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Lethal and sublethal effects towards zebrafish larvae of microcystins and other cyanopeptides produced by cyanobacteria
de Almeida Torres, M., Jones, M. R., vom Berg, C., Pinto, E., & Janssen, E. M. L. (2023). Lethal and sublethal effects towards zebrafish larvae of microcystins and other cyanopeptides produced by cyanobacteria. Aquatic Toxicology, 263, 106689 (11 pp.). https://doi.org/10.1016/j.aquatox.2023.106689
Cytotoxicity, accumulation and translocation of silver and silver sulfide nanoparticles in contact with rainbow trout intestinal cells
Opršal, J., Knotek, P., Zickler, G. A., Sigg, L., Schirmer, K., Pouzar, M., & Geppert, M. (2021). Cytotoxicity, accumulation and translocation of silver and silver sulfide nanoparticles in contact with rainbow trout intestinal cells. Aquatic Toxicology, 237, 105869 (11 pp.). https://doi.org/10.1016/j.aquatox.2021.105869
Uptake and effects of cerium(III) and cerium oxide nanoparticles to <i>Chlamydomonas reinhardtii</i>
Kosak née Röhder, L. A., Brandt, T., Sigg, L., & Behra, R. (2018). Uptake and effects of cerium(III) and cerium oxide nanoparticles to Chlamydomonas reinhardtii. Aquatic Toxicology, 197, 41-46. https://doi.org/10.1016/j.aquatox.2018.02.004
Toxicity of emerging antifouling biocides to non-target freshwater organisms from three trophic levels
Oliveira, I. B., Groh, K. J., Schönenberger, R., Barroso, C., Thomas, K. V., & Suter, M. J. F. (2017). Toxicity of emerging antifouling biocides to non-target freshwater organisms from three trophic levels. Aquatic Toxicology, 191, 164-174. https://doi.org/10.1016/j.aquatox.2017.07.019
Mercury tissue residue approach in <I>Chironomus riparius</I>: involvement of toxicokinetics and comparison of subcellular fractionation methods
Gimbert, F., Geffard, A., Guédron, S., Dominik, J., & Ferrari, B. J. D. (2016). Mercury tissue residue approach in Chironomus riparius: involvement of toxicokinetics and comparison of subcellular fractionation methods. Aquatic Toxicology, 171, 1-8. https://doi.org/10.1016/j.aquatox.2015.11.027
Tralopyril bioconcentration and effects on the gill proteome of the Mediterranean mussel <I>Mytilus galloprovincialis</I>
Oliveira, I. B., Groh, K. J., Stadnicka-Michalak, J., Schönenberger, R., Beiras, R., Barroso, C. M., … Suter, M. J. F. (2016). Tralopyril bioconcentration and effects on the gill proteome of the Mediterranean mussel Mytilus galloprovincialis. Aquatic Toxicology, 177, 198-210. https://doi.org/10.1016/j.aquatox.2016.05.026
Establishment of the first humpback whale fibroblast cell lines and their application in chemical risk assessment
Burkard, M., Whitworth, D., Schirmer, K., & Nash, S. B. (2015). Establishment of the first humpback whale fibroblast cell lines and their application in chemical risk assessment. Aquatic Toxicology, 167, 240-247. https://doi.org/10.1016/j.aquatox.2015.08.005
Early life exposure to PCB126 results in delayed mortality and growth impairment in the zebrafish larvae
Di Paolo, C., Groh, K. J., Zennegg, M., Vermeirssen, E. L. M., Murk, A. J., Eggen, R. I. L., … Schirmer, K. (2015). Early life exposure to PCB126 results in delayed mortality and growth impairment in the zebrafish larvae. Aquatic Toxicology, 169, 168-178. https://doi.org/10.1016/j.aquatox.2015.10.014
Stressor-induced proteome alterations in zebrafish: a meta-analysis of response patterns
Groh, K. J., & Suter, M. J. F. (2015). Stressor-induced proteome alterations in zebrafish: a meta-analysis of response patterns. Aquatic Toxicology, 159, 1-12. https://doi.org/10.1016/j.aquatox.2014.11.013
Acclimation of <I>Chlamydomonas reinhardtii</I> to ultraviolet radiation and its impact on chemical toxicity
Korkaric, M., Xiao, M., Behra, R., & Eggen, R. I. L. (2015). Acclimation of Chlamydomonas reinhardtii to ultraviolet radiation and its impact on chemical toxicity. Aquatic Toxicology, 167, 209-219. https://doi.org/10.1016/j.aquatox.2015.08.008
Multiple stressor effects in <I>Chlamydomonas reinhardtii</I> – toward understanding mechanisms of interaction between effects of ultraviolet radiation and chemical pollutants
