Unbiased shRNA screening, using a combination of FACS and high-throughput sequencing, enables identification of novel modifiers of Polycomb silencing

por Nishioka, Kenichi, Miyazaki, Hitomi, Soejima, Hidenobu
Publicado 2018

Placental Mesenchymal Dysplasia and Beckwith–Wiedemann Syndrome

por Soejima, Hidenobu, Hara, Satoshi, Ohba, Takashi, Higashimoto, Ken
Publicado 2022

Mbf1 ensures Polycomb silencing by protecting E(z) mRNA from degradation by Pacman

por Nishioka, Kenichi, Wang, Xian-Feng, Miyazaki, Hitomi, Soejima, Hidenobu, Hirose, Susumu
Publicado 2018

Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan

por TAKAMATSU, Yuichiro, HIGASHIMOTO, Ken, MAEDA, Toshiyuki, KAWASHIMA, Masatou, MATSUO, Muneaki, ABE, Tatsuya, MATSUSHIMA, Toshio, SOEJIMA, Hidenobu
Publicado 2017

Hypomethylation of a centromeric block of ICR1 is sufficient to cause Silver-Russell syndrome

por Higashimoto, Ken, Watanabe, Hijiri, Tanoue, Yuka, Tonoki, Hidefumi, Tokutomi, Tomoharu, Hara, Satoshi, Yatsuki, Hitomi, Soejima, Hidenobu
Publicado 2021

Growing oocyte-specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR

por Joh, Keiichiro, Matsuhisa, Fumikazu, Kitajima, Shuji, Nishioka, Kenichi, Higashimoto, Ken, Yatsuki, Hitomi, Kono, Tomohiro, Koseki, Haruhiko, Soejima, Hidenobu
Publicado 2018

ZAC, LIT1 (KCNQ1OT1) and p57(KIP2) (CDKN1C) are in an imprinted gene network that may play a role in Beckwith–Wiedemann syndrome

por Arima, Takahiro, Kamikihara, Tetsuya, Hayashida, Toshirou, Kato, Kiyoko, Inoue, Toshiaki, Shirayoshi, Yasuaki, Oshimura, Mitsuo, Soejima, Hidenobu, Mukai, Tunehiro, Wake, Norio
Publicado 2005

An analysis of the demographic history of the risk allele R4810K in RNF213 of moyamoya disease

por Koganebuchi, Kae, Sato, Kimitoshi, Fujii, Kiyotaka, Kumabe, Toshihiro, Haneji, Kuniaki, Toma, Takashi, Ishida, Hajime, Joh, Keiichiro, Soejima, Hidenobu, Mano, Shuhei, Ogawa, Motoyuki, Oota, Hiroki
Publicado 2021

TYK2 Promoter Variant Is Associated with Impaired Insulin Secretion and Lower Insulin Resistance in Japanese Type 2 Diabetes Patients

por Mori, Hitoe, Takahashi, Hirokazu, Mine, Keiichiro, Higashimoto, Ken, Inoue, Kanako, Kojima, Motoyasu, Kuroki, Shigetaka, Eguchi, Takahisa, Ono, Yasuhiro, Inuzuka, Sadataka, Soejima, Hidenobu, Nagafuchi, Seiho, Anzai, Keizo
Publicado 2021

Donor cord blood aging accelerates in recipients after transplantation

por Onizuka, Makoto, Imanishi, Tadashi, Harada, Kaito, Aoyama, Yasuyuki, Amaki, Jun, Toyosaki, Masako, Machida, Shinichiro, Kikkawa, Eri, Yamada, Sanetoshi, Nakabayashi, Kazuhiko, Hata, Kenichiro, Higashimoto, Ken, Soejima, Hidenobu, Ando, Kiyoshi
Publicado 2023

Ash1l Methylates Lys36 of Histone H3 Independently of Transcriptional Elongation to Counteract Polycomb Silencing

por Miyazaki, Hitomi, Higashimoto, Ken, Yada, Yukari, Endo, Takaho A., Sharif, Jafar, Komori, Toshiharu, Matsuda, Masashi, Koseki, Yoko, Nakayama, Manabu, Soejima, Hidenobu, Handa, Hiroshi, Koseki, Haruhiko, Hirose, Susumu, Nishioka, Kenichi
Publicado 2013

An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression

por Akiyama, Tokiho, Katsumura, Takafumi, Nakagome, Shigeki, Lee, Sang-il, Joh, Keiichiro, Soejima, Hidenobu, Fujimoto, Kazuma, Kimura, Ryosuke, Ishida, Hajime, Hanihara, Tsunehiko, Yasukouchi, Akira, Satta, Yoko, Higuchi, Shigekazu, Oota, Hiroki
Publicado 2017

Aberrant hypomethylation at imprinted differentially methylated regions is involved in biparental placental mesenchymal dysplasia

por Aoki, 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
Publicado 2022

Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer

por Hidaka, 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
Publicado 2018

DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2‐DMR0 as a DNA methylation‐dependent, P0 promoter‐specific enhancer

por Watanabe, 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
Publicado 2019

Comprehensive analyses of imprinted differentially methylated regions reveal epigenetic and genetic characteristics in hepatoblastoma

por Rumbajan, Janette Mareska, Maeda, Toshiyuki, Souzaki, Ryota, Mitsui, Kazumasa, Higashimoto, Ken, Nakabayashi, Kazuhiko, Yatsuki, Hitomi, Nishioka, Kenichi, Harada, Ryoko, Aoki, Shigehisa, Kohashi, Kenichi, Oda, Yoshinao, Hata, Kenichiro, Saji, Tsutomu, Taguchi, Tomoaki, Tajiri, Tatsuro, Soejima, Hidenobu, Joh, Keiichiro
Publicado 2013

Comprehensive and quantitative multilocus methylation analysis reveals the susceptibility of specific imprinted differentially methylated regions to aberrant methylation in Beckwit...

por Maeda, 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
Publicado 2014

Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment

por Court, Franck, Tayama, Chiharu, Romanelli, Valeria, Martin-Trujillo, Alex, Iglesias-Platas, Isabel, Okamura, Kohji, Sugahara, Naoko, Simón, Carlos, Moore, Harry, Harness, Julie V., Keirstead, Hans, Sanchez-Mut, Jose Vicente, Kaneki, Eisuke, Lapunzina, Pablo, Soejima, Hidenobu, Wake, Norio, Esteller, Manel, Ogata, Tsutomu, Hata, Kenichiro, Nakabayashi, Kazuhiko, Monk, David
Publicado 2014