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U. Kristina Walle

Department of Pharmacology

Medical University of South Carolina

Charleston

29425

USA

[email]@musc.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Department of Pharmacology, Medical University of South Carolina, Charleston, 29425, USA. 2000 - 2011

References

  1. Bioavailability of resveratrol. Walle, T. Ann. N. Y. Acad. Sci. (2011) [Pubmed]
  2. Methylation of dietary flavones increases their metabolic stability and chemopreventive effects. Walle, T. Int. J. Mol. Sci (2009) [Pubmed]
  3. Methoxylated flavones, a superior cancer chemopreventive flavonoid subclass? Walle, T. Semin. Cancer Biol. (2007) [Pubmed]
  4. Novel methoxylated flavone inhibitors of cytochrome P450 1B1 in SCC-9 human oral cancer cells. Walle, T., Walle, U.K. J. Pharm. Pharmacol. (2007) [Pubmed]
  5. Methylation of dietary flavones greatly improves their hepatic metabolic stability and intestinal absorption. Walle, T. Mol. Pharm. (2007) [Pubmed]
  6. Cancer chemopreventive properties of orally bioavailable flavonoids--methylated versus unmethylated flavones. Walle, T., Ta, N., Kawamori, T., Wen, X., Tsuji, P.A., Walle, U.K. Biochem. Pharmacol. (2007) [Pubmed]
  7. Improving metabolic stability of cancer chemoprotective polyphenols. Walle, T., Wen, X., Walle, U.K. Expert. Opin. Drug. Metab. Toxicol (2007) [Pubmed]
  8. Benzo[A]pyrene-induced oral carcinogenesis and chemoprevention: studies in bioengineered human tissue. Walle, T., Walle, U.K., Sedmera, D., Klausner, M. Drug Metab. Dispos. (2006) [Pubmed]
  9. Flavonoid glucosides are hydrolyzed and thus activated in the oral cavity in humans. Walle, T., Browning, A.M., Steed, L.L., Reed, S.G., Walle, U.K. J. Nutr. (2005) [Pubmed]
  10. The dietary polyphenol ellagic acid is a potent inhibitor of hOAT1. Whitley, A.C., Sweet, D.H., Walle, T. Drug Metab. Dispos. (2005) [Pubmed]
  11. Absorption and metabolism of flavonoids. Walle, T. Free Radic. Biol. Med. (2004) [Pubmed]
  12. High absorption but very low bioavailability of oral resveratrol in humans. Walle, T., Hsieh, F., DeLegge, M.H., Oatis, J.E., Walle, U.K. Drug Metab. Dispos. (2004) [Pubmed]
  13. Evidence of covalent binding of the dietary flavonoid quercetin to DNA and protein in human intestinal and hepatic cells. Walle, T., Vincent, T.S., Walle, U.K. Biochem. Pharmacol. (2003) [Pubmed]
  14. The beta-D-glucoside and sodium-dependent glucose transporter 1 (SGLT1)-inhibitor phloridzin is transported by both SGLT1 and multidrug resistance-associated proteins 1/2. Walle, T., Walle, U.K. Drug Metab. Dispos. (2003) [Pubmed]
  15. Disposition and metabolism of the flavonoid chrysin in normal volunteers. Walle, T., Otake, Y., Brubaker, J.A., Walle, U.K., Halushka, P.V. Br. J. Clin. Pharmacol (2001) [Pubmed]
  16. Carbon dioxide is the major metabolite of quercetin in humans. Walle, T., Walle, U.K., Halushka, P.V. J. Nutr. (2001) [Pubmed]
  17. Induction of UDP-glucuronosyltransferase UGT1A1 by the flavonoid chrysin in the human hepatoma cell line hep G2. Walle, T., Otake, Y., Galijatovic, A., Ritter, J.K., Walle, U.K. Drug Metab. Dispos. (2000) [Pubmed]
 
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