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收藏分享 收藏 分享 收藏 Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
Urakawa, Tatsuki; Soejima, Hidenobu; Yamoto, Kaori; Hara-Isono, Kaori; Nakamura, Akie; Kawashima, Sayaka; Narusawa, Hiromune; Kosaki, Rika; Nishimura, Yutaka; Yamazawa, Kazuki; Hattori, Tetsuo; Muramatsu, Yukako; Inoue, Takanobu; Matsubara, Keiko; Fukami, Maki; Saitoh, Shinji; Ogata, Tsutomu; Kagami, Masayo 分享 收藏 Whole-exome sequencing reveals causative genetic variants for several overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum全外显子组测序揭示了分子阴性beckwist-wiedemann谱中几种过度生长综合征的致病遗传变异Higashimoto, Ken; Sun, Feifei; Imagawa, Eri; Saida, Ken; Miyake, Noriko; Hara, Satoshi; Yatsuki, Hitomi; Kubiura-Ichimaru, Musashi; Fujita, Atsushi; Mizuguchi, Takeshi; Matsumoto, Naomichi; Soejima, Hidenobu 分享 收藏 Role of DNA methylation and histone H3 lysine 27 methylation in tissue-specific imprinting of mouse Grb10Yamasaki-Ishizaki, Yoko; Kayashima, Tomohiko; Mapendano, Christophe K.; Soejima, Hidenobu; Ohta, Tohru; Masuzaki, Hideaki; Kinoshita, Akira; Urano, Takeshi; Yoshiura, Ko-ichiro; Matsumoto, Naomichi; Ishimaru, Tadayuki; Mukai, Tsunehiro; Niikawa, Norio; Kishino, Tatsuya 分享 收藏 The mouse Murr1 gene is imprinted in the adult brain, presumably due to transcriptional interference by the antisense-oriented U2af1-rs1 geneWang, YD; Joh, K; Masuko, S; Yatsuki, H; Soejima, H; Nabetani, A; Beechey, CV; Okinami, S; Mukai, T 分享 收藏 Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasiaAoki, Saori; Higashimoto, Ken; Hidaka, Hidenori; Ohtsuka, Yasufumi; Aoki, Shigehisa; Mishima, Hiroyuki; Yoshiura, Koh-ichiro; Nakabayashi, Kazuhiko; Hata, Kenichiro; Yatsuki, Hitomi; Hara, Satoshi; Ohba, Takashi; Katabuchi, Hidetaka; Soejima, Hidenobu 分享 收藏 Short-term running exercise alters DNA methylation patterns in neuronal nitric oxide synthase and brain-derived neurotrophic factor genes in the mouse hippocampus and reduces anxiety-like behaviors短期跑步运动改变了小鼠海马神经元一氧化氮合酶和脑源性神经营养因子基因的DNA甲基化模式，并减少了焦虑样行为Tomiga, Yuki; Sakai, Kazuya; Ra, Song-Gyu; Kusano, Masaki; Ito, Ai; Uehara, Yoshinari; Takahashi, Hirokazu; Kawanaka, Kentaro; Soejima, Hidenobu; Higaki, Yasuki 分享 收藏 分享 收藏 DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancerWatanabe, Hidetaka; Higashimoto, Ken; Miyake, Noriko; Morita, Sumiyo; Horii, Takuro; Kimura, Mika; Suzuki, Takayuki; Maeda, Toshiyuki; Hidaka, Hidenori; Aoki, Saori; Yatsuki, Hitomi; Okamoto, Nobuhiko; Uemura, Tetsuji; Hatada, Izuho; Matsumoto, Naomichi; Soejima, Hidenobu 分享 收藏 IFPA meeting 2018 workshop report I: Reproduction and placentation among ocean-living species; placental imaging; epigenetics and extracellular vesicles in pregnancyAcharya, Ganesh; Bartolomei, Marisa; Carter, Anthony