2024 (4)

• Böhme, A., Simoneit, M., Ulrich, N., Schüürmann, G. (2024):
  Amino reactivity of aromatic aldehydes - Chemoassay analysis of mechanisms underlying their skin sensitization potency
  Naunyn-Schmiedebergs Arch. Pharmacol. 397 (Suppl. 1), S19 - P001 10.1007/s00210-024-02974-3
• Escher, B.I., Ahlheim, J., Böhme, A., Borchardt, D., Brack, W., Braun, G., Colbourne, J.K., Dann, J.P., Gessner, J., Jahnke, A., König, M., Klüver, N., Krauss, M., Lee, J., Li, X., Lips, S., Orsini, L., Rinke, K., Schmitt-Jansen, M., Scholz, S., Schulze, T., Spahr, S., Ulrich, N., Weitere, M., Varga, E. (2024):
  Mixtures of organic micropollutants exacerbated in vitro neurotoxicity of prymnesins and contributed to aquatic toxicity during a toxic algal bloom
  Nat. Water 2 (9), 889 - 898 10.1038/s44221-024-00297-4
• Menger, F., Römerscheid, M., Lips, S., Klein, O., Nabi, D., Gandrass, J., Joerss, H., Wendt-Potthoff, K., Bedulina, D., Zimmermann, T., Schmitt-Jansen, M., Huber, C., Böhme, A., Ulrich, N., Beck, A.J., Pröfrock, D., Achterberg, E.P., Jahnke, A., Hildebrandt, L. (2024):
  Screening the release of chemicals and microplastic particles from diverse plastic consumer products into water under accelerated UV weathering conditions
  J. Hazard. Mater. 477 , art. 135256 10.1016/j.jhazmat.2024.135256
• Simoneit, M., Böhme, A. (2024):
  Amino reactivity-based identification of respiratory sensitizers
  Naunyn-Schmiedebergs Arch. Pharmacol. 397 (Suppl. 1), S19 - P002 10.1007/s00210-024-02974-3

2023 (6)

• Böhme, A., Ulrich, N., Schüürmann, G. (2023):
  Amino chemoassay profiling of aromatic aldehydes–unraveling drivers of their skin sensitization potency
  Chem. Res. Toxicol. 36 (7), 1055 - 1070 10.1021/acs.chemrestox.3c00013
• Gerhards, M., Böhme, A., Schubert, K., Kodritsch, B., Ulrich, N. (2023):
  DNA adducts as link between in vitro and in vivo carcinogenicity – A case study with benzo[a]pyrene
  Curr. Res. Toxicol. 4 , art. 100097 10.1016/j.crtox.2022.100097
• Latz, M., Böhme, A., Ulrich, N. (2023):
  Reactivity-based identification of oxygen containing functional groups of chemicals applied as potential classifier in non-target analysis
  Sci. Rep. 13 , art. 22828 10.1038/s41598-023-50240-y
• Liess, M., Böhme, A., Gröning, J., Liebmann, L., Lück, M., Reemtsma, T., Römerscheid, M., Schade, U., Schwarz, B., Vormeier, P., Weisner, O. (2023):
  Belastung von kleinen Gewässern in der Agrarlandschaft mit Pflanzenschutzmittel-Rückständen – TV1 Datenanalyse
  zur Pilotstudie Kleingewässermonitoring 2018/2019 – Abschlussbericht. German monitoring of plant protection product residues in small streams – In depth analysis of the Kleingewässermonitoring from 2018/2019
  Texte Umweltbundesamt 63/2023
  Umweltbundesamt, Dessau-Roßlau, 244 S.
• Saleem, S., Böhme, A., Schüürmann, G. (2023):
  Baseline narcosis for the glass-vial 96-h growth inhibition of the nematode C. elegans and its use for identifying electrophilic and pro-electrophilic toxicity
  Environ. Sci. Technol. 57 (4), 1692 - 1700 10.1021/acs.est.2c05217
• Ulrich, N., Böhme, A., Strobel, A.B., Egert, T. (2023):
  Predicting partitioning from low density polyethylene to blood and adipose tissue by linear solvation energy relationship models
  J. Biomed. Mater. Res. Part B 111 (12), 2044 - 2054 10.1002/jbm.b.35304

2022 (4)

• Böhme, A., Moldrickx, J., Schüürmann, G. (2022):
  Amino reactivity of Schiff base forming aldehydes - Nonanimal assessment of their skin sensitization potency
  Naunyn-Schmiedebergs Arch. Pharmacol. 395 (Suppl. 1), S31 - S31 10.1007/s00210-022-02205-7
• Latz, M., Böhme, A., Ulrich, N. (2022):
  Spectra_reactivity - Version v1 [Data set]
  Zenodo 10.5281/zenodo.7429998
• Latz, M., Böhme, A., Ulrich, N. (2022):
  Spectra_reactivity - Version v2 [Data set]
  Zenodo 10.5281/zenodo.8213955
• Ulrich, N., Böhme, A. (2022):
  Rapid determination of serum albumin partition coefficients using affinity chromatography
  Environ. Adv. 9 , art. 100284 10.1016/j.envadv.2022.100284

