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Presence of red cell type NADH-methemoglobin reductase (NADH-diaphorase) in human non erythroid cells.

作者信息

Leroux A, Kaplan J C

出版信息

Biochem Biophys Res Commun. 1972 Nov 15;49(4):945-50. doi: 10.1016/0006-291x(72)90303-8.

DOI:10.1016/0006-291x(72)90303-8
PMID:4404857
Abstract
摘要

相似文献

1
Presence of red cell type NADH-methemoglobin reductase (NADH-diaphorase) in human non erythroid cells.人类非红细胞中红细胞型NADH-高铁血红蛋白还原酶（NADH-黄递酶）的存在。
Biochem Biophys Res Commun. 1972 Nov 15;49(4):945-50. doi: 10.1016/0006-291x(72)90303-8.
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Characterization of the purified NADPH-flavin reductase of human erythrocytes.人红细胞纯化的NADPH-黄素还原酶的特性分析。
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Reduction of methemoglobin through flavin at the physiological concentration by NADPH-flavin reductase of human erythrocytes.人红细胞的NADPH-黄素还原酶通过生理浓度的黄素还原高铁血红蛋白。
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Relationship between the pentose phosphate shunt and methemoglobin reductase activity in human erythrocytes: Effect of aging on methemoglobin reductase activity.
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Diaphorase P: a new fetal isozyme identified in human placenta.黄递酶P：在人胎盘中鉴定出的一种新的胎儿同工酶。
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引用本文的文献

1
Human FAD-dependent NAD(P)H diaphorase.人源黄素腺嘌呤二核苷酸（FAD）依赖的烟酰胺腺嘌呤二核苷酸（磷酸）（NAD(P)H）黄递酶
Biochem J. 1980 May 1;187(2):429-36. doi: 10.1042/bj1870429.
2
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.
3
Importance of oxidative metabolism in T cell cytotoxicity: a comparison of cloned T cells and spleen cells.
氧化代谢在T细胞细胞毒性中的重要性：克隆T细胞与脾细胞的比较
Immunology. 1983 Dec;50(4):645-50.
4
NADH cytochrome b5 reductase activity in lymphoid cell lines. Expression of the defect in epstein Barr virus transformed lymphoblastoid cell lines from patients with recessive congenital methemoglobinemia.淋巴样细胞系中的NADH细胞色素b5还原酶活性。隐性先天性高铁血红蛋白血症患者的爱泼斯坦-巴尔病毒转化淋巴母细胞系中缺陷的表达。
J Clin Invest. 1981 Jul;68(1):279-85. doi: 10.1172/jci110244.
5
Defective molecular variants of glucose-6-phosphate dehydrogenase and methaemoglobin reductase.葡萄糖-6-磷酸脱氢酶和高铁血红蛋白还原酶的缺陷分子变体。
J Clin Pathol Suppl (R Coll Pathol). 1974;8:134-41.
6
Assignment of NADH-cytochrome b5 reductase (DIA1 locus) to human chromosome 22.将NADH - 细胞色素b5还原酶（DIA1基因座）定位到人类第22号染色体上。
Hum Genet. 1978 Jun 27;42(3):233-9. doi: 10.1007/BF00291301.
7
Advances in hereditary red cell enzyme anomalies.遗传性红细胞酶异常的进展
Hum Genet. 1979;50(1):1-27. doi: 10.1007/BF00295584.