Mitochondrial genome mutations in 13 subunits of respiratory chain complexes in Chinese Han and Mongolian hypertensive individuals-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Mitochondrial genome mutations in 13 subunits of respiratory chain complexes in Chinese Han and Mongolian hypertensive individuals

Published:2017-11-26 Issue:7 Volume:29 Page:1090-1099
ISSN:2470-1394
Container-title:Mitochondrial DNA Part A
language:en
Short-container-title:Mitochondrial DNA Part A

Author:

Zhao Ying¹²,Chen Xi¹,Li Haide³,Zhu Chao¹,Li Yang¹⁴,Liu Yuqi¹⁴

Affiliation:

1. Department of Cardiology, Chinese PLA General Hospital, Beijing, China;

2. Outpatient Clinic of General Hospital of China Aviation, Beijing, China;

3. Department of Cardiology, Yishui Center Hospital of Shandong Province, Linyi, China;

4. Institute of Geriatric Cardiology, Chinese PLA General Hospital, Beijing, China

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.1080/24701394.2017.1407762

Reference32 articles.

1. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J

2. Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure

3. Epidemiology and genetics of hypertension.

4. Clinical Expression of Leber Hereditary Optic Neuropathy Is Affected by the Mitochondrial DNA–Haplogroup Background

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Consequences of Exposure to Hypobaric Hypoxia Associated with High Altitude on Spermatogenesis and Seminal Parameters: A Literature Review;Cells;2024-03-29

2. Mitochondrial DNA Is a Vital Driving Force in Ischemia-Reperfusion Injury in Cardiovascular Diseases;Oxidative Medicine and Cellular Longevity;2022-05-17

3. The Role of Mitochondrial DNA Mutations in Cardiovascular Diseases;International Journal of Molecular Sciences;2022-01-16

4. Variations of mitochondrial nd4 and nd5 genes and their association with temporal lobe epilepsy in a northern han chinese population;Annals of Indian Academy of Neurology;2021

5. Associations of mitochondrial DNA 3777–4679 region mutations with maternally inherited essential hypertensive subjects in China;BMC Medical Genetics;2020-05-15

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3