Korkaric, M., Behra, R., Fischer, B. B., Junghans, M., & Eggen, R. I. L. (2015). Multiple stressor effects in Chlamydomonas reinhardtii – toward understanding mechanisms of interaction between effects of ultraviolet radiation and chemical pollutants. Aquatic Toxicology, 162, 18-28. https://doi.org/10.1016/j.aquatox.2015.03.001
A primary FIsh Gill Cell System (FIGCS) for environmental monitoring of river waters
Minghetti, M., Schnell, S., Chadwick, M. A., Hogstrand, C., & Bury, N. R. (2014). A primary FIsh Gill Cell System (FIGCS) for environmental monitoring of river waters. Aquatic Toxicology, 154, 184-192. https://doi.org/10.1016/j.aquatox.2014.05.019
Influence of agglomeration of cerium oxide nanoparticles and speciation of cerium(III) on short term effects to the green algae <I>Chlamydomonas reinhardtii</I>
Röhder, L. A., Brandt, T., Sigg, L., & Behra, R. (2014). Influence of agglomeration of cerium oxide nanoparticles and speciation of cerium(III) on short term effects to the green algae Chlamydomonas reinhardtii. Aquatic Toxicology, 152, 121-130. https://doi.org/10.1016/j.aquatox.2014.03.027
Transient exposure to environmental estrogen affects embryonic development of brown trout (<I>Salmo trutta fario</I>)
Schubert, S., Peter, A., Schönenberger, R., Suter, M. J. F., Segner, H., & Burkhardt-Holm, P. (2014). Transient exposure to environmental estrogen affects embryonic development of brown trout (Salmo trutta fario). Aquatic Toxicology, 157, 141-149. https://doi.org/10.1016/j.aquatox.2014.10.007
Multiple-endpoint assay provides a detailed mechanistic view of responses to herbicide exposure in <I>Chlamydomonas reinhardtii</I>
Nestler, H., Groh, K. J., Schönenberger, R., Behra, R., Schirmer, K., Eggen, R. I. L., & Suter, M. J. F. (2012). Multiple-endpoint assay provides a detailed mechanistic view of responses to herbicide exposure in Chlamydomonas reinhardtii. Aquatic Toxicology, 110-111, 214-224. https://doi.org/10.1016/j.aquatox.2012.01.014
Acute toxicity of organic chemicals to <I>Gammarus pulex</I> correlates with sensitivity of <I>Daphnia magna</I> across most modes of action
Ashauer, R., Hintermeister, A., Potthoff, E., & Escher, B. I. (2011). Acute toxicity of organic chemicals to Gammarus pulex correlates with sensitivity of Daphnia magna across most modes of action. Aquatic Toxicology, 103(1-2), 38-45. https://doi.org/10.1016/j.aquatox.2011.02.002
Changes in gene transcription and whole organism responses in larval fathead minnow (<I>Pimephales promelas</I>) following short-term exposure to the synthetic pyrethroid bifenthrin
Beggel, S., Connon, R., Werner, I., & Geist, J. (2011). Changes in gene transcription and whole organism responses in larval fathead minnow (Pimephales promelas) following short-term exposure to the synthetic pyrethroid bifenthrin. Aquatic Toxicology, 105(1-2), 180-188. https://doi.org/10.1016/j.aquatox.2011.06.004
Sublethal responses to ammonia exposure in the endangered delta smelt; <I>Hypomesus transpacificus</I> (Fam. Osmeridae)
Connon, R. E., Deanovic, L. A., Fritsch, E. B., D'Abronzo, L. S., & Werner, I. (2011). Sublethal responses to ammonia exposure in the endangered delta smelt; Hypomesus transpacificus (Fam. Osmeridae). Aquatic Toxicology, 105(3-4), 369-377. https://doi.org/10.1016/j.aquatox.2011.07.002
Constitutive mRNA expression and protein activity levels of nine ABC efflux transporters in seven permanent cell lines derived from different tissues of rainbow trout (<I>Oncorhynchus mykiss</I>)
Fischer, S., Loncar, J., Zaja, R., Schnell, S., Schirmer, K., Smital, T., & Luckenbach, T. (2011). Constitutive mRNA expression and protein activity levels of nine ABC efflux transporters in seven permanent cell lines derived from different tissues of rainbow trout (Oncorhynchus mykiss). Aquatic Toxicology, 101(2), 438-446. https://doi.org/10.1016/j.aquatox.2010.11.010
Evolution of algal toxicity during (photo)oxidative degradation of diuron
Mestankova, H., Escher, B., Schirmer, K., von Gunten, U., & Canonica, S. (2011). Evolution of algal toxicity during (photo)oxidative degradation of diuron. Aquatic Toxicology, 101(2), 466-473. https://doi.org/10.1016/j.aquatox.2010.10.012