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Identification of regulatory factors for somatic imprinted DMR establishment and elucidation of their molecular mechanisms

Research Project

Project/Area Number 17K08687
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Human genetics
Research InstitutionSaga University

Principal Investigator

Soejima Hidenobu  佐賀大学, 医学部, 教授 (30304885)

Project Period (FY) 2017-04-01 – 2020-03-31
Project Status Completed (Fiscal Year 2019)
Budget Amount *help
¥4,680,000 (Direct Cost: ¥3,600,000、Indirect Cost: ¥1,080,000)
Fiscal Year 2019: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2018: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Keywords体細胞性インプリントDMR / DNAメチル化 / ゲノムインプリンティング / メチル化可変領域 / 遺伝子発現 / エピジェネティクス
Outline of Final Research Achievements

We screened regulatory factors for somatic imprinted DMR establishment within Igf2r/Airn domain using shRNA libraries. We found six genes as candidates. Second-order analyses revealed two genes as putative regulatory factors for the somatic DMR establishment. In addition, we generated model mice, in which candidate regions for DMR establishment were deleted, to clarify a mechanism of DMR establishment within Kcnq1ot1/Cdkn1c domain. Since DMR methylation did not change in the model mice, it was suggested that the regulatory region for DMR establishment did not exist within the deleted region. However, it was suggested that at least the enhancer for Cdkn1c would be included within the deleted region because Cdkn1c expression decreased in the model mice.

Academic Significance and Societal Importance of the Research Achievements

インプリント関連疾患では、配偶子形成過程で確立されるgDMRだけではなく、着床後に確立されるsDMRのメチル化も重要である。sDMRのメチル化を制御する因子の同定を目的に、Igf2r/Airn領域を対象に解析したところ、候補制御因子を2種類同定した。一方、Kcnq1ot1/Cdkn1c領域では、少なくともCdkn1cの候補エンハンサーの存在を突き止めた。インプリンティングの分子機構解明と疾患の病態解明に寄与する結果と考えられる。

Report

(4 results)
  • 2019 Annual Research Report   Final Research Report ( PDF )
  • 2018 Research-status Report
  • 2017 Research-status Report
  • Research Products

    (56 results)

All 2019 2018 2017 Other

All Journal Article (16 results) (of which Int'l Joint Research: 3 results,  Peer Reviewed: 16 results,  Open Access: 13 results,  Acknowledgement Compliant: 2 results) Presentation (35 results) (of which Int'l Joint Research: 4 results,  Invited: 11 results) Book (3 results) Remarks (2 results)

  • [Journal Article] The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome2019

    • Author(s)
      Sun Feifei、Higashimoto Ken、Awaji Atsuko、Ohishi Kenji、Nishizaki Naoto、Tanoue Yuka、Aoki Saori、Watanabe Hidetaka、Yatsuki Hitomi、Soejima Hidenobu
    • Journal Title

      Journal of Human Genetics

      Volume: 64 Issue: 9 Pages: 937-943

    • DOI

      10.1038/s10038-019-0634-0

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Habitual Light-intensity Physical Activity and ASC Methylation in a Middle-aged Population2019

    • Author(s)
      Nishida Y、Hara M、Higaki Y、Taguchi N、Nakamura K、Nanri H、Horita M、Shimanoe C、Yasukata J、Miyoshi N、Yamada Y、Higashimoto K、Soejima H、Tanaka K
    • Journal Title

      International Journal of Sports Medicine

      Volume: 40 Issue: 10 Pages: 670-677

    • DOI

      10.1055/a-0965-1374

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed
  • [Journal Article] One week, but not 12?hours, of cast immobilization alters promotor DNA methylation patterns in the nNOS gene in mouse skeletal muscle2019

    • Author(s)
      Tomiga Yuki、Ito Ai、Sudo Mizuki、Ando Soichi、Eshima Hiroaki、Sakai Kazuya、Nakashima Shihoko、Uehara Yoshinari、Tanaka Hiroaki、Soejima Hidenobu、Higaki Yasuki
    • Journal Title

      The Journal of Physiology

      Volume: 597 Issue: 21 Pages: 5145-5159

    • DOI

      10.1113/jp277019

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] DNA methylation analysis of multiple imprinted DMRs in Sotos syndrome reveals IGF2-DMR0 as a DNA methylation-dependent, P0 promoter-specific enhancer.2019

    • Author(s)
      Watanabe H, Higashimoto K, Miyake N, Morita S, Horii T, Kimura M, Suzuki T, Maeda T, Hidaka H, Aoki S, Yatsuki H, Okamoto N, Uemura T, Hatada I, Matsumoto N, Soejima H.
    • Journal Title

      FASEB J.

