Publications

2012年

  1. Hanaoka, N., Y. Murakami, M. Nagata, K. Horikawa, S. Nagakura, Y. Yonemura, S. Murata, T. Sonoki, T. Kinoshita and H. Nakakuma. 2012. Occupancy of whole blood cells by a single PIGA-mutant clone with HMGA2 amplification in a paroxysmal nocturnal haemoglobinuria patient having blood cells with NKG2D ligands. Br. J. Haematol., 160:114-116.
  2. Horiuchi, T., H. Ohi, I. Ohsawa, T. Fujita, M. Matsushita, N. Okada, T. Seya, T. Yamamoto, Y. Endo, M. Hatanaka, N. Wakamiya, M. Mizuno, M. Nakao, H. Okada, H. Tsukamoto, M. Matsumoto, N. Inoue, M. Nonaka and T. Kinoshita. 2012. Guideline for Hereditary Angioedema (HAE) 2010 by the Japanese Association for Complement Research. Allergol. Int., 61:559-62.
  3. Krawitz, P. M., Y. Murakami, J. Hecht, U. Kr殀er, S. E. Holder, G. R. Mortier, B. delle Chiaie, M. D. Thompson, T. Roscioli, S. Kielbasa, T. Kinoshita, S. Mundlos, P. N. Robinson and D. Horn. 2012. Mutations in PIGO, a member of the GPI anchor synthesis pathway, cause hyperphosphatasia with mental retardation. Am. J. Hum. Genet., 91:146-151.
  4. Loizides-Mangold, U., F. P. A. David, V. J. Nesatyy, T. Kinoshita and H. Riezman. 2012. GPI anchors regulate glycosphingolipid levels. J. Lipid Res., 53:1522-1534.
  5. Tarutani, M., K. Nakajima, Y. Uchida, M. Takaishi, N. Goto-Inoue, M. Setou T. Kinoshita, S. Sano, P. M. Elias and Y. Maeda. 2012. GPHR-dependent functions of the Golgi apparatus are essential for formation of lamellar granules and the skin barrier. J. Invest. Dermatol., 132:2019-2025.
  6. Hanaoka, N., Y. Murakami, M. Nagata, S. Nagakura, Y. Yonemura, T. Sonoki, T. Kinoshita and H. Nakakuma. 2012. Persistently high quality of life conferred by coexisting congenital deficiency of terminal complement C9 in a paroxysmal nocturnal hemoglobinuria patient. Blood, 119:3866-3868.
  7. Kanzawa, N., N. Shimozawa, R. J. A. Wanders, K. Ikeda, Y. Murakami, H. R. Waterham, S. Mukai, M. Fujita, Y. Maeda, R. Taguchi, Y. Fujiki and T. Kinoshita. 2012. Defective lipid remodeling of GPI anchors in peroxisomal disorders, Zellweger syndrome, and rhizomelic chondrodysplasia punctata. J. Lipid Res., 53:653-663.
  8. Murakami, Y., N. Kanzawa, K. Saito, P. M. Krawitz, S. Mundlos, P. N. Robinson, A. Karadimitris, Y. Maeda and T. Kinoshita. 2012. Mechanism for release of alkaline phosphatase caused by glycosylphosphatidylinositol deficiency in patients with hyperphosphatasia-mental retardation syndrome. J. Biol. Chem., 287:6318-6325.
  9. Fujita, M. and T. Kinoshita. 2012. GPI-anchor remodeling: potential functions of GPI-anchors in intracellular trafficking and membrane dynamics. Biochim. Biophys. Acta, 1821:1050-1058.
  10. Kinoshita, T. 2012. Paroxysmal nocturnal hemoglobinuria. In Encyclopedia of life sciences. 2nd Ed., John Wiley & Sons, Ltd., Chichester.
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