Publications

2015年

  1. Rong, Y., S. Nakamura, S., T. Hirata, D. Motooka, Y.S. Liu, Z.A. He, X.D.Gao, Y. Maeda, T. Kinoshita and M. Fujita. 2015. Genome-wide screening of genes required for glycosylphosphatidylinositol biosynthesis. PLoS One, 10:e0138553.
  2. Ilkovski, B. A., T. Pagnamenta, G. L. O'Grady, T. Kinoshita, M. F. Howard, M. Lek, B. Thomas, A. Turner, J. Christodoulou, D. Sillence, S. J.L. Knight, N. Popitsch, D. A. Keays, C. Anzilotti, A. Goriely, L. B. Waddell, F. Brilot, K. N. North, N. Kanzawa, D. G. MacArthur, J. C. Taylor, U. Kini1, Y. Murakami and N. F. Clarke. 2015. Mutations in PIGY: expanding the phenotype of inherited glycosylphosphatidylinositol (GPI) deficiencies. Hum. Mol. Genet., 24:6146-59.
  3. Hirata, T., M. Fujita, S. Nakamura, K. Gotoh, D. Motooka, Y. Murakami, Y. Maeda and T. Kinoshita. 2015. Post-Golgi anterograde transport requires GARP-dependent endosome-to-TGN retrograde transport. Mol. Biol. Cell, 26:3071-3084.
  4. Bosch, D.G.M, F.N. Boonstra, T. Kinoshita, J. de Ligt, F.P.M. Cremers, J.R. Lupski, Y. Murakami and B.B.A. de Vries. 2015. Cerebral visual impairment and intellectual disability caused by PGAP1 mutations. Eur. J. Hum. Genet., 23:1689-1693.
  5. Fujiwara, I., Y. Murakami, T. Niihori, J. Kanno, A. Hakoda, O. Sakamoto, N. Okamoto, R. Funayama, T. Nagashima, K. Nakayama, T. Kinoshita, S. Kure, Y. Matsubara, and Y. Aoki. Mutations in PIGL in a patient with Mabry syndrome. 2015. Am J Med Genet, 167A:777-785.
  6. Fujita, M., X.-D. Gao and T. Kinoshita. 2015. Glycan-mediated protein transport from the endoplasmic reticulum. In Sugar Chains. N. Taniguchi, T. Suzuki and K. Ohtsubo (eds.), p21-34. Springer.
  7. Kinoshita, T., 2015. Structural changes of GPI anchor after its attachment to proteins: functional significance. Adv. Exp. Med. Biol., 842:17-25.
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