Publications

2016年

  1. Ihara, S., S. Nakayama, Y. Murakami, E. Suzuki, M. Asakawa, T. Kinoshita and H. Sawa. 2016. PIGN prevents protein aggregation in the endoplasmic reticulum independently of its function in the GPI synthesis. J. Cell Sci., 130:602-613.
  2. Kolicheski, A. L., G. S. Johnson, T. Mhlanga-Mutangadura, J. F. Taylor, R. D. Schnabel, T. Kinoshita, Y. Murakami, D. P. O'Brien. 2016. A homozygous PIGN missense　mutation in soft coated wheatenterriers with a canine paroxysmal non-kinesigenic dyskinesia. Neurogenetics, in press.
  3. Lee, G-H., M. Fujita, K. Takaoka, Y. Murakami, Y. Fujihara, N. Kanzawa, K. Murakami, E. Kajikawa, Y. Takada, K. Saito, M. Ikawa, H. Hamada, Y. Maeda and T. Kinoshita. 2016. A GPI processing phospholipase A2, PGAP6, modulates Nodal signaling in embryos by shedding CRIPTO. J. Cell Biol., 215:705-718.
  4. Nakayama, H., H. Kurihara, Y. S. Morita, T. Kinoshita, L. Mauri, A. Prinetti, S. Sonnino, N. Yokoyama, H. Ogawa, K. Takamori and K. Iwabuchi. 2016. Lipoarabinomannan binding to lactosylceramide in lipid rafts is essential for the phagocytosis of mycobacteria by human neutrophils. Sci. Signal., 9: ra101.
  5. Edvardson, S.*, Y. Murakami*, T. T. M. Nguyen*, M. Shahrour*, A. St-Denis, A. Shaag, N. Damseh, S. Chiang Cern Cher, F. Le Deist, Y. Bryceson, B. Abu-Libdeh, P. M. Campeau, T. Kinoshita and O. Elpeleg. 2016. Mutations in the phosphatidylinositol glycan C (PIGC) gene are associated with epilepsy and intellectual disability. J. Med. Genet., in press.
  6. Hogrebe, M., Y. Murakami, M. Wild, M. Ahlmann, S. Biskup, K. Hoertnagel, M. Grueneberg, J. Reunert, T. Linden, T. Kinoshita and T. Marquardt. 2016. A novel mutation in PIGW causes glycosylphosphatidylinositol deficiency without hyperphosphatasia. Am. J. Med. Genet. A, in press.
  7. Nagae, M., T. Hirata, K. Morita-Matsumoto, R. Theiler, M. Fujita, T. Kinoshita and Y. Yamaguchi. 2016. 3D structure and interaction of p24ｲ and p24ｴ Golgi dynamics domains: implication for p24 complex formation and cargo transport. J. Mol. Biol., 428:4087-4099.
  8. Ninomiya, H., N. Obara, S. Chiba, K. Usuki, K. Nishiwaki, I. Matsumura, T. Shichishima, S. Okamoto, J. Nishimura, K. Ohyashiki, S. Nakao, K. Ando, Y. Kanda, T. Kawaguchi, H. Nakakuma, D. Harada, H.Akiyama, T. Kinoshita, K. Ozawa, M. Omine, Y. Kanakura. 2016. Interim analysis of post-marketing surveillance of eculizumab for paroxysmal nocturnal hemoglobinuria in Japan. Int. J. Hematol., in press.
  9. Knaus, A., T. Awaya, I. Helbig, Z. Afawi, M. Pendziwiat, J. Abu-Rachma, M. Thompson, D. Cole, S. Skinner, F. Annese, N. Canham, M. Schweiger, P. N. Robinson, S. Mundlos, T. Kinoshita, A. Munnich, Y. Murakami, D. Horn and P. Krawitz. 2016. Rare non-coding mutations extend the mutational spectrum in the PGAP3 subtype of Hyperphosphatasia with Mental Retardation Syndrome. Hum Mutat, 37:737-744.
  10. Hayashi, J. M., C.-Y. Luo, J. A. Mayfield, T. Hsu, T. Fukuda, A. L. Walfield, S. R. Giffen, J. Leszyk, C. E. Baer, O. T. Bennion, A. Madduri, S. A. Shaffer, B. B. Aldridge, C. M. Sassetti, S. J. Sandler, T. Kinoshita, D. B. Moody and Y. S. Morita. 2016. A spatially distinct and metabolically active membrane domain in Mycobacteria. Proc. Natl. Acad. Sci. USA, 113:5400-5405.
  11. Makrythanasis P., M. Kato, M. Zaki, H. Saitsu, K. Nakamura, F. Santoni, S. Miyatake, M. Nakashima, M. Y. Issa, M. Guipponi, A. Letourneau, C. Logan, N. Roberts, D. A. Parry, C. A. Johnson, N. Matsumoto, H. Hamamy, E. Sheridan, T. Kinoshita, S. E. Antonarakis and Y. Murakami. 2016. Pathogenic variants in PIGG cause intellectual disability with seizures and hypotonia. Am. J. Hum. Genet., 98:615-626.
  12. Kinoshita, T and M. Fujita. 2016. Biosynthesis of GPI-anchored proteins: special emphasis on GPI lipid remodeling. J Lipid Res, 57:6-24.
  13. Kinoshita, T. 2016. Glycosylphosphatidylinositol (GPI) Anchors: Biochemistry and Cell Biology: Introduction to a Thematic Review Series. J Lipid Res, 57:4-5.
  14. Nakagawa T, M., Taniguchi-Ikeda, Y. Murakami, S. Nakamura, D. Motooka, T. Emoto, W. Satake, M. Nishiyama, D. Toyoshima, N. Morisada, S. Takada, S. Tairaku, N. Okamoto, I. Morioka, H. Kurahashi, T. Toda, T. Kinoshita and K. Iijima. 2016. A novel PIGN mutation and prenatal diagnosis of inherited glycosylphosphatidylinositol deficiency. Am J Med Genet A. 170:183-188.
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