      Volume: 34 Issue: 1 Pages: 960-973

    • DOI

      10.1096/fj.201901757r

    • Related Report
      2019 Annual Research Report
    • Peer Reviewed / Open Access
  • [Journal Article] Beckwith-Wiedemann syndrome with asymmetric mosaic of paternal disomy causing hemihyperplasia2019

    • Author(s)
      Yamada Tomohiro、Sugiyama Goro、Higashimoto Ken、Nakashima Azusa、Nakano Hiroyuki、Sumida Tomoki、Soejima Hidenobu、Mori Yoshihide
    • Journal Title

      Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology

      Volume: 127 Issue: 3 Pages: e84-e88

    • DOI

      10.1016/j.oooo.2018.07.053

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Hepatoblastoma in an extremely low birth-weight infant with Beckwith?Wiedemann syndrome2018

    • Author(s)
      Kawasaki Yukako、Makimoto Masami、Samejima Azusa、Yoneda Noriko、Higashimoto Ken、Soejima Hidenobu、Yoshida Taketoshi
    • Journal Title

      Pediatrics & Neonatology

      Volume: 59 Issue: 5 Pages: 523-524

    • DOI

      10.1016/j.pedneo.2017.11.012

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Growing oocyte specific transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR2018

    • Author(s)
      Joh, K., Matsuhisa, F., Kitajima, S., Nishioka, K., Higashimoto, K., Yatsuki, H., Kono, T., Koseki, H., Soejima, H.
    • Journal Title

      Epigenetics & Chromatin

      Volume: 11 Issue: 1 Pages: 28-28

    • DOI

      10.1186/s13072-018-0200-6

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research
  • [Journal Article] Unbiased shRNA screening, using a combination of FACS and high-throughput sequencing, enables identification of novel modifiers of Polycomb silencing2018

    • Author(s)
      Nishioka Kenichi、Miyazaki Hitomi、Soejima Hidenobu
    • Journal Title

      Scientific Reports

      Volume: 8 Issue: 1 Pages: 12128-12128

    • DOI

      10.1038/s41598-018-30649-6

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Comprehensive methylation analysis of imprinting-associated differentially methylated regions in colorectal cancer.2018

    • Author(s)
      Hidaka H, Higashimoto K, Aoki S, Mishima H, Hayashida C, Maeda T, Koga Y, Yatsuki H, Joh K, Noshiro H, Iwakiri R, Kawaguchi A, Yoshiura KI, Fujimoto K, Soejima H.
    • Journal Title

      Clin Epigenetics

      Volume: 10 Issue: 1 Pages: 150-150

    • DOI

      10.1186/s13148-018-0578-9

    • Related Report
      2018 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Mbf1 ensures Polycomb silencing by protecting E(z) mRNA from degradation by Pacman2018

    • Author(s)
      Nishioka Kenichi、Wang Xian-Feng、Miyazaki Hitomi、Soejima Hidenobu、Hirose Susumu
    • Journal Title

      Development

      Volume: 145 Issue: 5 Pages: 162461-162461

    • DOI

      10.1242/dev.162461

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] The allele frequency of ALDH2*Glu504Lys and ADH1B*Arg47His for the Ryukyu islanders and their history of expansion among East Asians2017

    • Author(s)
      Koganebuchi, K., Haneji, K., Toma, T., Joh, K., Soejima, H., Fujimoto, K., Ishida, H., Ogawa, M., Hanihara, T., Harada, S., Kawamura, S. and *Oota, H.
    • Journal Title

