HuGE Literature Finder
Records 1-30
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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 |
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DDAH1 promoter -396 4N insertion variant is associated with increased risk of type 2 diabetes in a gender-dependent manner.
Molecular genetics & genomic medicine 2019 Nov e1011. Zhu Fasheng, Zhou Chi, Wen Zheng, Wang Dao W |
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Dimethylarginine Dimethylaminohydrolase 1 Polymorphisms and Venous Intimal Hyperplasia in Hemodialysis Patients.
American journal of nephrology 2019 Oct 1-11. Wu Chih-Cheng, Hsieh Mu-Yang, Lee Chih-Kuo, Chuang Shao-Yuan, Chung Ming-Yi, Lin Chih-Chi |
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DDAH1 and DDAH2 polymorphisms associate with asymmetrical dimethylarginine plasma levels in erectile dysfunction patients but not in healthy controls.
Nitric oxide : biology and chemistry 2019 Aug 92 11-17. Brites-Anselmi Guilhermo, Azevedo Ana Maria Milanez, Miyazaki Anderson Heiji Lima, Pinheiro Lucas Cezar, Coeli-Lacchini Fernanda Borchers, de Andrade Murilo Ferreira, Molina Carlos Augusto Fernandes, Tucci Silvio, Hirsch Emilio, Tanus-Santos Jose Eduardo, Lacchini Riccar |
Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease.
Current Alzheimer research 2019 16 (13): 1163-1174. Li Jin, Chen Feng, Zhang Qiushi, Meng Xianglian, Yao Xiaohui, Risacher Shannon L, Yan Jingwen, Saykin Andrew J, Liang Hong, Shen Li, |
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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 |
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Using clinical and genetic data to predict pulmonary hypertension in bronchopulmonary dysplasia.
Acta paediatrica (Oslo, Norway : 1992) 2018 Sep . Trittmann J K, Bartenschlag A, Zmuda E J, Frick J, Stewart W C L, Nelin L |
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The Methylenetetrahydrofolate Reductase C677T (rs1801133) and Apolipoprotein A5-1131T>C (rs662799) Polymorphisms, and Anemia Are Independent Risk Factors for Ischemic Stroke.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2018 May 27 (5): 1357-1362. Escobedo Jorge, Paz-Aragón Emmanuel, Vega-Rodríguez Luz Helena, Benítez Sanfeliz Miguel Alejandro, Estrada-Rodríguez Humberto, González-Figueroa Evangelina, Liceaga-Craviotto María Gabriela, Gutiérrez-Cuevas Jorge, Valladares-Salgado Adán, Cruz Migu |
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Relationship between asymmetric dimethylarginine, nitrite and genetic polymorphisms: Impact on erectile dysfunction therapy.
Nitric oxide : biology and chemistry 2017 Oct . Azevedo Ana Maria Milanez, Brites-Anselmi Guilhermo, Pinheiro Lucas Cezar, de Almeida Belo Vanessa, Coeli-Lacchini Fernanda Borchers, Molina Carlos Augusto Fernandes, de Andrade Murilo Ferreira, Tucci Silvio, Hirsch Emilio, Tanus-Santos Jose Eduardo, Lacchini Riccar |
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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 |
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Association between variation in the genes DDAH1 and DDAH2 and hypertension among Uygur, Kazakh and Han ethnic groups in China.
Sao Paulo medical journal = Revista paulista de medicina 2016 Jan 134 (3): 205-10. Wang Zhong, Chen Shaoze, Zhang Lina, Lu Guilin, Zhou Chengming, Wang Dao Wen, Wang Li, Badengmu Bayinbate, Zhai Zhihong, Qin Li |
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A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia.
Acta paediatrica (Oslo, Norway : 1992) 2015 Dec . Trittmann J K, Gastier-Foster J M, Zmuda E J, Frick J, Roger L K, Vieland V J, Chicoine L G, Nelin L |
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Genotype/allelic combinations as potential predictors of myocardial infarction.
Molecular biology reports 2015 Dec . Nasibullin Timur R, Timasheva Yanina R, Sadikova Regina I, Tuktarova Ilsiyar A, Erdman Vera V, Nikolaeva Irina E, Sabo Jan, Kruzliak Peter, Mustafina Olga |
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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 |
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Protective role of DDAH2 (rs805304) gene polymorphism in patients with myocardial infarction.
Experimental and molecular pathology 2014 Dec 97 (3): 393-8. Pérez-Hernández Nonanzit, Vargas-Alarcón Gilberto, Arellano-Zapoteco Rocio, Martínez-Rodríguez Nancy, Fragoso José Manuel, Aptilon-Duque Gad, Posadas-Sánchez Rosalinda, Posadas-Romero Carlos, Juárez-Cedillo Teresa, Domínguez-López María Lilia, Rodríguez-Pérez José Manu |
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Relationship between dimethylarginine dimethylaminohydrolase gene variants and asymmetric dimethylarginine in patients with rheumatoid arthritis.
