• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Kubiura Musashi  首浦 武作志 (一丸 武作志)

ORCIDConnect your ORCID iD *help
… Alternative Names

首浦 武作志  クビウラ ムサシ(イチマルムサシ)

一丸武作志

Less
Researcher Number 20827977
Other IDs
Affiliation (Current) 2026: 佐賀大学, 医学部, 助教
Affiliation (based on the past Project Information) *help 2024: 佐賀大学, 医学部, 助教
Review Section/Research Field
Principal Investigator
Basic Section 48040:Medical biochemistry-related
Except Principal Investigator
Medium-sized Section 45:Biology at organismal to population levels and anthropology, and related fields / Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords
Principal Investigator
シングルセル / エピゲノム / NSD1 / エピジェネティクス / シングルセル解析
Except Principal Investigator
霊長類 / ヒト / 精巣 / 生殖細胞 / シングルセル解析 … More / 免疫染色 / ヒト生殖細胞 / DNAメチル化確立 / 空間遺伝子発現 / 一細胞マルチオミクス / ヘテロ欠損マウス / ソトス症候群 / NSD1 Less
  • Research Projects

    (3 results)
  • Research Products

    (8 results)
  • Co-Researchers

    (4 People)
  •  Elucidation of molecular pathogenesis and establishment of therapeutic foundations for intellectual disabilities based on single-cell multiomics and spatial gene expression

    • Principal Investigator
      副島 英伸
    • Project Period (FY)
      2024 – 2027
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Saga University
  •  一細胞マルチオミクスを用いた体細胞分化過程におけるエピゲノム再確立の分子機構解明Principal Investigator

    • Principal Investigator
      首浦 武作志 (一丸武作志)
    • Project Period (FY)
      2024 – 2026
    • Research Category
      Grant-in-Aid for Early-Career Scientists
    • Review Section
      Basic Section 48040:Medical biochemistry-related
    • Research Institution
      Saga University
  •  ヒト雄性生殖細胞におけるDNAメチル化確立の解析

    • Principal Investigator
      渡部 聡朗
    • Project Period (FY)
      2024 – 2027
    • Research Category
      Fund for the Promotion of Joint International Research (International Collaborative Research)
    • Review Section
      Medium-sized Section 45:Biology at organismal to population levels and anthropology, and related fields
    • Research Institution
      National Center for Child Health and Development

All 2025 2024

All Journal Article Presentation

  • [Journal Article] DNMT1 can induce primary germ layer differentiation through de novo DNA methylation2024

    • Author(s)
      Ito Takamasa、Kubiura‐Ichimaru Musashi、Miura Fumihito、Tajima Shoji、Surani M. Azim、Ito Takashi、Yamaguchi Shinpei、Tada Masako
    • Journal Title

      Genes to Cells

      Volume: 29 Issue: 7 Pages: 549-566

    • DOI

      10.1111/gtc.13130

    • Peer Reviewed / Open Access / Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-23KJ1457, KAKENHI-PROJECT-24K18373
  • [Journal Article] Identification of responsible sequences which mutations cause maternal H19-ICR hypermethylation with Beckwith?Wiedemann syndrome-like overgrowth2024

    • Author(s)
      Hara Satoshi、Matsuhisa Fumikazu、Kitajima Shuji、Yatsuki Hitomi、Kubiura-Ichimaru Musashi、Higashimoto Ken、Soejima Hidenobu
    • Journal Title

      Communications Biology

      Volume: 7 Issue: 1 Pages: 1605-1605

    • DOI

      10.1038/s42003-024-07323-x

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-24K02422, KAKENHI-PROJECT-24K18373
  • [Presentation] ゲノムワイド父性片親性ヘテロダイソミーを示す核型46,XYのBeckwith-Wiedemannスペクトラムの一例.2025

    • Author(s)
      副島英伸、佐藤知彦、一丸(首浦)武作志、原聡史.
    • Organizer
      第47回日本小児遺伝学会学術集会
    • Data Source
      KAKENHI-PROJECT-24K02422
  • [Presentation] NSD1ヘテロ欠損はマウス新生児生存率を低下させる.2024

    • Author(s)
      一丸(首浦)武作志、原 聡史、八木 ひとみ、副島 英伸.
    • Organizer
      第47回日本分子生物学会
    • Data Source
      KAKENHI-PROJECT-24K02422
  • [Presentation] Exome sequencing reveals causative variants for overgrowth syndromes in molecularly negative Beckwith-Wiedemann spectrum.2024

    • Author(s)
      副島 英伸、東元 健、孫 菲菲、今川 英里、才田 謙、三宅 紀子、原 聡史、八木 ひとみ、一丸(首浦)武作志、藤田 京志、水口 剛、松本 直通.
    • Organizer
      日本人類遺伝学会第69回大会
    • Data Source
      KAKENHI-PROJECT-24K02422
  • [Presentation] NSD1ヘテロ欠損が胎仔・新生仔に与える影響2024

    • Author(s)
      一丸(首浦)武作志、原聡史、八木ひとみ、東元健、副島英伸
    • Organizer
      第17回日本エピジェネ手クス研究会年会
    • Data Source
      KAKENHI-PROJECT-24K18373
  • [Presentation] NSD1ヘテロ欠損はマウス新生児生存率を低下させる2024

    • Author(s)
      一丸(首浦)武作志、原聡史、八木ひとみ、副島英伸
    • Organizer
      第47回日本分子生物学会年会
    • Data Source
      KAKENHI-PROJECT-24K18373
  • [Presentation] NSD1ヘテロ欠損が胎仔・新生仔に与える影響.2024

    • Author(s)
      一丸(首浦)武作志、原聡史、八木ひとみ、東元健、副島英伸.
    • Organizer
      第17回日本エピジェネティクス研究会年会
    • Data Source
      KAKENHI-PROJECT-24K02422
  • 1.  副島 英伸 (30304885)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 5 results
  • 2.  原 聡史 (80739582)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 5 results
  • 3.  渡部 聡朗 (40715405)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 4.  富澤 信一 (00704628)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results

URL: 

Are you sure that you want to link your ORCID iD to your KAKEN Researcher profile?
* This action can be performed only by the researcher himself/herself who is listed on the KAKEN Researcher’s page. Are you sure that this KAKEN Researcher’s page is your page?

この研究者とORCID iDの連携を行いますか?
※ この処理は、研究者本人だけが実行できます。

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi