腺苷脱氨酶缺乏症与重症联合免疫缺陷病 - Suppr

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超能文献

Adenosine deaminase deficiency and severe combined immunodeficiency disease.

作者信息

Thompson L F, Seegmiller J E

出版信息

Adv Enzymol Relat Areas Mol Biol. 1980;51:167-210. doi: 10.1002/9780470122969.ch4.

DOI:10.1002/9780470122969.ch4

PMID:6255772

Abstract

摘要

相似文献

Adenosine deaminase deficiency and severe combined immunodeficiency disease.腺苷脱氨酶缺乏症与重症联合免疫缺陷病

Adv Enzymol Relat Areas Mol Biol. 1980;51:167-210. doi: 10.1002/9780470122969.ch4.

[Immunological failure caused by adenosine deaminase deficiency].[腺苷脱氨酶缺乏导致的免疫功能衰竭]

Acta Haematol Pol. 1979 Jul-Sep;10(3):205-10.

Intravenous deoxycytidine therapy in a patient with adenosine deaminase deficiency.腺苷脱氨酶缺乏症患者的静脉注射脱氧胞苷治疗。

Adv Exp Med Biol. 1984;165 Pt A:39-45. doi: 10.1007/978-1-4684-4553-4_8.

Progress in understanding the mechanism of immunodeficiency disease associated with defects in purine metabolism.嘌呤代谢缺陷相关免疫缺陷病发病机制的研究进展

Monogr Hum Genet. 1978;10:88-91. doi: 10.1159/000401572.

[Primary immunodeficiencies and purine metabolism].[原发性免疫缺陷与嘌呤代谢]

Rev Clin Esp. 1985 Oct;177(6):247-53.

A role for purine metabolism in the immune response: Adenosine-deaminase activity and deoxyadenosine catabolism.嘌呤代谢在免疫反应中的作用：腺苷脱氨酶活性与脱氧腺苷分解代谢。

Lancet. 1978 Jan 14;1(8055):60-3. doi: 10.1016/s0140-6736(78)90002-8.

Adenosine deaminase deficiency and severe combined immunodeficiency disease.腺苷脱氨酶缺乏症与重症联合免疫缺陷病

Life Sci. 1977 May 15;20(10):1645-50. doi: 10.1016/0024-3205(77)90337-x.

Purine metabolism in adenosine deaminase deficiency.腺苷脱氨酶缺乏症中的嘌呤代谢

Proc Natl Acad Sci U S A. 1976 Aug;73(8):2867-71. doi: 10.1073/pnas.73.8.2867.

Immune cell function and recycling of purines.免疫细胞功能与嘌呤的循环利用。

N Engl J Med. 1976 Dec 9;295(24):1375-6. doi: 10.1056/NEJM197612092952409.

Amelioration of neurologic abnormalities after "enzyme replacement" in adenosine deaminase deficiency.腺苷脱氨酶缺乏症“酶替代”治疗后神经功能异常的改善

N Engl J Med. 1980 Aug 14;303(7):377-80. doi: 10.1056/NEJM198008143030706.

引用本文的文献

Characterization of total adenosine deaminase activity (ADA) and its isoenzymes in saliva and serum in health and inflammatory conditions in four different species: an analytical and clinical validation pilot study.在四种不同物种中，健康和炎症条件下唾液和血清中总腺苷脱氨酶活性（ADA）及其同工酶的特征：一项分析和临床验证的初步研究。

BMC Vet Res. 2020 Oct 12;16(1):384. doi: 10.1186/s12917-020-02574-2.

Adenosine deaminase deficiency: unanticipated benefits from the study of a rare immunodeficiency.腺苷脱氨酶缺乏症：对一种罕见免疫缺陷疾病研究的意外收获。

J Immunol. 2012 Feb 1;188(3):933-5. doi: 10.4049/jimmunol.1103519.

Human ADA2 belongs to a new family of growth factors with adenosine deaminase activity.人ADA2属于具有腺苷脱氨酶活性的生长因子新家族。

Biochem J. 2005 Oct 1;391(Pt 1):51-7. doi: 10.1042/BJ20050683.

Adenosine deaminase deficiency with normal immune function. An acidic enzyme mutation.具有正常免疫功能的腺苷脱氨酶缺乏症。一种酸性酶突变。

J Clin Invest. 1983 Aug;72(2):483-92. doi: 10.1172/jci110996.

Sequence of human adenosine deaminase cDNA including the coding region and a small intron.包含编码区和一个小内含子的人腺苷脱氨酶cDNA序列。

Nucleic Acids Res. 1984 Mar 12;12(5):2439-46. doi: 10.1093/nar/12.5.2439.

Inherited disorders of purine metabolism--underlying molecular mechanisms.嘌呤代谢的遗传性疾病——潜在分子机制

Klin Wochenschr. 1984 Oct 15;62(20):953-62. doi: 10.1007/BF01728425.

Structure of adenosine deaminase mRNAs from normal and adenosine deaminase-deficient human cell lines.来自正常和腺苷脱氨酶缺陷型人类细胞系的腺苷脱氨酶mRNA的结构

Mol Cell Biol. 1984 Sep;4(9):1712-7. doi: 10.1128/mcb.4.9.1712-1717.1984.

Cloning of cDNA sequences of human adenosine deaminase.人腺苷脱氨酶cDNA序列的克隆

Proc Natl Acad Sci U S A. 1983 Dec;80(24):7481-5. doi: 10.1073/pnas.80.24.7481.

Adenosine deaminase (ADA) deficiency in cells derived from humans with severe combined immunodeficiency is due to an aberration of the ADA protein.患有严重联合免疫缺陷的人类细胞中腺苷脱氨酶（ADA）缺乏是由于ADA蛋白异常所致。

Nucleic Acids Res. 1984 Jan 25;12(2):1015-24. doi: 10.1093/nar/12.2.1015.

Adenosine deaminase messenger RNAs in lymphoblast cell lines derived from leukemic patients and patients with hereditary adenosine deaminase deficiency.来自白血病患者和遗传性腺苷脱氨酶缺乏症患者的淋巴母细胞系中的腺苷脱氨酶信使核糖核酸

J Clin Invest. 1983 Jun;71(6):1649-60. doi: 10.1172/jci110920.

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