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2. Padhi, Udit Narayan, Mulkalwar, Madhubala, Saikrishna, Lakkakula, Verma, Henu Kumar, Bhaskar, Lvks. . NOS3 gene intron 4 a/b polymorphism is associated with ESRD in autosomal dominant polycystic kidney disease patients. In Jornal brasileiro de nefrologia, 44, 224-231. doi:10.1590/2175-8239-JBN-2021-0089. https://pubmed.ncbi.nlm.nih.gov/35138322/
3. Vučić, N L J, Nikolić, Z Z, Vukotić, V D, Savić-Pavićević, D L J, Brajušković, G N. 2017. NOS3 gene variants and male infertility: Association of 4a/4b with oligoasthenozoospermia. In Andrologia, 50, . doi:10.1111/and.12817. https://pubmed.ncbi.nlm.nih.gov/28466478/
4. Pereira, Tiago V, Rudnicki, Martina, Cheung, Bernard M Y, Pereira, Alexandre C, Krieger, José E. . Three endothelial nitric oxide (NOS3) gene polymorphisms in hypertensive and normotensive individuals: meta-analysis of 53 studies reveals evidence of publication bias. In Journal of hypertension, 25, 1763-74. doi:. https://pubmed.ncbi.nlm.nih.gov/17762636/
5. Zeng, Zhen, Li, Lina, Zhang, Zhao, He, Lin, Shi, Yongyong. 2010. A meta-analysis of three polymorphisms in the endothelial nitric oxide synthase gene (NOS3) and their effect on the risk of diabetic nephropathy. In Human genetics, 127, 373-81. doi:10.1007/s00439-009-0783-x. https://pubmed.ncbi.nlm.nih.gov/20049477/
6. de Aragão Santos, Thaysa Walléria, Dos Santos Catena, Andriu, da Silva Mattos, Sandra, de Lima Filho, José Luiz, Gondim Martins, Danyelly Bruneska. 2020. The incidence of NOS3 gene polymorphisms on newborns with large and small birth weight. In Molecular biology reports, 47, 8545-8552. doi:10.1007/s11033-020-05897-3. https://pubmed.ncbi.nlm.nih.gov/33063148/
7. Isaiev, Oleksii, Serdiuk, Valerii, Ziablitsev, Denys. . PREDICTING THE OCCURRENCE OF PRIMARY OPEN-ANGLE GLAUCOMA DEPENDING ON THE GENETIC POLYMORPHISM ENDOTHELIAL NO SYNTHASE (NOS3) GENE. In Wiadomosci lekarskie (Warsaw, Poland : 1960), 75, 3087-3093. doi:10.36740/WLek202212133. https://pubmed.ncbi.nlm.nih.gov/36723332/
8. Zhou, Yan, Yu, Hongsong, Hou, Shengping, Kijlstra, Aize, Yang, Peizeng. 2016. Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese. In Molecular vision, 22, 311-8. doi:. https://pubmed.ncbi.nlm.nih.gov/27114698/
9. Aytac, Hasan M, Pehlivan, Mustafa, Oyaci, Yasemin, Pehlivan, Sacide. . Association of intron 4 VNTR polymorphism in the NOS3 gene with rapid cycling and treatment resistance in bipolar disorder: a case-control study. In Neurosciences (Riyadh, Saudi Arabia), 27, 229-236. doi:10.17712/nsj.2022.4.20220040. https://pubmed.ncbi.nlm.nih.gov/36252968/
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