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Association of ATP1A1 and dear single-nucleotide polymorphism haplotypes with essential hypertension: sex-specific and haplotype-specific effects.Circ Res. 2007 May 25;100(10):1522-9. doi: 10.1161/01.RES.0000267716.96196.60. Epub 2007 Apr 19.
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Association of novel promoter single nucleotide polymorphisms in vasopressin V1a receptor gene with essential hypertension in nonobese Japanese.J Hum Hypertens. 2007 Oct;21(10):825-7. doi: 10.1038/sj.jhh.1002227. Epub 2007 Jul 26.
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Differential gene expression of bradykinin receptors 1 and 2 in peripheral monocytes from patients with essential hypertension.J Hum Hypertens. 2014 Jul;28(7):450-5. doi: 10.1038/jhh.2013.133. Epub 2014 Jan 9.
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Functional promoter polymorphisms direct the expression of cystathionine gamma-lyase gene in mouse models of essential hypertension.J Mol Cell Cardiol. 2017 Jan;102:61-73. doi: 10.1016/j.yjmcc.2016.11.005. Epub 2016 Nov 16.
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Human dopamine beta-hydroxylase (DBH) regulatory polymorphism that influences enzymatic activity, autonomic function, and blood pressure.J Hypertens. 2010 Jan;28(1):76-86. doi: 10.1097/HJH.0b013e328332bc87.
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Aberrant methylation of the GCK gene body is associated with the risk of essential hypertension.Mol Med Rep. 2015 Aug;12(2):2390-4. doi: 10.3892/mmr.2015.3631. Epub 2015 Apr 16.
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The Orexin System and Hypertension.Cell Mol Neurobiol. 2018 Mar;38(2):385-391. doi: 10.1007/s10571-017-0487-z. Epub 2017 Mar 27.
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Effects of combined statin and ACE inhibitor therapy on endothelial function and blood pressure in essential hypertension - a randomised double-blind, placebo controlled crossover study.J Renin Angiotensin Aldosterone Syst. 2019 Jul-Sep;20(3):1470320319868890. doi: 10.1177/1470320319868890.
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Is there an association between T102C polymorphism of the serotonin receptor 2A gene and urinary incontinence?.Braz J Med Biol Res. 2007 Oct;40(10):1315-22. doi: 10.1590/s0100-879x2006005000151. Epub 2007 Jul 31.
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The gene polymorphism of LOX1 predicts the incidence of LVH in patients with essential hypertension.Cell Physiol Biochem. 2014;33(1):88-96. doi: 10.1159/000356652. Epub 2014 Jan 17.
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Chronic administration of sildenafil improves endothelial function in spontaneously hypertensive rats by decreasing COX-2 expression and oxidative stress.Life Sci. 2019 May 15;225:29-38. doi: 10.1016/j.lfs.2019.03.074. Epub 2019 Mar 30.
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Phenylethanolamine N-methyltransferase gene promoter haplotypes and risk of essential hypertension.Am J Hypertens. 2011 Nov;24(11):1222-6. doi: 10.1038/ajh.2011.124. Epub 2011 Aug 25.
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Polymorphisms and haplotype of ROCK2 associate with high altitude essential hypertension in native high altitude Ladakhi Indian population: a preliminary study.Clin Exp Hypertens. 2016;38(2):238-44. doi: 10.3109/10641963.2015.1081231. Epub 2016 Jan 28.
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A polymorphism in the norepinephrine transporter gene is associated with affective and cardiovascular disease through a microRNA mechanism.Mol Psychiatry. 2017 Jan;22(1):134-141. doi: 10.1038/mp.2016.40. Epub 2016 Apr 5.
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Cross talk between plasma membrane Na(+)/Ca (2+) exchanger-1 and TRPC/Orai-containing channels: key players in arterial hypertension.Adv Exp Med Biol. 2013;961:365-74. doi: 10.1007/978-1-4614-4756-6_31.
