[1]
|
Chauvet, C., Ménard, A., Xiao, C., Aguila, B., Blain, M., Roy, J. and Deng, A.Y. (2012) Novel genes as primary triggers for polygenic hypertension. Journal of Hypertension, 30, 81-86. doi:10.1097/HJH.0b013e32834dddb1
|
[2]
|
Simino, J., Shi, G., Kume, R., Schwander, K., Province, M.A., Gu, C.C., Kardia, S., Chakravarti, A., Ehret, G., Olshen, R.A., Turner, S.T., Ho, L.T., Zhu, X., Jaquish, C., Paltoo, D., Cooper, R.S., Weder, A., Curb, J.D., Boerwin-kle, E., Hunt, S.C. and Rao, D.C. (2011) Five blood pressure loci identified by an updated genome-wide link-age scan: Meta-analysis of the Family Blood Pressure Program. American Journal of Hypertension, 24, 347-354. doi:10.1038/ajh.2010.238
|
[3]
|
Johnson, M.D., He, L., Herman, D., Wakimoto, H., Wal-lace, C.A., Zidek, V., Mlejnek, P., Musilova, A., Simakova, M., Vorlicek, J., Kren, V., Viklicky, O., Qi, N.R., Wang, J., Seidman, C.E., Seidman, J., Kurtz, T.W., Aitman, T.J. and Pravenec, M. (2009) Dissection of chromosome 18 blood pressure and salt-sensitivity quan-titative trait loci in the spontaneously hypertensive rat. Hypertension, 54, 639-645.
doi:10.1161/HYPERTENSIONAHA.108.126664
|
[4]
|
Deng, A.Y. (2007) Genetic basis of polygenic hyperten-sion. Human Molecular Genetics, 16, R195-R202.
doi:10.1093/hmg/ddm126
|
[5]
|
Cowley Jr., A.W. (2006) The genetic dissection of essen-tial hypertension. Nature Reviews Genetics, 7, 829-840.
doi:10.1038/nrg1967
|
[6]
|
Twigger, S.N., Shimoyama, M., Bromberg, S., Kwitek, A.E., Jacob, H.J. and RGD Team (2007) The Rat Gen-ome Database, update 2007—Easing the path from dis-ease to data and back again. Nucleic Acids Research, 35, D658-D662. doi:10.1093/nar/gkl988
|
[7]
|
Tobin, M.D., Tomaszewski, M., Braund, P.S., Hajat, C., Raleigh, S.M., Palmer, T.M., Caulfield, M., Burton, P.R. and Samani, N.J. (2008) Common variants in genes un-derlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension, 51, 1658-1664.
doi:10.1161/HYPERTENSIONAHA.108.112664
|
[8]
|
Thomas, G.N., Critchley, J.A., Tomlinson, B., Cockram, C.S. and Chan, J.C. (2001) Relationships between the taqI polymorphism of the dopamine D2 receptor and blood pressure in hyperglycaemic and normoglycaemic Chinese subjects. Clinical Endocrinology, 55, 605-611.
|
[9]
|
Xiong, Q., Qiu, Y. and Gu, W. (2008) PGMapper: A web-based tool linking phenotype to genes. Bioinformat-ics, 24, 1011-1013. doi:10.1093/bioinformatics/btn002
|
[10]
|
Lander, E. and Kruglyak, L. (1995) Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results. Nature Genetics, 11, 241-247.
doi:10.1038/ng1195-241
|
[11]
|
Van Ooijen, J.W. (1992) Accuracy of mapping quan-titative trait loci in autogamous species. TAG Theoretical and Applied Genetics, 84, 9.
|
[12]
|
Yasui, N., Kajimoto, K., Sumiya, T., Okuda, T. and Iwai, N. (2007) The monocyte chemotactic protein-1 gene may contribute to hypertension in Dahl salt-sensitive rats. Hy-pertension Research, 30, 185-193.
