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Items: 1 to 20 of 95

1.

The Fusarium metabolite culmorin suppresses the in vitro glucuronidation of deoxynivalenol.

Woelflingseder L, Warth B, Vierheilig I, Schwartz-Zimmermann H, Hametner C, Nagl V, Novak B, Šarkanj B, Berthiller F, Adam G, Marko D.

Arch Toxicol. 2019 May 2. doi: 10.1007/s00204-019-02459-w. [Epub ahead of print]

PMID:
31049613
2.

Correction: Pestka, J.J., et al. Sex Is a Determinant for Deoxynivalenol Metabolism and Elimination in the Mouse. Toxins 2017, 9, 240.

Pestka JJ, Clark ES, Schwartz-Zimmermann HE, Berthiller F.

Toxins (Basel). 2019 Apr 26;11(5). pii: E238. doi: 10.3390/toxins11050238.

3.

Metabolism of nivalenol and nivalenol-3-glucoside in rats.

Schwartz-Zimmermann HE, Binder SB, Hametner C, Miró-Abella E, Schwarz C, Michlmayr H, Reiterer N, Labudova S, Adam G, Berthiller F.

Toxicol Lett. 2019 May 15;306:43-52. doi: 10.1016/j.toxlet.2019.02.006. Epub 2019 Feb 12.

4.

Untargeted LC-MS based 13C labelling provides a full mass balance of deoxynivalenol and its degradation products formed during baking of crackers, biscuits and bread.

Stadler D, Lambertini F, Bueschl C, Wiesenberger G, Hametner C, Schwartz-Zimmermann H, Hellinger R, Sulyok M, Lemmens M, Schuhmacher R, Suman M, Berthiller F, Krska R.

Food Chem. 2019 May 1;279:303-311. doi: 10.1016/j.foodchem.2018.11.150. Epub 2018 Dec 11.

PMID:
30611495
5.

Correction to: Glucuronidation of deoxynivalenol (DON) by different animal species: identification of iso-DON glucuronides and iso-deepoxy-DON glucuronides as novel DON metabolites in pigs, rats, mice, and cows.

Schwartz-Zimmermann HE, Hametner C, Nagl V, Fiby I, Macheiner L, Winkler J, Dänicke S, Clark E, Pestka JJ, Berthiller F.

Arch Toxicol. 2018 Oct;92(10):3245-3246. doi: 10.1007/s00204-018-2273-1.

PMID:
30088018
6.

The contribution of lot-to-lot variation to the measurement uncertainty of an LC-MS-based multi-mycotoxin assay.

Stadler D, Sulyok M, Schuhmacher R, Berthiller F, Krska R.

Anal Bioanal Chem. 2018 Jul;410(18):4409-4418. doi: 10.1007/s00216-018-1096-5. Epub 2018 May 1.

7.

UDP-Glucosyltransferases from Rice, Brachypodium, and Barley: Substrate Specificities and Synthesis of Type A and B Trichothecene-3-O-β-d-glucosides.

Michlmayr H, Varga E, Malachová A, Fruhmann P, Piątkowska M, Hametner C, Šofrová J, Jaunecker G, Häubl G, Lemmens M, Berthiller F, Adam G.

Toxins (Basel). 2018 Mar 6;10(3). pii: E111. doi: 10.3390/toxins10030111.

8.

Chemical synthesis of culmorin metabolites and their biologic role in culmorin and acetyl-culmorin treated wheat cells.

Weber J, Vaclavikova M, Wiesenberger G, Haider M, Hametner C, Fröhlich J, Berthiller F, Adam G, Mikula H, Fruhmann P.

Org Biomol Chem. 2018 Mar 28;16(12):2043-2048. doi: 10.1039/c7ob02460f. Epub 2018 Feb 21.

PMID:
29465119
9.

Less-toxic rearrangement products of NX-toxins are formed during storage and food processing.

Varga E, Wiesenberger G, Woelflingseder L, Twaruschek K, Hametner C, Vaclaviková M, Malachová A, Marko D, Berthiller F, Adam G.

Toxicol Lett. 2018 Mar 1;284:205-212. doi: 10.1016/j.toxlet.2017.12.016. Epub 2017 Dec 23.

10.

Determinants and Expansion of Specificity in a Trichothecene UDP-Glucosyltransferase from Oryza sativa.

Wetterhorn KM, Gabardi K, Michlmayr H, Malachova A, Busman M, McCormick SP, Berthiller F, Adam G, Rayment I.

