• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Defects of purine metabolism in immunodeficiency diseases.

作者信息

Hirschhorn R

出版信息

Prog Clin Immunol. 1977;3:67-83.

PMID:405713
Abstract
摘要

相似文献

1
Defects of purine metabolism in immunodeficiency diseases.免疫缺陷疾病中的嘌呤代谢缺陷
Prog Clin Immunol. 1977;3:67-83.
2
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.
3
Immunodeficiency syndromes associated with inherited metabolic disorders.
Clin Haematol. 1981 Feb;10(1):139-59.
4
Metabolic defects and immunodeficiency disorders.代谢缺陷与免疫缺陷疾病
N Engl J Med. 1983 Mar 24;308(12):714-6. doi: 10.1056/NEJM198303243081209.
5
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.
6
Correction of purine nucleoside phosphorylase deficiency by transplantation of allogeneic bone marrow from a sibling.通过移植同胞的异基因骨髓纠正嘌呤核苷磷酸化酶缺乏症。
J Pediatr. 1996 Mar;128(3):373-6. doi: 10.1016/s0022-3476(96)70285-8.
7
Partial deficiency of purine nucleoside phosphorylase: studies of purine and pyrimidine metabolism.嘌呤核苷磷酸化酶部分缺乏：嘌呤和嘧啶代谢研究
J Lab Clin Med. 1978 May;91(5):736-49.
8
Inborn errors of purine catabolism.嘌呤分解代谢的先天性缺陷。
Acta Paediatr Belg. 1981 Jan-Mar;34(1):3-12.
9
Overview of immunodeficiency diseases where bone marrow transplantation is feasible.
Bone Marrow Transplant. 1989 Dec;4 Suppl 4:132.
10
Genetic deficiencies of adenosine deaminase and purine nucleoside phosphorylase: overview, genetic heterogeneity and therapy.腺苷脱氨酶和嘌呤核苷磷酸化酶的遗传缺陷：概述、遗传异质性与治疗
Birth Defects Orig Artic Ser. 1983;19(3):73-81.

引用本文的文献

1
Bone marrow transplantation only partially restores purine metabolites to normal in adenosine deaminase-deficient patients.对于腺苷脱氨酶缺乏症患者，骨髓移植只能使嘌呤代谢产物部分恢复正常。
J Clin Invest. 1981 Dec;68(6):1387-93. doi: 10.1172/jci110389.
2
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.
3
Varicella pneumonia in a bone marrow-transplanted, immune-reconstituted adenosine deaminase-deficient patient with severe combined immunodeficiency disease.
患有严重联合免疫缺陷病的骨髓移植、免疫重建的腺苷脱氨酶缺乏患者的水痘肺炎。
J Clin Immunol. 1985 May;5(3):180-6. doi: 10.1007/BF00915509.
4
Restriction length polymorphism in the variable region of the Tcr locus linked to histocompatibility antigen H-8 on murine chromosome 14.
Immunogenetics. 1986;24(5):328-30. doi: 10.1007/BF00395539.
5
Insulin-dependent diabetes mellitus and severe atopic dermatitis in a child with adenosine deaminase deficiency.一名患有腺苷脱氨酶缺乏症儿童的胰岛素依赖型糖尿病和重度特应性皮炎。
Eur J Pediatr. 1992 Nov;151(11):811-4. doi: 10.1007/BF01957930.
6
Adenosine deaminase deficiency: another family with "silent" ADA allele and normal ADA activity in two heterozygotes.腺苷脱氨酶缺乏症：另一个家族中存在“沉默”的腺苷脱氨酶等位基因，两名杂合子的腺苷脱氨酶活性正常。
Am J Hum Genet. 1977 Nov;29(6):642-4.
7
Combined immunodeficiency and inborn errors of purine metabolism.联合免疫缺陷与嘌呤代谢先天性缺陷
Blut. 1978 Oct 13;37(4):173-81. doi: 10.1007/BF00996718.
8
Nucleoside phosphorylase 2 (Np-2) of mice.
Biochem Genet. 1978 Dec;16(11-12):1143-51. doi: 10.1007/BF00484535.