      American Journal of Human Biology

      Volume: 29 Issue: 2 Pages: 1-14

    • DOI

      10.1002/ajhb.22933

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] Long term survival of a patient with Perlman syndrome due to novel compound heterozygous missense mutations in RNB domain ofDIS3L22017

    • Author(s)
      Soma Noriko、Higashimoto Ken、Imamura Masaru、Saitoh Akihiko、Soejima Hidenobu、Nagasaki Keisuke
    • Journal Title

      Am J Med Genet Part A

      Volume: 173 Issue: 4 Pages: 1077-1081

    • DOI

      10.1002/ajmg.a.38111

    • Related Report
      2017 Research-status Report
    • Peer Reviewed
  • [Journal Article] Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome2017

    • Author(s)
      Eri Imagawa, Ken Higashimoto, Yasunari Sakai, Chikahiko Numakura, Nobuhiko Okamoto, Satoko Matsunaga, Akihide Ryo, Yoshinori Sato, Masafumi Sanefuji, Kenji Ihara, Yui Takada, Gen Nishimura, Hirotomo Saitsu, Takeshi Mizuguchi, Satoko Miyatake, Mitsuko Nakashima, Noriko Miyake, Hidenobu Soejima, Naomichi Matsumoto
    • Journal Title

      Human Mutation

      Volume: 印刷中 Issue: 6 Pages: 637-648

    • DOI

      10.1002/humu.23200

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access / Int'l Joint Research / Acknowledgement Compliant
  • [Journal Article] An ancestral haplotype of the human PERIOD2 gene associates with reduced sensitivity to light-induced melatonin suppression2017

    • Author(s)
      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
    • Journal Title

      PLoS One

      Volume: 12 Issue: 6 Pages: e0178373-e0178373

    • DOI

      10.1371/journal.pone.0178373

    • NAID

      120006891149

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan2017

    • Author(s)
      TAKAMATSU Yuichiro、HIGASHIMOTO Ken、MAEDA Toshiyuki、KAWASHIMA Masatou、MATSUO Muneaki、ABE Tatsuya、MATSUSHIMA Toshio、SOEJIMA Hidenobu
    • Journal Title

      Neurologia medico-chirurgica

      Volume: 57 Issue: 11 Pages: 607-611

    • DOI

      10.2176/nmc.oa.2017-0036

    • NAID

      130006201788

    • ISSN
      0470-8105, 1349-8029
    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access
  • [Journal Article] CTCF deletion syndrome: Clinical features and epigenetic delineation2017

    • Author(s)
      Hori I, Kawamura R, Nakabayashi K, Watanabe H, Higashimoto K, Tomikawa J, Ieda D, Ohashi K, Negishi Y, Hattori A, Sugio Y, Wakui K, Hata K, Soejima H, Kurosawa K, Saitoh S
    • Journal Title

      Journal of Medical Genetics

      Volume: 54 Issue: 12 Pages: 836-842

    • DOI

      10.1136/jmedgenet-2017-104854

    • Related Report
      2017 Research-status Report
    • Peer Reviewed / Open Access
  • [Presentation] ヒト疾患のエピゲノム2019

    • Author(s)
      副島英伸
    • Organizer
      日本人類遺伝学会第64回大会
    • Related Report
      2019 Annual Research Report
    • Invited
  • [Presentation] 先天異常症候群のエピゲノム異常2019

    • Author(s)
      副島英伸
    • Organizer
      日本人類遺伝学会第64回大会
    • Related Report
      2019 Annual Research Report
    • Invited
  • [Presentation] IGF2 overexpression due to IGF2-DMR0 hypomethylation in Sotos syndrome.2019

    • Author(s)
      Higashimoto K, Watanabe H, Miyake N, Morita S, Horii T, Maeda T, Hidaka H, Aoki S, Yatsuki H, Okamoto N, Hatada I, Matsumoto N, Soejima H.
    • Organizer
      The 59th Annual Meeting of The Japanese Teratology Society, The 13th World Congress of The International Cleft Lip and Palate Foundation
    • Related Report
      2019 Annual Research Report
    • Int'l Joint Research / Invited
  • [Presentation] Methylation anticipation extends to the outside of ICR1 in familial Beckwith-Wiedemann syndrome patients with ICR1 mutation.2019

