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Results:
1-7
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Results: 7
Authors:
Gregory, RI
Randall, TE
Johnson, CA
Khosla, S
Hatada, I
O'Neill, LP
Turner, BM
Feil, R
Citation: Ri. Gregory et al., DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1, MOL CELL B, 21(16), 2001, pp. 5426-5436
Authors:
Sotomaru, Y
Kawase, Y
Ueda, T
Obata, Y
Suzuki, H
Domeki, I
Hatada, I
Kono, T
Citation: Y. Sotomaru et al., Disruption of imprinted expression of U2afbp-rs/U2af1-rs1 gene in mouse parthenogenetic fetuses, J BIOL CHEM, 276(28), 2001, pp. 26694-26698
Authors:
Hatada, I
Morita, S
Obata, Y
Sotomaru, Y
Shimoda, M
Kono, T
Citation: I. Hatada et al., Identification of a new imprinted gene, Rian, on mouse chromosome 12 by fluorescent differential display screening, J BIOCHEM, 130(2), 2001, pp. 187-190
Authors:
Hatada, I
Mukai, T
Citation: I. Hatada et T. Mukai, Genomic imprinting and Beckwith-Wiedemann syndrome, HIST HISTOP, 15(1), 2000, pp. 309-312
Authors:
Schwienbacher, C
Angioni, A
Scelfo, R
Veronese, A
Calin, GA
Massazza, G
Hatada, I
Barbanti-Brodano, G
Negrini, M
Citation: C. Schwienbacher et al., Abnormal RNA expression of 11p15 imprinted genes and kidney developmental genes in Wilms' tumor, CANCER RES, 60(6), 2000, pp. 1521-1525
Authors:
Bhuiyan, ZA
Yatsuki, H
Sasaguri, T
Joh, K
Soejima, H
Zhu, XK
Hatada, I
Morisaki, H
Morisaki, T
Mukai, T
Citation: Za. Bhuiyan et al., Functional analysis of the p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome, HUM GENET, 104(3), 1999, pp. 205-210
Authors:
Lam, WWK
Hatada, I
Ohishi, S
Mukai, T
Joyce, JA
Cole, TRP
Donnai, D
Reik, W
Schofield, PN
Maher, ER
Citation: Wwk. Lam et al., Analysis of germline CDKN1C (p57(KIP2)) mutations in familial and sporadicBeckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation, J MED GENET, 36(7), 1999, pp. 518-523
Risultati:
1-7
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