A novel de novo point mutation of the OCT-binding site in the IGF2/H19-imprinting control region in a Beckwith-Wiedemann syndrome patient
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.
Published in Clinical genetics (01.12.2014)
Published in Clinical genetics (01.12.2014)
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Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome
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.
Published in Clinical genetics (01.09.2015)
Published in Clinical genetics (01.09.2015)
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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
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
Published in Journal of biochemistry (Tokyo) (01.11.2000)
Published in Journal of biochemistry (Tokyo) (01.11.2000)
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Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5 : long-stretches of unusually well conserved intronic sequences of Kvlqt1 between mouse and human
YATSUKI, H, WATANABE, H, KURATOMI, S, SASAKI, H, SAKAKI, Y, MUKAI, T, HATTORI, M, JOH, K, SOEJIMA, H, KOMODA, H, XIN, Z, ZHU, X, HIGASHIMOTO, K, NISHIMURA, M
Published in DNA research (30.06.2000)
Published in DNA research (30.06.2000)
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An NsiI RFLP in the human long QT intronic transcript 1 (LIT1)
Higashimoto, K, Soejima, H, Yatsuki, H, Katsuki, T, Mukai, T
Published in Journal of human genetics (01.03.2000)
Published in Journal of human genetics (01.03.2000)
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Journal Article
Expression and Sequence of the Only Detectable Aldolase in Chlamydomonas reinhardtii
Schnarrenberger, C., Pelzerreith, B., Yatsuki, H., Freund, S., Jacobshagen, S., Hori, K.
Published in Archives of biochemistry and biophysics (15.08.1994)
Published in Archives of biochemistry and biophysics (15.08.1994)
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High frequency of fusion transcripts of exon 11 and exon 4/5 in AF-4 gene is observed in cord blood, as well as leukemic cells from infant leukemia patients with t(4;11)(q21;q23)
YAMAMOTO, S, ZAITSU, M, ISHII, E, YATSUKI, H, MIZUTANI, S, EGUCHI, M, IHARA, K, OKAMURA, T, HARA, T, MIYAZAKI, S
Published in Leukemia (01.09.1998)
Published in Leukemia (01.09.1998)
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A Novel Human Homolog of a Dead-Box RNA Helicase Family
Kitajima, Y., Yatsuki, H., Zhang, R., Matsuhashi, S., Hori, K.
Published in Biochemical and biophysical research communications (15.03.1994)
Published in Biochemical and biophysical research communications (15.03.1994)
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Tissue-specific expression of rat aldolase A mRNAs. Three molecular species differing only in the 5'-terminal sequences
Mukai, T, Joh, K, Arai, Y, Yatsuki, H, Hori, K
Published in The Journal of biological chemistry (05.03.1986)
Published in The Journal of biological chemistry (05.03.1986)
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Nucleotide sequence of rat liver aldolase B messenger RNA
Tsutsumi, K, Mukai, T, Tsutsumi, R, Mori, M, Daimon, M, Tanaka, T, Yatsuki, H, Hori, K, Ishikawa, K
Published in The Journal of biological chemistry (10.12.1984)
Published in The Journal of biological chemistry (10.12.1984)
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The Mouse Murr1 Gene Is Imprinted in the Adult Brain, Presumably Due to Transcriptional Interference by the Antisense-Oriented U2af1-rs1 Gene
Wang, Youdong, Joh, Keiichiro, Masuko, Sadahiko, Yatsuki, Hitomi, Soejima, Hidenobu, Nabetani, Akira, Beechey, Colin V., Okinami, Satoshi, Mukai, Tsunehiro
Published in Molecular and Cellular Biology (01.01.2004)
Published in Molecular and Cellular Biology (01.01.2004)
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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 control region
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
Published in Genome research (01.12.2002)
Published in Genome research (01.12.2002)
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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
Higashimoto, Ken, Urano, Takeshi, Sugiura, Kazumitsu, Yatsuki, Hitomi, Joh, Keiichiro, Zhao, Wei, Iwakawa, Mayumi, Ohashi, Hirofumi, Oshimura, Mitsuo, Niikawa, Norio, Mukai, Tsunehiro, Soejima, Hidenobu
Published in American journal of human genetics (01.10.2003)
Published in American journal of human genetics (01.10.2003)
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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
Zhang, Zhongming, Joh, Keiichiro, Yatsuki, Hitomi, Wang, Youdong, Arai, Yuji, Soejima, Hidenobu, Higashimoto, Ken, Iwasaka, Tsuyoshi, Mukai, Tsunehiro
Published in Gene (17.01.2006)
Published in Gene (17.01.2006)
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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
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
Published in Genes & Genetic Systems (2008)
Published in Genes & Genetic Systems (2008)
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Characterization and Imprinting Status of OBPH1/Obph1 Gene: Implications for an Extended Imprinting Domain in Human and Mouse
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
Published in Genomics (San Diego, Calif.) (01.12.2002)
Published in Genomics (San Diego, Calif.) (01.12.2002)
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