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Biological Chemistry|August 16, 2023
Characterization of the active site in the thiocyanate-forming protein from Thlaspi arvense (TaTFP) using EPR spectroscopyHaleh Hashemi Haeri, Nicola Schneegans, Daniela Eisenschmidt-Bönn, et al.Plant Molecular Biology|August 12, 2015
The crystal structure of the thiocyanate-forming protein from Thlaspi arvense, a kelch protein involved in glucosinolate breakdownFrauke Gumz, Joern Krausze, Daniela Eisenschmidt, et al.Proceedings of the National Academy of Sciences of the United States of America|December 14, 2007
The genetic basis of a plant-insect coevolutionary key innovationChristopher W Wheat, Heiko Vogel, Ute Wittstock, et al.Plos One|November 13, 2025
Glucosinolate diversity in seven field-collected Brassicaceae speciesLisa Pormetter, Marina Pfalz, Mervic D Kagho, et al.The New Phytologist|November 29, 2018
Sequential regiospecific gem-diprenylation of tetrahydroxyxanthone by prenyltransferases from Hypericum spMohamed Nagia, Mariam Gaid, Eline Biedermann, et al.Plos One|April 27, 2012
Turning the 'mustard oil bomb' into a 'cyanide bomb': aromatic glucosinolate metabolism in a specialist insect herbivoreEinar J Stauber, Petrissa Kuczka, Maike van Ohlen, et al.Journal of Chemical Ecology|July 10, 2010
Differential effects of indole and aliphatic glucosinolates on lepidopteran herbivoresRené Müller, Martin de Vos, Joel Y Sun, et al.Phytochemistry|October 9, 2007
ESP and ESM1 mediate indol-3-acetonitrile production from indol-3-ylmethyl glucosinolate in ArabidopsisMeike Burow, Zhi-Yong Zhang, James A Ober, et al.Plant, Cell & Environment|February 29, 2024
Plant glucosinolate biosynthesis and breakdown pathways shape the rhizosphere bacterial/archaeal communityEleanor C M Chroston, Nina Bziuk, Einar J Stauber, et al.Proceedings of the National Academy of Sciences of the United States of America|March 31, 2004
Successful herbivore attack due to metabolic diversion of a plant chemical defenseUte Wittstock, Niels Agerbirk, Einar J Stauber, et al.Pageof 5