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I. Hatada

National Cardiovascular Center Research Institute

Osaka

Japan

[email]@ri.ncvc.go.jp

Name/email consistency: high

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Affiliations

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

References

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]
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]
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]