doi:10.1291/hypres.30.185
|
[13]
|
Denag, A.Y. (1998) Is the nitric oxide system involved in genetic hypertension in Dahl rats? Kidney International, 53, 1501-1511. doi:10.1046/j.1523-1755.1998.00933.x
|
[14]
|
Ye, P. and West, M.J. (2003) Cosegregation analysis of natriuretic peptide genes and blood pressure in the spon-taneously hypertensive rat. Clinical and Experimental Pharmacology and Physiology, 30, 930-936.
doi:10.1111/j.1440-1681.2003.03937.x
|
[15]
|
Suthanthiran, M., Li, B., Song, J.O., Ding, R., Sharma, V.K., Schwartz, J.E. and August, P. (2000) Transforming growth factor-beta-1 hyperexpression in African-Ameri-can hypertensives: A novel mediator of hypertension and/or target organ damage. Proceedings of the National Academy of Sciences, 97, 3479-3484.
|
[16]
|
Petretto, E., Sarwar, R., Grieve, I., Lu, H., Kumaran, M.K., Muckett, P.J., Mangion, J., Schroen, B., Benson, M., Punjabi, P.P., Prasad, S.K., Pennell, D.J., Kiesewetter, C., Tasheva, E.S., Corpuz, L.M., Webb, M.D., Conrad, G.W., Kurtz, T.W., Kren, V., Fischer, J., Hubner, N., Pinto, Y.M., Pravenec, M., Aitman, T.J. and Cook, S.A. (2008) Integrated genomic approaches implicate osteo-glycin (Ogn) in the regulation of left ventricular mass. Nature Genetics, 40, 546-552. doi:10.1038/ng.134
|
[17]
|
Frikke-Schmidt, R., Sing, C.F., Nordestgaard, B.G., Stef-fensen, R. and Tybjaerg-Hansen, A. (2007) Subsets of SNPs define rare genotype classes that predict ischemic heart disease. Human Genetics, 120, 865-877.
doi:10.1007/s00439-006-0233-y
|
[18]
|
Koo, B.K., Cho, Y.M., Park, B.L., Cheong, H.S., Shin, H.D., Jang, H.C., Kim, S.Y., Lee, H.K. and Park, K.S. (2007) Polymorphisms of KCNJ11 (Kir6.2 gene) are associated with Type 2 diabetes and hypertension in the Korean population. Diabetic Medicine, 24, 178-186.
doi:10.1111/j.1464-5491.2006.02050.x
|
[19]
|
Kokubo, Y., Tomoike, H., Tanaka, C., Banno, M., Okuda, T., Inamoto, N., Kamide, K., Kawano, Y. and Miyata, T. (2006) Association of sixty-one non-synonymous poly-merphisms in forty-one hypertension candidate genes with blood pressure variation and hypertension. Hyper-tension Research, 29, 611-619.
doi:10.1291/hypres.29.611
|
[20]
|
Iwai, N., Tago, N., Yasui, N., Kokubo, Y., Inamoto, N., Tomoike, H. and Shioji, K. (2004) Genetic analysis of 22 candidate genes for hypertension in the Japanese popu-lation. Journal of Hypertension, 22, 1119-1126.
doi:10.1097/00004872-200406000-00012
|
[21]
|
Busjahn, A., Aydin, A., Uhlmann, R., Krasko, C., B?h-ring, S., Szelestei, T., Feng, Y., Dahm, S., Sharma, A.M., Luft, F.C. and Lang, F. (2002) Serum-and glucocorti-coid-regulated kinase (SGK1) gene and blood pressure. Hypertension, 40, 256-260.
doi:10.1161/01.HYP.0000030153.19366.26
|
[22]
|
Trochen, N., Ganapathipillai, S., Ferrari, P., Frey, B.M. and Frey, F.J. (2004) Low prevalence of nonconservative mutations of serum and glucocorticoid-regulated kinase (SGK1) gene in hypertensive and renal patients. Ne-phrology Dialysis Transplantation, 19, 2499-2504.
