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340 related items for PubMed ID: 30284143

  • 1. AGXT2 and DDAH-1 genetic variants are highly correlated with serum ADMA and SDMA levels and with incidence of coronary artery disease in Egyptians.
    Amir M, Hassanein SI, Abdel Rahman MF, Gad MZ.
    Mol Biol Rep; 2018 Dec; 45(6):2411-2419. PubMed ID: 30284143
    [Abstract] [Full Text] [Related]

  • 2. Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.
    Seppälä I, Kleber ME, Lyytikäinen LP, Hernesniemi JA, Mäkelä KM, Oksala N, Laaksonen R, Pilz S, Tomaschitz A, Silbernagel G, Boehm BO, Grammer TB, Koskinen T, Juonala M, Hutri-Kähönen N, Alfthan G, Viikari JS, Kähonen M, Raitakari OT, März W, Meinitzer A, Lehtimäki T, AtheroRemo Consortium.
    Eur Heart J; 2014 Feb; 35(8):524-31. PubMed ID: 24159190
    [Abstract] [Full Text] [Related]

  • 3. Alanine-glyoxylate aminotransferase 2 (AGXT2) polymorphisms have considerable impact on methylarginine and β-aminoisobutyrate metabolism in healthy volunteers.
    Kittel A, Müller F, König J, Mieth M, Sticht H, Zolk O, Kralj A, Heinrich MR, Fromm MF, Maas R.
    PLoS One; 2014 Feb; 9(2):e88544. PubMed ID: 24586340
    [Abstract] [Full Text] [Related]

  • 4. Effects of AGXT2 variants on blood pressure and blood sugar among 750 older Japanese subjects recruited by the complete enumeration survey method.
    Yoshino Y, Kumon H, Mori T, Yoshida T, Tachibana A, Shimizu H, Iga JI, Ueno SI.
    BMC Genomics; 2021 Apr 20; 22(1):287. PubMed ID: 33879046
    [Abstract] [Full Text] [Related]

  • 5. Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine.
    Lüneburg N, Lieb W, Zeller T, Chen MH, Maas R, Carter AM, Xanthakis V, Glazer NL, Schwedhelm E, Seshadri S, Ikram MA, Longstreth WT, Fornage M, König IR, Loley C, Ojeda FM, Schillert A, Wang TJ, Sticht H, Kittel A, König J, Benjamin EJ, Sullivan LM, Bernges I, Anderssohn M, Ziegler A, Gieger C, Illig T, Meisinger C, Wichmann HE, Wild PS, Schunkert H, Psaty BM, Wiggins KL, Heckbert SR, Smith N, Lackner K, Lunetta KL, Blankenberg S, Erdmann J, Munzel T, Grant PJ, Vasan RS, Böger RH.
    Circ Cardiovasc Genet; 2014 Dec 20; 7(6):864-72. PubMed ID: 25245031
    [Abstract] [Full Text] [Related]

  • 6. Genetic variations in the alanine-glyoxylate aminotransferase 2 (AGXT2) gene and dimethylarginines levels in rheumatoid arthritis.
    Dimitroulas T, Hodson J, Panoulas VF, Sandoo A, Smith J, Kitas G.
    Amino Acids; 2017 Jun 20; 49(6):1133-1141. PubMed ID: 28357606
    [Abstract] [Full Text] [Related]

  • 7. Considerable impacts of AGXT2 V140I polymorphism on chronic heart failure in the Chinese population.
    Hu XL, Zhou JP, Kuang DB, Qi H, Peng LM, Yang TL, Li X, Zhang W, Zhou HH, Chen XP.
    Atherosclerosis; 2016 Aug 20; 251():255-262. PubMed ID: 27423328
    [Abstract] [Full Text] [Related]

  • 8. Association of the AGXT2 V140I polymorphism with risk for coronary heart disease in a Chinese population.
    Zhou JP, Bai YP, Hu XL, Kuang DB, Shi RZ, Xiong Y, Zhang W, Xia J, Chen BL, Yang TL, Chen XP.
    J Atheroscler Thromb; 2014 Aug 20; 21(10):1022-30. PubMed ID: 24834905
    [Abstract] [Full Text] [Related]

  • 9. Overexpression of alanine-glyoxylate aminotransferase 2 protects from asymmetric dimethylarginine-induced endothelial dysfunction and aortic remodeling.
    Rodionov RN, Jarzebska N, Burdin D, Todorov V, Martens-Lobenhoffer J, Hofmann A, Kolouschek A, Cordasic N, Jacobi J, Rubets E, Morawietz H, O'Sullivan JF, Markov AG, Bornstein SR, Hilgers K, Maas R, Pfluecke C, Chen Y, Bode-Böger SM, Hugo CPM, Hohenstein B, Weiss N.
    Sci Rep; 2022 Jun 07; 12(1):9381. PubMed ID: 35672381
    [Abstract] [Full Text] [Related]

