Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: 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 |
A genome-wide association study of the human metabolome in a community-based cohort.
Cell metabolism 2013 Jul 18 (1): 130-43. Rhee Eugene P, Ho Jennifer E, Chen Ming-Huei, Shen Dongxiao, Cheng Susan, Larson Martin G, Ghorbani Anahita, Shi Xu, Helenius Iiro T, O'Donnell Christopher J, Souza Amanda L, Deik Amy, Pierce Kerry A, Bullock Kevin, Walford Geoffrey A, Vasan Ramachandran S, Florez Jose C, Clish Clary, Yeh J-R Joanna, Wang Thomas J, Gerszten Robert |
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 on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
European heart journal 2014 Feb 35 (8): 524-31. Seppälä Ilkka, Kleber Marcus E, Lyytikäinen Leo-Pekka, Hernesniemi Jussi A, Mäkelä Kari-Matti, Oksala Niku, Laaksonen Reijo, Pilz Stefan, Tomaschitz Andreas, Silbernagel Günther, Boehm Bernhard O, Grammer Tanja B, Koskinen Tuomas, Juonala Markus, Hutri-Kähönen Nina, Alfthan Georg, Viikari Jorma S A, Kähonen Mika, Raitakari Olli T, März Winfried, Meinitzer Andreas, Lehtimäki Terho, |
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 |
Missense variants of the alanine:glyoxylate aminotransferase 2 gene are not associated with Japanese schizophrenia patients. Progress in neuro-psychopharmacology & biological psychiatry 2014 Aug 53 137-41. Yoshino Yuta, Abe Masao, Numata Shusuke, Ochi Shinichiro, Mori Yoko, Ishimaru Takashi, Kinoshita Makoto, Umehara Hidehiro, Yamazaki Kiyohiro, Mori Takaaki, Ohmori Tetsuro, Ueno Shu-ic |
Alanine-glyoxylate aminotransferase 2 (AGXT2) polymorphisms have considerable impact on methylarginine and ß-aminoisobutyrate metabolism in healthy volunteers. PloS one 2014 9 (2): e88544. Kittel Anja, Müller Fabian, König Jörg, Mieth Maren, Sticht Heinrich, Zolk Oliver, Kralj Ana, Heinrich Markus R, Fromm Martin F, Maas Ren |
Missense variants of the alanine: glyoxylate aminotransferase 2 gene correlated with carotid atherosclerosis in the Japanese population. Journal of biological regulators and homeostatic agents 0 28 (4): 605-14. Yoshino Y, Kohara K, Abe M, Ochi S, Mori Y, Yamashita K, Igase M, Tabara Y, Mori T, Miki T, Ueno |
Considerable impacts of AGXT2 V140I polymorphism on chronic heart failure in the Chinese population. Atherosclerosis 2016 08 251 255-262. Hu Xiao-Lei, Zhou Ji-Peng, Kuang Da-Bin, Qi Hong, Peng Li-Ming, Yang Tian-Lun, Li Xi, Zhang Wei, Zhou Hong-Hao, 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 |
AGXT2 rs37369 polymorphism predicts the renal function in patients with chronic heart failure. Gene 2017 Sep . Hu Xiao-Lei, Zeng Wen-Jing, Li Mu-Peng, Yang Yong-Long, Kuang Da-Bin, Li He, Zhang Yan-Jiao, Jiang Chun, Peng Li-Ming, Qi Hong, Zhang Ke, Chen Xiao-Pi |
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 |
Digenic mutations on SCAP and AGXT2 predispose to premature myocardial infarction. Oncotarget 2017 12 8 (59): 100141-100149. Gao Yuanfeng, Lee Chongyou, Song Junxian, Li Sufang, Cui Yuxia, Liu Yongzhen, Wang Jie, Lu Fengmin, Chen Ho |
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 |
Acute Aerobic Exercise Leads to Increased Plasma Levels of R- and S-?-Aminoisobutyric Acid in Humans. Frontiers in physiology 2019 10 1240. Stautemas Jan, Van Kuilenburg André B P, Stroomer Lida, Vaz Fred, Blancquaert Laura, Lefevere Filip B D, Everaert Inge, Derave W |
Sequence Variation in the DDAH1 Gene Predisposes for Delayed Cerebral Ischemia in Subarachnoidal Hemorrhage. Journal of clinical medicine 2020 Dec 9 (12): . Hannemann Juliane, Appel Daniel, Seeberger-Steinmeister Miriam, Brüning Tabea, Zummack Julia, Böger Rain |
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, |
Effects of AGXT2 variants on blood pressure and blood sugar among 750 older Japanese subjects recruited by the complete enumeration survey method. BMC genomics 2021 Apr 22 (1): 287. Yoshino Yuta, Kumon Hiroshi, Mori Takaaki, Yoshida Taku, Tachibana Ayumi, Shimizu Hideaki, Iga Jun-Ichi, Ueno Shu-Ic |
Association of Genes of the NO Pathway with Altitude Disease and Hypoxic Pulmonary Hypertension. Journal of clinical medicine 2021 12 10 (24): . Hannemann Juliane, Siques Patricia, Schmidt-Hutten Lena, Zummack Julia, Brito Julio, Böger Rain |
Functional AGXT2 SNP rs37369 Variant Is a Risk Factor for Diabetes Mellitus: Baseline Data From the Aidai Cohort Study in Japan. Canadian journal of diabetes 2022 Jun . Kumon Hiroshi, Miyake Yoshihiro, Yoshino Yuta, Iga Jun-Ichi, Tanaka Keiko, Senba Hidenori, Kimura Eizen, Higaki Takashi, Matsuura Bunzo, Kawamoto Ryuichi, Ueno Shu-Ic |
Cats with Genetic Variants of AGXT2 Respond Differently to a Dietary Intervention Known to Reduce the Risk of Calcium Oxalate Stone Formation. Genes 2022 Apr 13 (5): . Hall Jean A, Panickar Kiran S, Brockman Jeffrey A, Jewell Dennis |
Association of Variability in the DDAH1, DDAH2, AGXT2 and PRMT1 Genes with Circulating ADMA Concentration in Human Whole Blood. Journal of clinical medicine 2022 2 11 (4): . Hannemann Juliane, Zummack Julia, Hillig Jonas, Rendant-Gantzberg Leonard, Böger Rain |
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 |
Functional AGXT2 SNP rs180749 variant and depressive symptoms: Baseline data from the Aidai Cohort Study in Japan. Journal of neural transmission (Vienna, Austria : 1996) 2024 1 . Hiroshi Kumon, Yoshihiro Miyake, Yuta Yoshino, Jun-Ichi Iga, Keiko Tanaka, Hidenori Senba, Eizen Kimura, Takashi Higaki, Bunzo Matsuura, Ryuichi Kawamoto, Shu-Ichi Ue |
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- Page last updated:Apr 22, 2024
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