doi:10.1093/ndt/gfh417
|
[23]
|
Lazar, A., Zimmermann, T., Koch, W., Gründemann, D., Sch?mig, A., Kastrati, A. and Sch?mig, E. (2006) Lower prevalence of the OCT2 Ser270 allele in patients with essential hypertension. Clinical and Experimental Hy-pertension, 28, 645-653.
doi:10.1080/10641960600946411
|
[24]
|
Wang, L., Feng, Y., Zhang, Y., Zhou, H., Jiang, S., Niu, T., Wei, L.J., Xu, X., Xu, X. and Wang, X. (2006) Proly-lcarboxypeptidase gene, chronic hypertension, and risk of preeclampsia. American Journal of Obstetrics & Gyne-cology, 195, 162-171. doi:10.1016/j.ajog.2006.01.079
|
[25]
|
Tobin, M.D., Tomaszewski, M., Braund PS, Hajat C, Raleigh SM, Palmer TM, Caulfield, M., Burton, P.R. and Samani, N.J. (2008) Common variants in genes under-lying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension, 51, 1658-1664.
doi:10.1161/HYPERTENSIONAHA.108.112664
|
[26]
|
Büsst, C.J., Scurrah, K.J., Ellis, J.A. and Harrap, S.B. (2007) Selective genotyping reveals association between the epithelial sodium channel gamma-subunit and systolic blood pressure. Hypertension, 50, 672-678.
doi:10.1161/HYPERTENSIONAHA.107.089128
|
[27]
|
Iwai, N., Baba, S., Mannami, T., Katsuya, T., Higaki, J., Ogihara, T. and Ogata, J. (2001) Association of sodium channel gamma-subunit promoter variant with blood pressure. Hypertension, 38, 86-89.
doi:10.1161/01.HYP.38.1.86
|
[28]
|
Sáez, M.E., Martínez-Larrad, M.T., Ramírez-Lorca, R., González-Sánchez, J.L., Zabena, C., Martinez-Calatrava, M.J., González, A., Morón, F.J., Ruiz, A. and Serrano-Ríos, M. (2007) Calpain-5 gene variants are associated with diastolic blood pressure and cholesterol levels. BMC Medical Genetics, 8, 1.
|
[29]
|
Iwai, N., Kajimoto, K., Kokubo, Y. and Tomoike, H. (2006) Extensive genetic analysis of 10 candidate genes for hypertension in Japanese. Hypertension, 48, 901-907.
doi:10.1161/01.HYP.0000242485.23148.bb
|
[30]
|
Ji, Q., Ikegami, H., Fujisawa, T., Kawabata, Y., Ono, M., Nishino, M., Ohishi, M., Katsuya, T., Rakugi, H. and Ogihara, T. (2004) A common polymorphism of uncou-pling protein 2 gene is associated with hypertension. Journal of Hypertension, 22, 97-102.
doi:10.1097/00004872-200401000-00018
|
[31]
|
Matsunaga, T., Gu, N., Yamazaki, H., Tsuda, M., Adachi, T., Yasuda, K., Moritani, T., Tsuda, K., Nonaka, M. and Nishiyama, T. (2009) Association of UCP2 and UCP3 polymorphisms with heart rate variability in Japanese men. Journal of Hypertension, 27, 305-313.
doi:10.1097/HJH.0b013e32831ac967
|
[32]
|
Mar?ano, A.C., Burke, B., Gungadoo, J., Wallace, C., Kaisaki, P.J., Woon, P.Y., Farrall, M., Clayton, D., Brown, M., Dominiczak, A., Connell, J.M., Webster, J., Lathrop, M., Caulfield, M., Samani, N., Gauguier, D., Munroe, P.B. (2007) Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension. Journal of Medical Genetics, 44, 603-605.
