Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Hypertension and TGFB1[original query] |
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Association of transforming growth factor-beta1 gene polymorphisms with myocardial infarction in patients with angiographically proven coronary heart disease. Arteriosclerosis, thrombosis, and vascular biology 2006 May 26 (5): 1114-9. Koch Werner, Hoppmann Petra, Mueller Jakob C, Schömig Albert, Kastrati Adn |
Transforming growth factor-beta1 869T/C, but not interleukin-6 -174G/C, polymorphism associates with hypertension in rheumatoid arthritis. Rheumatology (Oxford, England) 2009 Feb 48 (2): 113-8. Panoulas V F, Douglas K M J, Smith J P, Stavropoulos-Kalinoglou A, Metsios G S, Nightingale P, Kitas G |
Genetic associations with hypoxemia and pulmonary arterial pressure in COPD. Chest 2009 Mar 135 (3): 737-44. Castaldi Peter J, Hersh Craig P, Reilly John J, Silverman Edwin |
Genetic modifiers of liver disease in cystic fibrosis. JAMA 2009 Sep 302 (10): 1076-83. Bartlett Jaclyn R, Friedman Kenneth J, Ling Simon C, Pace Rhonda G, Bell Scott C, Bourke Billy, Castaldo Giuseppe, Castellani Carlo, Cipolli Marco, Colombo Carla, Colombo John L, Debray Dominique, Fernandez Adriana, Lacaille Florence, Macek Milan, Rowland Marion, Salvatore Francesco, Taylor Christopher J, Wainwright Claire, Wilschanski Michael, Zemková Dana, Hannah William B, Phillips M James, Corey Mary, Zielenski Julian, Dorfman Ruslan, Wang Yunfei, Zou Fei, Silverman Lawrence M, Drumm Mitchell L, Wright Fred A, Lange Ethan M, Durie Peter R, Knowles Michael R, |
Evaluation of Transforming Growth Factor Beta-1 Gene 869T/C Polymorphism with Hypertension: A Meta-Analysis. International journal of hypertension 2011 2011 934265. Niu Wenqu |
Transforming growth factor ß1 +869T/C gene polymorphism and essential hypertension: a meta-analysis involving 2708 participants in the Chinese population. Internal medicine (Tokyo, Japan) 2011 50 (10): 1089-92. Yan-Yan |
Association of inflammatory gene polymorphisms with ischemic stroke in a Chinese Han population. Journal of neuroinflammation 2012 9 (1): 162. Zhao Nan, Liu Xin, Wang Yongqin, Liu Xiaoqiu, Li Jiana, Yu Litian, Ma Liyuan, Wang Shuyu, Zhang Hongye, Liu Lisheng, Zhao Jingbo, Wang Xing |
Association of rs1800471 polymorphism of TGFB1 gene with chronic kidney disease occurrence and progression and hypertension appearance. Archives of medical science : AMS 2013 Apr 9 (2): 230-7. Nabrdalik Katarzyna, Gumprecht Janusz, Adamczyk Piotr, Górczy?ska-Kosiorz Sylwia, Zywiec Joanna, Grzeszczak W?adys? |
Epistatic study reveals two genetic interactions in blood pressure regulation. BMC medical genetics 2013 14 (1): 2. Ndiaye Ndeye Coumba, Said El Shamieh, Stathopoulou Maria G, Siest Gérard, Tsai Michael Y, Visvikis-Siest Soph |
Altered erythrocyte membrane protein composition mirrors pleiotropic effects of hypertension susceptibility genes and disease pathogenesis. Journal of hypertension 2015 Sep . Polonikov Alexey V, Ushachev Dmitry V, Ivanov Vladimir P, Churnosov Mikhail I, Freidin Maxim B, Ataman Alexander V, Harbuzova Victoria Yu, Bykanova Marina A, Bushueva Olga Yu, Solodilova Maria |
Pathogenesis of intracranial aneurysm is mediated by proinflammatory cytokine TNFA and IFNG and through stochastic regulation of IL10 and TGFB1 by comorbid factors. Journal of neuroinflammation 2015 12 (1): 135. Sathyan Sanish, Koshy Linda V, Srinivas Lekshmi, Easwer H V, Premkumar S, Nair Suresh, Bhattacharya R N, Alapatt Jacob P, Banerjee Moin |
TGFB1 Functional Gene Polymorphisms (C-509T and T869C) in the Maternal Susceptibility to Pre-eclampsia in South Indian Women. Scandinavian journal of immunology 2015 Oct 82 (4): 390-7. Deepthi Goske, Chaithri Ponnaluri Kamakshi, Latha Prasanna, Usha Rani Vital, Rahman Police Fazul, Jahan Parve |
Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria.
