• 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

相似文献

1
G-T haplotype established by rs3785889-rs16941382 in gene is associated with coronary artery disease in Chinese Han population.基因中由rs3785889-rs16941382确定的G-T单倍型与中国汉族人群的冠状动脉疾病相关。
Oncotarget. 2017 Jul 17;8(47):82165-82173. doi: 10.18632/oncotarget.19280. eCollection 2017 Oct 10.
2
A haplotype of the GOSR2 gene is associated with myocardial infarction in Japanese men.GOSR2基因的一个单倍型与日本男性的心肌梗死有关。
Genet Test Mol Biomarkers. 2013 Jun;17(6):481-8. doi: 10.1089/gtmb.2012.0379. Epub 2013 May 15.
3
A haplotype of the GOSR2 gene is associated with essential hypertension in Japanese men.一个 GOSR2 基因的单体型与日本男性的原发性高血压有关。
Clin Biochem. 2013 Jun;46(9):760-5. doi: 10.1016/j.clinbiochem.2012.12.021. Epub 2013 Jan 11.
4
The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China.中国新疆汉族和维吾尔族人群中胆固醇吸收基因Numb多态性与冠状动脉疾病的关联
Lipids Health Dis. 2015 Sep 29;14:120. doi: 10.1186/s12944-015-0102-6.
5
A novel polymorphism of the GP78 gene is associated with coronary artery disease in Han population in China.GP78基因的一种新型多态性与中国汉族人群的冠状动脉疾病相关。
Lipids Health Dis. 2014 Sep 9;13:147. doi: 10.1186/1476-511X-13-147.
6
Association of G-protein coupled purinergic receptor P2Y2 with ischemic stroke in a Han Chinese population of North China.中国北方汉族人群中G蛋白偶联嘌呤能受体P2Y2与缺血性脑卒中的关联
Neural Regen Res. 2019 Mar;14(3):506-512. doi: 10.4103/1673-5374.245472.
7
Association between genetic polymorphism in NFKB1 and NFKBIA and coronary artery disease in a Chinese Han population.中国汉族人群中NFKB1和NFKBIA基因多态性与冠状动脉疾病的关联
Int J Clin Exp Med. 2015 Nov 15;8(11):21487-96. eCollection 2015.
8
Diplotypes of CYP2C9 gene is associated with coronary artery disease in the Xinjiang Han population for women in China.在中国新疆汉族女性人群中，CYP2C9基因的双倍型与冠状动脉疾病相关。
Lipids Health Dis. 2014 Sep 2;13:143. doi: 10.1186/1476-511X-13-143.
9
Genetic Variability of the Glucose-Dependent Insulinotropic Peptide Gene Is Involved in the Premature Coronary Artery Disease in a Chinese Population with Type 2 Diabetes.葡萄糖依赖性胰岛素促泌肽基因的遗传变异性与中国 2 型糖尿病患者的早发冠心病有关。
J Diabetes Res. 2018 Mar 25;2018:6820294. doi: 10.1155/2018/6820294. eCollection 2018.
10
A Case-Control Study of the Relationship Between SLC22A3-LPAL2-LPA Gene Cluster Polymorphism and Coronary Artery Disease in the Han Chinese Population.汉族人群中SLC22A3-LPAL2-LPA基因簇多态性与冠状动脉疾病关系的病例对照研究
Iran Red Crescent Med J. 2016 Jun 6;18(6):e35387. doi: 10.5812/ircmj.35387. eCollection 2016 Jun.

引用本文的文献

1
Getting Sugar Coating Right! The Role of the Golgi Trafficking Machinery in Glycosylation.恰到好处的糖衣！高尔基运输机制在糖基化中的作用。
Cells. 2021 Nov 23;10(12):3275. doi: 10.3390/cells10123275.
2
Congenital heart disease risk loci identified by genome-wide association study in European patients.全基因组关联研究在欧洲患者中鉴定出的先天性心脏病风险基因座。
J Clin Invest. 2021 Jan 19;131(2). doi: 10.1172/JCI141837.
3
Potential Impact of MicroRNA Gene Polymorphisms in the Pathogenesis of Diabetes and Atherosclerotic Cardiovascular Disease.微小RNA基因多态性在糖尿病和动脉粥样硬化性心血管疾病发病机制中的潜在影响
J Pers Med. 2019 Nov 25;9(4):51. doi: 10.3390/jpm9040051.
4
Apolipoprotein A1 is associated with SYNTAX score in patients with a non-ST segment elevation myocardial infarction.载脂蛋白 A1 与非 ST 段抬高型心肌梗死患者的 SYNTAX 评分相关。
Lipids Health Dis. 2019 Aug 7;18(1):159. doi: 10.1186/s12944-019-1101-9.
5
Association of polymorphisms in MALAT1 with risk of coronary atherosclerotic heart disease in a Chinese population.MALAT1 多态性与中国人群冠心病风险的关联。
Lipids Health Dis. 2018 Apr 10;17(1):75. doi: 10.1186/s12944-018-0728-2.

