• 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

New Insight to the Pathogenetic Mechanism of Kawasaki Disease (KD): the Relationship between Clinical Diversity and Genetic Heterogeneity.

作者信息

Yoo Byung Won

机构信息

Department of Clinical Pharmacology, Clinical Trial Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.

Division of Pediatric Cardiology, Department of Pediatrics, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Korean Circ J. 2019 Jan;49(1):109-112. doi: 10.4070/kcj.2018.0365. Epub 2018 Nov 13.

DOI:10.4070/kcj.2018.0365
PMID:30468043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6331318/
Abstract
摘要

相似文献

1
New Insight to the Pathogenetic Mechanism of Kawasaki Disease (KD): the Relationship between Clinical Diversity and Genetic Heterogeneity.川崎病（KD）发病机制的新见解：临床多样性与遗传异质性之间的关系
Korean Circ J. 2019 Jan;49(1):109-112. doi: 10.4070/kcj.2018.0365. Epub 2018 Nov 13.
2
Assessment of the Clinical Heterogeneity of Kawasaki Disease Using Genetic Variants of and .利用和的基因变异评估川崎病的临床异质性。
Korean Circ J. 2019 Jan;49(1):99-108. doi: 10.4070/kcj.2018.0224. Epub 2018 Oct 19.
3
Consortium-Based Genetic Studies of Kawasaki Disease in Korea: Korean Kawasaki Disease Genetics Consortium.韩国川崎病基于联盟的基因研究：韩国川崎病遗传学联盟
Korean Circ J. 2015 Nov;45(6):443-8. doi: 10.4070/kcj.2015.45.6.443. Epub 2015 Nov 25.
4
Kawasaki disease: A brief history.川崎病：简史
Pediatrics. 2000 Aug;106(2):E27. doi: 10.1542/peds.106.2.e27.
5
Pediatric Kawasaki Disease and Adult Human Immunodeficiency Virus Kawasaki-Like Syndrome Are Likely the Same Malady.小儿川崎病和成人人类免疫缺陷病毒相关性川崎样综合征可能是同一种疾病。
Open Forum Infect Dis. 2016 Sep 29;3(3):ofw160. doi: 10.1093/ofid/ofw160. eCollection 2016 Sep.
6
Behaviour sequelae following acute Kawasaki disease.急性川崎病后的行为后遗症
BMC Pediatr. 2005 May 25;5(1):14. doi: 10.1186/1471-2431-5-14.
7
Genetic variants of ADAM17 are implicated in the pathological process of Kawasaki disease and secondary coronary artery lesions via the TGF-β/SMAD3 signaling pathway.ADAM17的基因变异通过TGF-β/SMAD3信号通路参与川崎病及继发性冠状动脉病变的病理过程。
Eur J Pediatr. 2016 May;175(5):705-13. doi: 10.1007/s00431-016-2696-8. Epub 2016 Feb 1.
8
Variation in IL-21-secreting circulating follicular helper T cells in Kawasaki disease.川崎病患者外周血中分泌白介素 21 的滤泡辅助性 T 细胞的变化。
BMC Immunol. 2018 Dec 27;19(1):43. doi: 10.1186/s12865-018-0282-8.
9
Kawasaki disease - A common childhood vasculitis.川崎病——一种常见的儿童血管炎。
Indian J Rheumatol. 2015 Dec;10:S78-S83. doi: 10.1016/j.injr.2015.07.010. Epub 2015 Oct 1.
10
Update of genetic susceptibility in patients with Kawasaki disease.川崎病患者遗传易感性的最新进展。
Korean J Pediatr. 2015 Mar;58(3):84-8. doi: 10.3345/kjp.2015.58.3.84. Epub 2015 Mar 20.

本文引用的文献

1
Assessment of the Clinical Heterogeneity of Kawasaki Disease Using Genetic Variants of and .利用和的基因变异评估川崎病的临床异质性。
Korean Circ J. 2019 Jan;49(1):99-108. doi: 10.4070/kcj.2018.0224. Epub 2018 Oct 19.
2
Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease.FCGR2A基因His167Arg多态性与川崎病的男性特异性关联。
PLoS One. 2017 Sep 8;12(9):e0184248. doi: 10.1371/journal.pone.0184248. eCollection 2017.
3
Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease.全基因组关联研究确定了与川崎病冠状动脉瘤形成相关的新的易感基因。
PLoS One. 2016 May 12;11(5):e0154943. doi: 10.1371/journal.pone.0154943. eCollection 2016.
4
Association between the FCGR2A gene H131R polymorphism and risk of Kawasaki disease: a meta-analysis.FCGR2A基因H131R多态性与川崎病风险的关联：一项荟萃分析
Genet Mol Res. 2015 Jun 11;14(2):6256-64. doi: 10.4238/2015.June.9.12.
5
Absence of association of FCGR2A gene polymorphism rs1801274 with Kawasaki disease in Greek patients.希腊患者中FCGR2A基因多态性rs1801274与川崎病无关联。
Cardiol Young. 2015 Apr;25(4):681-3. doi: 10.1017/S1047951114000626. Epub 2014 Apr 28.
6
Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis.采用全基因组关联分析鉴定 KCNN2 为川崎病冠状动脉瘤的易感基因位点。
J Hum Genet. 2013 Aug;58(8):521-5. doi: 10.1038/jhg.2013.43. Epub 2013 May 16.
7
Do predictors of incomplete Kawasaki disease exist for infants?婴儿是否存在不完全川崎病的预测因素？
Pediatr Cardiol. 2013 Feb;34(2):286-90. doi: 10.1007/s00246-012-0440-3. Epub 2012 Sep 22.
8
A genome-wide association study identifies three new risk loci for Kawasaki disease.一项全基因组关联研究鉴定出川崎病的三个新风险位点。
Nat Genet. 2012 Mar 25;44(5):517-21. doi: 10.1038/ng.2220.
9
Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.通过全基因组关联分析鉴定出两个新的川崎病易感性基因座。
Nat Genet. 2012 Mar 25;44(5):522-5. doi: 10.1038/ng.2227.
10
[Association study of a functional SNP rs28493229 of ITPKC gene and Kawasaki disease in a Chinese population].[ITPKC基因功能性单核苷酸多态性rs28493229与中国人群川崎病的关联研究]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):644-8. doi: 10.3760/cma.j.issn.1003-9406.2011.06.010.