2021 (1)

• Böhme, A., Moldrickx, J., Schüürmann, G. (2021):
  Amino reactivity of glutardialdehyde and monoaldehydes - chemoassay profile vs skin sensitization potency
  Chem. Res. Toxicol. 34 (11), 2353 - 2365 10.1021/acs.chemrestox.1c00266

2020 (3)

• Böhme, A., Moldrickx, J., Schüürmann, G. (2020):
  Chemoassay profiling to characterize the skin sensitization potential and potency of organic electrophiles
  Naunyn-Schmiedebergs Arch. Pharmacol. 393 (Suppl. 1), 85 - 85 10.1007/s00210-020-01828-y
• Böhme, A., Werner, A., Moldrickx, J., Ebersbach, B., Mazik, M., Schüürmann, G. (2020):
  Chemoassay profiling of benzoates and salicylates to assess their skin sensitization potential
  Naunyn-Schmiedebergs Arch. Pharmacol. 393 (Suppl. 1), 85 - 85 10.1007/s00210-020-01828-y
• Sadik, A., Somarribas Patterson, L.F., Öztürk, S., Mohapatra, S.R., Panitz, V., Secker, P.F., Pfänder, P., Loth, S., Salem, H., Prentzell, M.T., Berdel, B., Iskar, M., Faessler, E., Reuter, F., Kirst, I., Kalter, V., Foerster, K.I., Jäger, E., Ramallo Guevara, C., Sobeh, M., Hielscher, T., Poschet, G., Reinhardt, A., Hassel, J.C., Zapatka, M., Hahn, U., von Deimling, A., Hopf, C., Schlichting, R., Escher, B.I., Burhenne, J., Haefeli, W.E., Ishaque, N., Böhme, A., Schäuble, S., Thedieck, K., Trump, S., Seiffert, M., Opitz, C.A. (2020):
  IL4I1 is a metabolic immune checkpoint that activates the AHR and promotes tumor progression
  Cell 182 (5), 1252 - 1270.e34 10.1016/j.cell.2020.07.038

2019 (1)

• Hovorka, S., Vrbka, P., Bermúdez-Salguero, C., Böhme, A. (2019):
  Air–water partitioning of C5 and C6 alkanones: Measurement, critical compilation, correlation, and recommended data
  J. Chem. Eng. Data 64 (12), 5765 - 5774 10.1021/acs.jced.9b00726

2017 (4)

• Escher, B.I., Hackermüller, J., Polte, T., Scholz, S., Aigner, A., Altenburger, R., Böhme, A., Bopp, S.K., Brack, W., Busch, W., Chadeau-Hyam, M., Covaci, A., Eisenträger, A., Galligan, J.J., Garcia-Reyero, N., Hartung, T., Hein, M., Herberth, G., Jahnke, A., Kleinjans, J., Klüver, N., Krauss, M., Lamoree, M., Lehmann, I., Luckenbach, T., Miller, G.W., Müller, A., Phillips, D.H., Reemtsma, T., Rolle-Kampczyk, U., Schüürmann, G., Schwikowski, B., Tan, Y.-M., Trump, S., Walter-Rohde, S., Wambaugh, J.F. (2017):
  From the exposome to mechanistic understanding of chemical-induced adverse effects
  Environ. Int. 99 , 97 - 106 10.1016/j.envint.2016.11.029
• Shafique, U., Schulze, S., Slawik, C., Böhme, A., Paschke, A., Schüürmann, G. (2017):
  Perfluoroalkyl acids in aqueous samples from Germany and Kenya
  Environ. Sci. Pollut. Res. 24 (12), 11031 - 11043 10.1007/s11356-016-7076-4
• Shafique, U., Schulze, S., Slawik, C., Chepchirchir, B.S., Böhme, A., Paschke, A., Schüürmann, G. (2017):
  Erratum to: Perfluoroalkyl acids in aqueous samples from Germany and Kenya
  Environ. Sci. Pollut. Res. 24 (12), 11044 - 11044 10.1007/s11356-016-7721-y
• Slawik, C., Rickmeyer, C., Brehm, M., Böhme, A., Schüürmann, G. (2017):
  Glutathione adduct patterns of Michael-acceptor carbonyls
  Environ. Sci. Technol. 51 (7), 4018 - 4026 10.1021/acs.est.6b04981

2016 (1)