本文引用的文献

1
Association of C5L2 genetic polymorphisms with coronary artery disease in a Han population in Xinjiang, China.中国新疆汉族人群中C5L2基因多态性与冠状动脉疾病的关联
Oncotarget. 2017 Jan 31;8(5):8590-8596. doi: 10.18632/oncotarget.14353.
2
Association between neutrophilic granulocyte percentage and depression in hospitalized patients with heart failure.心力衰竭住院患者中性粒细胞百分比与抑郁之间的关联。
BMC Psychiatry. 2016 Dec 13;16(1):446. doi: 10.1186/s12888-016-1161-6.
3
A promoter polymorphism in APJ gene is significantly associated with blood pressure changes and hypertension risk in Chinese women.APJ基因中的一个启动子多态性与中国女性的血压变化及高血压风险显著相关。
Oncotarget. 2016 Dec 27;7(52):86257-86265. doi: 10.18632/oncotarget.13370.
4
Combined Value of Red Blood Cell Distribution Width and Global Registry of Acute Coronary Events Risk Score for Predicting Cardiovascular Events in Patients with Acute Coronary Syndrome Undergoing Percutaneous Coronary Intervention.红细胞分布宽度与急性冠状动脉事件全球注册风险评分联合预测行经皮冠状动脉介入治疗的急性冠状动脉综合征患者心血管事件的价值
PLoS One. 2015 Oct 15;10(10):e0140532. doi: 10.1371/journal.pone.0140532. eCollection 2015.
5
Membrane proximal ectodomain cleavage of MUC16 occurs in the acidifying Golgi/post-Golgi compartments.MUC16的膜近端胞外结构域切割发生在酸性高尔基体/高尔基体后区室中。
Sci Rep. 2015 Jun 5;5:9759. doi: 10.1038/srep09759.
6
The golgi-associated PDZ domain protein PIST/GOPC stabilizes the β1-adrenergic receptor in intracellular compartments after internalization.高尔基体相关的PDZ结构域蛋白PIST/GOPC在内化后可稳定细胞内区室中的β1-肾上腺素能受体。
J Biol Chem. 2015 Mar 6;290(10):6120-9. doi: 10.1074/jbc.M114.605725. Epub 2015 Jan 22.
7
A genetic variant in the seed region of miR-4513 shows pleiotropic effects on lipid and glucose homeostasis, blood pressure, and coronary artery disease.miR-4513种子区域的一个基因变异对脂质和葡萄糖稳态、血压及冠状动脉疾病具有多效性影响。
Hum Mutat. 2014 Dec;35(12):1524-31. doi: 10.1002/humu.22706.
8
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.基因与年龄在血压调节中的相互作用：CHARGE、Global BPgen 和 ICBP 联盟的大规模研究。
Am J Hum Genet. 2014 Jul 3;95(1):24-38. doi: 10.1016/j.ajhg.2014.05.010. Epub 2014 Jun 19.
9
Lipoprotein-associated phospholipase A2 single-nucleotide polymorphisms and cardiovascular events in patients with coronary artery disease.脂蛋白相关磷脂酶A2单核苷酸多态性与冠心病患者的心血管事件
J Cardiovasc Med (Hagerstown). 2015 Jan;16(1):29-36. doi: 10.2459/JCM.0000000000000057.
10
A haplotype of the GOSR2 gene is associated with myocardial infarction in Japanese men.GOSR2基因的一个单倍型与日本男性的心肌梗死有关。
Genet Test Mol Biomarkers. 2013 Jun;17(6):481-8. doi: 10.1089/gtmb.2012.0379. Epub 2013 May 15.

基因中由rs3785889-rs16941382确定的G-T单倍型与中国汉族人群的冠状动脉疾病相关。

G-T haplotype established by rs3785889-rs16941382 in gene is associated with coronary artery disease in Chinese Han population.

作者信息

Pan Shuo, Guan Gong-Chang, Lv Ying, Liu Zhong-Wei, Liu Fu-Qiang, Zhang Yong, Zhu Shun-Ming, Zhang Rong-Huai, Zhao Na, Shi Shuang, Nakayama Tomohiro, Wang Jun-Kui

机构信息

First Department of Cardiology, People's Hospital of Shaanxi Province, Xi'an, People's Republic of China.

Division of Laboratory Medicine, Department of Pathology and Microbiology, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Oncotarget. 2017 Jul 17;8(47):82165-82173. doi: 10.18632/oncotarget.19280. eCollection 2017 Oct 10.

DOI:10.18632/oncotarget.19280
PMID:29137253
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5669879/
Abstract

OBJECTIVES

The aim of the present study is to assess the association between the human gene and coronary artery disease using a haplotype-based case-control study in Chinese Han population.

METHODS

A total of 283 coronary artery disease patients and 280 controls were genotyped for the human gene (rs197932, rs3785889, rs197922, rs17608766, and rs16941382). Data were analyzed for three separate groups: the total subjects, men, and women.

RESULTS

For the total subjects, the frequency of the G-T haplotype established by rs3785889-rs16941382 was significantly higher in the coronary artery disease patients as compared to the control subjects (=0.009). Multiple logistic regression analysis also confirmed that the subjects with G-T haplotype established by rs3785889-rs16941382 (homozygote) were found having significantly higher chance suffering from coronary artery disease than the ones without this haplotype (OR=1.887, =0.007).

CONCLUSIONS

The G-T haplotype established by rs3785889-rs16941382 may be a risk genetic marker for coronary artery disease patients in Chinese Han population.

摘要

目的

本研究旨在通过基于单倍型的病例对照研究，评估人类基因与中国汉族人群冠状动脉疾病之间的关联。

方法

对总共283例冠状动脉疾病患者和280例对照进行人类基因（rs197932、rs3785889、rs197922、rs17608766和rs16941382）的基因分型。对三个独立组进行数据分析：全部受试者、男性和女性。

结果

对于全部受试者，由rs3785889 - rs16941382确定的G - T单倍型在冠状动脉疾病患者中的频率显著高于对照受试者（P = 0.009）。多因素逻辑回归分析也证实，由rs3785889 - rs16941382确定的G - T单倍型（纯合子）受试者患冠状动脉疾病的几率显著高于无此单倍型的受试者（OR = 1.887，P = 0.007）。

结论

由rs3785889 - rs16941382确定的G - T单倍型可能是中国汉族人群冠状动脉疾病患者的一个风险遗传标记。