참고문헌
- Almasy, L., et al. (1999). Human pedigree-based quantitative-trait-locus mapping: localization of two genes influencing HDL-cholesterol metabolism. Am. J. Human Genetics 64, 1686-1693. https://doi.org/10.1086/302425
- Aouizerat, B.E., et al. (1999). A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11. Am. J. Human Genetics 65, 397-412. https://doi.org/10.1086/302490
- Arya, R., et al. (2002). Linkage of high-density lipoprotein-cholesterol concentrations to a locus on chromosome 9p in Mexican Americans. Nature Genetics 30, 102-105. https://doi.org/10.1038/ng810
- Barcat, D., et al. (2006). Combined hyperlipidemia/hyperalphalipoproteinemia associated with premature spontaneous atherosclerosis in mice lacking hepatic lipase and low density lipoprotein receptor. Atherosclerosis 188, 347-355. https://doi.org/10.1016/j.atherosclerosis.2005.11.022
- Bowry, V.W., Stanley, K.K., and Stocker, R. (1992). high-density-lipoprotein is the major carrier of lipid hydroperoxides in human blood-plasma from fasting donors. Proceedings of the National Academy of Sciences of the United States of America 89, 10316-10320. https://doi.org/10.1073/pnas.89.21.10316
- Brousseau, M.E., et al. (2004). Effects of an inhibitor of cholesteryl ester transfer protein on HDL cholesterol. N. Engl. J. Med. 350, 1505-1515. https://doi.org/10.1056/NEJMoa031766
- Coon, H., et al. (2001). Genome-wide linkage analysis of Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure study. Arteriosclerosis Thrombosis and Vascular Biology 21, 1969-1976. https://doi.org/10.1161/hq1201.100228
- Dastani, Z., et al. (2006). Genetics of high-density lipoproteins. Current Opinion in Cardiology 21, 329-335. https://doi.org/10.1097/01.hco.0000231403.94856.cd
- Forwood, J.K., Harley, V., and Jans, D.A. (2001). The C-terminal nuclear localization signal of the sex determining region Y (SRY) high mobility group domain mediates nuclear import through beta 1. Journal of Biological Chemistry 276, 46575-46582. https://doi.org/10.1074/jbc.M101668200
- Heath, S.C. (1997). Markov chain Monte Carlo segregation and linkage analysis for oligogenic models. American Journal of Human Genetics 61, 748-760. https://doi.org/10.1086/515506
- Imperatore, G., et al. (2000). A locus influencing total serum cholesterol on chromosome 19p - Results from an autosomal genomic scan of serum lipid concentrations in Pima Indians. Arteriosclerosis Thrombosis and Vascular Biology 20, 2651-2656. https://doi.org/10.1161/01.ATV.20.12.2651
- Inazu, A., et al. (1994). Genetic cholesteryl ester transfer protein-deficiency caused by 2 prevalent mutations as a major determinant of increased levels of high-density- lipoprotein cholesterol. Journal of Clinical Investigation 94, 1872-1882. https://doi.org/10.1172/JCI117537
- Klos, K.L., et al. (2001). Genome-wide linkage analysis reveals evidence of multiple regions that influence variation in plasma lipid and apolipoprotein levels associated with risk of coronary heart disease. Arteriosclerosis Thrombosis and Vascular Biology 21, 971-978. https://doi.org/10.1161/01.ATV.21.6.971
- Kuivenhoven, J.A., et al. (1997). Heterogeneity at the CETP gene locus - Influence on plasma CETP concentrations and HDL cholesterol levels. Arteriosclerosis Thrombosis and Vascular Biology 17, 560-568. https://doi.org/10.1161/01.ATV.17.3.560
- Mahaney, M.C., et al. (2003). A quantitative trait locus on chromosome 16q influences variation in plasma HDL-C levels in Mexican Americans. Arteriosclerosis Thrombosis and Vascular Biology 23, 339-345. https://doi.org/10.1161/01.ATV.0000051406.14162.6A
- Mari, M., and Cederbaum, A.I. (2001). Induction of catalase, alpha, and microsomal glutathione S-transferase in CYP2E1 overexpressing HepG2 cells and protection against short-term oxidative stress. Hepatology 33, 652-661. https://doi.org/10.1053/jhep.2001.22521
- Mcpeek, M.S., and Sun, L. (2000). Statistical tests for detection of misspecified relationships by use of genomescreen data. American Journal of Human Genetics 66, 1076-1094. https://doi.org/10.1086/302800
- Pajukanta, P., et al. (2003). Combined analysis of genome scans of Dutch and Finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q. American Journal of Human Genetics 72, 903-917. https://doi.org/10.1086/374177
- Peacock, J.M., et al. (2001). Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol - The NHLBI family heart study. Arteriosclerosis Thrombosis and Vascular Biology 21, 1823-1828. https://doi.org/10.1161/hq1101.097804
- Shoulders, C.C., Jones, E.L., and Naoumova, R.P. (2004). Genetics of familial combined hyperlipidemia and risk of coronary heart disease. Human Molecular Genetics 13, R149-R160. https://doi.org/10.1093/hmg/ddh069
- Wang, X.S., and Paigen, B. (2005). Genome-wide search for new genes controlling plasma lipid concentrations in mice and humans. Current Opinion in Lipidology 16, 127-137. https://doi.org/10.1097/01.mol.0000162317.09054.9d
- Yamashita, S., et al. (2000). Molecular mechanisms, lipoprotein abnormalities and atherogenicity of hyperalphalipoproteinemia. Atherosclerosis 152, 271-285. https://doi.org/10.1016/S0021-9150(00)00574-8
- Yancey, P.G., et al. (2003). Importance of different pathways of cellular cholesterol efflux. Arteriosclerosis Thrombosis and Vascular Biology 23, 712-719. https://doi.org/10.1161/01.ATV.0000057572.97137.DD
피인용 문헌
- Association between Prostaglandin-endoperoxide Synthase 2 (PTGS2) Polymorphisms and Blood Pressure in Korean Population vol.6, pp.3, 2008, https://doi.org/10.5808/GI.2008.6.3.110
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