尿中氧嘌呤排泄异常的受试者体内不稳定的次黄嘌呤-鸟嘌呤磷酸核糖转移酶 - Suppr | 超能文献

Unstable HPRTase in subjects with abnormal urinary oxypurine excretion.

作者信息

Balis M E, Yip L C, Yu T F, Gutman A B, Cox R, Dancis J

出版信息

Adv Exp Med Biol. 1973;41:195-202. doi: 10.1007/978-1-4684-3294-7_23.

DOI:10.1007/978-1-4684-3294-7_23

Abstract

摘要

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1

Unstable HPRTase in subjects with abnormal urinary oxypurine excretion.尿中氧嘌呤排泄异常的受试者体内不稳定的次黄嘌呤-鸟嘌呤磷酸核糖转移酶

Adv Exp Med Biol. 1973;41:195-202. doi: 10.1007/978-1-4684-3294-7_23.

2

Immunological studies of hypoxanthine-guanine phosphoribosyltransferase in Lesch-Nyhan syndrome.莱施-奈恩综合征中次黄嘌呤-鸟嘌呤磷酸核糖转移酶的免疫学研究。

Adv Exp Med Biol. 1973;41:187-94. doi: 10.1007/978-1-4684-3294-7_22.

3

Age-induced changes in adenosine monophosphate: pyrophosphate phosphoribosyltransferase and inosine monophosphate: pyrophosphate phosphoribosyltransferase from normal and Lesch-Nyhan erythrocytes.正常红细胞和莱施-奈恩红细胞中，年龄诱导的磷酸核糖焦磷酸腺苷转移酶及磷酸核糖焦磷酸次黄嘌呤核苷转移酶的变化。

Biochemistry. 1974 Jun 4;13(12):2558-61. doi: 10.1021/bi00709a013.

4

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.

5

Heterogeneity in the biochemical characteristics of red blood cell hypoxanthine-guanine phosphoribosyl transferase from two unrelated patients with the Lesch-Nyhan syndrome.两名无关的莱施-奈恩综合征患者红细胞次黄嘌呤-鸟嘌呤磷酸核糖基转移酶生化特性的异质性。

Biochem Genet. 1973 Jun;9(2):197-202. doi: 10.1007/BF00487450.

6

Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) deficiency: immunologic studies on the mutant enzyme.

Adv Exp Med Biol. 1973;41:177-85. doi: 10.1007/978-1-4684-3294-7_21.

7

Hypoxanthine-guanine phosphoribosyltransferase (HGPRT) deficiency: effect of dietary purines on enzyme activity.次黄嘌呤-鸟嘌呤磷酸核糖转移酶（HGPRT）缺乏症：膳食嘌呤对酶活性的影响。

Adv Exp Med Biol. 1973;41:203-9. doi: 10.1007/978-1-4684-3294-7_24.

8

Electrophoretic properties of hypoxanthine-guanine phosphoribosyl transferase in erythrocytes of subjects with Lesch-Nyhan syndrome.莱施-奈恩综合征患者红细胞中次黄嘌呤-鸟嘌呤磷酸核糖转移酶的电泳特性

Biochem Genet. 1972 Apr;6(2):139-46. doi: 10.1007/BF00486398.

9

Lesch-Nyhan syndrome: absence of the mutant enzyme in erythrocytes of a heterozygote for both normal and mutant hypoxanthine-guanine phosphoribosyl transferase.莱施-奈恩综合征：正常和突变型次黄嘌呤-鸟嘌呤磷酸核糖转移酶杂合子的红细胞中缺乏突变酶。

Biochem Genet. 1972 Feb;6(1):21-6. doi: 10.1007/BF00485961.

10

Resistance of erythrocyte adenine phosphoribosyltransferase in the Lesch-Nyhan syndrome to destabilization to heat by hypoxanthine.莱施-奈恩综合征中红细胞腺嘌呤磷酸核糖基转移酶对次黄嘌呤介导的热不稳定作用的抗性

Adv Exp Med Biol. 1973;41:215-20. doi: 10.1007/978-1-4684-3294-7_26.

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Disassembly of microtubules in the Lesch-Nyhan Syndrome? (Lesch-Nyhan syndrome and microtubules).莱施-奈恩综合征中的微管解聚？（莱施-奈恩综合征与微管）

Klin Wochenschr. 1979 Feb 15;57(4):181-6. doi: 10.1007/BF01477406.