M.; Chamley, Larry; Cotton, Charles F.; Hasegawa, Junichi; Hasegawa, Yuri; Hayakawa, Satoshi; Kawaguchi, Mari; Konwar, Chaini; Magawa, Shoichi; Miura, Kiyonori; Nishi, Hirotaka; Salomon, Carlos; Sato, Keiichi; Soejima, Hidenobu; Soma, Hiroaki; Sorensen, Anne; Takahashi, Hironori; Tomita, Taketeru; Whittington, Camilla M.; Yuan, Victor; O'Tierney-Ginn, Perrie 分享 收藏 Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancerHidaka, Hidenori; Higashimoto, Ken; Aoki, Saori; Mishima, Hiroyuki; Hayashida, Chisa; Maeda, Toshiyuki; Koga, Yasuo; Yatsuki, Hitomi; Joh, Keiichiro; Noshiro, Hirokazu; Iwakiri, Ryuichi; Kawaguchi, Atsushi; Yoshiura, Koh-ichiro; Fujimoto, Kazuma; Soejima, Hidenobu 分享 收藏 分享 收藏 分享 收藏 CTCF deletion syndrome: clinical features and epigenetic delineationHori, Ikumi; Kawamura, Rie; Nakabayashi, Kazuhiko; Watanabe, Hidetaka; Higashimoto, Ken; Tomikawa, Junko; Ieda, Daisuke; Ohashi, Kei; Negishi, Yutaka; Hattori, Ayako; Sugio, Yoshitsugu; Wakui, Keiko; Hata, Kenichiro; Soejima, Hidenobu; Kurosawa, Kenji; Saitoh, Shinji 分享 收藏 Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome编码polycomb抑制复合物2亚基的基因突变导致Weaver综合征Imagawa, Eri; Higashimoto, Ken; Sakai, Yasunari; Numakura, Chikahiko; Okamoto, Nobuhiko; Matsunaga, Satoko; Ryo, Akihide; Sato, Yoshinori; Sanefuji, Masafumi; Ihara, Kenji; Takada, Yui; Nishimura, Gen; Saitsu, Hirotomo; Mizuguchi, Takeshi; Miyatake, Satoko; Nakashima, Mitsuko; Miyake, Noriko; Soejima, Hidenobu; Matsumoto, Naomichi 分享 收藏 Identification of consensus motifs associated with mitotic recombination and clinical characteristics in patients with paternal uniparental isodisomy of chromosome 11Ohtsuka, Yasufumi; Higashimoto, Ken; Oka, Takehiko; Yatsuki, Hitomi; Jozaki, Kosuke; Maeda, Toshiyuki; Kawahara, Kozo; Hamasaki, Yuhei; Matsuo, Muneaki; Nishioka, Kenichi; Joh, Keiichiro; Mukai, Tsunehiro; Soejima, Hidenobu 分享 收藏 MOLECULAR GENETIC INVESTIGATION OF PLACENTAL MESENCHYMAL DYSPLASIAAoki, Saori; Higashimoto, Ken; Hidaka, Hidenori; Watanabe, Hidetaka; Ohtsuka, Yasufumi; Mishima, Hiroyuki; Yoshiura, Koh-ichiro; Yatsuki, Hitomi; Nishioka, Kenichi; Joh, Kei-ichiro; Ohba, Takashi; Katabuchi, Hidetaka; Soejima, Hidenobu 分享 收藏 Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwith-Wiedemann syndrome with epimutationsMaeda, Toshiyuki; Higashimoto, Ken; Jozaki, Kosuke; Yatsuki, Hitomi; Nakabayashi, Kazuhiko; Makita, Yoshio; Tonoki, Hidefumi; Okamoto, Nobuhiko; Takada, Fumio; Ohashi, Hirofumi; Migita, Makoto; Kosaki, Rika; Matsubara, Keiko; Ogata, Tsutomu; Matsuo, Muneaki; Hamasaki, Yuhei; Ohtsuka, Yasufumi; Nishioka, Kenichi; Joh, Keiichiro; Mukai, Tsunehiro; Hata, Kenichiro; Soejima, Hidenobu 分享 收藏 
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