Phone 615.343.8256
Office 3140 MRBIII
Nashville, TN 37232-8240
Email chris.wright@vanderbilt.edu
Fig. 2. YFP fluorescence in Ptf1aYFP/+ and Ptf1aYFP/YFP embryos. From "Pdx-1 and Ptf1a concurrently determine fate specification of pancreatic multipotent progrnitor cells."


 

The Wright laboratory research focuses on early embryonic development and organogenesis. Numerous papers from his group have been published in the fields of TGF-beta/BMP-like intercellular signaling in early embryos and of pancreas formation and maintenance with particular interests in multi-potential stem cells, endocrine and exocrine cell ontogeny, and plasticity and interconversion during development and metastasis.   Wright trainees have used a combination of molecular biological, genetic, biochemical and experimental embryological techniques to explore these issues in frog, mouse and zebrafish embryos.  Dr. Wright has published several solicited reviews and book chapters in both fields, and he and his lab members are extremely interested in broader issues such as the evolution of Nodal signaling pathways in gastrulation and left-right asymmetry during chordate and vertebrate evolution.  The lab also enjoys highly collaborative and productive relationships with several laboratories studying ascidians (e.g. Billie Swalla, Mike Levine), zebrafish (Marnie Halpern, Lila Solnica-Krezel), and other species.

 

For more information about Dr. Wright visit his Vanderbilt Faculty Page

NEWEST PUBLICATIONS

Pdx-1 and Ptf1a concurrently determine fate specification of pancreatic multipotent progrnitor cells.  Developmental Biology (2008) 316: 74-86

pdx-1 function is specifically required in embryonic beta cells to generate appropriate numbers of endocrine cell types and maintain glucose homeostasis.  Developmental Biology (2008) 314: 406-417

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Last modified: Friday, May 17, 2008 by Kim.Kane@vanderbilt.edu