doi:10.1136/jmg.2007.049718
|
[33]
|
Gaukrodger, N., Avery, P.J. and Keavney, B. (2008) Plasma potassium level is associated with common ge-netic variation in the beta-subunit of the epithelial sodium channel. American Journal of Physiology—Regulatory, Integrative and Comparative Physiology, 294, R1068-R1072. doi:10.1152/ajpregu.00732.2007
|
[34]
|
Jin, Y., Kuznetsova, T., Tikhonoff, V., Thijs, L., Hasenk-amp, S., B?umer, V., Stolarz-Skrzypek, K., Ryabikov, A., Richart, T., Malyutina, S., Nikitin, Y., Casiglia, E., Kawecka-Jaszcz, K., Olszanecka, A., Brand-Herrmann, S.M., Brand, E., Fagard, R., Staessen, J.A. and European Project on Genes in Hypertension (EPOGH) Investigators (2009) Left ventricular structure in relation to the human SAH gene in the European Project on Genes in Hyper-tension. Hypertension Research, 32, 145-151.
doi:10.1038/hr.2008.3
|
[35]
|
Tikhonoff, V., Staessen, J.A., Kuznetsova, T., Thijs, L., Hasenkamp, S., B?umer, V., Stolarz, K., Seidlerová, J., Filipovsky, J., Nikitin, Y., Peleska, J., Kawecka-Jaszcz, K., Casiglia, E., Brand-Herrmann, S.M., Brand, E. and European Project on Genes in Hypertension (EPOGH) Investigators (2008) SAH gene variants revisited in the European Project On Genes in Hypertension. Journal of Hypertension, 26, 244-250.
doi:10.1097/HJH.0b013e3282f2d36f
|
[36]
|
Yuan, Z., Su, Z., Miyoshi, T., Rowlan, J.S. and Shi, W. (2008) Quantitative trait locus analysis of circulating ad-hesion molecules in hyperlipidemic apolipoprotein E-de-ficient mice. Molecular Genetics and Genomics, 280, 375-383. Epub 2008 Aug 13.
doi:10.1007/s00438-008-0371-0
|
[37]
|
Okuda, T., Sumiya, T., Mizutani, K., Tago, N., Miyata, T., Tanabe, T., Kato, H., Katsuya, T., Higaki, J., Ogihara, T., Tsujita, Y. and Iwai, N. (2002) Analyses of differential gene expression in genetic hypertensive rats by microa-rray. Hypertension Research, 25, 249-255.
doi:10.1291/hypres.25.249
|
[38]
|
Tripodi, G., Modica, R., Stella, A., Bigatti, G., Bianchi, G. and Stella, P. (2005) Haplotype analysis of carnitine transporters and left ventricular mass in human essential hypertension. Journal of Renal Nutrition, 15, 2-7.
doi:10.1053/j.jrn.2004.09.035
|
[39]
|
Kohara, K., Tabara, Y., Nakura, J., Imai, Y., Ohkubo, T., Hata, A., Soma, M., Nakayama, T., Umemura, S., Hirawa, N., Ueshima, H., Kita, Y., Ogihara, T., Katsuya, T., Taka-hashi, N., Tokunaga, K. and Miki, T. (2008) Identification of hypertension-susceptibility genes and pathways by a systemic multiple candidate gene approach: The millennium genome project for hypertension. Hypertension Research, 31, 203-212. doi:10.1291/hypres.31.203
|
[40]
|
Kawaguchi, Y., Tochimoto, A., Hara, M., Kawamoto, M., Sugiura, T., Katsumata, Y., Okada, J., Kondo, H., Okubo, M. and Kamatani, N. (2006) NOS2 polymorphisms asso-ciated with the susceptibility to pulmonary arterial hy-pertension with systemic sclerosis: Contribution to the transcriptional activity. Arthritis Research & Therapy, 8, R104. doi:10.1186/ar1984
|
[41]
|
Jemaa, R., Ben, A.S., Kallel, A., Omar, S., Feki, M., El-asmi, M., Haj-Ta?eb, S., Sanhaji, H. and Kaabachi, N. (2009) Association between the -2518G/A polymorphism in the monocyte chemoattractant protein-1 (MCP-1) gene and hypertension in Tunisian patients. Clinical Biochemistry, 42, 34-37.