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The role of adenosine-related genes variants in susceptibility to essential hypertension.J Hypertens. 2004 Aug;22(8):1519-22. doi: 10.1097/01.hjh.0000133723.16947.6d.
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Variability in phenylephrine response and essential hypertension: a search for human alpha(1B)-adrenergic receptor polymorphisms.J Pharmacol Exp Ther. 1999 Nov;291(2):793-8.
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Genetic determinants of essential hypertension in the population of Tatars from Russia.J Hypertens. 2017 May;35 Suppl 1:S16-S23. doi: 10.1097/HJH.0000000000001332.
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Polymorphisms of APLN-APLNR system are associated with essential hypertension in Mexican-Mestizo individuals.Exp Mol Pathol. 2016 Aug;101(1):105-9. doi: 10.1016/j.yexmp.2016.07.007. Epub 2016 Jul 20.
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Association and interaction of -58C>T and 9 bp polymorphisms of BDKRB2 gene causing susceptibility to essential hypertension.Clin Exp Hypertens. 2012;34(3):230-5. doi: 10.3109/10641963.2011.631653. Epub 2012 Apr 2.
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Association of a BLVRA common polymorphism with essential hypertension and blood pressure in Kazaks.Clin Exp Hypertens. 2011;33(5):294-8. doi: 10.3109/10641963.2010.531854. Epub 2011 Jul 1.
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Association study of calcitonin-receptor-like receptor gene in essential hypertension.Am J Hypertens. 2005 Mar;18(3):403-8. doi: 10.1016/j.amjhyper.2004.10.016.
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Increased arterial pressure in mice with overexpression of the ADHD candidate gene calcyon in forebrain. PLoS One. 2019 Feb 12;14(2):e0211903. doi: 10.1371/journal.pone.0211903. eCollection 2019.
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CXCL13 polymorphism is associated with essential hypertension in Tatars from Russia.Mol Biol Rep. 2018 Oct;45(5):1557-1564. doi: 10.1007/s11033-018-4257-x. Epub 2018 Jul 17.
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Associations between CLCNKA_B tag SNPs with essential hypertension and interactions between genetic and environmental factors in an island population in China.Clin Exp Hypertens. 2015;37(7):519-25. doi: 10.3109/10641963.2015.1013124. Epub 2015 Apr 28.
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Association of CLCNKB haplotypes and hypertension in Mongolian and Han populations.Clin Exp Hypertens. 2012;34(7):482-7. doi: 10.3109/10641963.2012.666602. Epub 2012 May 11.
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Protective effect of the 1742(C/G) polymorphism of human cardiotrophin-1 against left ventricular hypertrophy in essential hypertension.J Hypertens. 2010 Nov;28(11):2219-26. doi: 10.1097/HJH.0b013e32833da326.
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Common polymorphisms in the CYP11B1 and CYP11B2 genes: evidence for a digenic influence on hypertension.Hypertension. 2013 Jan;61(1):232-9. doi: 10.1161/HYPERTENSIONAHA.112.200741. Epub 2012 Nov 12.
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Associations between ADRB1 and CYP2D6 gene polymorphisms and the response to -blocker therapy in hypertension.J Int Med Res. 2015 Jun;43(3):424-34. doi: 10.1177/0300060514563151. Epub 2015 Mar 30.
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A comprehensive study revealed SNP-SNP interactions and a sex-dependent relationship between polymorphisms of the CYP2J2 gene and hypertension risk.Hypertens Res. 2019 Feb;42(2):257-272. doi: 10.1038/s41440-018-0142-1. Epub 2018 Dec 5.
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Investigation of the association between dopamine D1 receptor gene polymorphisms and essential hypertension in a group of Turkish subjects.Clin Exp Hypertens. 2011;33(6):418-21. doi: 10.3109/10641963.2011.561898. Epub 2011 Jul 28.
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Ser9Gly polymorphism in the dopamine D3 receptor gene is not associated with essential hypertension in the Japanese.Med Sci Monit. 2002 Jan;8(1):CR1-4.
