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[Spontaneous and chloramphenicol-induced chromosome mutations and biochemical data in 2 cases with glutathione reductase deficiency (NAD(P)H: glutathione oxidoreductase, E.C.1.6.4.2.)].

作者信息

Hampel K E

出版信息

Humangenetik. 1969;7(4):305-13. doi: 10.1007/BF00283552.

DOI:10.1007/BF00283552
PMID:5365571
Abstract
摘要

相似文献

1
[Spontaneous and chloramphenicol-induced chromosome mutations and biochemical data in 2 cases with glutathione reductase deficiency (NAD(P)H: glutathione oxidoreductase, E.C.1.6.4.2.)].[2例谷胱甘肽还原酶缺乏症(NAD(P)H:谷胱甘肽氧化还原酶,E.C.1.6.4.2.)患者的自发及氯霉素诱导的染色体突变与生化数据]
Humangenetik. 1969;7(4):305-13. doi: 10.1007/BF00283552.
2
[Glutathione reductase deficiency with membrane defect in hereditary hemolytic anemia].遗传性溶血性贫血伴膜缺陷的谷胱甘肽还原酶缺乏症
Acta Haematol. 1976;56(1):47-57. doi: 10.1159/000207918.
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[Development of drug induced anemia in patients with glutathione reductase deficiency].[谷胱甘肽还原酶缺乏患者药物性贫血的发生]
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4
[Hemolytic anemias. Enzymopenic hemolytic anemias].[溶血性贫血。酶缺乏性溶血性贫血]
Internist (Berl). 1966 Jun;7(6):295-302.
5
[Study of intraerythrocytic enzymes in a family with spherocytosis (Minkowski-Chauffard hemolytic anemia)].
Rev Clin Esp. 1972 Nov 30;127(4):871-6.
6
[Erythrocyte glutathione-peroxidase deficiency and drug-induced hemolytic anemia. A further case].[红细胞谷胱甘肽过氧化物酶缺乏与药物性溶血性贫血。另一病例]
Presse Med (1893). 1970 Jan 24;78(4):171-4.
7
Observations on erythrocytic glutathione (GSH) and related enzymes during in vitro storage of blood from haemolytic anaemia patients.
Indian J Pathol Bacteriol. 1972 Jan;15(1):27-33.
8
[Superoxide dismutase activity in the platelets of myeloproliferative disorders and of hemolytic anemia with glutathione reductase deficiency (author's transl)].
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Acta Haematol. 1974;52(4):248-56. doi: 10.1159/000208248.
10
On the molecular basis of pyruvate kinase deficiency.丙酮酸激酶缺乏症的分子基础。
Biochim Biophys Acta. 1974 Dec 29;370(2):601-4. doi: 10.1016/0005-2744(74)90124-7.

引用本文的文献

1
[Transient pyruvate kinase- and glutathione reductase deficiency of erythrocytes in chronic idiopathic infantile pancytopenia].[慢性特发性婴儿全血细胞减少症中红细胞丙酮酸激酶和谷胱甘肽还原酶的短暂缺乏]
Klin Wochenschr. 1970 Dec 1;48(23):1407-14. doi: 10.1007/BF01488812.
2
Phenylbutazone, chloramphenicol and mammalian chromosomes.
Humangenetik. 1972;17(1):61-4. doi: 10.1007/BF01789601.

本文引用的文献

1
INHIBITION OF PROTEIN SYNTHESIS IN MAMMALIAN CELL-FREE SYSTEMS BY CHLORAMPHENICOL.氯霉素对哺乳动物无细胞系统中蛋白质合成的抑制作用。
J Exp Med. 1964 Aug 1;120(2):161-81. doi: 10.1084/jem.120.2.161.
2
Improved method for the determination of blood glutathione.测定血液中谷胱甘肽的改进方法。
J Lab Clin Med. 1963 May;61:882-8.
3
[A new enzymopenic hemolytic anemia with glutathione reductase deficiency].[一种伴有谷胱甘肽还原酶缺乏的新型酶缺乏性溶血性贫血]
Med Klin. 1962 Sep 7;57:1521-5.
4
Chromosome preparations of leukocytes cultured from human peripheral blood.从人外周血培养的白细胞的染色体标本制备。
Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.
5
Genetics of human cell lines. III. Incorporation of 5-bromo- and 5-iododeoxyuridine into the deoxyribonucleic acid of human cells and its effect on radiation sensitivity.人类细胞系的遗传学。III. 5-溴脱氧尿苷和5-碘脱氧尿苷掺入人类细胞的脱氧核糖核酸及其对辐射敏感性的影响。
J Exp Med. 1960 Sep 1;112(3):509-31. doi: 10.1084/jem.112.3.509.
6
The hemolytic effect of primaquine. II. The natural course of the hemolytic anemia and the mechanism of its self-limited character.伯氨喹的溶血作用。II. 溶血性贫血的自然病程及其自限性特征的机制。
J Lab Clin Med. 1954 Aug;44(2):171-6.
7
The regeneration of reduced glutathione in normal and glucose-6-phosphate dehydrogenase deficient human red blood cells.正常及葡萄糖-6-磷酸脱氢酶缺乏的人红细胞中还原型谷胱甘肽的再生
Blood. 1967 Mar;29(3):313-9.
8
[Erythrocyte isolation from blood with cotton].[用棉花从血液中分离红细胞]
Klin Wochenschr. 1966 Aug 15;44(16):983-4. doi: 10.1007/BF01711475.
9
[Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].
Humangenetik. 1966;2(3):287-316. doi: 10.1007/BF00395947.
10
[Glutathione reductase deficiency with hematological and neurologic disorders. (Autosomal dominant hereditary formation of a pathological enzyme)].伴有血液学和神经系统疾病的谷胱甘肽还原酶缺乏症。(病理性酶的常染色体显性遗传形成)
Klin Wochenschr. 1965 Apr 15;43(8):413-26. doi: 10.1007/BF01483846.