Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and AGXT2[original query] |
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A genome-wide association study of metabolic traits in human urine.
Nature genetics 2011 Jun 43 (6): 565-9. Suhre Karsten, Wallaschofski Henri, Raffler Johannes, Friedrich Nele, Haring Robin, Michael Kathrin, Wasner Christina, Krebs Alexander, Kronenberg Florian, Chang David, Meisinger Christa, Wichmann H-Erich, Hoffmann Wolfgang, Völzke Henry, Völker Uwe, Teumer Alexander, Biffar Reiner, Kocher Thomas, Felix Stephan B, Illig Thomas, Kroemer Heyo K, Gieger Christian, Römisch-Margl Werner, Nauck Matthi |
| Genetic and environmental determinants of dimethylarginines and association with cardiovascular disease in patients with type 2 diabetes. Diabetes care 2014 37 (3): 846-54. Anderssohn Maike, McLachlan Stela, Lüneburg Nicole, Robertson Christine, Schwedhelm Edzard, Williamson Rachel M, Strachan Mark W J, Ajjan Ramzi, Grant Peter J, Böger Rainer H, Price Jackie |
| Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine.
Circulation. Cardiovascular genetics 2014 Dec 7 (6): 864-72. Lüneburg Nicole, Lieb Wolfgang, Zeller Tanja, Chen Ming-Huei, Maas Renke, Carter Angela M, Xanthakis Vanessa, Glazer Nicole L, Schwedhelm Edzard, Seshadri Sudha, Ikram Mohammad Arfan, Longstreth William T, Fornage Myriam, König Inke R, Loley Christina, Ojeda Francisco M, Schillert Arne, Wang Thomas J, Sticht Heinrich, Kittel Anja, König Jörg, Benjamin Emelia J, Sullivan Lisa M, Bernges Isabel, Anderssohn Maike, Ziegler Andreas, Gieger Christian, Illig Thomas, Meisinger Christa, Wichmann H-Erich, Wild Philipp S, Schunkert Heribert, Psaty Bruce M, Wiggins Kerri L, Heckbert Susan R, Smith Nicholas, Lackner Karl, Lunetta Kathryn L, Blankenberg Stefan, Erdmann Jeanette, Munzel Thomas, Grant Peter J, Vasan Ramachandran S, Böger Rainer |
| Association of the AGXT2 V140I polymorphism with risk for coronary heart disease in a Chinese population. Journal of atherosclerosis and thrombosis 2014 21 (10): 1022-30. Zhou Ji-Peng, Bai Yong-Ping, Hu Xiao-Lei, Kuang Da-Bin, Shi Rui-Zheng, Xiong Yan, Zhang Wei, Xia Jian, Chen Bi-Lian, Yang Tian-Lun, Chen Xiao-Pi |
| Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke. Scientific reports 2016 6 23207. Seppälä Ilkka, Kleber Marcus E, Bevan Steve, Lyytikäinen Leo-Pekka, Oksala Niku, Hernesniemi Jussi A, Mäkelä Kari-Matti, Rothwell Peter M, Sudlow Cathie, Dichgans Martin, Mononen Nina, Vlachopoulou Efthymia, Sinisalo Juha, Delgado Graciela E, Laaksonen Reijo, Koskinen Tuomas, Scharnagl Hubert, Kähönen Mika, Markus Hugh S, März Winfried, Lehtimäki Ter |
| Effect of l-arginine, asymmetric dimethylarginine, and symmetric dimethylarginine on ischemic heart disease risk: A Mendelian randomization study. American heart journal 2016 Dec 182 54-61. Au Yeung Shiu Lun, Lin Shi Lin, Lam Hung San Hugh Simon, Schooling Catherine Ma |
| Genetic variations in the alanine-glyoxylate aminotransferase 2 (AGXT2) gene and dimethylarginines levels in rheumatoid arthritis. Amino acids 2017 Mar . Dimitroulas Theodoros, Hodson James, Panoulas Vasileios F, Sandoo Aamer, Smith Jacqueline, Kitas Geor |
| AGXT2 and DDAH-1 genetic variants are highly correlated with serum ADMA and SDMA levels and with incidence of coronary artery disease in Egyptians. Molecular biology reports 2018 Oct . Amir Mina, Hassanein Sally I, Abdel Rahman Mohamed F, Gad Mohamed |
| Disease-specific eQTL screening reveals an anti-fibrotic effect of AGXT2 in non-alcoholic fatty liver disease. Journal of hepatology 2021 Apr . Yoo Taekyeong, Joo Sae Kyung, Kim Hyo Jung, Kim Hyun Young, Sim Hyungtai, Lee Jieun, Kim Hee-Hoon, Jung Sunhee, Lee Youngha, Jamialahmadi Oveis, Romeo Stefano, Jeong Won-Il, Hwang Geum-Sook, Kang Keon Wook, Kim Jae Woo, Kim Won, Choi Murim, |
| Genetic and Metabolic Characteristics of Lean Nonalcoholic Fatty Liver Disease in a Korean Health Examinee Cohort. Gut and liver 2023 8 . Huiyul Park, Eileen L Yoon, Goh Eun Chung, Eun Kyung Choe, Jung Ho Bae, Seung Ho Choi, Mimi Kim, Woochang Hwang, Hye-Lin Kim, Sun Young Yang, Dae Won J |
| Whole-exome sequencing in moyamoya patients of Northern-European origin identifies gene variants involved in Nitric Oxide metabolism: A pilot study. Brain & spine 2023 6 3 101745. Markus K H Wiedmann, Ingunn V Steinsvåg, Tovy Dinh, Magnus D Vigeland, Pål G Larsson, Hanne Hjorthaug, Ying Sheng, Inger-Lise Mero, Kaja K Selm |
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