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Association of single nucleotide polymorphisms in endothelin family genes with the progression of atherosclerosis in patients with essential hypertension.J Hum Hypertens. 2007 Nov;21(11):883-92. doi: 10.1038/sj.jhh.1002234. Epub 2007 May 24.
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Quantitative association between a newly identified molecular variant in the endothelin-2 gene and human essential hypertension.J Hypertens. 1999 Sep;17(9):1281-7. doi: 10.1097/00004872-199917090-00007.
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Speckle-Tracking Echocardiographic Layer-Specific Strain Analysis on Subclinical Left Ventricular Dysfunction in Patients With Primary Aldosteronism.Am J Hypertens. 2019 Jan 15;32(2):155-162. doi: 10.1093/ajh/hpy175.
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Relationship between EPHX2 gene polymorphisms and essential hypertension in Uygur, Kazakh, and Han.Genet Mol Res. 2015 Apr 15;14(2):3474-80. doi: 10.4238/2015.April.15.11.
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Association of single nucleotide polymorphisms in the 3'UTR of ERAP1 gene with essential hypertension in the Northeastern Han Chinese.Gene. 2015 Apr 15;560(2):211-6. doi: 10.1016/j.gene.2015.02.005. Epub 2015 Feb 7.
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The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations.Hum Genet. 2009 Nov;126(5):655-66. doi: 10.1007/s00439-009-0714-x. Epub 2009 Jul 4.
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Association of ACE, FABP2 and GST genes polymorphism with essential hypertension risk among a North Indian population.Ann Hum Biol. 2015;42(5):461-9. doi: 10.3109/03014460.2014.968206. Epub 2014 Oct 30.
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Association between fatty acid binding protein 3 gene variants and essential hypertension in humans.Am J Hypertens. 2008 Jun;21(6):691-5. doi: 10.1038/ajh.2008.40. Epub 2008 Apr 10.
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Mutation of the follicle-stimulating hormone receptor gene 5'-untranslated region associated with female hypertension.Hypertension. 2006 Sep;48(3):512-8. doi: 10.1161/01.HYP.0000233877.84343.d7. Epub 2006 Jul 24.
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Associations between genetic variations in the FURIN gene and hypertension.BMC Med Genet. 2010 Aug 13;11:124. doi: 10.1186/1471-2350-11-124.
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Screening for the Gly40Ser mutation in the glucagon receptor gene among patients with type 2 diabetes or essential hypertension in Taiwan.Pancreas. 1999 Mar;18(2):151-5. doi: 10.1097/00006676-199903000-00006.
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Association between 1019C/T polymorphism in the connexin 37 gene and essential hypertension.Heart Lung Circ. 2014 Oct;23(10):924-9. doi: 10.1016/j.hlc.2014.02.016. Epub 2014 Mar 12.
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Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men.J Hypertens. 2006 Feb;24(2):325-30. doi: 10.1097/01.hjh.0000200512.40818.47.
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Association of an intronic variant of the heme oxygenase-1 gene with hypertension in northern Chinese Han population.Clin Exp Hypertens. 2009 Oct;31(7):534-43. doi: 10.3109/10641960902825461.
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The dominant models of KCNJ11 E23K and KCNMB1 E65K are associated with essential hypertension (EH) in Asian: Evidence from a meta-analysis.Medicine (Baltimore). 2019 Jun;98(23):e15828. doi: 10.1097/MD.0000000000015828.
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Common variation in KLKB1 and essential hypertension risk: tagging-SNP haplotype analysis in a case-control study.Hum Genet. 2007 May;121(3-4):327-35. doi: 10.1007/s00439-007-0340-4. Epub 2007 Feb 23.
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A rare variant at the KYNU gene is associated with kynureninase activity and essential hypertension in the Han Chinese population.Circ Cardiovasc Genet. 2011 Dec;4(6):687-94. doi: 10.1161/CIRCGENETICS.110.959064. Epub 2011 Oct 19.
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Apolipoprotein(a) gene polymorphism in the Korean population: is there any relevance to essential hypertension?.Med Princ Pract. 2002 Apr-Jun;11(2):69-74. doi: 10.1159/000058010.
