Hansruedi Glatt

发表

Potent inhibition of estrogen sulfotransferase by hydroxylated PCB metabolites: a novel pathway explaining the estrogenic activity of PCBs.

H. Glatt, D. Tibboel, C. Falany, 2000, Endocrinology.

Sulfotransferases in the bioactivation of xenobiotics.

H. Glatt, Hansruedi Glatt, 2000, Chemico-biological interactions.

Structure-activity relationship in the induction of chromosomal aberrations and spindle disturbances in Chinese hamster epithelial liver cells by regioisomeric phenanthrene quinones

H. Glatt, A. Seidel, A. Puliti, 1997, Cell Biology and Toxicology.

Biphenyl and fluorinated derivatives: liver enzyme-mediated mutagenicity detected in Salmonella typhimurium and Chinese hamster V79 cells.

H. Glatt, E. Anklam, L. Robertson, 1992, Mutation research.

Aneuploidy induction by benzo[a]pyrene and polyploidy induction by 7,12-dimethylbenz[a]anthracene in Chinese hamster cell lines V79-MZ and V79.

H. Glatt, T. Sofuni, H. Sakamoto, 1997, Mutagenesis.

Development and validation of alternative metabolic systems for mutagenicity testing in short-term assays.

H. Glatt, F. Palitti, A. Natarajan, 1996, Mutation research.

Stable expression of rat cytochrome P-450IA1 cDNA in V79 Chinese hamster cells and their use in mutagenicity testing.

H. Glatt, F. Oesch, A. Seidel, 1990, Molecular pharmacology.

Association between functional genetic polymorphisms of human sulfotransferases 1A1 and 1A2.

H. Glatt, H. Boeing, W. Meinl, 2000, Pharmacogenetics.

OCT1-dependent uptake of structurally diverse pyrrolizidine alkaloids in human liver cells is crucial for their genotoxic and cytotoxic effects

J. Küpper, J. Fahrer, M. Haas, 2023, Archives of Toxicology.

Detoxification of optically active bay- and fjord-region polycyclic aromatic hydrocarbon dihydrodiol epoxides by human glutathione transferase P1-1 expressed in Chinese hamster V79 cells.

H. Glatt, F. Oesch, A. Seidel, 1998, Carcinogenesis.

Inhibitors of mammalian melanocyte tyrosinase: in vitro comparisons of alkyl esters of gentisic acid with other putative inhibitors.

H. Glatt, V. Hearing, V. Virador, 1999, Biochemical pharmacology.

Sulfotransferases: genetics and role in toxicology.

H. Glatt, C. Falany, W. Meinl, 2000, Toxicology letters.

Genetically engineered V79 Chinese hamster cells metabolically activate the cytostatic drugs cyclophosphamide and ifosfamide.

H. Glatt, F. Oesch, A. Seidel, 1990, Environmental health perspectives.

Potent inhibition of estrogen sulfotransferase by hydroxylated metabolites of polyhalogenated aromatic hydrocarbons reveals alternative mechanism for estrogenic activity of endocrine disrupters.

H. Glatt, D. Tibboel, C. Falany, 2002, The Journal of clinical endocrinology and metabolism.

Species differences in enzymes controlling reactive epoxides.

H. Glatt, F. Oesch, Hansruedi Glatt, 1987, Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement.

Formation of DNA Adducts by 1-Methoxy-3-indolylmethylalcohol, a Breakdown Product of a Glucosinolate, in the Mouse: Impact of the SULT1A1 Status—Wild-Type, Knockout or Humanised

A. Ehlers, F. Schumacher, W. Meinl, 2024, International journal of molecular sciences.

Fruits and vegetables protect against the genotoxicity of heterocyclic aromatic amines activated by human xenobiotic-metabolizing enzymes expressed in immortal mammalian cells.

R. Edenharder, E. Muckel, S. Aderhold, 2010, Mutation research.

Protection by beverages, fruits, vegetables, herbs, and flavonoids against genotoxicity of 2-acetylaminofluorene and 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) in metabolically competent V79 cells.

H. Glatt, R. Edenharder, K. Platt, 2002, Mutation research.

Sulfation of thyroid hormone by estrogen sulfotransferase.

H. Glatt, D. Tibboel, C. Falany, 1999, The Journal of clinical endocrinology and metabolism.

Sulphotransferase-mediated toxification of chemicals in mouse models: effect of knockout or humanisation of SULT genes

W. Meinl, Hansruedi Glatt, 2024, Essays in biochemistry.