doi:10.1016/j.clinbiochem.2008.09.118
|
[42]
|
Quintana, L.F., Guzmán, B., Collado, S., Clària, J. and Poch, E. (2006) A coding polymorphism in the 12-lipo-xygenase gene is associated to essential hypertension and urinary 12(S)-HETE. Kidney International, 69, 526-530.
doi:10.1038/sj.ki.5000147
|
[43]
|
Omi, T., Kumada, M., Kamesaki, T., Okuda, H., Munkhtulga, L., Yanagisawa, Y., Utsumi, N., Gotoh, T., Hata, A., Soma, M., Umemura, S., Ogihara, T., Takahashi, N., Tabara, Y., Shimada, K., Mano, H., Kajii, E., Miki, T. and Iwamoto, S. (2006) An intronic variable number of tandem repeat polymorphisms of the cold-induced autoinflammatory syndrome 1 (CIAS1) gene modifies gene expression and is associated with essential hyper-tension. European Journal of Human Genetics, 14, 1295-1305. doi:10.1038/sj.ejhg.5201698
|
[44]
|
Timasheva, Y.R., Nasibullin, T.R., Zakirova, A.N. and Mustafina, O.E. (2008) Association of interleukin-6, interleukin-12, and interleukin-10 gene polymorphisms with essential hypertension in Tatars from Russia. Biochemical Genetics, 46, 64-74.
doi:10.1007/s10528-007-9130-x
|
[45]
|
Sink, K.M., Leng, X., Williamson, J., Kritchevsky, S.B., Yaffe, K., Kuller, L., Yasar, S., Atkinson, H., Robbins, M., Psaty, B. and Goff, D.C. Jr. (2009) Angiotensin-converting enzyme inhibitors and cognitive decline in older adults with hypertension: results from the Cardio-vascular Health Study. Archives of Internal Medicine, 169, 1195-1202. doi:10.1001/archinternmed.2009.175
|
[46]
|
Woo, S.W., Bang, S., Chung, M.W., Jin, S.K., Kim, Y.S. and Lee, S.H. (2009) Lack of association between ACE and bradykinin B2 receptor gene polymorphisms and ACE inhibitor-induced coughing in hypertensive Koreans. Journal of Clinical Pharmacy and Therapeutics, 34, 561-567. doi:10.1111/j.1365-2710.2009.01028.x
|
[47]
|
Kokubo, Y., Tomoike, H., Tanaka, C., Banno, M., Okuda, T., Inamoto, N., Kamide, K., Kawano, Y. and Miyata, T. (2006) Association of sixty-one non-synonymous poly-morphisms in forty-one hypertension candidate genes with blood pressure variation and hypertension. Hyper-tension Research, 29, 611-619.
doi:10.1291/hypres.29.611
|
[48]
|
Palijan, A., Lambert, R., Dutil, J., Sivo, Z. and Deng, A.Y. (2003) Comprehensive congenic coverage revealing mul-tiple blood pressure quantitative trait loci on Dahl rat chromosome 10. Hypertension, 42, 515-522.
doi:10.1161/01.HYP.0000090096.88509.15
|
[49]
|
Jung, J., Foroud, T.M., Eckert, G.J., Flury-Wetherill, L., Edenberg, H.J., Xuei, X., Zaidi, S.A. and Pratt, J.H. (2009) Association of the calcium-sensing receptor gene with blood pressure and urinary calcium in African-Americans. Journal of Clinical Endocrinology & Me-tabolism, 94, 1042-1048. doi:10.1210/jc.2008-1861
|
[50]
|
Tobin, M.D., Tomaszewski, M., Braund, P.S., Hajat, C., Raleigh, S.M., Palmer, T.M., Caulfield, M., Burton, P.R. and Samani, N.J. (2008) Common variants in genes un-derlying monogenic hypertension and hypotension and blood pressure in the general population. Hypertension, 51, 1658-1664.
