HuGE Literature Finder
Records 1-5
|
Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates.
Respiratory research 2019 Aug 20 (1): 174. Liu Xu, Mei Mei, Chen Xiang, Lu Yulan, Dong Xinran, Hu Liyuan, Hu Xiaojing, Cheng Guoqiang, Cao Yun, Yang Lin, Zhou Wenh |
|
Role of the transient receptor potential (TRP) channel gene expressions and TRP melastatin (TRPM) channel gene polymorphisms in obesity-related metabolic syndrome.
European review for medical and pharmacological sciences 2015 Apr 19 (8): 1388-97. Tabur S, Oztuzcu S, Duzen I V, Eraydin A, Eroglu S, Ozkaya M, Demiryürek A |
|
Molecular and clinical analysis of TRPC6 and AGTR1 genes in patients with pulmonary arterial hypertension.
Orphanet journal of rare diseases 2015 10 (1): 1. Pousada Guillermo, Baloira Adolfo, Valverde Dia |
|
Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis.
Contributions to nephrology 2013 181 91-100. Zhang Qianying, Ma Jun, Xie Jingyuan, Wang Zhaohui, Zhu Bin, Hao Xu, Yang Li, Ren Hong, Chen N |
|
A functional single-nucleotide polymorphism in the TRPC6 gene promoter associated with idiopathic pulmonary arterial hypertension.
Circulation 2009 May 119 (17): 2313-22. Yu Ying, Keller Steve H, Remillard Carmelle V, Safrina Olga, Nicholson Ann, Zhang Shenyuan L, Jiang Weihua, Vangala Nivruthi, Landsberg Judd W, Wang Jian-Ying, Thistlethwaite Patricia A, Channick Richard N, Robbins Ivan M, Loyd James E, Ghofrani Hossein A, Grimminger Friedrich, Schermuly Ralph T, Cahalan Michael D, Rubin Lewis J, Yuan Jason X |
- Page last reviewed:Oct 1, 2020
- Page last updated:Oct 21, 2020
- Content source: