Christopher V. E. Wright
                  Christopher Wright (Professor, Endowed Chair in the Department of Cell
                  and Developmental Biology) is Director of the Vanderbilt University Program
                  in Developmental Biology. His undergraduate education in England (1977-1980)
                  was at the University of Warwick, where he was trained in developmental
                  biology under Alan Colman and Hugh Woodland. His D. Phil. in Biochemistry
                  (University of Oxford, 1981-1984) with John Knowland was on purifying and
                  biophysically characterizing steroid receptor proteins. From 1985-1990,
                  Wright was lucky to do postdoctoral work with Eddy De Robertis on the just-discovered
                  vertebrate homeobox genes. He published the first description of Pdx1,
                  using immunodetection to show it labeling frog embryonic endoderm in the
                  presumptive pancreas, plus adjacent duodenum, stomach and biliary system.
                  Since joining Vanderbilt University in 1990, his lab has been amongst the
                  leaders in studies of the transcriptional regulators of pancreas organogenesis.
                  He has developed a translational focus on the differentiating ES cells
                  towards pancreatic endocrine fates, towards cell-based therapies. His mouse
                  genetic studies have determined that Pdx1 and Ptf1a are essential in multipotent
                  progenitors of the early anlagen, with later roles as differentiation/maintenance
                  factors in insulin-secreting beta cells (Pdx1), or enzyme-secreting acinar
                  cells (Ptf1a). From ~160 scientific publications, selected discoveries
                  include the first examples of lineage-switching triggered by inactivating
                  or reducing the level of Pdx1 and Ptf1a, and the cross-referencing of these
                  manipulations with effects on other stem/progenitor-regulatory factors.
                  Recent information supports the novel idea that MPC in the early pancreatic
                  epithelium are broadly communicating with each other to assess and establish
                  their identity and subsequent behavior. Also, that the endocrine trigger
                  factor, Ngn3, is expressed at low levels in cycling endocrine-biased progenitors,
                  and at higher levels when cells commit to become endocrine precursors.
                  Wright’s current goal is to move towards a high-resolution cell biological
                  dissection of pancreas differentiation. 
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