• 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

[Pulmonary arterial hypertension in a pedigree with bone morphogenetic protein receptor 2 c.282 mutation].

作者信息

Song J R, Zhang J W, Li B, Deng M J, Cao Y S

机构信息

First Clinical Medical College of Gansu University of Chinese Medicine (Gansu Provincial Hospital), Lanzhou 730000, China.

Department of Cardiology, Gansu Provincial Hospital, Lanzhou 730000, China.

出版信息

Zhonghua Xin Xue Guan Bing Za Zhi. 2023 Jul 24;51(7):769-772. doi: 10.3760/cma.j.cn112148-20220620-00484.

DOI:10.3760/cma.j.cn112148-20220620-00484
PMID:37460431
Abstract
摘要

相似文献

1
[Pulmonary arterial hypertension in a pedigree with bone morphogenetic protein receptor 2 c.282 mutation].[伴有骨形态发生蛋白受体2基因c.282突变的家系中的肺动脉高压]
Zhonghua Xin Xue Guan Bing Za Zhi. 2023 Jul 24;51(7):769-772. doi: 10.3760/cma.j.cn112148-20220620-00484.
2
Different Cytokine Patterns in BMPR2-Mutation-Positive Patients and Patients With Pulmonary Arterial Hypertension Without Mutations and Their Influence on Survival.BMPR2 突变阳性患者与无突变的肺动脉高压患者的不同细胞因子模式及其对生存的影响。
Chest. 2022 Jun;161(6):1651-1656. doi: 10.1016/j.chest.2022.01.019. Epub 2022 Jan 19.
3
Idiopathic pulmonary arterial hypertension associated with a novel frameshift mutation in the bone morphogenetic protein receptor II gene and enhanced bone morphogenetic protein signaling: A case report.与骨形态发生蛋白受体II基因新的移码突变及骨形态发生蛋白信号增强相关的特发性肺动脉高压:一例报告
Medicine (Baltimore). 2019 Oct;98(42):e17594. doi: 10.1097/MD.0000000000017594.
4
Genetics of pulmonary arterial hypertension.肺动脉高压的遗传学。
Clin Chest Med. 2013 Dec;34(4):651-63. doi: 10.1016/j.ccm.2013.08.003.
5
Letter by Kataoka et al Regarding Article, "Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension: A View on the Right Ventricle".
Circulation. 2016 Aug 30;134(9):e115-6. doi: 10.1161/CIRCULATIONAHA.116.022841.
6
Response by van der Bruggen et al to Letter Regarding Article, "Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension: A View on the Right Ventricle".范德布鲁根等人对关于“肺动脉高压中骨形态发生蛋白受体2型突变:对右心室的看法”一文的信件的回复
Circulation. 2016 Aug 30;134(9):e117-8. doi: 10.1161/CIRCULATIONAHA.116.024173.
7
Codependence of Bone Morphogenetic Protein Receptor 2 and Transforming Growth Factor-β in Elastic Fiber Assembly and Its Perturbation in Pulmonary Arterial Hypertension.骨形态发生蛋白受体2与转化生长因子-β在弹性纤维组装中的相互依存关系及其在肺动脉高压中的紊乱
Arterioscler Thromb Vasc Biol. 2017 Aug;37(8):1559-1569. doi: 10.1161/ATVBAHA.117.309696. Epub 2017 Jun 15.
8
At the X-Roads of Sex and Genetics in Pulmonary Arterial Hypertension.在肺动脉高压的性与遗传学交汇处。
Genes (Basel). 2020 Nov 20;11(11):1371. doi: 10.3390/genes11111371.
9
From bone morphogenic protein receptor II mutations to heritable pulmonary arterial hypertension-the long and winding road.
J Heart Lung Transplant. 2017 Feb;36(2):134-135. doi: 10.1016/j.healun.2016.08.002. Epub 2016 Aug 17.
10
Better off blue: BMPR-2 mutation, arteriovenous malformation, and pulmonary arterial hypertension.蓝色更有利:骨形态发生蛋白受体2突变、动静脉畸形与肺动脉高压
Am J Respir Crit Care Med. 2014 Jun 1;189(11):1435-6. doi: 10.1164/rccm.201311-2019IM.