黑腹果蝇ma-1和ry突变体的拟表型：4-羟基吡唑并（3,4-d）嘧啶对体内黄嘌呤脱氢酶的抑制作用 - Suppr

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Phenocopies of the ma-1 and ry mutants of Drosophila melanogaster: inhibition in vivo of xanthine dehydrogenase by 4-hydroxypyrazolo(3,4-d)pyrimidine.

作者信息

Keller E C, Glassman E

出版信息

Nature. 1965 Oct 9;208(5006):202-3. doi: 10.1038/208202a0.

DOI:10.1038/208202a0

PMID:5884262

Abstract

摘要

相似文献

Phenocopies of the ma-1 and ry mutants of Drosophila melanogaster: inhibition in vivo of xanthine dehydrogenase by 4-hydroxypyrazolo(3,4-d)pyrimidine.黑腹果蝇ma-1和ry突变体的拟表型：4-羟基吡唑并（3,4-d）嘧啶对体内黄嘌呤脱氢酶的抑制作用

Nature. 1965 Oct 9;208(5006):202-3. doi: 10.1038/208202a0.

Effects of the inhibitor of xanthine dehydrogenase, 4-hydroxypyrazolo(3,4 d)pyrimidine (or HPP) on the red eye pigments of Drosophila melanogaster.黄嘌呤脱氢酶抑制剂4-羟基吡唑并（3,4-d）嘧啶（或HPP）对黑腹果蝇红眼色素的影响。

Experientia. 1967 Mar 15;23(3):186-7. doi: 10.1007/BF02136276.

Abnormalities of the eye pigments (pteridins and ommochromes) induced in Drosophila melanogaster by the inhibitor of xanthine dehydrogenase 4-hydroxypyrazole (3,4 d) pyrimidine.黄嘌呤脱氢酶抑制剂4-羟基吡唑（3,4-d）嘧啶在黑腹果蝇中诱导产生的眼色素（蝶啶和眼色素）异常。

Experientia. 1967 Dec 15;23(12):1020-1. doi: 10.1007/BF02136423.

Xanthine oxidase activity in human tissues and its inhibition by allopurinol (4-hydroxypyrazolo[3,4-d] pyrimidine).人体组织中的黄嘌呤氧化酶活性及其被别嘌呤醇（4-羟基吡唑并[3,4-d]嘧啶）的抑制作用。

J Lab Clin Med. 1965 Oct;66(4):688-97.

Inhibition of uric acid biosynthesis in the chick embryo and chicken by a xanthine oxidase inhibitor, 4-hydroxypyrazolo(3,4d)pyrimidine.

J Pharmacol Exp Ther. 1965 Sep;149(3):417-22.

Electrophoretic variants of xanthine dehydrogenase in Drosophila melanogaster. II. Enzyme kinetics.黑腹果蝇中黄嘌呤脱氢酶的电泳变体。II. 酶动力学

Biochim Biophys Acta. 1967 Sep 12;146(1):35-44. doi: 10.1016/0005-2744(67)90071-x.

Nutritional control of xanthine dehydrogenase. I. The effect in adult Drosophila melanogaster of feeding a high protein diet to larvae.黄嘌呤脱氢酶的营养调控。I. 给幼虫喂食高蛋白饮食对成年黑腹果蝇的影响。

Biochim Biophys Acta. 1970 May 12;208(2):294-303. doi: 10.1016/0304-4165(70)90248-5.

In vitro complementation between non-allelic mutants deficient in xanthine dehydrogenase. II. The absence of the ma-l+ factor in lxd mutant flies.黄嘌呤脱氢酶缺陷的非等位突变体之间的体外互补作用。II. lxd突变果蝇中不存在ma-l+因子。

Biochem Biophys Res Commun. 1964 Oct 14;17(3):242-7. doi: 10.1016/0006-291x(64)90391-2.

Urate-null rosy mutants of Drosophila melanogaster are hypersensitive to oxygen stress.黑腹果蝇的尿酸盐缺失型玫瑰色突变体对氧应激高度敏感。

Proc Natl Acad Sci U S A. 1992 May 15;89(10):4343-7. doi: 10.1073/pnas.89.10.4343.

The conversion of 4-hydroxypyrazolo[3,4-d]pyrimidine (allopurinol) into 4,6-dihroxypyrazolo[3,4-d]pyrimidine (Oxipurinol) in vivo in the absence of xanthine-oxen oxidoreductase.在缺乏黄嘌呤氧化还原酶的情况下，4-羟基吡唑并[3,4-d]嘧啶（别嘌呤醇）在体内转化为4,6-二羟基吡唑并[3,4-d]嘧啶（氧嘌呤醇）。

Biochem J. 1969 May;112(4):527-32. doi: 10.1042/bj1120527.

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rosy Function is required for juvenile hormone effects in Drosophila melanogaster.在黑腹果蝇中，rosy功能是保幼激素发挥作用所必需的。

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Experientia. 1967 Dec 15;23(12):1020-1. doi: 10.1007/BF02136423.

Experientia. 1967 Mar 15;23(3):186-7. doi: 10.1007/BF02136276.

Xanthine dehydrogenase in the biosynthesis of the eye pterin pigments of Drosophila melanogaster.黄嘌呤脱氢酶在黑腹果蝇眼蝶呤色素生物合成中的作用

Experientia. 1971 Apr 15;27(4):382-3. doi: 10.1007/BF02137260.

Concentration-affinity equivalence in gene regulation: convergence of genetic and environmental effects.基因调控中的浓度-亲和力等效性：遗传与环境效应的趋同

Proc Natl Acad Sci U S A. 1988 Jul;85(13):4784-8. doi: 10.1073/pnas.85.13.4784.

The effects of recessive lethal Notch mutations of Drosophila melanogaster on flavoprotein enzyme activities whose inhibitions cause Notch-like phenocopies.黑腹果蝇隐性致死Notch突变对黄素蛋白酶活性的影响，这些酶活性的抑制会导致Notch样拟表型。

Biochem Genet. 1987 Feb;25(1-2):7-25. doi: 10.1007/BF00498948.

Molybdenum hydroxylases in Drosophila. III. Further characterization of the low xanthine dehydrogenase gene.果蝇中的钼羟化酶。III. 低黄嘌呤脱氢酶基因的进一步特征分析。

Biochem Genet. 1986 Aug;24(7-8):509-27. doi: 10.1007/BF00504332.

Lethal mutations flanking the 68C glue gene cluster on chromosome 3 of Drosophila melanogaster.果蝇3号染色体上68C黏胶基因簇侧翼的致死突变。

Genetics. 1986 Apr;112(4):785-802. doi: 10.1093/genetics/112.4.785.

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