三磷酸吡啶核苷酸-高铁血红蛋白还原酶缺乏症：一种新的红细胞酶缺陷。 - Suppr

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超能文献

TPNH-methemoglobin reductase deficiency: a new red-cell enzyme defect.

作者信息

Sass M D, Caruso C J, Farhangi M

出版信息

J Lab Clin Med. 1967 Nov;70(5):760-7.

PMID:4383300

Abstract

摘要

相似文献

TPNH-methemoglobin reductase deficiency: a new red-cell enzyme defect.三磷酸吡啶核苷酸-高铁血红蛋白还原酶缺乏症：一种新的红细胞酶缺陷。

J Lab Clin Med. 1967 Nov;70(5):760-7.

[Heterozygous NADH-methemoglobin reductase defect with methemoglobinemia in an infant (author's transl)].婴儿杂合子NADH-高铁血红蛋白还原酶缺陷伴高铁血红蛋白血症（作者译）

Z Kinderheilkd. 1973 Nov 19;115(4):273-81.

DPNH-methemoglobin reductase deficiency and hereditary methemoglobinemia.二磷酸吡啶核苷酸-高铁血红蛋白还原酶缺乏症与遗传性高铁血红蛋白血症。

Semin Hematol. 1971 Oct;8(4):417-37.

Mechanism of the TPNH-linked reduction of methemoglobin by methylene blue.

Clin Chim Acta. 1969 Apr;24(1):77-85. doi: 10.1016/0009-8981(69)90143-0.

Observations on the role of TPNH dehydrogenase in human red cells.关于三磷酸吡啶核苷酸脱氢酶在人体红细胞中的作用的观察

Clin Chim Acta. 1968 Jul;21(1):101-3. doi: 10.1016/0009-8981(68)90016-8.

Congenital methemoglobinemia due to DPNH-methemoglobin reductase deficiency: another inherited defect of red blood cell metabolism found in Thailand.

J Med Assoc Thai. 1970 May;53(5):322-36.

[Metabolism of red blood cells. I. Oxidation-reduction systems of red blood cells and their anomalies].[红细胞的代谢。I. 红细胞的氧化还原系统及其异常]

Przegl Lek. 1972;29(2):313-20.

[Familial NADH diaphorase deficiency].[家族性烟酰胺腺嘌呤二核苷酸黄递酶缺乏症]

Nouv Rev Fr Hematol. 1972 Jul-Aug;12(4):560-3.

Red cell enzyme deficiencies: a review.红细胞酶缺乏症：综述

Am J Med Technol. 1972 Nov;38(11):454-61.

Acatalasemia.

Adv Hum Genet. 1971;2:143-99.

引用本文的文献

PharmGKB summary: methylene blue pathway.药物基因组学知识库总结：亚甲蓝途径。

Pharmacogenet Genomics. 2013 Sep;23(9):498-508. doi: 10.1097/FPC.0b013e32836498f4.

Evidence that biliverdin-IX beta reductase and flavin reductase are identical.胆绿素-IXβ还原酶和黄素还原酶相同的证据。

Biochem J. 1996 Jun 1;316 ( Pt 2)(Pt 2):385-7. doi: 10.1042/bj3160385.

Electrophoretic and functional variants of NADH-methemoglobin reductase in hereditary methemoglobinemia.遗传性高铁血红蛋白血症中NADH-高铁血红蛋白还原酶的电泳及功能变体

J Clin Invest. 1971 Jan;50(1):196-202. doi: 10.1172/JCI106473.

Comparative studies on the effects of toluidine blue and methylene blue on the reduction of ferrihaemoglobin in man and dog.甲苯胺蓝和亚甲蓝对人和狗高铁血红蛋白还原作用的比较研究。

Eur J Clin Pharmacol. 1972 Mar;4(2):115-8. doi: 10.1007/BF00562507.

Activity of NADH- and NADPH-dependent methemoglobin reductases in erythrocytes from fetal to adult age. A parallel assessment.从胎儿到成人阶段红细胞中NADH和NADPH依赖性高铁血红蛋白还原酶的活性。一项平行评估。

Klin Wochenschr. 1971 Sep 1;49(17):972-7. doi: 10.1007/BF01489462.

Inherited methemoglobinemia (enzyme deficiencies).遗传性高铁血红蛋白血症（酶缺乏症）。

Humangenetik. 1970;9(3):217-8. doi: 10.1007/BF00279219.

Drug- and chemical-induced methaemoglobinaemia. Clinical features and management.药物和化学物质诱发的高铁血红蛋白血症。临床特征与处理

Med Toxicol. 1986 Jul-Aug;1(4):253-60. doi: 10.1007/BF03259842.

Characterization of NADPH-dependent methemoglobin reductase as a heme-binding protein present in erythrocytes and liver.将NADPH依赖性高铁血红蛋白还原酶鉴定为红细胞和肝脏中存在的一种血红素结合蛋白。

Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2130-4. doi: 10.1073/pnas.89.6.2130.

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