Browsing by Author "Demay, Marie"

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    • Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossification 

      Dey, D.; Bagarova, J.; Hatsell, S. J.; Armstrong, K. A.; Huang, L.; Ermann, J.; Vonner, A. J.; Shen, Y.; Mohedas, Agustin Humberto; Lee, A.; Eekhoff, E. M. W.; van Schie, A.; Demay, Marie Bernadette; Keller, C.; Wagers, Amy Jo; Economides, A. N.; Yu, P. B. (American Association for the Advancement of Science (AAAS), 2016)
      Fibrodysplasia ossificans progressiva (FOP), a congenital HO syndrome caused by gain-of-function mutations of bone morphogenetic protein (BMP) type I receptor ACVR1, manifests with progressive ossification of diverse tissues ...