참고문헌
- Benard G, Karbowski M. Mitochondrial fusion and division: Regulation and role in cell viability. Semin Cell Dev Biol. 2009. 20: 365-374. https://doi.org/10.1016/j.semcdb.2008.12.012
- Cerveny KL, Tamura Y, Zhang Z, Jensen RE, Sesaki H. Regulation of mitochondrial fusion and division. Trends Cell Biol. 2007. 17: 563-569. https://doi.org/10.1016/j.tcb.2007.08.006
- Chan DC. Mitochondrial fusion and fission in mammals. Annu Rev Cell Dev Biol. 2006. 22: 79-99. https://doi.org/10.1146/annurev.cellbio.22.010305.104638
- Cho YS, Go MJ, Kim YJ, Heo JY, Oh JH, Ban HJ, Yoon D, Lee MH, Kim DJ, Park M, Cha SH, Kim JW, Han BG, Min H, Ahn Y, Park MS, Han HR, Jang HY, Cho EY, Lee JE, Cho NH, Shin C, Park T, Park JW, Lee JK, Cardon L, Clarke G, McCarthy MI, Lee JY, Lee JK, Oh B, Kim HL. A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Nat Genet. 2009. 41: 527-534. https://doi.org/10.1038/ng.357
- Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, Novartis Institutes of BioMedical Research. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007. 316: 1331-1336. https://doi.org/10.1126/science.1142358
- Fox CS, Heard-Costa N, Cupples LA, Dupuis J, Vasan RS, Atwood LD. Genome-wide association to body mass index and waist circumference: The Framingham heart study 100K project. BMC Med Genet. 2007. 8 Suppl 1: S18. https://doi.org/10.1186/1471-2350-8-S1-S18
- Gamm DM, Baude EJ, Uhler MD. The major catalytic subunit isoforms of cAMP-dependent protein kinase have distinct biochemical properties in vitro and in vivo. J Biol Chem. 1996. 271: 15736-15742. https://doi.org/10.1074/jbc.271.26.15736
- Hang L, Thundyil J, Lim KL. Mitochondrial dysfunction and parkinson disease: A parkin-AMPK alliance in neuroprotection. Ann N Y Acad Sci. 2015. 1350: 37-47. https://doi.org/10.1111/nyas.12820
- Hiura Y, Tabara Y, Kokubo Y, Okamura T, Miki T, Tomoike H, Iwai N. A genome-wide association study of hypertension-related phenotypes in a Japanese population. Circ J. 2010. 74: 2353-2359. https://doi.org/10.1253/circj.CJ-10-0353
- Hoppins S, Lackner L, Nunnari J. The machines that divide and fuse mitochondria. Annu Rev Biochem. 2007. 76: 751-780. https://doi.org/10.1146/annurev.biochem.76.071905.090048
- Huber N, Guimaraes S, Schrader M, Suter U, Niemann A. Charcot-Marie-tooth disease-associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission. EMBO Rep. 2013. 14: 545-552. https://doi.org/10.1038/embor.2013.56
- In SK, Hyun TK, Kim E-J, Lee EJ. A comparative study of the concentration of salivary and blood glucose in normal and diabetic subjects. Journal of Experimental & Biomedical Sciences. 2013. 19: 105-111.
- Jin HS, Kim J, Lee SJ, Kim K, Go MJ, Lee JY, Lee HJ, Song J, Jeon BT, Roh GS, Kim SJ, Kim BY, Hong KW, Yoo YH, Oh B, Kang Y, Jeong SY. The PARK2 gene is involved in the maintenance of pancreatic beta-cell functions related to insulin production and secretion. Mol Cell Endocrinol. 2014. 382: 178-189. https://doi.org/10.1016/j.mce.2013.09.031
- Jin HJ, Kim J, Kyung TK, Ho JS. Application of an efficient method for isolation of mitochondria from biological samples. Biomedical Science Letters. 2014. 20: 180-184. https://doi.org/10.15616/BSL.2014.20.3.180
- Kabzinska D, Kotruchow K, Cegielska J, Hausmanowa-Petrusewicz I, Kochanski A. A severe recessive and a mild dominant form of Charcot-Marie-tooth disease associated with a newly identified Glu222Lys GDAP1 gene mutation. Acta Biochim Pol. 2014. 61: 739-744.