    • Author(s)
      Sun F, Higashimoto K, Soejima H.
    • Organizer
      European Society of Human Genetics Conference 2019
    • Related Report
      2019 Annual Research Report
  • [Presentation] Atypical DNA methylation defects of ICR1 cause two opposite imprinting disorders, Beckwith-Wiedemann syndrome and Silver-Russell syndrome.2019

    • Author(s)
      Soejima H, Sun F, Tanoue Y, Yatsuki H, Higashimoto K.
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] IGF2-DMR0はDNAメチル化依存的なIGF2 P0プロモーター特異的エンハンサーである-ソトス症候群のインプリントDMRのDNAメチル化解析から-2019

    • Author(s)
      東元健、渡邊英孝、三宅紀子、森田純代、堀居拓郎、畑田出穂、松本直通、副島英伸.
    • Organizer
      第42回日本分子生物学会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] The extent of DNA methylation anticipation due to a genetic defect in ICR1 in Beckwith-Wiedemann syndrome.2019

    • Author(s)
      Sun F, Higashimoto K, Soejima H.
    • Organizer
      日本人類遺伝学会第64回大会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 乳癌と卵巣癌を合併する症例の検討.2019

    • Author(s)
      大隈恵美、橋口真理子、山本徒子、西山哲、光貴子、中尾佳史、副島英伸、横山正俊.
    • Organizer
      日本人類遺伝学会第64回大会
    • Related Report
      2019 Annual Research Report
  • [Presentation] 本邦の間葉性異形成胎盤症例における妊娠高血圧症候群の発症に関する検討―PMD全国調査の副次的解析―.2019

    • Author(s)
      小寺千聡、大場 隆、副島英伸、片渕秀隆.
    • Organizer
      第40回日本妊娠高血圧学会学術集会
    • Related Report
      2019 Annual Research Report
  • [Presentation] FACSと次世代シークエンサーを用いたshRNAライブラリースクリーニングによるポリコームサイレンシング制御因子の探索2019

    • Author(s)
      西岡憲一、宮_仁美、副島英伸.
    • Organizer
      第13回日本エピジェネティクス研究会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] DNA methylation anticipation due to ICR1 mutation in familial Beckwith-Wiedemann syndrome patients.2019

    • Author(s)
      Sun F, Higashimoto K, Soejima H. The extended
    • Organizer
      第13回日本エピジェネティクス研究会年会
    • Related Report
      2019 Annual Research Report
  • [Presentation] HBOCの遺伝カウンセリング2019

    • Author(s)
      副島英伸
    • Organizer
      第11回佐賀乳腺フォーラム
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] 眼瞼腫脹を契機に神経芽細胞腫が判明したBeckwith-Wiedemann症候群の女児.2018

    • Author(s)
      米田堅佑、川口晃司、高橋郁子、小倉妙美、堀越泰雄、宮林和紀、左藤由梨亜、東元健、副島英伸、渡邉健一郎
    • Organizer
      第121回日本小児科学会学術集会
    • Related Report
      2018 Research-status Report
  • [Presentation] エピジェネティクス_基礎と疾患_2018

    • Author(s)
      副島英伸
    • Organizer
      第42回日本産婦人科栄養・代謝研究会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] Beckwith-Wiedemann症候群とゲノムインプリンティング2018

    • Author(s)
      副島英伸
    • Organizer
      第175回染色体研究会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] 超早産児で出生した11p15.5重複によるBeckwith-Wiedemann症候群の一例2018

    • Author(s)
      香田翼、三崎真衣子、柴田暁男、川本久美、東元健、副島英伸、竹島泰弘
    • Organizer
      日本人類遺伝学会第63回大会 2017.10.10-13. パシフィコ横浜(ポスターP-195、プログラム・抄録集 p152/p353)
    • Related Report
      2018 Research-status Report
  • [Presentation] エピゲノム―基礎と疾患―2018

