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1. Hogan P, Dall T, Nikolov P. American Diabetes Association. Economic costs of diabetes in the US in 2002. Diabetes Care 2003;26:917–932 |
Sách, tạp chí |
|
2. Knowler WC, Barrett-Connor E, Fowler SE, et al. Diabetes Prevention Program Research Group. Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N Engl J Med 2002;346:393–403 |
Sách, tạp chí |
|
3. Zimmet P, Lefebvre P. The global NIDDM epidemic. Treating the disease and ignoring the symptom. Diabetologia 1996;39:1247–1248 |
Sách, tạp chí |
|
4. Wild S, Roglic G, Green A, Sicree R, King H. Global prevalence of diabetes: estimates for the year 2000 and projections for 2030.Diabetes Care 2004;27:1047–1053 |
Sách, tạp chí |
|
5. Hedley AA, Ogden CL, Johnson CL, Carroll MD, Curtin LR, Flegal KM. Prevalence of overweight and obesity among US children, adolescents and adults, 1999–2002. JAMA 2004;291:2847–2850 |
Sách, tạp chí |
|
6. Schulze MB, Manson JE, Ludwig DS, et al. Sugar-sweetened beverages, weight gain, and incidence of type 2 diabetes in young and middle-aged women. JAMA 2004;292:927–934 |
Sách, tạp chí |
|
7. Caroli M, Argentieri L, Cardone M, Masi A. Role of television in childhood obesity prevention. Int J Obes Relat Metab Disord 2004;28 (Suppl 3):S104–S108 |
Sách, tạp chí |
Tiêu đề: |
Int J Obes Relat Metab Disord |
|
8. DeFronzo RA. Pathogenesis of type 2 diabetes mellitus. Med Clin North Am 2004;88:787–835 |
Sách, tạp chí |
Tiêu đề: |
Med Clin North Am |
|
9. Barnett AH, Eff C, Leslie RD, Pyke DA. Diabetes in identical twins. A study of 200 pairs. Diabetologia 1981;20:87–93 |
Sách, tạp chí |
|
10. van den Ouweland JM, Lemkes HH, Trembath RC, et al. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene. Diabetes. 1994;43:746–751 |
Sách, tạp chí |
|
11. Inoue H, Tanizawa Y, Wasson J, et al. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome). Nat Genet 1998;20:143–148 |
Sách, tạp chí |
|
12. Porter JR, Barrett TG. Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure. J Med Genet 2005;42:893–902 |
Sách, tạp chí |
|
13. Bell GI, Polonsky KS. Diabetes mellitus and genetically programmed defects in beta-cell function. Nature 2001;414:788–791 |
Sách, tạp chí |
|
14. Hanis CL, Boerwinkle E, Chakraborty R, et al. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet 1996;13:161–166 |
Sách, tạp chí |
|
15. Horikawa Y, Oda N, Cox NJ, et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus.Nat Genet 2000;26:163–175 |
Sách, tạp chí |
|
16. Marshall C, Hitman GA, Partridge CJ, et al. Evidence that an isoform of calpain-10 is a regulator of exocytosis in pancreatic beta-cells. Mol Endocrinol 2005;19:213–224 |
Sách, tạp chí |
|
17. Gunton JE, Kulkarni RN, Yim S, et al. Loss of ARNT/HIF1beta mediates altered gene expression and pancreatic-islet dysfunction in human type 2 diabetes. Cell. 2005;122:337–349 |
Sách, tạp chí |
|
18. Porzio O, Federici M, Hribal ML, et al. The Gly972-->Arg amino acid polymorphism in IRS-1 impairs insulin secretion in pancreatic beta cells. J Clin Invest 1999;104:357–364 |
Sách, tạp chí |
|
19. Florez JC, Sjogren M, Burtt N, et al. Association testing in 9,000 people fails to confirm the association of the insulin receptor substrate-1 G972R polymorphism with type 2 diabetes. Diabetes 2004;53:3313–3318 |
Sách, tạp chí |
|
20. Grant SF, Thorleifsson G, Reynisdottir I, et al. Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes.Nat Genet 2006;38:320–323 |
Sách, tạp chí |
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