Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 10, 2023. (Total: 223917Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 7 (of 7 Records)

Query Trace: Hypertension and TRPC6[original query]
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
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
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
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
TRPC6 Mutational Analysis in Iranian Children With Focal Segmental Glomerulosclerosis.
Iranian journal of kidney diseases 2019 1 12 (6): 341-349.
Gheissari Alaleh, Meamar Rokhsareh, Kheirollahi Majid, Rouigari Maedeh, Dehbashi Moein, Dehghani Leila, Abedini Am
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. GWAS Catalog
JAMA cardiology 2023 6 .
Jaakko S Tyrmi, Tea Kaartokallio, A Inkeri Lokki, Tiina Jääskeläinen, Eija Kortelainen, Sanni Ruotsalainen, Juha Karjalainen, Samuli Ripatti, Anna Kivioja, Triin Laisk, Johannes Kettunen, Anneli Pouta, Katja Kivinen, Eero Kajantie, Seppo Heinonen, Juha Kere, Hannele Laivuori,
TOP