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Martin von Bergen

Researcher at Helmholtz Centre for Environmental Research - UFZ

Publications -  395
Citations -  19405

Martin von Bergen is an academic researcher from Helmholtz Centre for Environmental Research - UFZ. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 58, co-authored 346 publications receiving 15305 citations. Previous affiliations of Martin von Bergen include Max Planck Society & Leipzig University.

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Insight Into the Molecular Mechanisms Underpinning the Mycoremediation of Multiple Metals by Proteomic Technique

TL;DR: The comparative fungal proteomics displayed the remarkable inherent intracellular and extracellular mechanism of metal resistance and tolerance potential of A. fumigatus PD-18 and provides valuable insights toward the growing research in comprehending the metal microbe interactions in the presence of multimetal.
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Evaluation of Population and Individual Variances of Urinary Phthalate Metabolites in terms of Epidemiological Studies

TL;DR: The results showed that by accounting for the contribution of daily variance, the standard deviations of the log-transformed phthalate values of the cohort samples are reduced but still larger than daily standard deviation values, with the exception of MCPrP concentrations.
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Microbial community functioning during plant litter decomposition

TL;DR: In this article , the authors performed a correlative network analysis on the results of direct infusion HR-MS DOM analysis and cross-validated functional predictions from 16S rRNA gene amplicon sequencing and with DOM and metaproteomic analyses.
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Proteomic Characterization of the Cellular Effects of AhR Activation by Microbial Tryptophan Catabolites in Endotoxin-Activated Human Macrophages.

TL;DR: In this article, the authors analyzed proteomic changes in macrophages after treatment with the tryptophan metabolites indole-3-acetic acid (I3AA) or indole 3-aldehyde (IAld), as well as the prototypic exogenous AhR-ligand benzo(a)pyrene (BaP) in the absence and presence of lipopolysaccharide (LPS) to identify affected cellular processes and pathways.