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Journal Abstract Search

272 related items for PubMed ID: 24562681

  • 1. Genetic association studies of endothelial nitric oxide synthase gene polymorphisms in women with unexplained recurrent pregnancy loss: a systematic and meta-analysis.
    Cao Y, Zhang Z, Xu J, Wang J, Yuan W, Shen Y, Du J.
    Mol Biol Rep; 2014 Jun; 41(6):3981-9. PubMed ID: 24562681
    [Abstract] [Full Text] [Related]

  • 2. Association of endothelial nitric oxide synthase gene variants (-786 T>C, intron 4 b/a VNTR and 894 G>T) with idiopathic recurrent pregnancy loss: A case-control study with haplotype and in silico analysis.
    Azani A, Hosseinzadeh A, Azadkhah R, Zonouzi AAP, Zonouzi AP, Aftabi Y, Khani H, Heidary L, Danaii S, Bargahi N, Pouladi N, Hosseini SM.
    Eur J Obstet Gynecol Reprod Biol; 2017 Aug; 215():93-100. PubMed ID: 28605668
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  • 3. Association study between methylenetetrahydrofolate reductase polymorphisms and unexplained recurrent pregnancy loss: a meta-analysis.
    Cao Y, Xu J, Zhang Z, Huang X, Zhang A, Wang J, Zheng Q, Fu L, Du J.
    Gene; 2013 Feb 10; 514(2):105-11. PubMed ID: 23201418
    [Abstract] [Full Text] [Related]

  • 4. Endothelial nitric oxide (eNOS) gene G894T and VNTR polymorphisms are closely associated with the risk of ischemic stroke development for Asians: meta-analysis of epidemiological studies.
    Guo X.
    Mol Biol Rep; 2014 Feb 10; 41(4):2571-83. PubMed ID: 24573998
    [Abstract] [Full Text] [Related]

  • 5. The association of Intron 4 VNTR and Glu298Asp polymorphisms of the nitric oxide synthetase 3 gene and vasculogenic erectile dysfunction in Turkish men.
    Arda E, Ay A, Akdere H, Akdeniz E.
    Syst Biol Reprod Med; 2019 Oct 10; 65(5):383-389. PubMed ID: 30977424
    [Abstract] [Full Text] [Related]

  • 6. Endothelial nitric oxide synthase gene polymorphisms and risk of erectile dysfunction: An updated meta-analysis of genetic association studies.
    Yao HX, Ma FZ, Tan YY, Liu LY.
    Int J Surg; 2018 Jun 10; 54(Pt A):141-148. PubMed ID: 29654965
    [Abstract] [Full Text] [Related]

  • 7. Endothelial nitric oxide synthase gene polymorphisms in recurrent spontaneous abortions.
    Karvela M, Papadopoulou S, Tsaliki E, Konstantakou E, Hatzaki A, Florentin-Arar L, Lamnissou K.
    Arch Gynecol Obstet; 2008 Oct 10; 278(4):349-52. PubMed ID: 18299866
    [Abstract] [Full Text] [Related]

  • 8. A meta-analysis for association of eNOS VNTR 4b/a,  - 786 T > C and + 894G > T polymorphisms with risk of recurrent pregnancy loss.
    Golestanpour H, Bahrami R, Dastgheib SA, Tabatabaei RS, Javaheri A, Karimi-Zarchi M, Mirjalili SR, Neamatzadeh H.
    Arch Gynecol Obstet; 2021 Nov 10; 304(5):1135-1151. PubMed ID: 34387724
    [Abstract] [Full Text] [Related]

  • 9. Genetic analysis of eNOS gene polymorphisms in association with recurrent miscarriage among North Indian women.
    Parveen F, Faridi RM, Alam S, Agrawal S.
    Reprod Biomed Online; 2011 Jul 10; 23(1):124-31. PubMed ID: 21565555
    [Abstract] [Full Text] [Related]

  • 10. An updated meta-analysis of endothelial nitric oxide synthase gene: three well-characterized polymorphisms with ischemic stroke.
    Yao YS, Chang WW, Jin YL, He LP.
    Gene; 2013 Oct 10; 528(2):84-92. PubMed ID: 23845784
    [Abstract] [Full Text] [Related]

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  • 12. Genetic association studies of angiogenesis- and vasoconstriction-related genes in women with recurrent pregnancy loss: a systematic review and meta-analysis.
    Su MT, Lin SH, Chen YC.
    Hum Reprod Update; 2011 Oct 10; 17(6):803-12. PubMed ID: 21642294
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  • 15. The Endothelial Nitric Oxide Synthase Gene T-786C Polymorphism Increases Myocardial Infarction Risk: A Meta-Analysis.
    Kong XZ, Zhang ZY, Wei LH, Li R, Yu J.
    Med Sci Monit; 2017 Feb 11; 23():759-766. PubMed ID: 28188309
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  • 17. Association between eNOS gene polymorphisms and the risk of unexplained recurrent spontaneous abortion in Yunnan province, China.
    Zou L, Dong W, Ai Y, Li Y, Cheng Y, Feng Y.
    Technol Health Care; 2024 Feb 11; 32(3):1871-1879. PubMed ID: 37840513
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  • 19. Association between endothelial nitric oxide synthase Glu298Asp gene polymorphism and diabetic nephropathy susceptibility.
    Zhou TB, Xu HL, Yin SS.
    Ren Fail; 2013 Feb 11; 35(1):173-8. PubMed ID: 23113598
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