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Judith Maria Rollinger

Institute of Pharmacy/Pharmacognosy and Center for Molecular Biosciences Innsbruck

University of Innsbruck

Innsbruck

Austria

[email]@uibk.ac.at

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Institute of Pharmacy/Pharmacognosy and Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, Austria. 2001 - 2010

References

  1. 11beta-Hydroxysteroid dehydrogenase 1 inhibiting constituents from Eriobotrya japonica revealed by bioactivity-guided isolation and computational approaches. Rollinger, J.M., Kratschmar, D.V., Schuster, D., Pfisterer, P.H., Gumy, C., Aubry, E.M., Brandstötter, S., Stuppner, H., Wolber, G., Odermatt, A. Bioorg. Med. Chem. (2010) [Pubmed]
  2. Computational techniques for lead discovery from nature. Rollinger, J.M. Curr. Pharm. Des. (2010) [Pubmed]
  3. In silico target fishing for rationalized ligand discovery exemplified on constituents of Ruta graveolens. Rollinger, J.M., Schuster, D., Danzl, B., Schwaiger, S., Markt, P., Schmidtke, M., Gertsch, J., Raduner, S., Wolber, G., Langer, T., Stuppner, H. Planta Med. (2009) [Pubmed]
  4. Structure-based virtual screening for the discovery of natural inhibitors for human rhinovirus coat protein. Rollinger, J.M., Steindl, T.M., Schuster, D., Kirchmair, J., Anrain, K., Ellmerer, E.P., Langer, T., Stuppner, H., Wutzler, P., Schmidtke, M. J. Med. Chem. (2008) [Pubmed]
  5. Taspine: bioactivity-guided isolation and molecular ligand-target insight of a potent acetylcholinesterase inhibitor from Magnolia x soulangiana. Rollinger, J.M., Schuster, D., Baier, E., Ellmerer, E.P., Langer, T., Stuppner, H. J. Nat. Prod. (2006) [Pubmed]
  6. Venturia inaequalis-inhibiting Diels-Alder adducts from Morus root bark. Rollinger, J.M., Spitaler, R., Menz, M., Marschall, K., Zelger, R., Ellmerer, E.P., Schneider, P., Stuppner, H. J. Agric. Food Chem. (2006) [Pubmed]
  7. Strategies for efficient lead structure discovery from natural products. Rollinger, J.M., Langer, T., Stuppner, H. Curr. Med. Chem. (2006) [Pubmed]
  8. Discovering COX-inhibiting constituents of Morus root bark: activity-guided versus computer-aided methods. Rollinger, J.M., Bodensieck, A., Seger, C., Ellmerer, E.P., Bauer, R., Langer, T., Stuppner, H. Planta Med. (2005) [Pubmed]
  9. New insights into the acetylcholinesterase inhibitory activity of Lycopodium clavatum. Rollinger, J.M., Ewelt, J., Seger, C., Sturm, S., Ellmerer, E.P., Stuppner, H. Planta Med. (2005) [Pubmed]
  10. Application of the in combo screening approach for the discovery of non-alkaloid acetylcholinesterase inhibitors from Cichorium intybus. Rollinger, J.M., Mocka, P., Zidorn, C., Ellmerer, E.P., Langer, T., Stuppner, H. Curr. Drug. Discov. Technol (2005) [Pubmed]
  11. Combining ethnopharmacology and virtual screening for lead structure discovery: COX-inhibitors as application example. Rollinger, J.M., Haupt, S., Stuppner, H., Langer, T. J. Chem. Inf. Comput. Sci (2004) [Pubmed]
  12. Acetylcholinesterase inhibitory activity of scopolin and scopoletin discovered by virtual screening of natural products. Rollinger, J.M., Hornick, A., Langer, T., Stuppner, H., Prast, H. J. Med. Chem. (2004) [Pubmed]
  13. Lignans, phenylpropanoids and polyacetylenes from Chaerophyllum aureum L. (Apiaceae). Rollinger, J.M., Zidorn, C., Dobner, M.J., Ellmerer, E.P., Stuppner, H. Z. Naturforsch., C, J. Biosci. (2003) [Pubmed]
  14. Crystal forms of torasemide: new insights. Rollinger, J.M., Gstrein, E.M., Burger, A. Eur. J. Pharm. Biopharm (2002) [Pubmed]
  15. Polymorphism of racemic felodipine and the unusual series of solid solutions in the binary system of its enantiomers. Rollinger, J.M., Burger, A. J. Pharm. Sci (2001) [Pubmed]
 
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