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A study of lipoprotein lipase gene intron 8 polymorphisms in Chinese Han race essential hypertension patients.Int J Cardiol. 2005 Mar 18;99(2):263-7. doi: 10.1016/j.ijcard.2004.01.015.
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Lanosterol Synthase Gene Polymorphisms and Changes in Endogenous Ouabain in the Response to Low Sodium Intake.Hypertension. 2016 Feb;67(2):342-8. doi: 10.1161/HYPERTENSIONAHA.115.06415. Epub 2015 Dec 14.
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Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension.Hum Genet. 2001 Oct;109(4):408-15. doi: 10.1007/s004390100565.
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Chronic treatment with C-type natriuretic peptide impacts differently in the aorta of normotensive and hypertensive rats.Pflugers Arch. 2019 Aug;471(8):1103-1115. doi: 10.1007/s00424-019-02287-y. Epub 2019 Jun 11.
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Association of NPRA and NPRC gene variants and hypertension in Mongolian population.Genet Mol Res. 2015 Dec 28;14(4):18494-502. doi: 10.4238/2015.December.23.37.
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Association of NPR3 polymorphism with risk of essential hypertension in a Chinese population.J Clin Pharm Ther. 2017 Oct;42(5):554-560. doi: 10.1111/jcpt.12549. Epub 2017 May 11.
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Risk of new-onset autoimmune diseases in primary aldosteronism: a nation-wide population-based study.J Hypertens. 2020 Apr;38(4):745-754. doi: 10.1097/HJH.0000000000002300.
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Cotransporters, WNKs and hypertension: an update.Curr Opin Nephrol Hypertens. 2008 Mar;17(2):186-92. doi: 10.1097/MNH.0b013e3282f5244e.
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The obesity-related polymorphism PCSK1 rs6235 is associated with essential hypertension in the Han Chinese population.Hypertens Res. 2012 Oct;35(10):994-9. doi: 10.1038/hr.2012.79. Epub 2012 May 17.
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Association of polymorphisms in prolylcarboxypeptidase and chymase genes with essential hypertension in the Chinese Han population.J Renin Angiotensin Aldosterone Syst. 2013 Sep;14(3):263-70. doi: 10.1177/1470320312448949. Epub 2012 Jun 7.
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Influence of PRKCH gene polymorphism on antihypertensive response to amlodipine and telmisartan.Clin Exp Hypertens. 2017;39(8):726-731. doi: 10.1080/10641963.2017.1324475. Epub 2017 Jun 22.
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Association of genetic variations of the prostasin gene with essential hypertension in the Xinjiang Kazakh population.Chin Med J (Engl). 2011 Jul;124(14):2107-12.
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Association between prostaglandin E2 receptor gene and essential hypertension.Prostaglandins Leukot Essent Fatty Acids. 2007 Jul;77(1):15-20. doi: 10.1016/j.plefa.2007.04.004. Epub 2007 Jul 20.
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Rare SNP rs12731181 in the miR-590-3p Target Site of the Prostaglandin F2 Receptor Gene Confers Risk for Essential Hypertension in the Han Chinese Population.Arterioscler Thromb Vasc Biol. 2015 Jul;35(7):1687-95. doi: 10.1161/ATVBAHA.115.305445. Epub 2015 May 14.
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The RGS2 (-391, C>G) genetic variation correlates to antihypertensive drug responses in Chinese patients with essential hypertension.PLoS One. 2015 Apr 7;10(4):e0121483. doi: 10.1371/journal.pone.0121483. eCollection 2015.
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Sympathetic nervous system, genes and human essential hypertension.Curr Neurovasc Res. 2005 Oct;2(4):303-17. doi: 10.2174/156720205774322575.
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E-selectin gene in essential hypertension: a case-control study.Eur J Clin Invest. 2018 Jan;48(1). doi: 10.1111/eci.12868. Epub 2017 Dec 13.