Biochemistry. 2017 Dec 19;56(50):6585-6596. doi: 10.1021/acs.biochem.7b01007. Epub 2017 Nov 30.

PMID:
29140092
11.

Corrigendum to "Formulation and processing factors affecting trichothecene mycotoxins within industrial biscuit-making" [Food Chem. (2017) 597-603].

Generotti S, Cirlini M, Šarkanj B, Sulyok M, Berthiller F, Dall'Asta C, Suman M.

Food Chem. 2018 Apr 1;244:414. doi: 10.1016/j.foodchem.2017.10.061. Epub 2017 Oct 20. No abstract available.

PMID:
29120802
12.

Mycotoxin profiling of 1000 beer samples with a special focus on craft beer.

Peters J, van Dam R, van Doorn R, Katerere D, Berthiller F, Haasnoot W, Nielen MWF.

PLoS One. 2017 Oct 5;12(10):e0185887. doi: 10.1371/journal.pone.0185887. eCollection 2017.

13.

Sex Is a Determinant for Deoxynivalenol Metabolism and Elimination in the Mouse.

Pestka JJ, Clark ES, Schwartz-Zimmermann HE, Berthiller F.

Toxins (Basel). 2017 Aug 4;9(8). pii: E240. doi: 10.3390/toxins9080240. Erratum in: Toxins (Basel). 2019 Apr 26;11(5):.

14.

Glucuronidation of deoxynivalenol (DON) by different animal species: identification of iso-DON glucuronides and iso-deepoxy-DON glucuronides as novel DON metabolites in pigs, rats, mice, and cows.

Schwartz-Zimmermann HE, Hametner C, Nagl V, Fiby I, Macheiner L, Winkler J, Dänicke S, Clark E, Pestka JJ, Berthiller F.

Arch Toxicol. 2017 Dec;91(12):3857-3872. doi: 10.1007/s00204-017-2012-z. Epub 2017 Jun 21. Erratum in: Arch Toxicol. 2018 Oct;92(10):3245-3246.

15.

A barley UDP-glucosyltransferase inactivates nivalenol and provides Fusarium Head Blight resistance in transgenic wheat.

Li X, Michlmayr H, Schweiger W, Malachova A, Shin S, Huang Y, Dong Y, Wiesenberger G, McCormick S, Lemmens M, Fruhmann P, Hametner C, Berthiller F, Adam G, Muehlbauer GJ.

J Exp Bot. 2017 Apr 1;68(9):2187-2197. doi: 10.1093/jxb/erx109.

16.

Formulation and processing factors affecting trichothecene mycotoxins within industrial biscuit-making.

Generotti S, Cirlini M, Šarkanj B, Sulyok M, Berthiller F, Dall'Asta C, Suman M.

Food Chem. 2017 Aug 15;229:597-603. doi: 10.1016/j.foodchem.2017.02.115. Epub 2017 Mar 1. Erratum in: Food Chem. 2018 Apr 1;244:414.

17.

Synthesis of Mono- and Di-Glucosides of Zearalenone and α-/β-Zearalenol by Recombinant Barley Glucosyltransferase HvUGT14077.

Michlmayr H, Varga E, Lupi F, Malachová A, Hametner C, Berthiller F, Adam G.

Toxins (Basel). 2017 Feb 9;9(2). pii: E58. doi: 10.3390/toxins9020058.

18.

Metabolism of Zearalenone and Its Major Modified Forms in Pigs.

Binder SB, Schwartz-Zimmermann HE, Varga E, Bichl G, Michlmayr H, Adam G, Berthiller F.

Toxins (Basel). 2017 Feb 8;9(2). pii: E56. doi: 10.3390/toxins9020056.

19.

Metabolism of HT-2 Toxin and T-2 Toxin in Oats.

Meng-Reiterer J, Bueschl C, Rechthaler J, Berthiller F, Lemmens M, Schuhmacher R.

Toxins (Basel). 2016 Dec 5;8(12). pii: E364.

20.

Study on the uptake and deglycosylation of the masked forms of zearalenone in human intestinal Caco-2 cells.

Cirlini M, Barilli A, Galaverna G, Michlmayr H, Adam G, Berthiller F, Dall'Asta C.

Food Chem Toxicol. 2016 Dec;98(Pt B):232-239. doi: 10.1016/j.fct.2016.11.003. Epub 2016 Nov 2.

PMID:
27816555

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