doi:10.1161/HYPERTENSIONAHA.108.112664
|
[51]
|
Wessel, J., Topol, E.J., Ji, M., Meyer, J. and McCarthy, J.J. (2004) Replication of the association between the thrombospondin-4 A387P polymorphism and myocardial infarction. American Heart Journal, 147, 905-909.
doi:10.1016/j.ahj.2003.12.013
|
[52]
|
Gigante, B., Bellis, A., Visconti, R., Marino, M., Morisco, C., Trimarco, V., Galasso, G., Piscione, F., De Luca, N., Prince, J.A., de Faire, U. and Trimarco, B. (2007) Retrospective analysis of coagulation factor II receptor (F2R) sequence variation and coronary heart disease in hypertensive patients. Arteriosclerosis, Thrombosis, and Vascular Biology, 27, 1213-1219.
doi:10.1161/ATVBAHA.107.140541
|
[53]
|
Pitzalis, M.V., Sarzani, R., Dessì-Fulgheri, P., Iacoviello, M., Forleo, C., Lucarelli, K., Pietrucci, F., Salvi, F., Sorrentino, S., Romito, R., Guida, P., Rappelli, A. and Rizzon, P. (2003) Allelic variants of natriuretic peptide receptor genes are associated with family history of hypertension and cardiovascular phenotype. Journal of Hypertension, 21, 1491-1496.
doi:10.1097/00004872-200308000-00012
|
[54]
|
Horan, M., Newsway, V., Yasmin, Lewis, M.D., Easter, T.E., Rees, D.A., Mahto, A., Millar, D.S., Procter, A.M., Scanlon, M.F., Wilkinson, I.B., Hall, I.P., Wheatley, A., Blakey, J., Bath, P.M., Cockcroft, J.R., Krawczak, M. and Cooper, D.N. (2006) Genetic variation at the growth hormone (GH1) and growth hormone receptor (GHR) loci as a risk factor for hypertension and stroke. Human Genetics, 119, 527-540. doi:10.1007/s00439-006-0166-5
|
[55]
|
Rice, T., Rankinen, T., Province, M.A., Chagnon, Y.C., Pérusse, L., Borecki, I.B., Bouchard, C. and Rao, D.C. (2000) Genome-wide linkage analysis of systolic and diastolic blood pressure: The Québec Family Study. Circulation, 102, 1956-1963.
doi:10.1161/01.CIR.102.16.1956
|
[56]
|
Capoluongo, E., Onder, G., Concolino, P., Russo, A., Santonocito, C., Bernabei, R., Zuppi, C., Ameglio, F. and Landi, F. (2009) GSTM1-null polymorphism as possible risk marker for hypertension: results from the aging and longevity study in the Sirente Geographic Area (ilSIRENTE study). Clinica Chimica Acta, 399, 92-96.
doi:10.1016/j.cca.2008.09.017
|
[57]
|
Woon, P.Y., Kaisaki, P.J., Bragan?a, J., Bihoreau, M.T., Levy, J.C., Farrall, M. and Gauguier, D. (2007) Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetes. Proceedings of the National Academy of Sciences, 104, 14412-14417.
doi:10.1073/pnas.0703247104
|
[58]
|
Liu, J., Li, M., Qi, M.L., Liu, X.L., Li, Y.H., Fu, L.Y. and Zhao, Y.Y. (2007) Association of -63A/C polymorphism of glutathione S-transferase M3 gene with essential hypertension in Chinese population. Chinese Journal of Medical Genetics, 24, 582-585.
