Lack of Association of the Mitochondrial DNA 5178 A/C Polymorphism with Hypertension in a Korean Population |
Kang, Byung-Yong
(Research Institute for life Science, Sahmyook University)
Kim, Seon-Jeong (Dept. of Life Science, Sahmyook University) Jang, Dai-Ho (Dept. of Life Science, Sahmyook University) Kim, Hyun-Hee (Dept. of Life Science, Sahmyook University) Lee, Kang-Oh (Dept. of Life Science, Sahmyook University) |
1 | Cann RL, Stoneking M and Wilson AC. Mitochondrial DNA and human evolution. Nature 1987; 325: 31-36 DOI ScienceOn |
2 | Dimauro S and Schon EA. Mitochondrial DNA mutations in human disease, Am. J. Med. Genet. 2001; 106: 18-26 DOI PUBMED ScienceOn |
3 | Kokaze A, Ishikawa M, Matsunaga N, Yoshida M, Sekine Y, Teruya K, Takeda N, Sumiya Y, Uchida Y and Takashima Y. Association of the mitochondrial DNA 5178 A/C polymorphism with serum lipid levels in the Japanese population, Hum. Genet. 2001; 109: 521-525 DOI ScienceOn |
4 | Shoji M, Tsutaya S, Kasai T and Yasujima M. Implication of single nucleotide polymorphisms in association study: mitochondrial variations as another genetic markers for hypertension, Rinsho. Byori. 2002; 50: 497-501 |
5 | Thorburn DR and Dahl H-HM. Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options, Am. J. Med. Genet. 2001; 106: 102-114 DOI PUBMED ScienceOn |
6 | Kokaze A, Ishikawa M, Matsunaga N, Yoshida M, Sekine Y, Teruya K, Takeda N, Satoh M, Sumiya Y, Uchida Y and Takashima Y. Association of the longevity-associated mitochondrial DNA 5178 A/C polymorphism with serum protein fraction levels in healthy Japanese women, Exp. Gerontol. 2002; 37: 931-936 DOI ScienceOn |
7 | Inoue I, Nakajima T, Williams CS, Quackenbush J, Puryear R, Powers M, Cheng T, Ludwig EH, Sharma AM, Hata A, Jeunemaitre X and Lalouel JM. A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro, J. Clin. Invest. 1997; 99: 1786-1797 DOI ScienceOn |
8 | Kurtz TW and Spence MA. Genetics of essential hypertension, Am. J. Med. 1993; 94: 77-84 DOI ScienceOn |
9 | Longini IM Jr, Higgins MW, Hinton PC, Moll PP and Keller JB, Environmental and genetic sources of familial aggregation of blood pressure in Tecumseh, Michigan. Am. J. Epidemiol. 1984; 120: 131-144 DOI |
10 | Fridewald WT, Levy RI and Friedrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma without the use of the preparative ultracentrifuge, Clin. Chern. 1972; 18: 499-502 |
11 | Tanaka M, Gong J-S, Zhang J, Yoneda M and Yagi K. Mitochondrial genotype associated with longevity, Lancet 1998; 351: 185-186 DOI ScienceOn |
12 | Bae JS, Kang BY, Lee KO, Yoon TJ, Kim JH and Kim KT. Haplotype distribution of the receptor gene in Korean essential ypertensives. J. Toxicol. Pub. Health. 2002; 18: 233-240 |
13 | Jeunemaitre X, Soubrier F, Kotelevtsev Y, Lifton R, Williams C, Charm A, Hunt S, Hopkins P, Williams R, Lalouel JM and Corvol P. Molecular basis of human hypertension: the role of angiotensinogen, Cell 1992; 71: 169-180 DOI ScienceOn |
14 | Soma M, Nakayama T and Katuo K. Nitric oxide synthase gene polymorphism and its influence on cardiovascular disease, Curro Opin. Nephrol. Hypertens. 1999; 8: 83-87 DOI ScienceOn |
15 | Casari G, Barlassina C, Cusi D, Zagato L, Muirhead R, Righetti M, Nembri P, Amar K, Gatti M, Macciardi F, Binelli G and Bianchi G, Association of the locus with essential hypertension, Hypertension 1995; 25: 320-326 DOI |
16 | Lifton RP. Molecular genetics of human blood pressure variation, Science 1996; 272: 676-680 DOI PUBMED ScienceOn |
17 | Frossard PM, Obineche EN, Elshahat YI, Lestringant GG, John A and Parvez SH. Association study of mutation to A in the promoter of the human apolipoprotein AI gene and essential hypertension, Biogenic Amines 1998; 14: 91-100 |
18 | Niemi A-K, Hervonen A, Hurme M, Karhunen PJ, Jylha M and Majamaa K. Mitochondrial DNA polymorphisms associated with longevity in a Finnish population, Hum. Genet. 2003; 112: 29-33 DOI ScienceOn |
19 | Dahl H-HM and Thorburn DR. Mitochondrial diseases: beyond the magic circle, Am. J. Med. Genet. 2001; 106: 1-3 DOI PUBMED ScienceOn |
20 | Anderson S, Bankier AT, Barrel BG, DeBruijin M, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith A, Staden R and Young IG. Sequence and organization of the human mitochondrial genome, Nature 1981; 290: 457-465 DOI ScienceOn |
21 | Ward R, Familial aggregation and genetic epidemiology of blood pressure. In: Laragh JH, Brenner BM (eds). Hypertension, Pathophysiology, Diagnosis and Management. Raven Press: New York, 1990; 81-100 |
22 | Matsunaga H, Tanaka Y, Tanaka M, Gong J-S, Zhang J, Nomiyama T, Ogawa O, Ogihara T, Yamada Y, Yagi K and Kawamori R. Antiatherogenic mitochondrial genotype in patients with type 2 diabetes, Diabetes Care 2001; 24: 500-503 DOI ScienceOn |
23 | Orth M and Schapira AHV. Mitochondria and degenerative disorders, Am. J. Med. Genet. 2001; 106: 27-36 DOI ScienceOn |
24 | Cusi D, Barlassina C, Azzani T, Casari G, Citterio L, Devoto M, Glorioso N, Lanzani C, Manunta P, Righetti M, Rivera R, Stella P, Troffa C, Zagato L and Bianchi G. Polymorphisms of -adducin and salt sensitivity in patients with essential hypertension, Lancet 1997; 349: 1353-1357 |
25 | Lifton RP and Jeunemaitre X. Finding genes that cause human hypertension, J. Hypertens. 1993; 11: 231-236 DOI ScienceOn |
26 | Raha S and Robinson BH. Mitochondria, oxygen free radicals and apoptosis, Am. J. Med. Genet. 2001; 106: 62-70 DOI ScienceOn |
27 | Shin JH, Kang, BY, Lee KH, Lee CC and Kim KT. Association between genetic variation in the human factor VII gene and essential hypertension in Korean population. Environ, Mutagens Carcinogens 2001; 21: 106-112 |
28 | Bostein D, White RL, Skolnick M and Davis RW. Construction of a genetic linkage map in man using restriction fragment length polymorphisms, Am. J. Hum. Genet. 1980; 32: 314-331 |
29 | Biron P, Mongeau JG and Bertrand D. Familial aggregation of blood pressure in 558 adopted children, Can. Med. Assoc. J. 1976; 115: 773-774 |