.人类红细胞中一种NADP(H)结合蛋白(FX)定量水平的基因变异。
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Heterogeneity of glucose-6-phosphate dehydrogenase enzymopathies in the GDR.德意志民主共和国葡萄糖-6-磷酸脱氢酶酶病的异质性
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引用本文的文献

1
Association between Glucose-6-Phosphate Dehydrogenase Deficiency and Asthma.葡萄糖-6-磷酸脱氢酶缺乏症与哮喘之间的关联
J Clin Med. 2021 Nov 29;10(23):5639. doi: 10.3390/jcm10235639.
2
Tolerability of tiaprofenic acid in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Drugs. 1988;35 Suppl 1:107-10. doi: 10.2165/00003495-198800351-00024.
3
[Toxic hemolytic anemias].[中毒性溶血性贫血]
Blut. 1976 Aug;33(2):73-82. doi: 10.1007/BF00999869.
4
Investigations on the organization of genetic loci in Drosophila melanogaster: lethal mutations affecting 6-phosphogluconate dehydrogenase and their suppression.黑腹果蝇基因位点组织的研究:影响6-磷酸葡萄糖酸脱氢酶的致死突变及其抑制作用。
Mol Gen Genet. 1977 Jun 8;153(2):191-8. doi: 10.1007/BF00264735.
5
Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphism.“正常”人红细胞葡萄糖-6-磷酸脱氢酶的遗传异质性:一种等电点多态性。
Proc Natl Acad Sci U S A. 1979 Feb;76(2):852-6. doi: 10.1073/pnas.76.2.852.
6
Biochemical mechanisms of glucose-6-phosphate dehydrogenase deficiency.葡萄糖-6-磷酸脱氢酶缺乏症的生化机制
Proc Natl Acad Sci U S A. 1978 Apr;75(4):1979-83. doi: 10.1073/pnas.75.4.1979.
7
Parallel occurrence of oxidant-sensitivity and decreased inhibition by NADPH in G-6-PD Lublin and G-6-PD Poxnań.葡萄糖-6-磷酸脱氢酶卢布林型和葡萄糖-6-磷酸脱氢酶波兹南型中氧化敏感性与NADPH抑制作用降低的平行出现。
Hum Genet. 1977 Dec 29;40(1):107-11. doi: 10.1007/BF00280837.