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 - Suppr

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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

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.

[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.

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.

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.

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.

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.

[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.

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.

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.

[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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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.

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.

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.

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.

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.

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.

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