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Dr. Matthew P. Scott is the tenth president of the Carnegie Institution for Science. His tenure began September 1, 2014. Scott was Professor of Developmental Biology, Genetics, Bioengineering, and Biology at the Stanford University School of Medicine prior to his Carnegie appointment. Scott did his undergraduate and graduate work at M.I.T., with Prof. Mary Lou Pardue as his Ph.D. thesis advisor. He moved to Indiana University for his postdoctoral work as a Helen Hay Whitney fellow with Profs. Thomas Kaufman and Barry Polisky. After setting up his own lab at the University of Colorado, Boulder, Dr. Scott went to Stanford in 1990 to join the newly formed Department of Developmental Biology, and the Department of Genetics. His research focused on genes that control development, and how damage to these genes leads to birth defects, cancer, and neurodegeneration. He discovered the “homeobox,” an evolutionarily conserved component of many genes that control development. His lab group discovered the genetic basis of the most common human cancer, basal cell carcinoma, and of the most common childhood malignant brain tumor, medulloblastoma. Scott served as Associate Chair and Chair of the Department of Developmental Biology for a total of six years. He chaired the multidisciplinary Bio-X program at Stanford from 2001-2007 and was Co-chair of the Center for Children’s Brain Tumors. He is a member of the American Academy of Arts and Sciences, the National Academy of Sciences, and the Institute of Medicine, and he served as president of the Society for Developmental Biology. His awards include the Passano Award (1990), the Conklin Medal of the Society for Developmental Biology (2004), and the Pasarow Award in Cancer Research (2013). 〔(【引用サイトリンク】 title=President Matthew P. Scott )〕 While at Stanford University Dr. Scott studied how embryonic and later development is governed by proteins that control gene activity and cell signaling processes.〔(【引用サイトリンク】 title=Scott lab homepage at Stanford University )〕 〔(【引用サイトリンク】 title=HHMI Scientist Bio: Matthew P. Scott, Ph.D. )〕 He independently discovered homeobox genes in Drosophila melanogaster working with Amy J. Weiner at Indiana University. Among his laboratory's many subsequent discoveries, he is recognized for the cloning of the patched gene family and demonstration that a human homolog PTCH1 is a key tumor suppressor gene for the Hedgehog signaling pathway as well as the causative gene for the nevoid basal cell carcinoma syndrome, or Gorlin syndrome.〔 〕〔 〕 ==Biography== Scott served on the faculty of the Department of Molecular, Cellular, and Developmental Biology at the University of Colorado starting in 1983. He moved to Stanford University in 1990 to join the faculty of the Department of Developmental Biology and the Department of Genetics. From 2002-2007 he was Chair of Bio-X, Stanford's interdisciplinary biosciences program.〔(【引用サイトリンク】 title=Biography: Matthew Scott )〕 He is married to Stanford developmental geneticist Margaret T. Fuller. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「Matthew P. Scott」の詳細全文を読む スポンサード リンク
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