[Normal activity of hypoxanthine-guanine-phosphoribosyl transferase in adults with primary gout].

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作者信息

Ropers H H, Mertz D P

出版信息

Klin Wochenschr. 1973 Mar 15;51(6):283-4. doi: 10.1007/BF01467817.

DOI:10.1007/BF01467817

PMID:4698395

Abstract

摘要

相似文献

[Normal activity of hypoxanthine-guanine-phosphoribosyl transferase in adults with primary gout].

Klin Wochenschr. 1973 Mar 15;51(6):283-4. doi: 10.1007/BF01467817.

Phosphoribosyl transferase activity in normal subjects, gout patients, and children with mental retardation.正常受试者、痛风患者及智力发育迟缓儿童的磷酸核糖转移酶活性。

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Hypoxanthine-guanine phosphoribosyl transferase deficiency. Our experience.次黄嘌呤-鸟嘌呤磷酸核糖转移酶缺乏症。我们的经验。

Adv Exp Med Biol. 1973;41:271-9. doi: 10.1007/978-1-4684-3294-7_32.

Diminished affinity for purine substrates as a basis for gout with mild deficiency of hypoxanthine-guanine phosphoribosyltransferase.次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶轻度缺乏导致痛风的基础：对嘌呤底物的亲和力降低

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Increased PP-ribose-P synthetase activity: a genetic abnormality leading to excessive purine production and gout.磷酸核糖焦磷酸合成酶活性增加：一种导致嘌呤过度生成和痛风的基因异常。

Adv Exp Med Biol. 1973;41:307-15. doi: 10.1007/978-1-4684-3294-7_37.

[Phosphoribosylpyrophosphate synthetase anomalies in 2 cases of gout beginning at an early age].

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Gout with purine overproduction due to increased phosphoribosylpyrophosphate synthetase activity.由于磷酸核糖焦磷酸合成酶活性增加导致嘌呤产生过多的痛风。

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Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase associated with gout and uric acid lithiasis.与痛风和尿酸结石相关的次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶部分缺乏症。

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Human hypoxanthine-guanine phosphoribosyltransferase: studies on the normal and mutant forms of the enzyme.

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引用本文的文献

[Glutamine synthetase activity in the liver in primary gout (author's transl)].

Klin Wochenschr. 1974 Apr 15;52(8):396-7. doi: 10.1007/BF01468439.

本文引用的文献

A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.一种尿酸代谢与中枢神经系统功能的家族性疾病。

Am J Med. 1964 Apr;36:561-70. doi: 10.1016/0002-9343(64)90104-4.

On the determination of creatinine in plasma by the Jaffé reaction, after adsorption to Lloyd's reagent.通过Jaffé反应，在吸附到劳埃德试剂后，对血浆中肌酐进行测定。

Scand J Clin Lab Invest. 1954;6(4):325-34. doi: 10.3109/00365515409134871.

Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis.与一种X连锁人类神经疾病及嘌呤过度合成相关的酶缺陷。

Science. 1967 Mar 31;155(3770):1682-4. doi: 10.1126/science.155.3770.1682.

Hypoxanthine-guanine phosphoribosyltransferase deficiency in the Lesch-Nyhan syndrome and gout.莱施-奈恩综合征和痛风中的次黄嘌呤-鸟嘌呤磷酸核糖转移酶缺乏症。

Fed Proc. 1968 Jul-Aug;27(4):1047-52.

Rarity of X-linked partial hypoxanthine-guanine phosphoribosyltransferase deficiency in a large gouty population.

Ann Intern Med. 1972 Feb;76(2):255-64. doi: 10.7326/0003-4819-76-2-255.

[Changes between 1948 and 1970 in the epidemiology and clinical features of primary gout].

Dtsch Med Wochenschr. 1973 Feb 2;98(5):183-8. doi: 10.1055/s-0028-1106774.

Simplified methods for the measurement and electrophoretic demonstration of hypoxanthine-guanine phosphoribosyl transferase. Evidence for dimeric enzyme structure in various mammals.

Humangenetik. 1972;17(1):69-74. doi: 10.1007/BF01789603.

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