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Interaction of alpha(1)-Na,K-ATPase and Na,K,2Cl-cotransporter genes in human essential hypertension.Hypertension. 2001 Aug;38(2):204-9. doi: 10.1161/01.hyp.38.2.204.
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Urate transporter gene SLC22A12 polymorphisms associated with obesity and metabolic syndrome in Caucasians with hypertension.Kidney Blood Press Res. 2012;35(6):477-82. doi: 10.1159/000337370. Epub 2012 Jun 8.
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Lower prevalence of the OCT2 Ser270 allele in patients with essential hypertension.Clin Exp Hypertens. 2006 Oct;28(7):645-53. doi: 10.1080/10641960600946411.
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Association of SLC6A9 gene variants with human essential hypertension.J Atheroscler Thromb. 2009 Jun;16(3):201-6. doi: 10.5551/jat.e125. Epub 2009 Jun 25.
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Association of the gene polymorphisms of BMPR2, ACVRL1, SMAD9 and their interactions with the risk of essential hypertension in the Chinese Han population.Biosci Rep. 2019 Jan 25;39(1):BSR20181217. doi: 10.1042/BSR20181217. Print 2019 Jan 31.
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Association of with-no-lysine kinase 1 and Serine/Threonine kinase 39 gene polymorphisms and haplotypes with essential hypertension in Tibetans.Environ Mol Mutagen. 2018 Mar;59(2):151-160. doi: 10.1002/em.22140. Epub 2017 Sep 25.
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Differences in TRPC3 and TRPC6 channels assembly in mesenteric vascular smooth muscle cells in essential hypertension.J Physiol. 2017 Mar 1;595(5):1497-1513. doi: 10.1113/JP273327. Epub 2016 Dec 29.
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Association of ACE, ACE2 and UTS2 polymorphisms with essential hypertension in Han and Dongxiang populations from north-western China.J Int Med Res. 2006 May-Jun;34(3):272-83. doi: 10.1177/147323000603400306.
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Susceptiveness of Vitamin K epOxide Reductase Complex Subunit 1 Gene Polymorphism in Essential Hypertension.Genet Test Mol Biomarkers. 2017 May;21(5):292-297. doi: 10.1089/gtmb.2016.0311. Epub 2017 Mar 10.
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Association of WNK1 exon 1 polymorphisms with essential hypertension in Hani and Yi minorities of China.J Genet Genomics. 2011 Apr 20;38(4):165-71. doi: 10.1016/j.jgg.2011.03.004. Epub 2011 Apr 13.
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Single nucleotide polymorphism of adiponectin +276 G/T is associated with the susceptibility to essential hypertension in a Turkish population.Clin Exp Hypertens. 2016;38(8):686-690. doi: 10.1080/10641963.2016.1200607. Epub 2016 Dec 9.
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ADRB3 Gene Trp64Arg Polymorphism and Essential Hypertension: A Meta-Analysis Including 9,555 Subjects.Front Genet. 2018 Apr 4;9:106. doi: 10.3389/fgene.2018.00106. eCollection 2018.
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Association between single-nucleotide polymorphisms in six hypertensive candidate genes and hypertension among northern Han Chinese individuals.Hypertens Res. 2014 Dec;37(12):1068-74. doi: 10.1038/hr.2014.124. Epub 2014 Aug 7.
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Neprilysin Inhibitors and Bradykinin.Front Med (Lausanne). 2018 Sep 19;5:257. doi: 10.3389/fmed.2018.00257. eCollection 2018.
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GNB3 C825T and ACE I/D polymorphisms on the sodium-proton exchanger and the prevalence of essential hypertension in males.Arch Med Res. 2006 Jan;37(1):150-7. doi: 10.1016/j.arcmed.2005.05.012.
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Catestatin: A Master Regulator of Cardiovascular Functions.Curr Med Chem. 2018;25(11):1352-1374. doi: 10.2174/0929867324666170425100416.
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Angiotensin II type 1 receptor gene polymorphism and essential hypertension in Serbian population.Clin Chim Acta. 2003 Jan;327(1-2):181-5. doi: 10.1016/s0009-8981(02)00340-6.
