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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Katalin Monostory

Chemical Research Center

Hungarian Academy of Sciences

Budapest

Hungary

[email]@chemres.hu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Chemical Research Center, Hungarian Academy of Sciences, Budapest, Hungary. 2005 - 2011
  • Department of Biochemical Pharmacology, Chemical Research Center, Hungarian Academy of Sciences, P.O. Box 17, Hungary. 2004 - 2005
  • P.O. Box 17, Budapest, H-1525 Hungary, Hungary. 2003

References

  1. Steroid regulation of drug-metabolizing cytochromes P450. Monostory, K., Dvorak, Z. Curr. Drug Metab. (2011) [Pubmed]
  2. Hormonal regulation of CYP1A expression. Monostory, K., Pascussi, J.M., Kóbori, L., Dvorak, Z. Drug Metab. Rev. (2009) [Pubmed]
  3. Drug interaction potential of 2-((3,4-dichlorophenethyl)(propyl)amino)-1-(pyridin-3-yl)ethanol (LK-935), the novel nonstatin-type cholesterol-lowering agent. Monostory, K., Pascussi, J.M., Szabó, P., Temesvári, M., Köhalmy, K., Acimovic, J., Kocjan, D., Kuzman, D., Wilzewski, B., Bernhardt, R., Kóbori, L., Rozman, D. Drug Metab. Dispos. (2009) [Pubmed]
  4. The effect of synthetic glucocorticoid, dexamethasone on CYP1A1 inducibility in adult rat and human hepatocytes. Monostory, K., Kohalmy, K., Prough, R.A., Kóbori, L., Vereczkey, L. FEBS Lett. (2005) [Pubmed]
  5. Role of CYP2E1 in deramciclane metabolism. Monostory, K., Köhalmy, K., Hazai, E., Vereczkey, L., Kóbori, L. Drug Metab. Dispos. (2005) [Pubmed]
  6. Biotransformation of deramciclane in primary hepatocytes of rat, mouse, rabbit, dog, and human. Monostory, K., Kohalmy, K., Ludányi, K., Czira, G., Holly, S., Vereczkey, L., Urmös, I., Klebovich, I., Kóbori, L. Drug Metab. Dispos. (2005) [Pubmed]
  7. Inhibition of cytochrome P450 enzymes participating in p-nitrophenol hydroxylation by drugs known as CYP2E1 inhibitors. Monostory, K., Hazai, E., Vereczkey, L. Chem. Biol. Interact. (2004) [Pubmed]
  8. GYKI-47261, a new AMPA [2-amino-3-(3-hydroxymethylisoxazole-4-yl)propionic acid] antagonist, is a CYP2E1 inducer. Tamási, V., Hazai, E., Porsmyr-Palmertz, M., Ingelman-Sundberg, M., Vereczkey, L., Monostory, K. Drug Metab. Dispos. (2003) [Pubmed]
 
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