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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

I. Hatada

National Cardiovascular Center Research Institute




Name/email consistency: high



  • National Cardiovascular Center Research Institute, Osaka, Japan. 1996 - 1997
  • Department of Bioscience, National Cardiovascular Center Research Institute, 5-7-1, Fujishiro-dai, Japan. 1997


  1. Aberrant methylation of an imprinted gene U2af1-rs1(SP2) caused by its own transgene. Hatada, I., Nabetani, A., Arai, Y., Ohishi, S., Suzuki, M., Miyabara, S., Nishimune, Y., Mukai, T. J. Biol. Chem. (1997) [Pubmed]
  2. New p57KIP2 mutations in Beckwith-Wiedemann syndrome. Hatada, I., Nabetani, A., Morisaki, H., Xin, Z., Ohishi, S., Tonoki, H., Niikawa, N., Inoue, M., Komoto, Y., Okada, A., Steichen, E., Ohashi, H., Fukushima, Y., Nakayama, M., Mukai, T. Hum. Genet. (1997) [Pubmed]
  3. An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome. Hatada, I., Ohashi, H., Fukushima, Y., Kaneko, Y., Inoue, M., Komoto, Y., Okada, A., Ohishi, S., Nabetani, A., Morisaki, H., Nakayama, M., Niikawa, N., Mukai, T. Nat. Genet. (1996) [Pubmed]
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