Recent Publications

Gene expression profiling and differentiation assessment in primary human hepatocyte cultures, established hepatoma cell lines, and human liver tissues full paper...

Gene Expression Profiling of Extracellular Matrix as an Effector of Human Hepatocyte Phenotype in Primary Cell Culture full paper...

Transactivation of a DR-1 PPRE by a human constitutive androstane receptor variant expressed from internal protein translation start sites full paper...

CAR2 Displays Unique Ligand Binding and RXR Heterodimerization Characteristics full paper...

Relative Activation of Human Pregnane X Receptor versus Constitutive Androstane Receptor Defines Distinct Classes of CYP2B6 and CYP3A4 Inducers full paper ...

Alternative Promoters Determine Tissue-Specific Expression Profiles of the Human Microsomal Epoxide Hydrolase Gene (EPHX1) full paper...

Retinoid X Receptor-α Dependent Transactivation by a Naturally Occurring Structural Variant of Human Constitutive Androstane Receptor (NR1I3) full paper...

Alternatively spliced isoforms of the human constitutive androstane receptorfull paper...

Variability in Human Sensitivity to 1,3-Butadiene: Influence of Polymorphisms in the 5'-Flanking Region of the Microsomal Epoxide Hydrolase Gene (EPHX1) full paper...


The research area of our laboratory is that of Molecular Toxicology. Our research centers on the study of human variability in chemical detoxication, an area termed 'toxicogenomics.' Detoxication pathways under investigation include the cytochrome P450 oxidation and epoxide hydrolase metabolism systems. We are working to characterize genetic differences within enzymes and within their respective regulatory networks that dictate interindividual responses to drug and chemical exposure. The regulatory pathways involved include certain members of the nuclear receptor superfamily, such as the constitutive androstane receptor, or CAR. These ‘xenobiotic' receptors function to sense the chemical environment in cells and then adjust the levels of biotransformation activity to accommodate specific exposure situations. The receptor control circuits exhibit diversity within cells, tissues and among individuals, in part due to the use of alternative RNA splicing mechanisms – an area of research focus of the laboratory. Transgenic mouse, primary cell culture and stem cell models are used in these investigations.

-Dr. Curtis Omiecinski

 

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