两兄弟患有与终末期肾衰竭相关的p47-吞噬细胞氧化酶缺陷慢性肉芽肿病。 - Suppr | 超能文献

Two brothers with p47-phox-deficient chronic granulomatous disease associated with end-stage renal failure.

作者信息

Yamazaki H, Nishi S, Chou T, Nakagawa Y, Shimada H, Nunoi H, Imajoh-Ohmi S, Yoshioka K, Arakawa M

机构信息

Department of Medicine (II), Niigata University School of Medicine, Japan.

出版信息

Nephrol Dial Transplant. 1995 Dec;10(12):2334-6. doi: 10.1093/ndt/10.12.2334.

DOI:10.1093/ndt/10.12.2334

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

Two brothers with p47-phox-deficient chronic granulomatous disease associated with end-stage renal failure.两兄弟患有与终末期肾衰竭相关的p47-吞噬细胞氧化酶缺陷慢性肉芽肿病。

Nephrol Dial Transplant. 1995 Dec;10(12):2334-6. doi: 10.1093/ndt/10.12.2334.

2

Treatment with rhG-CSF for osteomyelitis in a patient with p47-phox-deficient chronic granulomatous disease.

Ann Hematol. 1997 Nov-Dec;75(5-6):243-6. doi: 10.1007/s002770050351.

3

Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiency.慢性肉芽肿病中Alu重复序列诱导的缺失：不仅是p67-吞噬氧化酶缺乏的原因，也是p47-吞噬氧化酶缺乏的原因。

Ann Hematol. 2013 Jul;92(7):1003-4. doi: 10.1007/s00277-012-1661-5. Epub 2012 Dec 29.

4

Visceral leishmaniasis and other severe infections in an adult patient with p47-phox-deficient chronic granulomatous disease.一名患有p47-吞噬细胞氧化酶缺陷型慢性肉芽肿病的成年患者出现内脏利什曼病及其他严重感染

Infection. 2000 May-Jun;28(3):171-4. doi: 10.1007/s150100050074.

5

[An autopsy case of chronic granulomatous disease diagnosed by biopsy].[一例经活检诊断的慢性肉芽肿病尸检病例]

Kansenshogaku Zasshi. 1997 Jul;71(7):668-71. doi: 10.11150/kansenshogakuzasshi1970.71.668.

6

CRISPR/Cas9-generated p47-deficient cell line for Chronic Granulomatous Disease gene therapy vector development.CRISPR/Cas9 基因编辑技术构建 p47 缺陷细胞系用于慢性肉芽肿病基因治疗载体的开发。

Sci Rep. 2017 Mar 13;7:44187. doi: 10.1038/srep44187.

7

In vitro molecular reconstitution of the respiratory burst in B lymphoblasts from p47-phox-deficient chronic granulomatous disease.来自 p47-吞噬氧化酶缺陷型慢性肉芽肿病患者 B 淋巴母细胞呼吸爆发的体外分子重建

J Clin Invest. 1993 Jan;91(1):201-7. doi: 10.1172/JCI116171.

8

Assembly of the phagocyte NADPH oxidase: binding of Src homology 3 domains to proline-rich targets.吞噬细胞NADPH氧化酶的组装：Src同源3结构域与富含脯氨酸的靶点的结合。

Proc Natl Acad Sci U S A. 1994 Oct 25;91(22):10650-4. doi: 10.1073/pnas.91.22.10650.

9

Protein delivery by Pseudomonas type III secretion system: Ex vivo complementation of p67(phox)-deficient chronic granulomatous disease.铜绿假单胞菌III型分泌系统介导的蛋白质递送：p67(phox)缺陷型慢性肉芽肿病的体外互补

Biochem Biophys Res Commun. 2000 Sep 7;275(3):854-8. doi: 10.1006/bbrc.2000.3399.

10

A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease.一个p47-吞噬细胞氧化酶假基因携带了导致p47-吞噬细胞氧化酶缺陷型慢性肉芽肿病的最常见突变。

J Clin Invest. 1997 Oct 15;100(8):1907-18. doi: 10.1172/JCI119721.

引用本文的文献

1

Diabetes, renal and cardiovascular disease in p47 phox-/- chronic granulomatous disease.p47phox-/- 慢性肉芽肿病中的糖尿病、肾脏和心血管疾病。

J Clin Immunol. 2013 May;33(4):725-30. doi: 10.1007/s10875-013-9871-8. Epub 2013 Feb 6.

2

Prostatic abscess in a pediatric patient with chronic granulomatous disease: report of a unique case and review of the literature.儿童慢性肉芽肿病患者的前列腺脓肿：1 例独特病例报告及文献复习。

J Pediatr Surg. 2012 Feb;47(2):400-3. doi: 10.1016/j.jpedsurg.2011.11.003.