참고문헌
- 당뇨병의 진단 및 분류 권고안 : 당뇨병의 분류 ; 당뇨병의 분류. 임상당뇨병, 대한당뇨병학회 8: 31-33, 2007.
- 김응진, 민헌기, 최영길, 이태희, 허갑범, 신순현. 당뇨병학. 서울, 고려의학, pp 493-495, 498, 1998.
- Barroso, I. Genetics of Type 2 diabetes. Diabet Med. 22: 517-535, 2005. https://doi.org/10.1111/j.1464-5491.2005.01550.x
- Florez, J.C., Hirschhorn, J. and Altshuler, D. The inherited basis of diabetes mellitus: implications for the genetic analysis of complex traits. Annu Rev Genomics Hum Gene. t4: 257-291, 2003.
- Lander, E.S. and Schork, N.J. Genetic dissection of complex traits. Science. 265: 2037-2048, 1994. https://doi.org/10.1126/science.8091226
- Consortium(2003). The International HapMap Project. Nature. 426: 789-796, 2003. https://doi.org/10.1038/nature02168
- 당뇨병의 진단과 분류 (Diagnosis and Classification of Diabetes). 임상 당뇨병, 대한당뇨병학회 6: 132-139, 2005.
- Frayling, T.M. Genome-wide association studies provide new insights into type 2 diabetes aetiology. Nat Rev Genet. 8: 657-662, 2007.
- Scott, L.J., Mohlke, K.L., Bonnycastle, L.L., Willer, C.J., Li, Y., Duren, W.L., Erdos, M.R., Stringham, H.M., Chines, P.S., Jackson, A.U., et al. A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Science. 316: 1341-1345, 2007. https://doi.org/10.1126/science.1142382
- Saxena, R., Voight, B.F., Lyssenko, V., Burtt, N.P., de Bakker, P.I., Chen, H., Roix, J.J., Kathiresan, S., Hirschhorn, J.N., Daly, M.J., et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 316: 1331-1336, 2007. https://doi.org/10.1126/science.1142358
- Frazer, K.A., Ballinger, D.G., Cox, D.R., Hinds, D.A., Stuve, L.L., Gibbs, R.A., Belmont, J.W., Boudreau, A., Hardenbol, P., Leal, S.M., et al. A second generation human haplotype map of over 3.1million SNPs. Nature. 449: 851-861, 2007. https://doi.org/10.1038/nature06258
- Zeggini, E., Weedon, M.N., Lindgren, C.M., Frayling, T.M., Elliott, K.S., Lango, H., Timpson, N.J., Perry, J.R., Rayner, N.W., Freathy, R.M., et al. Replication of genome-wide association signals in UK sample sreveals risk loci for type 2 diabetes. Science. 316: 1336-1341, 2007. https://doi.org/10.1126/science.1142364
- Peters, T., Ausmeier, K. and Ruther, U. Cloning of Fatso (Fto), a novel gene deleted by the Fused toes (Ft) mouse mutation. Mamm Genome. 10: 983-986, 1999. https://doi.org/10.1007/s003359901144
- Gerken, T., Girard, C.A., Tung, Y.C., Webby, C.J., Saudek, V., Hewitson, K.S., Yeo, G.S., McDonough, M.A., Cunliffe, S., McNeill, L.A., et al. The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase. Science. 318: 1469-1472, 2007. https://doi.org/10.1126/science.1151710
- Sanchez-Pulido, L. and Andrade-Navarro, M.A. The FTO (fat mass and obesity associated) gene codes for a novel member of the non-heme dioxygenase superfamily. BMC Biochem. 8: 23, 2007. https://doi.org/10.1186/1471-2091-8-23
- Frayling, T.M., Timpson, N.J., Weedon, M.N., Zeggini, E., Freathy, R.M., Lindgren, C.M., Perry, J.R., Elliott, K.S., Lango, H., Rayner, N.W., et al. A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science. 316: 889-894, 2007. https://doi.org/10.1126/science.1141634
- Sampietro, J., Dahlberg, C.L., Cho, U.S., Hinds, T.R., Kimelman, D. and Xu, W. Crystal structure of a beta-catenin/BCL9/Tcf4 complex. Mol Cell. 24: 293-300, 2006. https://doi.org/10.1016/j.molcel.2006.09.001
- Poy, F., Lepourcelet, M., Shivdasani, R.A. and Eck, M.J. Structure of a human Tcf4-beta-catenin complex. Nat Struct Biol. 8: 1053-1057, 2001. https://doi.org/10.1038/nsb720
- Duval, A., Rolland, S., Tubacher, E., Bui, H., Thomas, G. and Hamelin, R. The human T-cell transcription factor-4 gene: structure, extensive characterization of alternative splicings, and mutational analysis in colorectal cancer cell lines. Cancer Res. 60: 3872-3879, 2000.
- Grant, S.F., Thorleifsson, G., Reynisdottir, I., Benediktsson, R., Manolescu, A., Sainz, J., Helgason, A., Stefansson, H., Emilsson, V., Helgadottir, A., et al. Variant of transcription factor 7-like2 (TCF7L2) gene confers risk of type 2 diabetes. NatGenet. 38: 320-323, 2006.
- Florez, J.C., Jablonski, K.A., Bayley, N., Pollin, T.I., de Bakker, P.I., Shuldiner, A.R., Knowler, W.C., Nathan, D.M. and Altshuler, D. TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program. N Engl J Med. 355: 241-250, 2006. https://doi.org/10.1056/NEJMoa062418
- 정은희, 조은희, 배윤정, 김윤지, 민원기, 고은희, 김민선, 박중열, 이기업. 저밀도 지단백 콜레스테롤 직접 측정값과 Friedewald 계산값의 비교. 임상당뇨병, 대한당뇨병학회 8: 253-260, 2007.
- Ng, M.C., Park, K.S., Oh, B., Tam, C.H., Cho, Y.M., Shin, H.D., Lam, V.K., Ma, R.C., So, W.Y., Cho, Y.S., et al. Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. Diabetes. 57: 2226-2233, 2008. https://doi.org/10.2337/db07-1583
- Kimchi-Sarfaty C., Oh, J.M., Kim, I.W., Sauna, Z.E., Calcagno, A.M., Ambudkar, S.V., Gottesman, M.M. A "silent" polymorphism in the MDR1 gene changes substrate specificity. Science. 315: 525-528, 2007. https://doi.org/10.1126/science.1135308