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Camalexin (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Camalexin" in German language version.

refsWebsite
Global rank German rank
4doi.org
2nd place
3rd place
1biomol.com
low place
low place
1nih.gov
4th place
7th place

biomol.com (Global: low place; German: low place)

  • Camalexin. Produktinformationen. Biomol GmbH, abgerufen am 29. Februar 2024.

doi.org (Global: 2nd place; German: 3rd place)

  • Erich Glawischnig: Camalexin. In: Phytochemistry. Band 68, Nr. 4, Februar 2007, S. 401–406, doi:10.1016/j.phytochem.2006.12.005.
  • Thomas Rauhut, Erich Glawischnig: Evolution of camalexin and structurally related indolic compounds. In: Phytochemistry. Band 70, Nr. 15–16, Oktober 2009, S. 1638–1644, doi:10.1016/j.phytochem.2009.05.002.
  • Erich Glawischnig, Bjarne Gram Hansen, Carl Erik Olsen, Barbara Ann Halkier: Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis. In: Proceedings of the National Academy of Sciences. Band 101, Nr. 21, 25. Mai 2004, S. 8245–8250, doi:10.1073/pnas.0305876101, PMID 15148388, PMC 419588 (freier Volltext).
  • Ngoc Huu Nguyen, Patricia Trotel-Aziz, Christophe Clément, Philippe Jeandet, Fabienne Baillieul, Aziz Aziz: Camalexin accumulation as a component of plant immunity during interactions with pathogens and beneficial microbes. In: Planta. Band 255, Nr. 6, Juni 2022, doi:10.1007/s00425-022-03907-1.

nih.gov (Global: 4th place; German: 7th place)

ncbi.nlm.nih.gov

  • Erich Glawischnig, Bjarne Gram Hansen, Carl Erik Olsen, Barbara Ann Halkier: Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis. In: Proceedings of the National Academy of Sciences. Band 101, Nr. 21, 25. Mai 2004, S. 8245–8250, doi:10.1073/pnas.0305876101, PMID 15148388, PMC 419588 (freier Volltext).