182
Views
17
CrossRef citations to date
0
Altmetric
Original Articles

Association of ACE gene A2350G and I/D polymorphisms with essential hypertension in the northernmost province of China

, , , , &
Pages 32-38 | Received 17 Oct 2016, Accepted 30 Jan 2017, Published online: 27 Nov 2017

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (1)

Mariyana Hristova, Spaska Stanilova & Lyuba Miteva. (2019) Serum concentration of renin-angiotensin system components in association with ACE I/D polymorphism among hypertensive subjects in response to ACE inhibitor therapy. Clinical and Experimental Hypertension 41:7, pages 662-669.
Read now

Articles from other publishers (16)

I Putu Sudayasa, Fera Husdaningsih & La Ode Alifariki. (2023) Polymorphism of Gene ACE I/D and Family History of Hypertension as Predisposition of Hypertension. Malaysian Journal of Medicine and Health Sciences 19:3, pages 171-177.
Crossref
Li Wang, Ting-ting Song & Chang-wu Dong. (2023) Association between Interactions among ACE Gene Polymorphisms and Essential Hypertension in Patients in the Hefei Region, Anhui, China. Journal of the Renin-Angiotensin-Aldosterone System 2023, pages 1-8.
Crossref
Zhenyun Wang, Juanjuan Hou, Hongjun Zheng, Dan Wang, Weihua Tian, Dan ZhangJiamin Yan. (2023) Genetic and phenotypic frequency distribution of ACE, ADRB1, AGTR1, CYP2C9*3, CYP2D6*10, CYP3A5*3, NPPA and factors associated with hypertension in Chinese Han hypertensive patients. Medicine 102:10, pages e33206.
Crossref
Wang Li & Dong Changwu. (2022) A homozygote for rs12709426 of the ACE gene in patients with essential hypertension: a case report. A homozygote for rs12709426 of the ACE gene in patients with essential hypertension: a case report.
Chong Wan, Rui-Yi Zong & Xing-Shu Chen. (2022) The new mechanism of cognitive decline induced by hypertension: High homocysteine-mediated aberrant DNA methylation. Frontiers in Cardiovascular Medicine 9.
Crossref
T. А. Mulerova, N. I. Morozova, E. D. Bazdyrev, T. F. Gaziev, E. V. Indukaeva, D. P. Tsygankova & O. V. Nakhratova. (2022) Genetic approaches in the choice of therapy for hypertension in the population of Mountain Shoria. "Arterial’naya Gipertenziya" ("Arterial Hypertension") 29:1, pages 58-67.
Crossref
Yu Cai, Sinong Zhang, Jiaxing Zhang, Xiaonan Liu, Kang Ma, Wei Xu, Xianghai Deng, Jiangcun Yang, Ting Ma, Chao Jiang, Wenli Hui & Yali Cui. (2022) Visual Detection of ACE I/D Polymorphism Using T-ARMS-PCR Combined with a Lateral Flow Assay and Its Clinical Application . Analytical Chemistry 94:11, pages 4686-4694.
Crossref
T A Mulerova, M Yu Ogarkov, D P Tsygankova, Yu V Kazachek, O M Polikutina & O L Barbarash. (2021) Ethnicity as a model for the development of cardiovascular diseases and their risk factors in epidemiological studies. Kazan medical journal 102:5, pages 736-746.
Crossref
Zhigang Ren, Benchen Rao, Siqi Xie, Ang Li, Lijun Wang, Guangying Cui, Tiantian Li, Hang Yan, Zujiang Yu & Suying Ding. (2020) A novel predicted model for hypertension based on a large cross-sectional study. Scientific Reports 10:1.
Crossref
Yanrui Wu, Xingming Pan & Xiaoxiao Jin. (2020) Haplotype-based association study between PRCP gene polymorphisms and essential hypertension in Hani minority group from a remote region of China. Journal of the Renin-Angiotensin-Aldosterone System 21:4, pages 147032032098131.
Crossref
Yanrui Wu, Hongju Yang & Chunjie Xiao. (2020) Genetic association study of prolylcarboxypeptidase polymorphisms with susceptibility to essential hypertension in the Yi minority of China: A case–control study based on an isolated population. Journal of the Renin-Angiotensin-Aldosterone System 21:2, pages 147032032091958.
Crossref
O. S. Pavlova, S. E. Ogurtsova, M. M. Liventseva, T. H. Lakotko, I. Y. Korobko, V. I. Shyshko & A. G. Mrochek. (2019) Association of the I/D polymorphism of angiotensinconverting enzyme gene with the development of essential hypertension. The Siberian Medical Journal 34:3, pages 87-96.
Crossref
Pimphen Charoen, Jakris Eu-ahsunthornwattana, Nisakron Thongmung, Pedro A. Jose, Piyamitr Sritara, Prin Vathesatogkit & Chagriya Kitiyakara. (2019) Contribution of Four Polymorphisms in Renin-Angiotensin-Aldosterone-Related Genes to Hypertension in a Thai Population. International Journal of Hypertension 2019, pages 1-8.
Crossref
He Sun, Jun-Ting Zhang, Xue-Rong Xie, Tao Li, Xue-Yan Li, Ning-Ning Wang, Jing-Ping Li, Zhi-Hui Deng & Chang-Chun Qiu. (2018) Association of uncoupling protein gene polymorphisms with essential hypertension in a northeastern Han Chinese population. Journal of Human Hypertension 33:7, pages 524-530.
Crossref
T. A. MulerovaS. A. Maksimov, M. Yu. OgarkovO. V. Gruzdeva, A. V. Ponasenko, V. N. MaksimovM. I. VoyevodaE. S. FilimonovG. V. Artamonova. (2018) Associations of Cardiovascular Risk Factors and Genetic Markers with Development of Arterial Hypertension in the Population of Mountain Shoriya. Rational Pharmacotherapy in Cardiology 14:5, pages 678-686.
Crossref
Mariangela Torreglosa Ruiz Cintra, Marly Aparecida Spadotto Balarin, Sarah Cristina Sato Vaz Tanaka, Vanessa Iorrana Mota da Silva, Alessandra Bernadete Trovó de Marqui, Elisabete Aparecida Mantovani Rodrigues de Resende, Marco Fábio Prata Lima & Mariana Kefálas Oliveira Gomes. (2018) Polycystic ovarian syndrome: rs1799752 polymorphism of ACE gene. Revista da Associação Médica Brasileira 64:11, pages 1017-1022.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.