• Böhme, A., Laqua, A., Schüürmann, G. (2016):
  Chemoavailability of organic electrophiles: impact of hydrophobicity and reactivity on their aquatic excess toxicity
  Chem. Res. Toxicol. 29 (6), 952 - 962 10.1021/acs.chemrestox.5b00398

2014 (1)

• Fenclová, D., Blahut, A., Vrbka, P., Dohnal, V., Böhme, A. (2014):
  Temperature dependence of limiting activity coefficients, Henry's law constants, and related infinite dilution properties of C4–C6 isomeric n-alkyl ethanoates/ethyl n-alkanoates in water. Measurement, critical compilation, correlation, and recommended data
  Fluid Phase Equilib. 375 , 347 - 359 10.1016/j.fluid.2014.05.023

2013 (1)

• Böhme, A., Zhang, W., Schüürmann, G. (2013):
  Identification of potential skin sensitizers based on non-animal chemoassay and in vitro bioassay information
  Abstr. Paper Am. Chem. Soc. 246 , 336-ENVR

2012 (3)

• Blaschke, U., Eismann, K., Böhme, A., Paschke, A., Schüürmann, G. (2012):
  Structural alerts for the excess toxicity of acrylates, methacrylates, and propiolates derived from their short-term and long-term bacterial toxicity
  Chem. Res. Toxicol. 25 (1), 170 - 180 10.1021/tx200395k
• Bönisch, U., Böhme, A., Kohajda, T., Mögel, I., Schütze, N., von Bergen, M., Simon, J.C., Lehmann, I., Polte, T. (2012):
  Volatile organic compounds enhance allergic airway inflammation in an experimental mouse model
  PLoS One 7 (7), e39817 10.1371/journal.pone.0039817
• Thaens, D., Heinzelmann, D., Böhme, A., Paschke, A., Schüürmann, G. (2012):
  Chemoassay screening of DNA-reactive mutagenicity with 4-(4-nitrobenzyl)pyridine  –  application to epoxides, oxetanes, and sulfur heterocycles
  Chem. Res. Toxicol. 25 (10), 2092 - 2102 10.1021/tx3001412

2011 (1)

• Mögel, I., Baumann, S., Böhme, A., Kohajda, T., von Bergen, M., Simon, J.-C., Lehmann, I. (2011):
  The aromatic volatile organic compounds toluene, benzene and styrene induce COX-2 and prostaglandins in human lung epithelial cells via oxidative stress and p38 MAPK activation
  Toxicology 289 (1), 28 - 37 10.1016/j.tox.2011.07.006

2010 (4)

• Böhme, A., Schramm, F., Wondrousch, D., Schüürmann, G. (2010):
  Alternativmethoden zur toxikologischen Bewertung chemischer Stoffe
  Zeitschrift für Freunde und Förderer der Technischen Universität Bergakademie Freiberg 17 (Sonderdruck), 117 - 121
• Böhme, A., Thaens, D., Schramm, F., Paschke, A., Schüürmann, G. (2010):
  Thiol reactivity and its impact on the ciliate toxicity of α,β-unsaturated aldehydes, ketones, and esters
  Chem. Res. Toxicol. 23 (12), 1905 - 1912 10.1021/tx100226n
• Dohnal, V., Vrbka, P., Rehák, K., Böhme, A., Paschke, A. (2010):
  Activity coefficients and partial molar excess enthalpies at infinite dilution for four esters in water
  Fluid Phase Equilib. 295 (2), 194 - 200 10.1016/j.fluid.2010.05.010
• Wondrousch, D., Böhme, A., Thaens, D., Ost, N., Schüürmann, G. (2010):
  Local electrophilicity predicts toxicity-relevant reactivity of Michael acceptors
  J. Phys. Chem. Lett. 1 (10), 1605 - 1610 10.1021/jz100247x

2009 (2)

• Böhme, A., Thaens, D., Paschke, A., Schüürmann, G. (2009):
  Kinetic glutathione chemoassay-A non-animal component of integrated testing strategies to identify compounds with an electrophilic potential for reactive toxicity
  Toxicol. Lett. 189 (Suppl. 1), S62 - S62 10.1016/j.toxlet.2009.06.308
• Böhme, A., Thaens, D., Paschke, A., Schüürmann, G. (2009):
  Kinetic glutathione chemoassay to quantify thiol reactivity of organic electrophiles - application to α,β-unsaturated ketones, acrylates, and propiolates
  Chem. Res. Toxicol. 22 (4), 742 - 750 10.1021/tx800492x

2008 (1)

• Böhme, A., Paschke, A., Vrbka, P., Dohnal, V., Schüürmann, G. (2008):
  Determination of temperature-dependent Henry's law constant of four oxygenated solutes in water using headspace solid phases microextraction technique
  J. Chem. Eng. Data 53 (12), 2873 - 2877 10.1021/je800623x