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Medical College of Georgia |
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Research Emphasis We use the zebrafish (Danio rerio) embryo as a model vertebrate system because of its rapid development, optical clarity and amenability to both embryological and genetic manipulations. Importantly, the vestibular portion of the fish inner ear is functionally and structurally similar to that of mammals. Our laboratory is characterizing several mutant lines of fish with defects affecting development and function of the inner ear. Utilizing the zebrafish core facility, we are generating transgenic zebrafish that express green fluorescent protein (a gene reporter that can be visualized in live embryos) under the control of inner ear specific gene promoter elements. These transgenic fish will aid in the analysis of mutants as well as provide new information about patterns of gene expression, cell lineage and cell fates in the developing otic vesicle. Projects in our lab utilize molecular (PCR, cloning, in situ hybridization), cell biological (microinjection, fate mapping), and genomic (positional cloning) technologies. Education Postdoctoral Training Awards and Honors: Selected Publications: *Kenny, A.P.,*Kozlowski, D.J., Oleksyn, D.W., Angerer, L., Angerer, R.C.
1999. SpSoxB1, a maternally encoded transcription factor
asymmetrically distributed among early sea urchin blastomeres.
Development 126: 5473-5483.
Kelly, C., Chin, A.J., Leatherman, J., Kozlowski, D.J., Weinberg, E.W. 2000. Maternally controlled b-catenin-mediated signaling is required for organizer formation in the zebrafish. Development 127: 3899-3911. Gee, K.R., Weinberg, E.S., Kozlowski, D.J. 2001. Caged Q-Rhodamine Dextran: A new Photoactivated Fluorescent Tracer. Bioorganic & Medicinal Chemistry Letters 11: 2181-2183. |
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Cellular Biology and Anatomy December 13, 2005 |