C. Sengstag

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DNA recombination induced by aflatoxin B1 activated by cytochrome P450 1A enzymes

C. Sengstag, F. Würgler, 1994, Molecular carcinogenesis.

Using SUC2-HIS4C reporter domain to study topology of membrane proteins in Saccharomyces cerevisiae.

C. Sengstag, 2000, Methods in enzymology.

Targeting of heterologous membrane proteins into proliferated internal membranes in Saccharomyces cerevisiae

C. Sengstag, F. Würgler, Nicola E. Wittenkindt, 1995, Yeast.

Genetic and biochemical evaluation of eucaryotic membrane protein topology: multiple transmembrane domains of Saccharomyces cerevisiae 3-hydroxy-3-methylglutaryl coenzyme A reductase

R. Schekman, J. Rine, C. Sengstag, 1990 .

Constitutive and inducible expression of human cytochrome P450IA1 in yeast Saccharomyces cerevisiae: an alternative enzyme source for in vitro studies.

A. Hinnen, C. Sengstag, F. Würgler, 1990, Biochemical and biophysical research communications.

Heterocyclic aromatic amines efficiently induce mitotic recombination in metabolically competent Saccharomyces cerevisiae strains.

C. Sengstag, G. Paladino, B. Weibel, 1999, Carcinogenesis.

The potential use of mutation spectra in cancer related genes in genetic toxicology: a statement of a GUM working group.

F. Staedtler, A. Hartwig, C. Sengstag, 2001, Mutation research.

Caffeine, estradiol, and progesterone interact with human CYP1A1 and CYP1A2. Evidence from cDNA-directed expression in Saccharomyces cerevisiae.

C. Sengstag, F. Würgler, H. Eugster, 1992, Drug metabolism and disposition: the biological fate of chemicals.

Genotoxicity of aflatoxin B1: evidence for a recombination-mediated mechanism in Saccharomyces cerevisiae.

C. Sengstag, M. Fasullo, B. Weibel, 1996, Cancer research.

The molecular mechanism of aflatoxin B1–induced liver cancer: Is mitotic recombination involved?

C. Sengstag, 1997, Molecular carcinogenesis.

Functional expression of fused enzymes between human cytochrome P4501A1 and human NADPH-cytochrome P450 oxidoreductase in Saccharomyces cerevisiae.

N. Wittekindt, C. Sengstag, F. Würgler, 1995, DNA and cell biology.

Identification oftheSequences inHMG-CoA Reductase Required forKarmellae Assembly

C. Sengstag, 1995 .

Nucleic Acids Research

A. Hinnen, C. Sengstag, 2022 .

Characterization of the trp5-27 allele used to monitor drug-induced mitotic gene conversion in the Saccharomyces cerevisiae tester strain D7.

C. Sengstag, F. Würgler, A. Ehrenhofer-Murray, 1994, Mutagenesis.

High promutagen activating capacity of yeast microsomes containing human cytochrome P-450 1A and human NADPH-cytochrome P-450 reductase.

C. Sengstag, F. Würgler, H. Eugster, 1994, Carcinogenesis.

Reciprocal mitotic recombination is the predominant mechanism for the loss of a heterozygous gene in saccharomyces cerevisiae

C. Sengstag, F. Würgler, G. Acuña, 1994, Environmental and molecular mutagenesis.

Heterologous expression of human microsomal epoxide hydrolase in Saccharomyces cerevisiae. Study of the valpromide-carbamazepine epoxide interaction.

A. Hinnen, C. Sengstag, F. Würgler, 1991, Biochemical pharmacology.

Codon 249 of the human TP53 tumor suppressor gene is no hot spot for aflatoxin B1 in a heterologous background.

C. Sengstag, B. Weibel, J. Mörbe, 1999, Mutation research.

A cloned DNA fragment from bacteriophage P1 enhances IS2 insertion

C. Sengstag, W. Arber, 1987, Molecular and General Genetics MGG.

Functional co-expression of human oxidoreductase and cytochrome P450 1A1 in Saccharomyces cerevisiae results in increased EROD activity.

C. Sengstag, F. Würgler, H. Eugster, 1992, Biochemical and biophysical research communications.

Liver carcinogen aflatoxin B1 as an inducer of mitotic recombination in a human cell line

C. Sengstag, P. Stettler, Christian Sengstag, 2001, Molecular carcinogenesis.

The Next Generation Scientist program: capacity-building for future scientific leaders in low- and middle-income countries

M. Ramsay, K. Chibale, C. Masimirembwa, 2018, BMC medical education.

Saccharomyces cerevisiae: an alternative source for human microsomal liver enzymes and its use in drug interaction studies.