|
[59]
|
Delles, C., Padmanabhan, S., Lee, W.K., Miller, W.H., McBride, M.W., McClure, J.D., Brain, N.J., Wallace, C., Mar?ano, A.C., Schmieder, R.E., Brown, M.J., Caulfield, M.J., Munroe, P.B., Farrall, M., Webster, J., Connell, J.M. and Dominiczak, A.F. (2008) Glutathione S-transferase variants and hypertension. Journal of Hypertension, 26, 1343-1352. doi:10.1097/HJH.0b013e3282fe1d67
|
[60]
|
Motone, M., Katsuya, T., Ishikawa, K., Iwashima, Y., Sugimoto, K., Yamamoto, K., Fu, Y., Matsuo, A., Ohishi, M., Rakugi, H. and Ogihara, T. (2004) Association be-tween hepatocyte growth factor gene polymorphism and essential hypertension. Hypertension Research, 27, 247-251. doi:10.1291/hypres.27.247
|
[61]
|
Takiuchi, S., Mannami, T., Miyata, T., Kamide, K., Ta-naka, C., Kokubo, Y., Koyama, Y., Inamoto, N., Katsuya, T., Iwai, N., Kawano, Y., Ogihara, T. and Tomoike, H. (2004) Identification of 21 single nucleotide polymer-phisms in human hepatocyte growth factor gene and as-sociation with blood pressure and carotid atherosclerosis in the Japanese population. Atherosclerosis, 173, 301-307.
doi:10.1016/j.atherosclerosis.2003.12.020
|
[62]
|
Genelhu, V.A., Celoria, B.M., Pimentel, M.M., Duarte, S.F., Cabello, P.H. and Francischetti, E.A. (2009) Asso-ciation of a common variant of the leptin gene with blood pressure in an obese Brazilian population. American Journal of Hypertension, 22, 577-580.
doi:10.1038/ajh.2009.7
|
[63]
|
Hou, X.W., Wang, L.F., Wang, N., Pang, D., Hui, B., Zhou, Y.L. and He, X. (2008) The G501C polymorphism of oxidized LDL receptor gene [OLR-1] is associated with susceptibility and serum C-reactive protein concen-tration in Chinese essential hypertensives. Clinica Chi-mica Acta, 388, 200-203. doi:10.1016/j.cca.2007.11.016
|
[64]
|
Lan?a, V., Alcantara, P., Braz-Nogueira, J. and Bicho, M.P. (2004) Cytochrome P450 1A1 (CYP1A1) T6325C polymorphism might modulate essential hypertension-associated stroke risk. Revista Portuguesa de Cardiologia, 23, 343-355.
|
[65]
|
Corbetta, S., Eller-Vainicher, C., Frigerio, M., Valaperta, R., Costa, E., Vicentini, L., Baccarelli, A., Beck-Peccoz, P. and Spada, A. (2009) Analysis of the 206 M polymer-phic variant of the SLC26A6 gene encoding a Cloxalate transporter in patients with primary hyperparathyroidism. European Journal of Endocrinology, 160, 283-288.
doi:10.1530/EJE-08-0623
|
[66]
|
Wen, G., Wessel, J., Zhou, W., Ehret, G.B., Rao, F., Stridsberg, M., Mahata, S.K., Gent, P.M., Das, M., Coo-per, R.S., Chakravarti, A., Zhou, H., Schork, N.J., O’Connor, D.T. and Hamilton, B.A. (2007) An ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertension. Human Molecular Genetics, 16, 1752-1764.
doi:10.1093/hmg/ddm123
|
[67]
|
Dries, D.L., Victor, R.G., Rame, J.E., Cooper, R.S., Wu, X., Zhu, X., Leonard, D., Ho, S.I., Wu, Q., Post, W. and Drazner, M.H. (2005) Corin gene minor allele defined by 2 missense mutations is common in blacks and associated with high blood pressure and hypertension. Circulation, 112, 2403-2410.
