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Franz Berthiller

Showing results (81-90 of 129) with videos related to

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Analytica Chimica Acta|January 9, 2025
Modular comparison of untargeted metabolomics processing stepsMarkus Aigensberger, Christoph Bueschl, Ezequias Castillo-Lopez, et al.
The Journal of Biological Chemistry|September 13, 2003
Detoxification of the Fusarium mycotoxin deoxynivalenol by a UDP-glucosyltransferase from Arabidopsis thalianaBrigitte Poppenberger, Franz Berthiller, Doris Lucyshyn, et al.
Biochemistry|October 8, 2016
Crystal Structure of Os79 (Os04g0206600) from Oryza sativa: A UDP-glucosyltransferase Involved in the Detoxification of DeoxynivalenolKarl M Wetterhorn, Sean A Newmister, Rachell K Caniza, et al.
Analytical and Bioanalytical Chemistry|January 4, 2024
Comparison of LC-MS-based methods for the determination of carboxylic acids in animal matricesHeidi E Schwartz-Zimmermann, Manuel Hündler, Nicole Reiterer, et al.
Analytical and Bioanalytical Chemistry|May 4, 2015
Simultaneous determination of major type A and B trichothecenes, zearalenone and certain modified metabolites in Finnish cereal grains with a novel liquid chromatography-tandem mass spectrometric methodAlexis V Nathanail, Jenna Syvähuoko, Alexandra Malachová, et al.
Analytical and Bioanalytical Chemistry|September 17, 2009
A reference-gene-based quantitative PCR method as a tool to determine Fusarium resistance in wheatKurt Brunner, Maria P Kovalsky Paris, Guadalupe Paolino, et al.
Organic & Biomolecular Chemistry|June 7, 2014
Methylthiodeoxynivalenol (MTD): insight into the chemistry, structure and toxicity of thia-Michael adducts of trichothecenesPhilipp Fruhmann, Theresa Weigl-Pollack, Hannes Mikula, et al.
Journal of Agricultural and Food Chemistry|March 24, 2009
Occurrence of deoxynivalenol and its major conjugate, deoxynivalenol-3-glucoside, in beer and some brewing intermediatesMarta Kostelanska, Jana Hajslova, Milena Zachariasova, et al.
Journal of Agricultural and Food Chemistry|January 7, 2014
Zearalenone-16-O-glucoside: a new masked mycotoxinMaria Paula Kovalsky Paris, Wolfgang Schweiger, Christian Hametner, et al.
Molecular Nutrition & Food Research|October 11, 2012
Masked mycotoxins: a reviewFranz Berthiller, Colin Crews, Chiara Dall'Asta, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Analytica Chimica Acta|January 9, 2025
Modular comparison of untargeted metabolomics processing stepsMarkus Aigensberger, Christoph Bueschl, Ezequias Castillo-Lopez, et al.
The Journal of Biological Chemistry|September 13, 2003
Detoxification of the Fusarium mycotoxin deoxynivalenol by a UDP-glucosyltransferase from Arabidopsis thalianaBrigitte Poppenberger, Franz Berthiller, Doris Lucyshyn, et al.
Biochemistry|October 8, 2016
Crystal Structure of Os79 (Os04g0206600) from Oryza sativa: A UDP-glucosyltransferase Involved in the Detoxification of DeoxynivalenolKarl M Wetterhorn, Sean A Newmister, Rachell K Caniza, et al.
Analytical and Bioanalytical Chemistry|January 4, 2024
Comparison of LC-MS-based methods for the determination of carboxylic acids in animal matricesHeidi E Schwartz-Zimmermann, Manuel Hündler, Nicole Reiterer, et al.
Analytical and Bioanalytical Chemistry|May 4, 2015
Simultaneous determination of major type A and B trichothecenes, zearalenone and certain modified metabolites in Finnish cereal grains with a novel liquid chromatography-tandem mass spectrometric methodAlexis V Nathanail, Jenna Syvähuoko, Alexandra Malachová, et al.
Analytical and Bioanalytical Chemistry|September 17, 2009
A reference-gene-based quantitative PCR method as a tool to determine Fusarium resistance in wheatKurt Brunner, Maria P Kovalsky Paris, Guadalupe Paolino, et al.
Organic & Biomolecular Chemistry|June 7, 2014
Methylthiodeoxynivalenol (MTD): insight into the chemistry, structure and toxicity of thia-Michael adducts of trichothecenesPhilipp Fruhmann, Theresa Weigl-Pollack, Hannes Mikula, et al.
Journal of Agricultural and Food Chemistry|March 24, 2009
Occurrence of deoxynivalenol and its major conjugate, deoxynivalenol-3-glucoside, in beer and some brewing intermediatesMarta Kostelanska, Jana Hajslova, Milena Zachariasova, et al.
Journal of Agricultural and Food Chemistry|January 7, 2014
Zearalenone-16-O-glucoside: a new masked mycotoxinMaria Paula Kovalsky Paris, Wolfgang Schweiger, Christian Hametner, et al.
Molecular Nutrition & Food Research|October 11, 2012
Masked mycotoxins: a reviewFranz Berthiller, Colin Crews, Chiara Dall'Asta, et al.
Pageof 13