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Characterization of mutant subunits of human purine nucleoside phosphorylase.

作者信息

Gudas L J, Zannis V I, Clift S M, Ammann A J, Staal G E, Martin D W

出版信息

J Biol Chem. 1978 Dec 25;253(24):8916-24.

PMID:102643
Abstract
摘要

相似文献

1
Characterization of mutant subunits of human purine nucleoside phosphorylase.人嘌呤核苷磷酸化酶突变亚基的特性分析
J Biol Chem. 1978 Dec 25;253(24):8916-24.
2
Purine nucleoside phosphorylase deficiency; genetic studies in a Dutch family.嘌呤核苷磷酸化酶缺乏症；一个荷兰家族的遗传学研究。
Adv Exp Med Biol. 1980;122A:367-73. doi: 10.1007/978-1-4615-9140-5_60.
3
Clinico-biochemical and molecular studies of purine nucleoside phosphorylase deficiency.
Adv Exp Med Biol. 1989;253A:73-9. doi: 10.1007/978-1-4684-5673-8_11.
4
Purification and characterization of human erythrocyte purine nucleoside phosphorylase and its subunits.
J Biol Chem. 1978 Jan 25;253(2):504-10.
5
Purine nucleoside phosphorylase deficiency: altered kinetic properties of a mutant enzyme.
Science. 1977 Sep 9;197(4308):1084-6. doi: 10.1126/science.407651.
6
Prenatal exclusion of purine nucleoside phosphorylase deficiency.
Eur J Pediatr. 1986 Apr;145(1-2):51-3. doi: 10.1007/BF00441852.
7
Purine nucleoside phosphorylase deficiency: improved metabolic and immunologic function with erythrocyte transfusions.嘌呤核苷磷酸化酶缺乏症：红细胞输注改善代谢和免疫功能
N Engl J Med. 1980 Oct 23;303(17):973-7. doi: 10.1056/NEJM198010233031705.
8
Cellular immunodeficiency associated with nucleoside phosphorylase deficiency. Immunologic and biochemical studies.
Clin Immunol Immunopathol. 1977 Sep;8(2):247-53. doi: 10.1016/0090-1229(77)90114-3.
9
Purine nucleoside phosphorylase deficiency: biochemical properties and heterogeneity in two families.嘌呤核苷磷酸化酶缺乏症：两个家族中的生化特性及异质性
Arthritis Rheum. 1979 May;22(5):524-31. doi: 10.1002/art.1780220513.
10
Human erythrocyte purine nucleoside phosphorylase: molecular weight and physical properties. A Theorell-Chance catalytic mechanism.
J Biol Chem. 1979 Oct 10;254(19):9927-32.

引用本文的文献

1
Characterization of the subunit composition of HGPRTase from human erythrocytes and cultured fibroblasts.人红细胞和培养成纤维细胞中次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶亚基组成的表征
Biochem Genet. 1980 Feb;18(1-2):1-19. doi: 10.1007/BF00504356.
2
Heterogeneity of the molecular defect in human dihydropteridine reductase deficiency.人类二氢蝶啶还原酶缺乏症分子缺陷的异质性
Biochem J. 1981 Sep 15;198(3):677-82. doi: 10.1042/bj1980677.
3
Cloning of human purine-nucleoside phosphorylase cDNA sequences by complementation in Escherichia coli.通过在大肠杆菌中互补克隆人嘌呤核苷磷酸化酶cDNA序列。
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4281-5. doi: 10.1073/pnas.80.14.4281.
4
Ecto-5'-nucleotidase activity in human T cell subsets. Decreased numbers of ecto-5'-nucleotidase positive cells from both OKT4+ and OKT8+ cells in patients with hypogammaglobulinemia.人T细胞亚群中的外切5'-核苷酸酶活性。低丙种球蛋白血症患者中OKT4+和OKT8+细胞中外切5'-核苷酸酶阳性细胞数量减少。
J Clin Invest. 1983 Apr;71(4):892-9. doi: 10.1172/jci110843.
5
The biochemical basis of immunodeficiency disease.免疫缺陷疾病的生化基础。
Eur J Pediatr. 1980 Oct;135(1):13-20. doi: 10.1007/BF00445887.
6
Human purine nucleoside phosphorylase cDNA sequence and genomic clone characterization.人类嘌呤核苷磷酸化酶cDNA序列及基因组克隆特征分析。
Nucleic Acids Res. 1984 Jul 25;12(14):5779-87. doi: 10.1093/nar/12.14.5779.
7
Molecular analysis of mutations in a patient with purine nucleoside phosphorylase deficiency.一名嘌呤核苷磷酸化酶缺乏症患者突变的分子分析。
Am J Hum Genet. 1992 Oct;51(4):763-72.
8
Characterization of the subunits of purine nucleoside phosphorylase from cultured normal human fibroblasts.
Biochem Genet. 1979 Aug;17(7-8):621-30. doi: 10.1007/BF00502122.