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(1) ÂÛ»ù¹ü·ÏÅý¼À´µ¥Õ¥©¡¼¥é¥à¥Û¡¼¥à¥Ú¡¼¥¸¡§http://plaza.umin.ac.jp/~fskel/cgi-bin/wiki/wiki.cgi?page=FrontPage

(2) Millan JL, Narisawa S, Lemire I, et al: Enzyme replacement therapy for murine hypophosphatasia. J Bone Mener Res 2008;23:777-787

(3) Whyte MP, Greenberg CR, Salman NJ, et al: Enzyme-replacement therapy in life-threatening Hypophosphatasia. New Engl J Med 2012;366:904-913

(4) Taketani T, Kanai R, Abe M, et al: Therapy-related Ph+ leukemia after both bone marrow and mesenchymal stem cell transplantation for hypophosphatasia. Pediatr Int 2013;55:e52-55

(5) Vrecenak JD, Flake AW: In utero hematopoietic cell transplantation – recent progress and the potential for clinical application. Cytotherapy 2013;15:525-535

(6) Le Blanc K, Gotherstom C, Ringden O, et al: Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta. Transplantation 2005;79:1607-1614

(7) Yamamoto M, Conget P, Allers C, et al: Intrauterine transfusion (IUT) of mesenchymal stem cells in two fetuses with severe fractures led to no postnatal fractures up to 1- and 2- years of age. Ultrasound Obstet Gynecol 2007;30:650

(8) Kunisaki SM: Congenital anomalies – treatment options based on amniotic fluid-derived stem cells. Organogenesis 2012;8:89-95

(9) Outani H, Okada M, Yamashita A, et al: Direct induction of chondrogenic cells from human dermal fibroblast culture by defined factors. PLoS ONE 2013;8(10): e77365. doi:10.1371/journal.pone.0077365

(10) Sugano H, Matsumoto T, Miyake K, et al: Successful gene therapy in utero for lethal murine hypophosphatasia. Hum Gene Ther 2012;23:399-406

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