    • Author(s)
      副島英伸
    • Organizer
      日本人類遺伝学会第63回大会
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] FACSと次世代シークエンサーを用いたshRNAライブラリースクリーニングによるポリコームサイレンシング制御因子の探索2018

    • Author(s)
      西岡憲一、宮崎仁美、副島英伸
    • Organizer
      第41回日本分子生物学会年会
    • Related Report
      2018 Research-status Report
  • [Presentation] 佐賀大学におけるHBOCの遺伝カウンセリング2018

    • Author(s)
      副島英伸
    • Organizer
      BRCA遺伝子変異陽性乳癌診療セミナー in Saga
    • Related Report
      2018 Research-status Report
    • Invited
  • [Presentation] NSD1 haploinsufficiency evokes DNA hypomethylation at imprinted DMRs and the increased expression of imprinted genes.2018

    • Author(s)
      Watanabe H, Higashimoto K, Nagano Y, Kurokawa M, Uemura T, Soejima H
    • Organizer
      EURAPS Research Meeting 2018.
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research
  • [Presentation] Transcription-dependent de novo DNA methylation at the imprinted Zrsr1-DMR occurs in the growing oocyte, but not in early embryonic cells.2018

    • Author(s)
      Soejima H, Matsuhisa F, Kitajima S, Nishioka K, Higashimoto K, Yatsuki H, Kono T, Koseki, H Joh K.
    • Organizer
      European Society of Human Genetics Conference 2018.
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research
  • [Presentation] Beckwith-Wiedemann syndrome and placental mesenchymal dysplasia.2018

    • Author(s)
      Soejima H.
    • Organizer
      International Federation of Placenta Associations (IFPA 2018 Tokyo Meeting)
    • Related Report
      2018 Research-status Report
    • Int'l Joint Research / Invited
  • [Presentation] Mbf1はPacmanからE(z) mRNAを保護することでポリコームサイレンシングの堅牢性を担保している2017

    • Author(s)
      西岡憲一、宮崎仁美、副島英伸、広瀬進
    • Organizer
      第11回日本エピジェネティクス研究会年会
    • Related Report
      2017 Research-status Report
  • [Presentation] マウスCommd1とZrsr1のゲノムインプリンティング機構の研究2017

    • Author(s)
      城 圭一郎、西岡憲一、北嶋修司、松久葉一、古関明彦、河野友宏、副島英伸
    • Organizer
      第11回日本エピジェネティクス研究会年会
    • Related Report
      2017 Research-status Report
  • [Presentation] 大腸癌におけるインプリントDMRの包括的メチル化解析2017

    • Author(s)
      樋高秀憲、東元健、青木早織、渡邊英孝、前田寿幸、古賀靖大、岩切龍一、能城浩和、藤本一眞、副島英伸
    • Organizer
      第11回日本エピジェネティクス研究会年会
    • Related Report
      2017 Research-status Report
  • [Presentation] NSD1ハプロ不全はDNAメチル化インプリント異常と遺伝子発現異常を惹起する2017

    • Author(s)
      渡邊英孝、東元健、三宅紀子、前田寿幸、樋高秀憲、青木早織、八木ひとみ、西岡憲一、城圭一郎、松本直通、副島英伸
    • Organizer
      第11回日本エピジェネティクス研究会年会
    • Related Report
      2017 Research-status Report
  • [Presentation] ゲノムインプリンティングのoverviewとBeckwith-Wiedemann症候群2017

    • Author(s)
      副島英伸
    • Organizer
      日本人類遺伝学会第62回大会
    • Related Report
      2017 Research-status Report
    • Invited
  • [Presentation] NSD1ハプロ不全はDNAメチル化インプリント異常と遺伝子発現異常を惹起する2017

    • Author(s)
      渡邊英孝、東元健、三宅紀子、前田寿幸、樋高秀憲、青木早織、八木ひとみ、西岡憲一、城圭一郎、松本直通、副島英伸
    • Organizer
      日本人類遺伝学会第62回大会
    • Related Report
      2017 Research-status Report
  • [Presentation] ポリコーム抑制複合体2の構成蛋白質の遺伝子変異がWeaver症候群を引き起こす2017