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Analysis of VNTRs in the solute carrier family 6, member 18 (SLC6A18) and lack of association with hypertension.DNA Cell Biol. 2008 Oct;27(10):559-67. doi: 10.1089/dna.2008.0755.
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The contribution of CYP2C gene subfamily involved in epoxygenase pathway of arachidonic acids metabolism to hypertension susceptibility in Russian population.Clin Exp Hypertens. 2017;39(4):306-311. doi: 10.1080/10641963.2016.1246562. Epub 2017 May 17.
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Endothelin 1 type a receptor antagonism prevents vascular dysfunction and hypertension induced by 11beta-hydroxysteroid dehydrogenase inhibition: role of nitric oxide.Circulation. 2001 Jun 26;103(25):3129-35. doi: 10.1161/01.cir.103.25.3129.
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Haplotype-based case-control study of the human CYP4F2 gene and essential hypertension in Japanese subjects.Hypertens Res. 2008 Sep;31(9):1719-26. doi: 10.1291/hypres.31.1719.
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Polymorphisms of the Flavin containing monooxygenase 3 (FMO3) gene do not predispose to essential hypertension in Caucasians.BMC Med Genet. 2005 Dec 2;6:41. doi: 10.1186/1471-2350-6-41.
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Association of HSD3B1 and HSD3B2 gene polymorphisms with essential hypertension, aldosterone level, and left ventricular structure.Eur J Endocrinol. 2010 Oct;163(4):671-80. doi: 10.1530/EJE-10-0428. Epub 2010 Jul 21.
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Associations of CYP4A11 gene-gene and gene-smoking interactions with essential hypertension in the male eastern Chinese Han population.Clin Exp Hypertens. 2017;39(5):448-453. doi: 10.1080/10641963.2016.1267201. Epub 2017 May 23.
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Two medium-chain acyl-coenzyme A synthetase genes, SAH and MACS1, are associated with plasma high-density lipoprotein cholesterol levels, but they are not associated with essential hypertension.J Hypertens. 2004 Oct;22(10):1903-7. doi: 10.1097/00004872-200410000-00012.
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Combined SSCP and heteroduplex analysis of the human plasma membrane Ca(2+)-ATPase isoform 1 in patients with essential hypertension.Biochem Biophys Res Commun. 1999 Aug 2;261(2):515-20. doi: 10.1006/bbrc.1999.1064.
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CLCNKB-T481S and essential hypertension in a Ghanaian population.J Hypertens. 2009 Feb;27(2):298-304. doi: 10.1097/hjh.0b013e3283140c9e.
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The C718T polymorphism in the 3'-untranslated region of glutathione peroxidase-4 gene is a predictor of cerebral stroke in patients with essential hypertension.Hypertens Res. 2012 May;35(5):507-12. doi: 10.1038/hr.2011.213. Epub 2011 Dec 8.
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Novel genetic variation in exon 28 of FBN1 gene is associated with essential hypertension.Am J Hypertens. 2011 Jun;24(6):687-93. doi: 10.1038/ajh.2011.21. Epub 2011 Feb 17.
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Association between the C3F-gene and essential hypertension.Clin Sci (Lond). 1981 Dec;61 Suppl 7:363s-365s. doi: 10.1042/cs061363s.
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Haptoglobin polymorphism, a genetic risk factor in coronary artery bypass surgery.Atherosclerosis. 1997 Jul 25;132(2):215-9. doi: 10.1016/s0021-9150(97)00089-0.
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Lack of association of functional variants in alpha-ENaC gene and essential hypertension in two ethnic groups in China.Kidney Blood Press Res. 2008;31(4):268-73. doi: 10.1159/000151286. Epub 2008 Aug 15.
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Association of SCNN1B promoter methylation with essential hypertension.Mol Med Rep. 2016 Dec;14(6):5422-5428. doi: 10.3892/mmr.2016.5905. Epub 2016 Oct 31.