Atherosclerosis 2014 Nov 237 (1): 38-44. Dimitroulas Theodoros, Sandoo Aamer, Hodson James, Smith Jacqueline, Panoulas Vasileios F, Kitas George |
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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, |
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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 |
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Genetic variation in the dimethylarginine dimethylaminohydrolase 1 gene (DDAH1) is related to asymmetric dimethylarginine (ADMA) levels, but not to endothelium-dependent vasodilation.
Vascular medicine (London, England) 2013 Aug 18 (4): 192-9. Lind Lars, Ingelsson Erik, Kumar Jitender, Syvänen Ann-Christine, Axelsson Tomas, Teerlink T |
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Common genetic variants in the endothelial system predict blood pressure response to sodium intake: the GenSalt study.
American journal of hypertension 2013 May 26 (5): 643-56. Defagó Maria Daniela, Gu Dongfeng, Hixson James E, Shimmin Lawrence C, Rice Treva K, Gu Charles C, Jaquish Cashell E, Liu De-Pei, He Jiang, Kelly Tanika |
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Elevation of serum asymmetrical and symmetrical dimethylarginine in patients with advanced glaucoma.
Investigative ophthalmology & visual science 2012 Apr 53 (4): 1923-7. Javadiyan Shahrbanou, Burdon Kathryn P, Whiting Malcolm J, Abhary Sotoodeh, Straga Tania, Hewitt Alex W, Mills Richard A, Craig Jamie |
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ADMA, SDMA and L-arginine/ADMA ratio but not DDAH genetic polymorphisms are reliable predictors of diabetic nephropathy progression as identified by competing risk analysis.
Kidney & blood pressure research 2012 36 (1): 200-8. Tanhäuserová Veronika, Tomandl Josef, Pácal Lukáš, Klepárník Martin, Malúšková Denisa, Bartáková Vendula, Kuricová Katarína, Reho?ová Jitka, St?pánková So?a, Svojanovský Jan, Olšovský Jind?ich, B?lobrádková Jana, Krusová Darja, Jurajda Michal, Mužík Jan, Pavlík Tomáš, Ka?ková Kate?i |
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Genetic variants, endothelial function, and risk of preeclampsia among American Indians.
Hypertension in pregnancy 2012 31 (1): 1-10. Best Lyle G, Nadeau Melanie, Bercier Shellee, Dauphinais Sara, Davis Jacob, Davis Kylie, Poitra Shyleen, Anderson Cindy |
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The association of dimethylarginine dimethylaminohydrolase 1 gene polymorphism with type 2 diabetes: a cohort study.
Cardiovascular diabetology 2011 10 (1): 16. Lu Tse-Min, Lin Shing-Jong, Lin Ming-Wei, Hsu Chiao-Po, Chung Ming- |
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The ALDH2 Glu504Lys polymorphism is associated with coronary artery disease in Han Chinese: Relation with endothelial ADMA levels.
Atherosclerosis 2010 Aug 211 (2): 545-50. Guo Yi-Jie, Chen Lei, Bai Yong-Ping, Li Ling, Sun Ji, Zhang Guo-Gang, Yang Tian-Lun, Xia Jian, Li Yuan-Jian, Chen Xiao-Pi |
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A novel loss-of-function DDAH1 promoter polymorphism is associated with increased susceptibility to thrombosis stroke and coronary heart disease.
Circulation research 2010 Apr 106 (6): 1145-52. Ding Hu, Wu Bin, Wang Hu, Lu Zhilan, Yan Jiangtao, Wang Xiaojing, Shaffer John R, Hui Rutai, Wang Dao W |
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Circulating methylarginine levels and the decline in renal function in patients with chronic kidney disease are modulated by DDAH1 polymorphisms.
Kidney international 2010 Mar 77 (5): 459-67. Caplin Ben, Nitsch Dorothea, Gill Herpreet, Hoefield Richard, Blackwell Scott, MacKenzie Douglas, Cooper Jackie A, Middleton Rachel J, Talmud Philippa J, Veitch Peter, Norman Jill, Wheeler David C, Leiper James |
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Sequence variation in DDAH1 and DDAH2 genes is strongly and additively associated with serum ADMA concentrations in individuals with type 2 diabetes.
PloS one 2010 5 (3): e9462. Abhary Sotoodeh, Burdon Kathryn P, Kuot Abraham, Javadiyan Shahrbanou, Whiting Malcolm J, Kasmeridis Nicholas, Petrovsky Nikolai, Craig Jamie |
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Haplotypic association of DDAH1 with susceptibility to pre-eclampsia.
Molecular human reproduction 2005 Jan 11 (1): 73-7. Akbar Fareeza, Heinonen Seppo, Pirskanen Mia, Uimari Pekka, Tuomainen Tomi-Pekka, Salonen Jukka |
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Relationship between DDAH gene variants and serum ADMA level in individuals with type 1 diabetes.
Journal of diabetes and its complications 0 26 (3): 195-8. Fogarty Rhys D, Abhary Sotoodeh, Javadiyan Shahrbanou, Kasmeridis Nicholas, Petrovsky Nikolai, Whiting Malcolm J, Craig Jamie E, Burdon Kathryn |
- Page last reviewed:Oct 1, 2020
- Page last updated:Apr 22, 2021
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