- Mason CC, Hanson RL, Knowler WC. Progression to type 2 diabetes characterized by moderate then rapid glucose increases. Diabetes. 2007. 56: 2054-2061. https://doi.org/10.2337/db07-0053
- McBride HM, Neuspiel M, Wasiak S. Mitochondria: More than just a powerhouse. Curr Biol. 2006. 16: R551-560. https://doi.org/10.1016/j.cub.2006.06.054
- Ober C, Nord AS, Thompson EE, Pan L, Tan Z, Cusanovich D, Sun Y, Nicolae R, Edelstein C, Schneider DH, Billstrand C, Pfaffinger D, Phillips N, Anderson RL, Philips B, Rajagopalan R, Hatsukami TS, Rieder MJ, Heagerty PJ, Nickerson DA, Abney M, Marcovina S, Jarvik GP, Scanu AM, Nicolae DL. Genome-wide association study of plasma lipoprotein (a) levels identifies multiple genes on chromosome 6q. J Lipid Res. 2009. 50: 798-806. https://doi.org/10.1194/jlr.M800515-JLR200
- Otera H, Ishihara N, Mihara K. New insights into the function and regulation of mitochondrial fission. Biochim Biophys Acta. 2013. 1833: 1256-1268. https://doi.org/10.1016/j.bbamcr.2013.02.002
- Paternoster L, Evans DM, Nohr EA, Holst C, Gaborieau V, Brennan P, Gjesing AP, Grarup N, Witte DR, Jorgensen T, Linneberg A, Lauritzen T, Sandbaek A, Hansen T, Pedersen O, Elliott KS, Kemp JP, St Pourcain B, McMahon G, Zelenika D, Hager J, Lathrop M, Timpson NJ, Smith GD, Sorensen TI. Genome-wide population-based association study of extremely overweight young adults--the GOYA study. PLoS One. 2011. 6: e24303. https://doi.org/10.1371/journal.pone.0024303
- Pollin TI, Damcott CM, Shen H, Ott SH, Shelton J, Horenstein RB, Post W, McLenithan JC, Bielak LF, Peyser PA, Mitchell BD, Miller M, O'Connell JR, Shuldiner AR. A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Science. 2008. 322: 1702-1705. https://doi.org/10.1126/science.1161524
- Prokopenko I, Langenberg C, Florez JC, Saxena R, Soranzo N, Thorleifsson G, Loos RJ, Manning AK, Jackson AU, Aulchenko Y, Potter SC, Erdos MR, Sanna S, Hottenga JJ, Wheeler E, Kaakinen M, Lyssenko V, Chen WM, Ahmadi K, Beckmann JS, Bergman RN, Bochud M, Bonnycastle LL, Buchanan TA, Cao A, Cervino A, Coin L, Collins FS, Crisponi L, de Geus EJ, Dehghan A, Deloukas P, Doney AS, Elliott P, Freimer N, Gateva V, Herder C, Hofman A, Hughes TE, Hunt S, Illig T, Inouye M, Isomaa B, Johnson T, Kong A, Krestyaninova M, Kuusisto J, Laakso M, Lim N, Lindblad U, Lindgren CM, McCann OT, Mohlke KL, Morris AD, Naitza S, Orru M, Palmer CN, Pouta A, Randall J, Rathmann W, Saramies J, Scheet P, Scott LJ, Scuteri A, Sharp S, Sijbrands E, Smit JH, Song K, Steinthorsdottir V, Stringham HM, Tuomi T, Tuomilehto J, Uitterlinden AG, Voight BF, Waterworth D, Wichmann HE, Willemsen G, Witteman JC, Yuan X, Zhao JH, Zeggini E, Schlessinger D, Sandhu M, Boomsma DI, Uda M, Spector TD, Penninx BW, Altshuler D, Vollenweider P, Jarvelin MR, Lakatta E, Waeber G, Fox CS, Peltonen L, Groop LC, Mooser V, Cupples LA, Thorsteinsdottir U, Boehnke M, Barroso I, Van Duijn C, Dupuis J, Watanabe RM, Stefansson K, McCarthy MI, Wareham NJ, Meigs JB, Abecasis GR. Variants in MTNR1B influence fasting glucose levels. Nat Genet. 2009. 41: 77-81. https://doi.org/10.1038/ng.290
- Rabbee N, Speed TP. A genotype calling algorithm for affymetrix SNP arrays. Bioinformatics. 2006. 22: 7-12. https://doi.org/10.1093/bioinformatics/bti741
- Watanabe RM, Valle T, Hauser ER, Ghosh S, Eriksson J, Kohtamaki K, Ehnholm C, Tuomilehto J, Collins FS, Bergman RN, Boehnke M. Familiality of quantitative metabolic traits in finnish families with non-insulin-dependent diabetes mellitus. Finland-United States investigation of NIDDM genetics (FUSION) study investigators. Hum Hered. 1999. 49: 159-168. https://doi.org/10.1159/000022865