Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Syndrome and TGFB1[original query] |
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| Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients. Human genetics 2003 Dec 114 (1): 87-98. McCarthy Jeanette J, Meyer Joanne, Moliterno David J, Newby L Kristin, Rogers William J, Topol Eric J, |
| Transforming growth factor-beta receptor-3 is associated with pulmonary emphysema. American journal of respiratory cell and molecular biology 2009 Sep 41 (3): 324-31. Hersh Craig P, Hansel Nadia N, Barnes Kathleen C, Lomas David A, Pillai Sreekumar G, Coxson Harvey O, Mathias Rasika A, Rafaels Nicholas M, Wise Robert A, Connett John E, Klanderman Barbara J, Jacobson Francine L, Gill Ritu, Litonjua Augusto A, Sparrow David, Reilly John J, Silverman Edwin K, |
| Moyamoya vasculopathy shows a genetic mutational gradient decreasing from East to West. Journal of neurosurgical sciences 2016 Oct . Raso Alessandro, Biassoni Roberto, Mascelli Samantha, Nozza Paolo, Ugolotti Elisabetta, DI Marco Eddi, DE Marco Patrizia, Merello Elisa, Cama Armando, Pavanello Marco, Capra Valer |
| Transforming growth factor-? signaling pathway-associated genes SMAD2 and TGFBR2 are implicated in metabolic syndrome in a Taiwanese population. Scientific reports 2017 Oct 7 (1): 13589. Lin Eugene, Kuo Po-Hsiu, Liu Yu-Li, Yang Albert C, Tsai Shih-J |
| Functional dyspepsia susceptibility is associated with TGFB1 gene polymorphisms (RS4803455, RS1800469) in H pylori-negative Chinese population. Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society 2019 Aug e13681. Cheung Cynthia K Y, Lan Lin Lin, Chan Yawen, Yuen Kay, Cheong Pui Kuan, Fang Fanny, Wu Justin C |
| 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 |
| GWAS of Hematuria. Clinical journal of the American Society of Nephrology : CJASN 2022 4 17 (5): 672-683. Gagliano Taliun Sarah A, Sulem Patrick, Sveinbjornsson Gardar, Gudbjartsson Daniel F, Stefansson Kari, Paterson Andrew D, Barua Moumi |
| Systematic review of reported association studies of monogenic genes and bladder cancer risk and confirmation analysis in a large population cohort. BJUI compass 2023 2 4 (2): 156-163. Mian Abrar, Wei Jun, Shi Zhuqing, Rifkin Andrew S, Zheng S Lilly, Glaser Alexander P, Kearns James T, Helfand Brian T, Xu Jianfe |
| Influence of Genetic Polymorphisms on the Age at Cancer Diagnosis in a Homogenous Lynch Syndrome Cohort of Individuals Carrying the MLH1:c.1528C>T South African Founder Variant. Biomedicines 2024 10 12 (10): . Lutricia Ndou, Ramadhani Chambuso, Ursula Algar, Paul Goldberg, Adam Boutall, Raj Rames |
- Page last reviewed:Feb 1, 2024
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