A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient von Higashimoto, K., Jozaki, K., Kosho, T., Matsubara, K., Fuke, T., Yamada, D., Yatsuki, H., Maeda, T., Ohtsuka, Y., Nishioka, K., Joh, K., Koseki, H., Ogata, T., Soejima, H.

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Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome von Ohtsuka, Y., Higashimoto, K., Sasaki, K., Jozaki, K., Yoshinaga, H., Okamoto, N., Takama, Y., Kubota, A., Nakayama, M., Yatsuki, H., Nishioka, K., Joh, K., Mukai, T., Yoshiura, K.-i., Soejima, H.

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Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours von Satoh, Y, Nakadate, H, Nakagawachi, T, Higashimoto, K, Joh, K, Masaki, Z, Uozumi, J, Kaneko, Y, Mukai, T, Soejima, H

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Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer von Higashimoto, K., Soejima, H., Saito, T., Okumura, K., Mukai, T.

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Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancer von Nakagawachi, Tetsuji, Soejima, Hidenobu, Urano, Takeshi, Zhao, Wei, Higashimoto, Ken, Satoh, Yuji, Matsukura, Shiroh, Kudo, Shinichi, Kitajima, Yoshihiko, Harada, Haruhito, Furukawa, Koichi, Matsuzaki, Hideki, Emi, Mitsuru, Nakabeppu, Yusaku, Miyazaki, Kohji, Sekiguchi, Mutsuo, Mukai, Tsunehiro

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A Novel Imprinted Gene, KCNQ1DN, within the WT2 Critical Region of Human Chromosome 11p15.5 and Its Reduced Expression in Wilms' Tumors von Xin, Zhenghan, Soejima, Hidenobu, Higashimoto, Ken, Yatsuki, Hitomi, Zhu, Xike, Satoh, Yuji, Masaki, Zenjiro, Kaneko, Yasuhiko, Jinno, Yoshihiro, Fukuzawa, Ryuji, Hata, Jun-ichi, Mukai, Tsunehiro

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Primary palmar hyperhidrosis locus maps to 14q11.2-q13 von Higashimoto, Ikuyo, Yoshiura, Koh-ichiro, Hirakawa, Naomi, Higashimoto, Ken, Soejima, Hidenobu, Totoki, Tadahide, Mukai, Tsunehiro, Niikawa, Norio

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Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer von Soejima, Hidenobu, Nakagawachi, Tetsuji, Zhao, Wei, Higashimoto, Ken, Urano, Takeshi, Matsukura, Shiroh, Kitajima, Yoshihiko, Takeuchi, Makoto, Nakayama, Masahiro, Oshimura, Mitsuo, Miyazaki, Kohji, Joh, Keiichiro, Mukai, Tsunehiro

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An NsiI RFLP in the human long QT intronic transcript 1 (LIT1) von Higashimoto, K., Soejima, H., Yatsuki, H., Katsuki, T., Mukai, T.

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Essential Role of Histone H3 Lys9 Di-Methylation and MeCP2 Binding in MGMT Silencing with Poor DNA Methylation of the Promoter CpG Island von Zhao, Wei, Soejima, Hidenobu, Higashimoto, Ken, Nakagawachi, Tetsuji, Urano, Takeshi, Kudo, Shinichi, Matsukura, Shiroh, Matsuo, Shuzo, Joh, Keiichiro, Mukai, Tsunehiro

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Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene von Higashimoto, K., Soejima, H., Katsuki, T., Mukai, T.

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Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting contr... von Yatsuki, Hitomi, Joh, Keiichiro, Higashimoto, Ken, Soejima, Hidenobu, Arai, Yuji, Wang, Youdong, Hatada, Izuho, Obata, Yayoi, Morisaki, Hiroko, Zhang, Zhongming, Nakagawachi, Tetsuji, Satoh, Yuji, Mukai, Tsunehiro

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Loss of CpG Methylation Is Strongly Correlated with Loss of Histone H3 Lysine 9 Methylation at DMR-LIT1 in Patients with Beckwith-Wiedemann Syndrome von Higashimoto, Ken, Urano, Takeshi, Sugiura, Kazumitsu, Yatsuki, Hitomi, Joh, Keiichiro, Zhao, Wei, Iwakawa, Mayumi, Ohashi, Hirofumi, Oshimura, Mitsuo, Niikawa, Norio, Mukai, Tsunehiro, Soejima, Hidenobu

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MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products von Yakabe, S.(Saga Univ. (Japan). Faculty of Medicine), Soejima, H, Yatsuki, H, Tominaga, H, Zhao, W, Higashimoto, K, Joh, K, Kudo, S, Miyazaki, K, Mukai, T

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Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice von Zhang, Zhongming, Joh, Keiichiro, Yatsuki, Hitomi, Wang, Youdong, Arai, Yuji, Soejima, Hidenobu, Higashimoto, Ken, Iwasaka, Tsuyoshi, Mukai, Tsunehiro

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Imprinting disruption of the CDKN1CIKCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer von Higashimoto, K, Soejima, H, Saito, T, Okumura, K, Mukai, T

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Characterization and Imprinting Status of OBPH1/Obph1 Gene: Implications for an Extended Imprinting Domain in Human and Mouse von Higashimoto, Ken, Soejima, Hidenobu, Yatsuki, Hitomi, Joh, Keiichiro, Uchiyama, Michiko, Obata, Yayoi, Ono, Ryuichi, Wang, Youdong, Xin, Zhenghan, Zhu, Xike, Masuko, Sadahiko, Ishino, Fumitoshi, Hatada, Izuho, Jinno, Yoshihiro, Iwasaka, Tsuyoshi, Katsuki, Takeshi, Mukai, Tsunehiro

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Genetic and epigenetic alterations on the short arm of chromosome I I are involved in a majority of sporadic Wilms' tumours von SATOH, Y, NAKADATE, H, NAKAGAWACHI, T, HIGASHIMOTO, K, JOH, K, MASAKI, Z, UOZUMI, J, KANEKO, Y, MUKAI, T, SOEJIMA, H

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Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting contr... von Yatsuki, Hitomi, Joh, Keiichiro, Higashimoto, Ken, Soejima, Hidenobu, Arai, Yuji, Wang, Youdong, Hatada, Izuho, Obata, Yayoi, Morisaki, Hiroko, Zhang, Zhonming, Nakagawachi, Tetsuji, Satoh, Yuji, Mukai, Tsunehiro

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A Case of AIDS Patient Who Was Hard to Diagnose from an Initial Symptom of Interstitial Pneumonitis von HAKODA, Shigeru, HIGASHIMOTO, Kazuyoshi, KIUCHI, Shunichirou, KITAZAWA, Yasuhide, YONEZU, Seibun, FUJITA, Yoshiko, OKAMURA, Akiharu, TANAKA, Takaya

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