Feng, Xiaodong_ Xie, Hong-Guang - Applying pharmacogenomics in therapeutics-CRC Press (2016)
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Pharmacogenomics and Alternative Medicine
267
Answer Key
1. bcd
2. abcd
3. ad
4. acd
5. abcd
REFERENCES
1. Teut, M. and K. Linde. Scientific case research in complementary and alternative
medicine—A review. Complement Ther Med, 2013;21(4):388–95.
2. Weeks, L.C. and T. Strudsholm. A scoping review of research on complementary and
alternative medicine (CAM) and the mass media: Looking back, moving forward. BMC
Complement Altern Med, 2008;8:43.
3. Tanwar, V.S., et al. Common variant in FUT2 gene is associated with levels of vitamin
B(12) in Indian population. Gene, 2013;515(1):224–8.
4. Bender. Nutritional biochemistry of the vitamins. Cambridge, UK: Cambridge
University Press; 2003.
5. Diop-Bove, N., et al. A novel deletion mutation in the proton-coupled folate transporter
(PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption. Gene,
2013;527(2):673–4.
6. Wang, Q., et al. The first Chinese case report of hereditary folate malabsorption with a
novel mutation on SLC46A1. Brain Dev, 2015;37(1):163–7.
7. Von Castel-Dunwoody, K.M., et al. Transcobalamin 776C→G polymorphism negatively
affects vitamin B-12 metabolism. Am J Clin Nutr, 2005;81(6):1436–41.
8. Cahill, L.E. and A. El-Sohemy. Vitamin C transporter gene polymorphisms, dietary
vitamin C and serum ascorbic acid. J Nutrigenet Nutrigenomics, 2009;2(6):292–301.
9. Dalgard, C., et al. Variation in the sodium-dependent vitamin C transporter 2 gene
is associated with risk of acute coronary syndrome among women. PLoS One, 2013;
8(8):e70421.
10. Pani, M.A., et al. Vitamin D 1alpha-hydroxylase (CYP1alpha) polymorphism in Graves’
disease, Hashimoto’s thyroiditis and type 1 diabetes mellitus. Eur J Endocrinol, 2002;
146(6):777–81.
11. Al-oanzi, Z.H., et al. Vitamin D-binding protein gene microsatellite polymorphism
influences BMD and risk of fractures in men. Osteoporos Int, 2008;19(7):951–60.
12. Girona, J., et al. The apolipoprotein A5 gene −1131T→C polymorphism affects
vitamin E plasma concentrations in type 2 diabetic patients. Clin Chem Lab Med, 2008;
46(4):453–7.
13. Testa, R., et al. Effect of 4G/5G PAI-1 polymorphism on the response of PAI-1 activity
to vitamin E supplementation in type 2 diabetic patients. Diabetes Nutr Metab, 2004;
17(4):217–21.
14. Zuchinali, P., et al. Influence of VKORC1 gene polymorphisms on the effect of oral
vitamin K supplementation in over-anticoagulated patients. J Thromb Thrombolysis,
2014;37:338–44.
15. McNulty, H., et al. Nutrition throughout life: Folate. Int J Vitam Nutr Res, 2012;82(5):
348–54.
16. Torre, M.L., et al. MTHFR C677T polymorphism, folate status and colon cancer risk in
acromegalic patients. Pituitary, 2014;17:257–66.
17. Coppede, F., V. Lorenzoni, and L. Migliore. The reduced folate carrier (RFC-1) 80A>G
polymorphism and maternal risk of having a child with Down syndrome: A metaanalysis.
Nutrients, 2013;5(7):2551–63.