C. Sengstag, H. Eugster, 1993, Toxicology.

A nuclear mutation that post-transcriptionally blocks accumulation of a yeast mitochondrial gene product can be suppressed by a mitochondrial gene rearrangement.

C. Sengstag, T. Fox, P. Müller, 1984, Journal of molecular biology.

The Saccharomyces cerevisiae SGE1 gene product: a novel drug-resistance protein within the major facilitator superfamily

C. Sengstag, F. Würgler, A. Ehrenhofer-Murray, 1994, Molecular and General Genetics MGG.

The Sge1 protein of Saccharomyces cerevisiae is a membrane‐associated multidrug transporter

C. Sengstag, A. Ehrenhofer-Murray, Monika U. Keller Seitz, 1998, Yeast.

Transcriptional response of yeast to aflatoxin B1: recombinational repair involving RAD51 and RAD1.

U. Certa, C. Sengstag, F. Würgler, 2004, Molecular biology of the cell.

The role of mitotic recombination in carcinogenesis.

C. Sengstag, 1994, Critical reviews in toxicology.

Rearrangements in minisatellite sequences induced by aflatoxin B1 in a metabolically competent strain of Saccharomyces cerevisiae.

C. Wild, C. Sengstag, C. Kaplanski, 1998, Carcinogenesis.

A genetic system to detect mitotic recombination between repeated chromosomal sequences in Drosophila Schneider line 2 cells.

C. Sengstag, F. Würgler, S. Bärtsch, 1997, Mutation research.

Identification of the sequences in HMG-CoA reductase required for karmellae assembly.

M. Parrish, J. Rine, C. Sengstag, 1995, Molecular biology of the cell.

Gene 68, a new bacteriophage T4 gene which codes for the 17K prohead core protein is involved in head size determination.

T. Bickle, E. Kellenberger, C. Sengstag, 1984, Journal of molecular biology.

Metabolism of promutagens catalyzed by Drosophila melanogaster CYP6A2 enzyme in Saccharomyces cerevisiae

C. Sengstag, F. Würgler, C. Saner, 1996, Environmental and molecular mutagenesis.

A plasmid system to monitor gene conversion and reciprocal recombination in vitro.

C. Sengstag, F. Würgler, T. Oppliger, 1993, Mutation research.

Evolutionary relevance of genetic rearrangements involving plasmids.

B. Dalrymple, P. Caspers, C. Sengstag, 1985, Basic life sciences.

Expression of human microsomal epoxide hydrolase in Saccharomyces cerevisiae reveals a functional role in aflatoxin B1 detoxification.

D. Eaton, C. Sengstag, E. Kelly, 2002, Toxicological sciences : an official journal of the Society of Toxicology.

Mutations in liver DNA of lacI transgenic mice (Big Blue) following subchronic exposure to 2-acetylaminofluorene.

C. Schlatter, C. Sengstag, S. Shephard, 1993, Mutation research.

IS2 insertion is a major cause of spontaneous mutagenesis of the bacteriophage P1: non‐random distribution of target sites.

C. Sengstag, W. Arber, 1983, EMBO Journal.

Ectopic mitotic recombination in Drosophila probed with bacterial beta-galactosidase gene-based reporter transgenes.

C. Sengstag, F. Würgler, S. Bärtsch, 1997, Nucleic acids research.

Genetic and biochemical evaluation of eucaryotic membrane protein topology: multiple transmembrane domains of Saccharomyces cerevisiae 3-hydroxy-3-methylglutaryl coenzyme A reductase

R. Schekman, J. Rine, C. Sengstag, 1990, Molecular and cellular biology.

The sequence of the Saccharomyces cerevisiae gene PHO2 codes for a regulatory protein with unusual aminoacid composition

C. Sengstag, A. Hinnen, A. Hinnen, 1987, Nucleic Acids Res..

Postnatal ontogeny of hippocampal expression of the mineralocorticoid and glucocorticoid receptors in the common marmoset monkey

J. Feldon, A. Jongen-Rêlo, E. Fuchs, 2005, The European journal of neuroscience.

The Next Generation Scientist program: capacity-building for future scientific leaders in low- and middle-income countries

Goonaseelan Pillai, Bernhards Ogutu, Christian Sengstag, 2018, BMC Medical Education.