    • Author(s)
      今川英里、東元健、酒井康成、沼倉周彦、岡本伸彦、松永智子、梁明秀、佐藤由典、實藤雅文、井原健二、高田結、西村玄、才津浩智、水口剛、宮武聡子、中島光子、三宅紀子、副島英伸、松本直通
    • Organizer
      日本人類遺伝学会第62回大会
    • Related Report
      2017 Research-status Report
  • [Presentation] 間葉性異形成胎盤とインプリンティング異常2017

    • Author(s)
      副島英伸
    • Organizer
      第25回日本胎盤学会学術集会
    • Related Report
      2017 Research-status Report
    • Invited
  • [Presentation] Mbf1はPacmanからE(z) mRNAを保護することでポリコームサイレンシングの堅牢性を担保している2017

    • Author(s)
      西岡憲一、宮崎仁美、副島英伸、広瀬進
    • Organizer
      2017年度生命科学系学会合同年次大会
    • Related Report
      2017 Research-status Report
  • [Presentation] マウスCommd1とZrsr1のゲノムインプリンティング機構の研究2017

    • Author(s)
      城 圭一郎、西岡憲一、北嶋修司、松久葉一、古関明彦、河野友宏、副島英伸
    • Organizer
      2017年度生命科学系学会合同年次大会
    • Related Report
      2017 Research-status Report
  • [Presentation] Beckwith-Wiedemann症候群に合併した後縦隔神経芽腫の1例2017

    • Author(s)
      川口晃司、卜部馨介、高橋郁子、小倉妙美、堀越泰雄、東元 健、副島英伸、渡邉健一郎
    • Organizer
      第73回東海小児がん研究会
    • Related Report
      2017 Research-status Report
  • [Presentation] NSD1 haploinsufficiency evokes DNA hypomethylation at imprinted DMRs and the increased expression of imprinted genes2017

    • Author(s)
      Watanabe H, Higashimoto K, Miyake N, Maeda T, Hidaka H, Aoki S, Matsumoto N, Soejima H
    • Organizer
      The 67th Annual Meeting of the American Society of Human Genetics
    • Related Report
      2017 Research-status Report
  • [Presentation] Germline mutations associated with polycomb repressive complex 2 cause Weaver syndrome2017

    • Author(s)
      Imagawa E, Higashimoto K, Sakai Y, Numakura C, Okamoto N, Matsunaga S, Ryo A, Sato Y, Sanefuji M, Ihara K, Takada Y, Nishimura G, Saitsu H, Mizuguchi T, Miyatake S, Nakashima M, Miyake N, Soejima H, Matsumoto N
    • Organizer
      The 67th Annual Meeting of the American Society of Human Genetics
    • Related Report
      2017 Research-status Report
  • [Book] 基礎と臨床の両側面からみた胎盤学2019

    • Author(s)
      日本胎盤学会
    • Total Pages
      448
    • Publisher
      メジカルビュー社
    • ISBN
      9784758317627
    • Related Report
      2019 Annual Research Report
  • [Book] コアカリ準拠臨床遺伝学テキストノート 第6講義エピジェネティクス2018

    • Author(s)
      副島英伸
    • Total Pages
      192
    • Publisher
      診断と治療社
    • Related Report
      2018 Research-status Report
  • [Book] DNA and Histone Methylation as Cancer Targets2017

    • Author(s)
      Higashimoto K, Joh K, Soejima H
    • Total Pages
      622
    • Publisher
      Humana Press
    • Related Report
      2017 Research-status Report
  • [Remarks] 佐賀大学医学部分子生命科学講座分子遺伝学・エピジェネティクス分野

    • URL

      http://www.biomol.med.saga-u.ac.jp/mbg/index.htm

    • Related Report
      2019 Annual Research Report 2017 Research-status Report
  • [Remarks] 佐賀大学医学部分子生命科学講座分子遺伝学・エピジェネティクス分野

    • URL

      http://www.biomol.med.saga-u.ac.jp/mbg/

    • Related Report
      2018 Research-status Report

URL: 

Published: 2017-04-28   Modified: 2021-02-19  

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