田山千春 (Chiharu Tayama) - マイポータル

基本情報

所属: 国立成育医療研究センター研究所周産期病態研究部研究員

研究者番号: 60774445
J-GLOBAL ID: 202101006102418990
researchmap会員ID: R000031232

論文

Placenta-specific epimutation at H19-DMR among common pregnancy complications: its frequency and effect on the expression patterns of H19 and IGF2.

Yuko Yamaguchi, Chiharu Tayama, Junko Tomikawa, Rina Akaishi, Hiromi Kamura, Kentaro Matsuoka, Norio Wake, Hisanori Minakami, Kiyoko Kato, Takahiro Yamada …

Clinical epigenetics 11(1) 113-113 2019年8月1日
Characterization of parent-of-origin methylation using the Illumina Infinium MethylationEPIC array platform.

Jose R Hernandez Mora, Chiharu Tayama, Marta Sánchez-Delgado, Ana Monteagudo-Sánchez, Kenichiro Hata, Tsutomu Ogata, Jose Medrano, Maria E Poo-Llanillo, Carlos Simón, Sebastian Moran …

Epigenomics 10(7) 941-954 2018年7月
Human Oocyte-Derived Methylation Differences Persist in the Placenta Revealing Widespread Transient Imprinting.

Marta Sanchez-Delgado, Franck Court, Enrique Vidal, Jose Medrano, Ana Monteagudo-Sánchez, Alex Martin-Trujillo, Chiharu Tayama, Isabel Iglesias-Platas, Ivanela Kondova, Ronald Bontrop …

PLoS genetics 12(11) e1006427 2016年11月
Imprinting control regions (ICRs) are marked by mono-allelic bivalent chromatin when transcriptionally inactive.

Stéphanie Maupetit-Méhouas, Bertille Montibus, David Nury, Chiharu Tayama, Michel Wassef, Satya K Kota, Anne Fogli, Fabiana Cerqueira Campos, Kenichiro Hata, Robert Feil …

Nucleic acids research 44(2) 621-35 2016年1月29日
Absence of Maternal Methylation in Biparental Hydatidiform Moles from Women with NLRP7 Maternal-Effect Mutations Reveals Widespread Placenta-Specific Imprinting.

Marta Sanchez-Delgado, Alejandro Martin-Trujillo, Chiharu Tayama, Enrique Vidal, Manel Esteller, Isabel Iglesias-Platas, Nandita Deo, Olivia Barney, Ken Maclean, Kenichiro Hata …

PLoS genetics 11(11) e1005644 2015年11月
Integration of transcriptome and methylome analysis of aldosterone-producing adenomas.

Masanori Murakami, Takanobu Yoshimoto, Kazuhiko Nakabayashi, Kyoichiro Tsuchiya, Isao Minami, Ryotaro Bouchi, Hajime Izumiyama, Yasuhisa Fujii, Kosei Abe, Chiharu Tayama …

European journal of endocrinology 173(2) 185-95 2015年8月
Genomic, Epigenomic, and Transcriptomic Profiling towards Identifying Omics Features and Specific Biomarkers That Distinguish Uterine Leiomyosarcoma and Leiomyoma at Molecular Levels.

Tomoko Miyata, Kenzo Sonoda, Junko Tomikawa, Chiharu Tayama, Kohji Okamura, Kayoko Maehara, Hiroaki Kobayashi, Norio Wake, Kiyoko Kato, Kenichiro Hata …

Sarcoma 2015 412068-412068 2015年
HBx induces hypomethylation of distal intragenic CpG islands required for active expression of developmental regulators.

Sun-Min Lee, Young-gun Lee, Jae-Bum Bae, Jung Kyoon Choi, Chiharu Tayama, Kenichiro Hata, Yungdae Yun, Je-Kyung Seong, Young-Joon Kim

Proceedings of the National Academy of Sciences of the United States of America 111(26) 9555-60 2014年7月1日
Genome-wide parent-of-origin DNA methylation analysis reveals the intricacies of human imprinting and suggests a germline methylation-independent mechanism of establishment.

Franck Court, Chiharu Tayama, Valeria Romanelli, Alex Martin-Trujillo, Isabel Iglesias-Platas, Kohji Okamura, Naoko Sugahara, Carlos Simón, Harry Moore, Julie V Harness …

Genome research 24(4) 554-69 2014年4月
Molecular and clinical studies in 138 Japanese patients with Silver-Russell syndrome.

Tomoko Fuke, Seiji Mizuno, Toshiro Nagai, Tomonobu Hasegawa, Reiko Horikawa, Yoko Miyoshi, Koji Muroya, Tatsuro Kondoh, Chikahiko Numakura, Seiji Sato …

PloS one 8(3) e60105 2013年
Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes.

Kazuhiko Nakabayashi, Alex Martin Trujillo, Chiharu Tayama, Cristina Camprubi, Wataru Yoshida, Pablo Lapunzina, Aurora Sanchez, Hidenobu Soejima, Hiroyuki Aburatani, Genta Nagae …

Human molecular genetics 20(16) 3188-97 2011年8月15日

MISC

KLF14欠損マウスにおける肥満誘導時の白色脂肪組織リモデリング異常

田山千春, 高梨理絵子, 富川順子, 大喜多肇, 松本健治, 秦健一郎, 岡村匡史, 中林一彦

生命科学系学会合同年次大会 2017年度 [1P-1163] 2017年12月

共同研究・競争的資金等の研究課題

代謝カスケード調節遺伝子KLF14の転写制御機構・生理機能の解明

日本学術振興会科学研究費助成事業基盤研究(C) 2013年4月 - 2017年3月

中林一彦, 高田修治, 冨川順子, 田山千春, 菅原直子