  • 10. 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.
    Tanhäuserová V, Tomandl J, Pácal L, Klepárník M, Malúšková D, Bartáková V, Kuricová K, Rehořová J, Stěpánková S, Svojanovský J, Olšovský J, Bělobrádková J, Krusová D, Jurajda M, Mužík J, Pavlík T, Kaňková K.
    Kidney Blood Press Res; 2012 Jun 07; 36(1):200-8. PubMed ID: 23147199
    [Abstract] [Full Text] [Related]

  • 11. Genetic variation in the dimethylarginine dimethylaminohydrolase 1 gene (DDAH1) is related to asymmetric dimethylarginine (ADMA) levels, but not to endothelium-dependent vasodilation.
    Lind L, Ingelsson E, Kumar J, Syvänen AC, Axelsson T, Teerlink T.
    Vasc Med; 2013 Aug 07; 18(4):192-9. PubMed ID: 23892448
    [Abstract] [Full Text] [Related]

  • 12. Age-related changes in ADMA-DDAH-NO pathway in rat liver subjected to partial ischemia followed by global reperfusion.
    Trocha M, Merwid-Ląd A, Chlebda-Sieragowska E, Szuba A, Pieśniewska M, Fereniec-Gołębiewska L, Kwiatkowska J, Szeląg A, Sozański T.
    Exp Gerontol; 2014 Feb 07; 50():45-51. PubMed ID: 24269305
    [Abstract] [Full Text] [Related]

  • 13. Assessment of serum levels of asymmetric dimethylarginine, symmetric dimethylarginine and L-arginine in coronary artery disease.
    Gad MZ, Hassanein SI, Abdel-Maksoud SM, Shaban GM, Abou-Aisha K, Elgabarty HA.
    Biomarkers; 2010 Dec 07; 15(8):746-52. PubMed ID: 20936901
    [Abstract] [Full Text] [Related]

  • 14. Role of alanine:glyoxylate aminotransferase 2 in metabolism of asymmetric dimethylarginine in the settings of asymmetric dimethylarginine overload and bilateral nephrectomy.
    Rodionov RN, Martens-Lobenhoffer J, Brilloff S, Hohenstein B, Jarzebska N, Jabs N, Kittel A, Maas R, Weiss N, Bode-Böger SM.
    Nephrol Dial Transplant; 2014 Nov 07; 29(11):2035-42. PubMed ID: 25002409
    [Abstract] [Full Text] [Related]

  • 15. Human alanine-glyoxylate aminotransferase 2 lowers asymmetric dimethylarginine and protects from inhibition of nitric oxide production.
    Rodionov RN, Murry DJ, Vaulman SF, Stevens JW, Lentz SR.
    J Biol Chem; 2010 Feb 19; 285(8):5385-91. PubMed ID: 20018850
    [Abstract] [Full Text] [Related]

  • 16. Associations of functional alanine-glyoxylate aminotransferase 2 gene variants with atrial fibrillation and ischemic stroke.
    Seppälä I, Kleber ME, Bevan S, Lyytikäinen LP, Oksala N, Hernesniemi JA, Mäkelä KM, Rothwell PM, Sudlow C, Dichgans M, Mononen N, Vlachopoulou E, Sinisalo J, Delgado GE, Laaksonen R, Koskinen T, Scharnagl H, Kähönen M, Markus HS, März W, Lehtimäki T.
    Sci Rep; 2016 Mar 17; 6():23207. PubMed ID: 26984639
    [Abstract] [Full Text] [Related]

  • 17. Missense variants of the alanine: glyoxylate aminotransferase 2 gene correlated with carotid atherosclerosis in the Japanese population.
    Yoshino Y, Kohara K, Abe M, Ochi S, Mori Y, Yamashita K, Igase M, Tabara Y, Mori T, Miki T, Ueno S.
    J Biol Regul Homeost Agents; 2014 Mar 17; 28(4):605-14. PubMed ID: 25620171
    [Abstract] [Full Text] [Related]

  • 18. The Second Life of Methylarginines as Cardiovascular Targets.
    Jarzebska N, Mangoni AA, Martens-Lobenhoffer J, Bode-Böger SM, Rodionov RN.
    Int J Mol Sci; 2019 Sep 17; 20(18):. PubMed ID: 31533264
    [Abstract] [Full Text] [Related]

  • 19. Dimethylarginine Dimethylaminohydrolase 1 Polymorphisms and Venous Intimal Hyperplasia in Hemodialysis Patients.
    Wu CC, Hsieh MY, Lee CK, Chuang SY, Chung MY, Lin CC.
    Am J Nephrol; 2019 Sep 17; 50(6):454-464. PubMed ID: 31639806
    [Abstract] [Full Text] [Related]

  • 20. AGXT2: An unnegligible aminotransferase in cardiovascular and urinary systems.
    Hu XL, Li MP, Song PY, Tang J, Chen XP.
    J Mol Cell Cardiol; 2017 Dec 17; 113():33-38. PubMed ID: 28970090
    [Abstract] [Full Text] [Related]

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