A new assay method for hypoxanthine-guanine phosphoribosyltransferase.
作者信息
Chow D C, Kawahara F S, Saunders T, Sorensen L B
出版信息
J Lab Clin Med. 1970 Nov;76(5):733-8.
PMID:5477333
Abstract
摘要
相似文献
1
A new assay method for hypoxanthine-guanine phosphoribosyltransferase.一种次黄嘌呤-鸟嘌呤磷酸核糖转移酶的新检测方法。
J Lab Clin Med. 1970 Nov;76(5):733-8.
2
[From Lesch-Nyhan disease to primary gout].[从莱施-奈恩病到原发性痛风]
Rev Eur Etud Clin Biol. 1970 Jun-Jul;15(6):605-9.
3
Lesch-Nyhan syndrome.莱施-奈恩综合征
Paediatr Univ Tokyo. 1970 Dec;18:25-31.
4
[Lesh-Nyhan syndrome. A congenital defect of purine metabolism with the clinical symptoms of gout and central nervous disorders].[莱施-奈恩综合征。一种嘌呤代谢的先天性缺陷，伴有痛风和中枢神经系统紊乱的临床症状]
Dtsch Med Wochenschr. 1970 May 8;95(19):1077-80.
5
[Congenital disorder of purine metabolism].[嘌呤代谢先天性疾病]
Nihon Rinsho. 1970 May;28(5):1550-76.
6
Lesch-Nyhan syndrome: altered kinetic properties of mutant enzyme.莱施-奈恩综合征：突变酶的动力学特性改变
Science. 1971 Feb 19;171(3972):689-91. doi: 10.1126/science.171.3972.689.
7
8
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: intermediate enzyme deficiency in heterozygote red cells.次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶部分缺乏：杂合子红细胞中的中间酶缺乏
Ann Intern Med. 1972 Feb;76(2):285-7. doi: 10.7326/0003-4819-76-2-285.
9
Seminars on Lesch-Nyhan syndrome. Aspects of purine metabolism.莱施-奈恩综合征研讨会。嘌呤代谢的各个方面。
Fed Proc. 1968 Jul-Aug;27(4):1067-74.
10
Hypoxanthine-guanine phosphoribosyltransferase: characteristics of the mutant enzyme in erythrocytes from patients with the Lesch-Nyhan syndrome.次黄嘌呤-鸟嘌呤磷酸核糖转移酶：莱施-奈恩综合征患者红细胞中突变酶的特征
J Clin Invest. 1972 Jul;51(7):1805-12. doi: 10.1172/JCI106982.
引用本文的文献
1
Hypoxanthine-guanine phosphoribosyl transferase deficiency.次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶缺乏症
Hum Genet. 1976 Feb 29;31(2):127-50. doi: 10.1007/BF00296142.
2
Molecular and tissue-specific heterogeneity in HPRT deficiency.次黄嘌呤磷酸核糖转移酶缺乏症中的分子和组织特异性异质性。
Biochem Genet. 1978 Dec;16(11-12):1187-202. doi: 10.1007/BF00484539.
Zotero 插件