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Genetic association of rs1800780 (AG) polymorphism of the eNOS gene with susceptibility to essential hypertension in a Chinese Han population.Biochem Genet. 2014 Feb;52(1-2):71-8. doi: 10.1007/s10528-013-9628-3. Epub 2013 Nov 29.
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Endothelial Gata5 transcription factor regulates blood pressure.Nat Commun. 2015 Nov 30;6:8835. doi: 10.1038/ncomms9835.
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Association of genetic polymorphisms of ACADSB and COMT with human hypertension.J Hypertens. 2007 Jan;25(1):103-10. doi: 10.1097/HJH.0b013e3280103a40.
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Polymorphisms in four candidate genes in young patients with essential hypertension.Acta Paediatr. 2006 Mar;95(3):353-8. doi: 10.1080/08035250500434777.
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Association between the C34T polymorphism of the AMPD1 gene and essential hypertension in Malaysian patients.Genet Mol Res. 2016 Jun 20;15(2). doi: 10.4238/gmr.15026241.
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A comprehensive contribution of genes for aryl hydrocarbon receptor signaling pathway to hypertension susceptibility.Pharmacogenet Genomics. 2017 Feb;27(2):57-69. doi: 10.1097/FPC.0000000000000261.
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Seven lessons from two candidate genes in human essential hypertension: angiotensinogen and epithelial sodium channel.Hypertension. 1999 Jun;33(6):1324-31. doi: 10.1161/01.hyp.33.6.1324.
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The human ATF1 rs11169571 polymorphism increases essential hypertension risk through modifying miRNA binding.FEBS Lett. 2015 Jul 22;589(16):2087-93. doi: 10.1016/j.febslet.2015.06.029. Epub 2015 Jul 3.
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Association of ATP1B1 single-nucleotide polymorphisms with blood pressure and hypertension in a Chinese population.Clin Chim Acta. 2009 Sep;407(1-2):47-50. doi: 10.1016/j.cca.2009.06.026. Epub 2009 Jun 27.
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Investigation of the Met-267 Arg exchange in isoform 1 of the human plasma membrane calcium pump in patients with essential hypertension by the amplification-created restriction site technique.J Mol Med (Berl). 1997 Jan;75(1):62-6. doi: 10.1007/s001090050088.
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Mitochondrial DNA 7908-8816 region mutations in maternally inherited essential hypertensive subjects in China.BMC Med Genomics. 2018 Oct 16;11(1):89. doi: 10.1186/s12920-018-0408-0.
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Association of single nucleotide polymorphisms in the 5' upstream region of the C4BPA gene with essential hypertension in a northeastern Han Chinese population.Mol Med Rep. 2017 Aug;16(2):1289-1297. doi: 10.3892/mmr.2017.6736. Epub 2017 Jun 9.
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Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study.Pharmacogenomics. 2014 Sep;15(13):1643-52. doi: 10.2217/pgs.14.119.
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Association of CAPN10 gene with insulin sensitivity, glucose tolerance and renal function in essential hypertensive patients.Clin Chim Acta. 2010 Aug 5;411(15-16):1126-31. doi: 10.1016/j.cca.2010.04.012. Epub 2010 Apr 18.
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High sodium-low potassium environment and hypertension.Am J Cardiol. 1976 Nov 23;38(6):768-85. doi: 10.1016/0002-9149(76)90356-8.
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Effects of sodium nitrite on renal function and blood pressure in hypertensive vs. healthy study participants: a randomized, placebo-controlled, crossover study.J Hypertens. 2018 Mar;36(3):666-679. doi: 10.1097/HJH.0000000000001598.
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A common genetic variant of FCN3/CD164L2 is associated with essential hypertension in a Chinese population.Clin Exp Hypertens. 2012;34(5):377-82. doi: 10.3109/10641963.2012.665538. Epub 2012 Apr 3.
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A novel CYBA variant, the -675A/T polymorphism, is associated with essential hypertension.J Hypertens. 2007 Aug;25(8):1620-6. doi: 10.1097/HJH.0b013e3281ac211d.
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