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Journal Abstract Search

196 related items for PubMed ID: 26823875

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  • 2. The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide synthase 3 gene polymorphisms.
    Ilguy S, Cilingir O, Bilgec MD, Ozalp O, Erzurumluoglu Gokalp E, Arslan S, Tekin N, Aydemir O, Erol N, Colak E, Gursoy H.
    Ophthalmic Genet; 2021 Dec; 42(6):725-731. PubMed ID: 34346275
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  • 3. Endothelial nitric oxide synthase gene T-786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity.
    Rusai K, Vannay A, Szebeni B, Borgulya G, Fekete A, Vásárhelyi B, Tulassay T, Szabó AJ.
    Mol Vis; 2008 Feb 05; 14():286-90. PubMed ID: 18334945
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  • 4. Endothelial nitric oxide synthase genotypes in the etiology of retinopathy of prematurity in premature infants.
    Yanamandra K, Napper D, Pramanik A, Bocchini JA, Dhanireddy R.
    Ophthalmic Genet; 2010 Dec 05; 31(4):173-7. PubMed ID: 20809776
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  • 5. Functional Variations in the NOS3 Gene Are Associated With Erectile Dysfunction Susceptibility, Age of Onset and Severity in a Han Chinese Population.
    Yang B, Liu L, Peng Z, Lu D, Ren Z, Liu S, Yang X, Liao J, Dong Q.
    J Sex Med; 2017 Apr 05; 14(4):551-557. PubMed ID: 28268155
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  • 9. Association of NOS2 and NOS3 gene polymorphisms with susceptibility to type 2 diabetes mellitus and diabetic nephropathy in the Chinese Han population.
    Chen F, Li YM, Yang LQ, Zhong CG, Zhuang ZX.
    IUBMB Life; 2016 Jul 05; 68(7):516-25. PubMed ID: 27192959
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  • 11. [Single nucleotide polymorphisms in NOS3 A-922G, T-786C and G894T: a correlation study of the distribution of their allelic combinations with hypertension in chinese Han population].
    Ma HX, Xie ZX, Niu YH, Li ZY, Zhou P.
    Yi Chuan; 2006 Jan 05; 28(1):3-10. PubMed ID: 16469708
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  • 14. 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
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  • 18. Promoter polymorphism T-786C, 894G→T at exon 7 of endothelial nitric oxide synthase gene are associated with risk of osteoporosis in Sichuan region male residents.
    Gu Z, Zhang Y, Qiu G.
    Int J Clin Exp Pathol; 2015 Oct 10; 8(11):15270-4. PubMed ID: 26823879
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  • 19. Functional G894T (rs1799983) polymorphism and intron-4 VNTR variant of nitric oxide synthase (NOS3) gene are susceptibility biomarkers of obesity among Tunisians.
    Nasr HB, Dimassi S, M'hadhbi R, Debbabi H, Kortas M, Tabka Z, Chahed K.
    Obes Res Clin Pract; 2016 Oct 10; 10(4):465-75. PubMed ID: 25956856
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