Nature communications 2019 Sep 10 (1): 4130. Teumer Alexander, Li Yong, Ghasemi Sahar, Prins Bram P, Wuttke Matthias, Hermle Tobias, Giri Ayush, Sieber Karsten B, Qiu Chengxiang, Kirsten Holger, Tin Adrienne, Chu Audrey Y, Bansal Nisha, Feitosa Mary F, Wang Lihua, Chai Jin-Fang, Cocca Massimiliano, Fuchsberger Christian, Gorski Mathias, Hoppmann Anselm, Horn Katrin, Li Man, Marten Jonathan, Noce Damia, Nutile Teresa, Sedaghat Sanaz, Sveinbjornsson Gardar, Tayo Bamidele O, van der Most Peter J, Xu Yizhe, Yu Zhi, Gerstner Lea, Ärnlöv Johan, Bakker Stephan J L, Baptista Daniela, Biggs Mary L, Boerwinkle Eric, Brenner Hermann, Burkhardt Ralph, Carroll Robert J, Chee Miao-Li, Chee Miao-Ling, Chen Mengmeng, Cheng Ching-Yu, Cook James P, Coresh Josef, Corre Tanguy, Danesh John, de Borst Martin H, De Grandi Alessandro, de Mutsert Renée, de Vries Aiko P J, Degenhardt Frauke, Dittrich Katalin, Divers Jasmin, Eckardt Kai-Uwe, Ehret Georg, Endlich Karlhans, Felix Janine F, Franco Oscar H, Franke Andre, Freedman Barry I, Freitag-Wolf Sandra, Gansevoort Ron T, Giedraitis Vilmantas, Gögele Martin, Grundner-Culemann Franziska, Gudbjartsson Daniel F, Gudnason Vilmundur, Hamet Pavel, Harris Tamara B, Hicks Andrew A, Holm Hilma, Foo Valencia Hui Xian, Hwang Shih-Jen, Ikram M Arfan, Ingelsson Erik, Jaddoe Vincent W V, Jakobsdottir Johanna, Josyula Navya Shilpa, Jung Bettina, Kähönen Mika, Khor Chiea-Chuen, Kiess Wieland, Koenig Wolfgang, Körner Antje, Kovacs Peter, Kramer Holly, Krämer Bernhard K, Kronenberg Florian, Lange Leslie A, Langefeld Carl D, Lee Jeannette Jen-Mai, Lehtimäki Terho, Lieb Wolfgang, Lim Su-Chi, Lind Lars, Lindgren Cecilia M, Liu Jianjun, Loeffler Markus, Lyytikäinen Leo-Pekka, Mahajan Anubha, Maranville Joseph C, Mascalzoni Deborah, McMullen Barbara, Meisinger Christa, Meitinger Thomas, Miliku Kozeta, Mook-Kanamori Dennis O, Müller-Nurasyid Martina, Mychaleckyj Josyf C, Nauck Matthias, Nikus Kjell, Ning Boting, Noordam Raymond, Connell Jeffrey O', Olafsson Isleifur, Palmer Nicholette D, Peters Annette, Podgornaia Anna I, Ponte Belen, Poulain Tanja, Pramstaller Peter P, Rabelink Ton J, Raffield Laura M, Reilly Dermot F, Rettig Rainer, Rheinberger Myriam, Rice Kenneth M, Rivadeneira Fernando, Runz Heiko, Ryan Kathleen A, Sabanayagam Charumathi, Saum Kai-Uwe, Schöttker Ben, Shaffer Christian M, Shi Yuan, Smith Albert V, Strauch Konstantin, Stumvoll Michael, Sun Benjamin B, Szymczak Silke, Tai E-Shyong, Tan Nicholas Y Q, Taylor Kent D, Teren Andrej, Tham Yih-Chung, Thiery Joachim, Thio Chris H L, Thomsen Hauke, Thorsteinsdottir Unnur, Tönjes Anke, Tremblay Johanne, Uitterlinden André G, van der Harst Pim, Verweij Niek, Vogelezang Suzanne, Völker Uwe, Waldenberger Melanie, Wang Chaolong, Wilson Otis D, Wong Charlene, Wong Tien-Yin, Yang Qiong, Yasuda Masayuki, Akilesh Shreeram, Bochud Murielle, Böger Carsten A, Devuyst Olivier, Edwards Todd L, Ho Kevin, Morris Andrew P, Parsa Afshin, Pendergrass Sarah A, Psaty Bruce M, Rotter Jerome I, Stefansson Kari, Wilson James G, Susztak Katalin, Snieder Harold, Heid Iris M, Scholz Markus, Butterworth Adam S, Hung Adriana M, Pattaro Cristian, Köttgen An |
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 |
Genetic Variants Associated with Chronic Kidney Disease in a Spanish Population. Scientific reports 2020 Jan 10 (1): 144. Corredor Zuray, Filho Miguel Inácio da Silva, Rodríguez-Ribera Lara, Velázquez Antonia, Hernández Alba, Catalano Calogerina, Hemminki Kari, Coll Elisabeth, Silva Irene, Diaz Juan Manuel, Ballarin José, Vallés Prats Martí, Calabia Martínez Jordi, Försti Asta, Marcos Ricard, Pastor Susa |
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- Page last updated:Mar 18, 2024
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