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Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.

作者信息

Kaplan J C, Beutler E

出版信息

Nature. 1968 Jan 20;217(5125):256-8. doi: 10.1038/217256a0.

DOI:10.1038/217256a0
PMID:4384274
Abstract
摘要

相似文献

1
Electrophoretic study of glutathione reductase in human erythrocytes and leucocytes.
Nature. 1968 Jan 20;217(5125):256-8. doi: 10.1038/217256a0.
2
[Erythrocyte diaphorases and glutathione reductase].
Expos Annu Biochim Med. 1969;29:77-99.
3
[Study of NADH-diaphorase activity of leukocytes in congenital recessive methemoglobinemia].
C R Acad Hebd Seances Acad Sci D. 1970 May 4;18:2223-4.
4
Heterogeneity of the enzymatic defect in congenital methemoglobinemia.
N Engl J Med. 1969 Oct 23;281(17):919-22. doi: 10.1056/NEJM196910232811702.
5
Effect of primaquine on erythrocytes with NADH-methaemoglobin reductase deficiency and low glutathione reductase activity.伯氨喹对伴有NADH-高铁血红蛋白还原酶缺乏和低谷胱甘肽还原酶活性的红细胞的影响。
Br J Haematol. 1972 Sep;23(3):333-41. doi: 10.1111/j.1365-2141.1972.tb08880.x.
6
Leukocyte diaphorase deficiency in congenital methemoglobinemia: a valuable prognostic indicator.
Biol Neonate. 1977;32(3-4):193-6. doi: 10.1159/000241016.
7
Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girl.一名西班牙女孩患先天性高铁血红蛋白还原酶（细胞色素b5还原酶）缺乏症并伴有智力发育迟缓
Acta Haematol. 1978;59(6):348-53. doi: 10.1159/000207786.
8
Electrophoresis of red cell NADH- and NADPH-diaphorases in normal subjects and patients with congenital methemoglobinemia.正常受试者和先天性高铁血红蛋白血症患者红细胞NADH-和NADPH-黄递酶的电泳分析
Biochem Biophys Res Commun. 1967 Nov 30;29(4):605-10. doi: 10.1016/0006-291x(67)90529-3.
9
Alteration of NADH-diaphorase and cytochrome b5 reductase activities of erythrocytes, platelets, and leucocytes in hereditary methaemoglobinaemia with and without mental retardation.伴有和不伴有智力迟钝的遗传性高铁血红蛋白血症患者红细胞、血小板和白细胞中NADH-黄递酶及细胞色素b5还原酶活性的改变
J Med Genet. 1982 Jun;19(3):204-9. doi: 10.1136/jmg.19.3.204.
10
Studies on methemoglobin reductase. I. Comparative studies of diaphorases from normal and methemoglobinemic erythrocytes.高铁血红蛋白还原酶的研究。I. 正常红细胞和高铁血红蛋白血症红细胞中黄递酶的比较研究。
J Biol Chem. 1972 Jan 25;247(2):550-5.

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1
Cisplatin Resistance and Redox-Metabolic Vulnerability: A Second Alteration.顺铂耐药性与氧化还原代谢脆弱性：第二个改变。
Int J Mol Sci. 2021 Jul 9;22(14):7379. doi: 10.3390/ijms22147379.
2
Properties and physiological function of a glutathione reductase purified from spinach leaves by affinity chromatography.用亲和层析法从菠菜叶中纯化得到的谷胱甘肽还原酶的性质和生理功能。
Planta. 1978 Jan;139(1):9-17. doi: 10.1007/BF00390803.
3
Purification and characterization of glutathione reductase isozymes specific for the state of cold hardiness of red spruce.
红云杉抗寒状态特异性谷胱甘肽还原酶同工酶的纯化与特性分析
Plant Physiol. 1994 May;105(1):205-13. doi: 10.1104/pp.105.1.205.
4
Alterations in the prooxidant and antioxidant status of human leukemic T-lymphocyte MOLT4 cells treated with potassium chromate.用铬酸钾处理的人白血病T淋巴细胞MOLT4细胞的促氧化剂和抗氧化剂状态的改变。
Mol Cell Biochem. 1995 Jan 12;142(1):61-70. doi: 10.1007/BF00928914.
5
[Glyoxalase I (GLO) in human tissues (author's transl)].人组织中的乙二醛酶I（GLO）（作者译）
Z Rechtsmed. 1980;85(3):165-8. doi: 10.1007/BF02116315.
6
Effect of flavin compounds on glutathione reductase activity: in vivo and in vitro studies.黄素化合物对谷胱甘肽还原酶活性的影响：体内和体外研究
J Clin Invest. 1969 Oct;48(10):1957-66. doi: 10.1172/JCI106162.
7
[Family studies on glutathione reductase deficiency in human erythrocytes].[人类红细胞谷胱甘肽还原酶缺乏症的家系研究]
Humangenetik. 1968;6(2):163-70. doi: 10.1007/BF00297725.
8
NADH diaphorase: an inherited variant associated with normal methemoglobin reduction.NADH 脱氢酶：一种与高铁血红蛋白正常还原相关的遗传性变异体。
Am J Hum Genet. 1970 Jan;22(1):100-4.
9
[Properties of erythrocyte glutathione reductase from normal and enzyme-deficient subjects (author's transl)].[正常人和酶缺乏受试者红细胞谷胱甘肽还原酶的特性（作者译）]
Klin Wochenschr. 1973 Dec 15;51(24):1177-84. doi: 10.1007/BF01468553.
10
Survey of several red cell and serum genetic markers in a Peruvian population.秘鲁人群中几种红细胞和血清遗传标记的调查。
Am J Hum Genet. 1972 Mar;24(2):111-23.