先天性高铁血红蛋白血症中的高铁血红蛋白还原酶（细胞色素b5还原酶）缺乏症。 - Suppr

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超能文献

Methemoglobin reductase (cytochrome b5 reductase) deficiency in congenital methemoglobinemia.

作者信息

Kitao T, Sugita Y, Yoneyama Y, Hattori K

出版信息

Blood. 1974 Dec;44(6):879-84.

PMID:4138943

Abstract

摘要

相似文献

Methemoglobin reductase (cytochrome b5 reductase) deficiency in congenital methemoglobinemia.先天性高铁血红蛋白血症中的高铁血红蛋白还原酶（细胞色素b5还原酶）缺乏症。

Blood. 1974 Dec;44(6):879-84.

Membrane-bound cytochrome b5 reductase (methemoglobin reductase) in human erythrocytes. Study in normal and methemoglobinemic subjects.人红细胞中的膜结合细胞色素b5还原酶（高铁血红蛋白还原酶）。对正常人和高铁血红蛋白血症患者的研究。

J Clin Invest. 1981 Jan;67(1):149-55. doi: 10.1172/JCI110007.

Concentration of NADH-cytochrome b5 reductase in erythrocytes of normal and methemoglobinemic individuals measured with a quantitative radioimmunoblotting assay.用定量放射免疫印迹分析法测定正常人和高铁血红蛋白血症患者红细胞中NADH-细胞色素b5还原酶的浓度。

J Clin Invest. 1987 Nov;80(5):1296-302. doi: 10.1172/JCI113205.

Serine-proline replacement at residue 127 of NADH-cytochrome b5 reductase causes hereditary methemoglobinemia, generalized type.NADH-细胞色素b5还原酶第127位残基的丝氨酸-脯氨酸置换导致遗传性高铁血红蛋白血症，全身性类型。

Blood. 1990 Apr 1;75(7):1408-13.

Studies on methemoglobin reductase. Immunochemical similarity of soluble methemoglobin reductase and cytochrome b5 of human erythrocytes with NADH-cytochrome b5 reductase and cytochrome b5 of rat liver microsomes.高铁血红蛋白还原酶的研究。人红细胞可溶性高铁血红蛋白还原酶及细胞色素b5与大鼠肝微粒体NADH - 细胞色素b5还原酶及细胞色素b5的免疫化学相似性。

Arch Biochem Biophys. 1976 Feb;172(2):600-7. doi: 10.1016/0003-9861(76)90113-2.

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.

Exponential decay of cytochrome b5 and cytochrome b5 reductase during senescence of erythrocytes: relation to the increased methemoglobin content.红细胞衰老过程中细胞色素b5和细胞色素b5还原酶的指数衰减：与高铁血红蛋白含量增加的关系。

J Biochem. 1983 Mar;93(3):931-4. doi: 10.1093/jb/93.3.931.

[Polyacrylamide gel isoelectric focusing for the study of erythrocyte methemoglobin reductase].

Probl Gematol Pereliv Krovi. 1982 Nov;27(11):56-8.

Analyis of met-form haemoglobins in human erythrocytes of normal adults and of a patient with hereditary methaemoglobinaemia due to deficiency of NADH-cytochrome b5 reductase.正常成年人及一名因烟酰胺腺嘌呤二核苷酸（NADH）-细胞色素b5还原酶缺乏导致遗传性高铁血红蛋白血症患者的人红细胞中高铁血红蛋白的分析。

Biochem J. 1979 Aug 1;181(2):505-7. doi: 10.1042/bj1810505.

[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.

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Cureus. 2023 Mar 10;15(3):e35974. doi: 10.7759/cureus.35974. eCollection 2023 Mar.

Isolated Diaphorase From Bovine Erythrocyte Cannot Reduce Oxidized Cytoglobin (Metcygb).从牛红细胞中分离出的黄递酶不能还原氧化型细胞红蛋白（高铁细胞红蛋白）。

Rep Biochem Mol Biol. 2022 Jul;11(2):289-298. doi: 10.52547/rbmb.11.2.289.

Crystal structures of the naturally fused CS and cytochrome b reductase (bR) domains of Ncb5or reveal an expanded CS fold, extensive CS-bR interactions and productive binding of the NAD(P) nicotinamide ring.天然融合的 CS 和细胞色素 b 还原酶 (bR) 结构域的 Ncb5or 晶体结构揭示了扩展的 CS 折叠、广泛的 CS-bR 相互作用以及 NAD(P) 烟酰胺环的有效结合。

Acta Crystallogr D Struct Biol. 2019 Jul 1;75(Pt 7):628-638. doi: 10.1107/S205979831900754X. Epub 2019 Jun 26.

Congenital methemoglobinemia misdiagnosed as polycythemia vera: Case report and review of literature.误诊为真性红细胞增多症的先天性高铁血红蛋白血症：病例报告及文献复习

Hematol Rep. 2018 Mar 2;10(1):7221. doi: 10.4081/hr.2018.7221.

Structure Guided Chemical Modifications of Propylthiouracil Reveal Novel Small Molecule Inhibitors of Cytochrome b5 Reductase 3 That Increase Nitric Oxide Bioavailability.丙硫氧嘧啶的结构导向化学修饰揭示了细胞色素b5还原酶3的新型小分子抑制剂，可提高一氧化氮的生物利用度。

J Biol Chem. 2015 Jul 3;290(27):16861-72. doi: 10.1074/jbc.M114.629964. Epub 2015 May 22.

Polymorphisms in the carcinogen detoxification genes CYB5A and CYB5R3 and breast cancer risk in African American women.致癌物解毒基因CYB5A和CYB5R3的多态性与非裔美国女性的乳腺癌风险

Cancer Causes Control. 2014 Nov;25(11):1513-21. doi: 10.1007/s10552-014-0454-7. Epub 2014 Sep 16.

Congenital methemoglobinemia in a dog with a promoter deletion and a nonsynonymous coding variant in the gene encoding cytochrome b₅.一只患有启动子缺失和编码细胞色素b₅基因非同义编码变异的犬先天性高铁血红蛋白血症

J Vet Intern Med. 2014 Sep-Oct;28(5):1626-31. doi: 10.1111/jvim.12423. Epub 2014 Aug 21.

Evaluation of polymorphisms in the sulfonamide detoxification genes NAT2, CYB5A, and CYB5R3 in patients with sulfonamide hypersensitivity.评价磺胺类药物过敏患者中磺胺类药物解毒基因 NAT2、CYB5A 和 CYB5R3 的多态性。

Pharmacogenet Genomics. 2012 Oct;22(10):733-40. doi: 10.1097/FPC.0b013e328357a735.

Methemoglobinemia in a young man.一名年轻男性的高铁血红蛋白血症。

Tex Heart Inst J. 2008;35(1):76-7.

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.

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