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148 related items for PubMed ID: 38765527

  • 21. Association study of dimethylarginine dimethylaminohydrolase 2 gene polymorphisms and coronary heart disease.
    Xu AG, Xu RM, Lu CQ, Li DD, Xu QF, Guo J, Fu X, Zhao W, Yao MY.
    Mol Med Rep; 2012 Nov; 6(5):1103-6. PubMed ID: 22923027
    [Abstract] [Full Text] [Related]

  • 22. Relationship between dimethylarginine dimethylaminohydrolase gene variants and asymmetric dimethylarginine in patients with rheumatoid arthritis.
    Dimitroulas T, Sandoo A, Hodson J, Smith J, Panoulas VF, Kitas GD.
    Atherosclerosis; 2014 Nov; 237(1):38-44. PubMed ID: 25194333
    [Abstract] [Full Text] [Related]

  • 23. Protective role of DDAH2 (rs805304) gene polymorphism in patients with myocardial infarction.
    Pérez-Hernández N, Vargas-Alarcón G, Arellano-Zapoteco R, Martínez-Rodríguez N, Fragoso JM, Aptilon-Duque G, Posadas-Sánchez R, Posadas-Romero C, Juárez-Cedillo T, Domínguez-López ML, Rodríguez-Pérez JM.
    Exp Mol Pathol; 2014 Dec; 97(3):393-8. PubMed ID: 25236572
    [Abstract] [Full Text] [Related]

  • 24. A comparison of maternal serum levels of endothelial nitric oxide synthase, asymmetric dimethylarginine, and homocysteine in normal and preeclamptic pregnancies.
    Laskowska M, Laskowska K, Terbosh M, Oleszczuk J.
    Med Sci Monit; 2013 Jun 05; 19():430-7. PubMed ID: 23739294
    [Abstract] [Full Text] [Related]

  • 25. The role of nitric oxide synthase inhibition by asymmetric dimethylarginine in the pathophysiology of preeclampsia.
    Böger RH, Diemert A, Schwedhelm E, Lüneburg N, Maas R, Hecher K.
    Gynecol Obstet Invest; 2010 Jun 05; 69(1):1-13. PubMed ID: 19828999
    [Abstract] [Full Text] [Related]

  • 26. Asymmetric dimethylarginine levels in preeclampsia - Systematic review and meta-analysis.
    Németh B, Murányi E, Hegyi P, Mátrai P, Szakács Z, Varjú P, Hamvas S, Tinusz B, Budán F, Czimmer J, Bérczi B, Erőss B, Gyöngyi Z, Kiss I.
    Placenta; 2018 Sep 05; 69():57-63. PubMed ID: 30213485
    [Abstract] [Full Text] [Related]

  • 27. The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
    Salimi S, Saravani M, Yaghmaei M, Fazlali Z, Mokhtari M, Naghavi A, Farajian-Mashhadi F.
    Arch Gynecol Obstet; 2015 Jun 05; 291(6):1303-12. PubMed ID: 25480409
    [Abstract] [Full Text] [Related]

  • 28. Ex vivo gene transferring of human dimethylarginine dimethylaminohydrolase-2 improved endothelial dysfunction in diabetic rat aortas and high glucose-treated endothelial cells.
    Lu CW, Guo Z, Feng M, Wu ZZ, He ZM, Xiong Y.
    Atherosclerosis; 2010 Mar 05; 209(1):66-73. PubMed ID: 19775692
    [Abstract] [Full Text] [Related]

  • 29. Role of asymmetric dimethylarginine in vascular injury in transgenic mice overexpressing dimethylarginie dimethylaminohydrolase 2.
    Hasegawa K, Wakino S, Tatematsu S, Yoshioka K, Homma K, Sugano N, Kimoto M, Hayashi K, Itoh H.
    Circ Res; 2007 Jul 20; 101(2):e2-10. PubMed ID: 17601800
    [Abstract] [Full Text] [Related]

  • 30. Common genetic variation in DDAH2 is associated with intracerebral haemorrhage in a Chinese population: a multi-centre case-control study in China.
    Bai Y, Chen J, Sun K, Xin Y, Liu J, Hui R.
    Clin Sci (Lond); 2009 Aug 17; 117(7):273-9. PubMed ID: 19250061
    [Abstract] [Full Text] [Related]

