Courses Taught
                                                   
                                                
                                                
                                                   
                                                   
About
                                                   
                                                
                                                
                                                   
                                                   My research interests center on inflammation, the response to injury and infection,
                                                      and my goals are to elucidate the molecular mechanisms that regulate activity of inflammatory
                                                      mediators called eicosanoids. The current focus of this work involves analysis of
                                                      a gene designated CYP4F3 (cytochrome P450 4F3) that generates two distinct enzymes
                                                      by alternative splicing. One of these enzymes is expressed in neutrophils where it
                                                      inactivates the inflammatory mediator LTB4, and I am investigating the possibility
                                                      that it protects against inflammatory disease. The second enzyme is expressed in liver
                                                      and is induced by the cholesterol-lowering drugs called statins, although the consequences
                                                      for statin users are unknown.
                                                   
                                                   My specific objectives are to identify regulatory sites in the gene that control tissue-specific
                                                      CYP4F3 transcription and splicing. We will use this information to search for interventions
                                                      that alter physiology by modifying CYP4F3 expression.
                                                   
                                                   At a broader level, I am interested in exploring the functions of a CYP4F multi-gene
                                                      family that contribute to inflammation, lipid homeostasis, and drug metabolism.