Publication List
2000
Original Research Papers
Watanabe, T., Yoshimura, A., Mishima, Y., Endo, Y., Shiroishi, T., Koide, T., Sasaki, H., Asakura, H. & Kominami, R.
Differential chromatin packaging of genomic imprinted region between expressed and non-expressed alleles.
Hum. Mol. Genet. 9, 3029-3035 (2000)
PubMed

Ueda, T., Abe, K., Miura, A., Yuzuriha, M., Zubair M., Noguchi, M., Niwa, K., Kawase, Y., Kono, T., Matsuda, Y., Fujimoto, H., Shibata, H., Hayashizaki, Y. & Sasaki, H.
The paternal methylation imprint of the mouse H19 locus is acquired in the gonocyte stage during fetal testis development.
Genes Cells 5, 649-659 (2000)
PubMed

Yatsuki, H., Watanabe, H., Hattori, M., Joh, K., Soejima, H., Komoda, H., Xin, Z., Zhu, X., Higashimoto, K., Nishimura, M., Kuratomi, S., Sasaki, H., Sakaki, Y. & Mukai, T.
Sequence-based structural features between Kvlqt1 and Tapa1 in mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region in human 11p15.5: long-stretches of unusually well conserved intronic sequence of Kvlqt1 between mouse and human.
DNA Res. 7, 195-206 (2000)
PubMed

Ishihara, K., Hatano, N., Furuumi, H., Kato, R., Iwaki, T., Miura, K., Jinno, Y. & Sasaki, H.
Comparative genomic sequencing identifies novel tissue-specific enhancers and sequence elements for methylation-sensitive factors implicated in Igf2/H19 imprinting.
Genome Res. 10, 664-671 (2000)
PubMed

Sado, T., Fenner, M. H., Tan, S-S., Tam, P., Shioda, T., & Li, E.
X-inactivation in the mouse embryo deficient for Dnmt1: Distinct effect of hypomethylation on imprinted and random X-inactivation.
Dev. Biol. 225, 294-303, (2000)
PubMed

Reviewsh
Sasaki, H., Ishihara, K. & Kato, R.
Mechanisms of Igf2/H19 imprinting: DNA methylation, chromatin and long-distance gene regulation.
J. Biochem. 127, 711-715 (2000)
PubMed

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