doi:10.1161/CIRCULATIONAHA.105.568881
|
[68]
|
Wang, W., Liao, X., Fukuda, K., Knappe, S., Wu, F., Dries, D.L., Qin, J. and Wu, Q. (2008) Corin variant as-sociated with hypertension and cardiac hypertrophy ex-hibits impaired zymogen activation and natriuretic pep-tide processing activity. Circulation Research, 103, 502-508. doi:10.1161/CIRCRESAHA.108.177352
|
[69]
|
Naganuma, T., Nakayama, T., Sato, N., Fu, Z., Soma, M., Aoi, N. and Usami, R. (2008) A haplotype-based case-control study examining human extracellular superoxide dismutase gene and essential hypertension. Hypertension Research, 31, 1533-1540. doi:10.1291/hypres.31.1533
|
[70]
|
Manunta, P. and Bianchi, G. (2006) Pharmacogenomics and pharmacogenetics of hypertension: Update and per-spectives--The adducin paradigm. Journal of the Ameri-can Society of Nephrology, 17, S30-S35.
doi:10.1681/ASN.2005121346
|
[71]
|
Mandò, C., Antonazzo, P., Tabano, S., Zanutto, S., Pileri, P., Somigliana, E., Colleoni, F., Martinelli, A., Zolin, A., Benedetto, C., Marozio, L., Neri, I., Facchinetti, F., Miozzo, M. and Cetin, I. (2009) Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension. Reproductive Sciences, 16, 819-826. doi:10.1177/1933719109336612
|
[72]
|
Cohn, H.I., Xi, Y., Pesant, S., Harris, D.M., Hyslop, T., Falkner, B. and Eckhart, A.D. (2009) G protein-coupled receptor kinase 2 expression and activity are associated with blood pressure in black Americans. Hypertension, 54, 71-76.
doi:10.1161/HYPERTENSIONAHA.108.125955
|
[73]
|
Yamada, Y., Matsuo, H., Segawa, T., Watanabe, S., Kato, K., Hibino, T., Yokoi, K., Ichihara, S., Metoki, N., Yo-shida, H., Satoh, K. and Nozawa, Y. (2006) Assessment of the genetic component of hypertension. American Journal of Hypertension, 19, 1158-1165.
doi:10.1016/j.amjhyper.2006.04.010
|
[74]
|
Seasholtz, T.M., Wessel, J., Rao, F., Rana, B.K., Khan-drika, S., Kennedy, B.P., Lillie, E.O., Ziegler, M.G., Smith, D.W., Schork, N.J., Brown, J.H. and O’Connor, D.T. (2006) Rho kinase polymorphism influences blood pressure and systemic vascular resistance in human twins: role of heredity. Hypertension, 47, 937-947.
doi:10.1161/01.HYP.0000217364.45622.f0
|
[75]
|
Murray, F., Patel, H.H., Suda, R.Y., Zhang, S., This-tlethwaite, P.A., Yuan, J.X. and Insel, P.A. (2007) Ex-pression and activity of cAMP phosphodiesterase iso-forms in pulmonary artery smooth muscle cells from pa-tients with pulmonary hypertension: role for PDE1. American Journal of Physiology—Lung Cellular and Molecular Physiology, 292, L294-L303.
doi:10.1152/ajplung.00190.2006
|
[76]
|
Lee, J., Kim, S., Kim, J., Jeong, M.H., Oh, Y. and Choi, K.C. (2006) Increased expression of renal aquaporin wa-ter channels in spontaneously hypertensive rats. Kidney and Blood Pressure Research, 29, 18-23.
doi:10.1159/000092483
|
[77]
|
Liaw, C.W., Lovenberg, T.W., Barry, G., Oltersdorf, T., Grigoriadis, D.E. and De Souza, E.B. (1996) Cloning and characterization of the human corticotropin-releasing factor-2 receptor complementary deoxyribonucleic acid. Endocrinology, 137, 72-77. doi:10.1210/en.137.1.72
|
[78]
|
Briscoe, R.J., Cabrera, C.L., Baird, T.J., Rice, K.C. and Woods, J.H. (2000) Antalarmin blockade of corticotropin releasing hormone-induced hypertension in rats. Brain Research, 881, 204-207.
doi:10.1016/S0006-8993(00)02742-6
|