  • 31. [Relationship between changes of endogenous nitric oxide synthase inhibitor and hydrolase and initiation of pre-eclampsia].
    Huang YY, Yao XB, Lu XH, Liu HS, Chen DJ.
    Zhonghua Fu Chan Ke Za Zhi; 2009 Apr 17; 44(4):249-52. PubMed ID: 19570459
    [Abstract] [Full Text] [Related]

  • 32. Haplotypic association of DDAH1 with susceptibility to pre-eclampsia.
    Akbar F, Heinonen S, Pirskanen M, Uimari P, Tuomainen TP, Salonen JT.
    Mol Hum Reprod; 2005 Jan 17; 11(1):73-7. PubMed ID: 15501905
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  • 33. Estimation of asymmetric dimethylarginine (ADMA), placental growth factor (PLGF) and pentraxin 3 (PTX 3) in women with preeclampsia.
    Garg P, Jaryal AK, Kachhawa G, Deepak KK, Kriplani A.
    Pregnancy Hypertens; 2018 Oct 17; 14():245-251. PubMed ID: 29548740
    [Abstract] [Full Text] [Related]

  • 34. Accelerated onset of senescence of endothelial progenitor cells in patients with type 2 diabetes mellitus: role of dimethylarginine dimethylaminohydrolase 2 and asymmetric dimethylarginine.
    Yuan Q, Hu CP, Gong ZC, Bai YP, Liu SY, Li YJ, Jiang JL.
    Biochem Biophys Res Commun; 2015 Mar 20; 458(4):869-76. PubMed ID: 25701782
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  • 35. Gene transfer of dimethylarginine dimethylaminohydrolase-2 improves the impairments of DDAH/ADMA/NOS/NO pathway in endothelial cells induced by lysophosphatidylcholine.
    Feng M, Liu L, Guo Z, Xiong Y.
    Eur J Pharmacol; 2008 Apr 14; 584(1):49-56. PubMed ID: 18342305
    [Abstract] [Full Text] [Related]

  • 36. Dimethylarginine dimethylaminohydrolase 2 regulates nitric oxide synthesis and hemodynamics and determines outcome in polymicrobial sepsis.
    Lambden S, Kelly P, Ahmetaj-Shala B, Wang Z, Lee B, Nandi M, Torondel B, Delahaye M, Dowsett L, Piper S, Tomlinson J, Caplin B, Colman L, Boruc O, Slaviero A, Zhao L, Oliver E, Khadayate S, Singer M, Arrigoni F, Leiper J.
    Arterioscler Thromb Vasc Biol; 2015 Jun 14; 35(6):1382-92. PubMed ID: 25857313
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  • 37. Polymorphism (-499C/G) in DDAH2 promoter may act as a protective factor for metabolic syndrome: A case-control study in Azar-Cohort population.
    Faramarzi E, Aftabi Y, Ansarin K, Somi MH, Gilani N, Seyedrezazadeh E.
    Arch Endocrinol Metab; 2021 Nov 03; 65(4):443-449. PubMed ID: 34283907
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  • 38. Effects of NAMPT polymorphisms and haplotypes on circulating visfatin/NAMPT levels in hypertensive disorders of pregnancy.
    Luizon MR, Belo VA, Palei AC, Amaral LM, Lacchini R, Sandrim VC, Duarte G, Cavalli RC, Tanus-Santos JE.
    Hypertens Res; 2015 May 03; 38(5):361-6. PubMed ID: 25716650
    [Abstract] [Full Text] [Related]

  • 39. DDAH2 alleviates myocardial fibrosis in diabetic cardiomyopathy through activation of the DDAH/ADMA/NOS/NO pathway in rats.
    Zhu ZD, Ye JM, Fu XM, Wang XC, Ye JY, Wu XR, Hua P, Liao YQ, Xuan W, Duan JL, Li WY, Fu H, Xia ZH, Zhang X.
    Int J Mol Med; 2019 Feb 03; 43(2):749-760. PubMed ID: 30569164
    [Abstract] [Full Text] [Related]

  • 40. Polymorphisms in endothelial nitric oxide synthase gene in early and late severe preeclampsia.
    Alpoim PN, Gomes KB, Pinheiro Mde B, Godoi LC, Jardim LL, Muniz LG, Sandrim VC, Fernandes AP, Dusse LM.
    Nitric Oxide; 2014 Nov 15; 42():19-23. PubMed ID: 25106888
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