Kitazawa Moe 北澤萌恵

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KITAZAWA Moe 北澤萌恵

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Researcher Number	40801965
Other IDs
Affiliation (Current)	2025: 山梨大学, 大学院総合研究部, 客員研究員 2025: 東京科学大学, その他の部局等, 非常勤講師
Affiliation (based on the past Project Information) *help	2024: 山梨大学, 大学院総合研究部, 客員研究員 2019 – 2023: 東京医科歯科大学, 難治疾患研究所, 助教 2022: 東京医科歯科大学, 統合研究機構, プロジェクト助教
Review Section/Research Field	Principal Investigator Basic Section 44020:Developmental biology-related / 0702:Biology at cellular to organismal levels, and related fields Except Principal Investigator Medium-sized Section 44:Biology at cellular to organismal levels, and related fields
Keywords	Principal Investigator 進化 / 脳構造 / 獲得遺伝子 / 真獣類 / 発生生物学 / 筋肉形成 / 鏡-緒方症候群 / miRNA / 行動解析 / 脳機能 … More / Peg11/Rtl1 / ヒト14番染色体二倍体症候群 / ゲノムインプリンティング疾患 / 脳 / 骨格筋 / 真獣類特異的遺伝子 / Rtl1 / Peg11 … More Except Principal Investigator 哺乳類の個体発生 / 哺乳類進化 / KOダナート / 母子免疫寛容 / 胎盤形成 / 有袋類でのKO動物作製 / 有袋類の胎盤 / 脳機能 / 母子免疫反応 / LTRレトロトランスポゾン / PEG10の機能 / 有袋類の胎盤形成 / 哺乳類の胎盤進化 / 胎盤形成と母子免疫 / TS細胞 / iPS細胞 / レトロウイルス / 獲得遺伝子 / PEG10 / 胎盤 / 有袋類 / 胎生進化 / 哺乳類 Less

真獣類特異的獲得遺伝子Peg11/Rtl1の脳構造形成における機能解析Principal Investigator
- Principal Investigator
  
  北澤萌恵
- Project Period (FY)
  2023 – 2026
- Research Category
  
  Grant-in-Aid for Early-Career Scientists
- Review Section
  
  Basic Section 44020:Developmental biology-related
- Research Institution
  University of Yamanashi
  Tokyo Medical and Dental University
Development of in vivo knockdown treatment for PEG11 in Kagami-Ogata syndromePrincipal Investigator
- Principal Investigator
  
  KITAZAWA Moe
- Project Period (FY)
  2019 – 2020
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Review Section
  
  0702:Biology at cellular to organismal levels, and related fields
- Research Institution
  Tokyo Medical and Dental University
Functional analysis of PEG10 in marsupial placenta formation
- Principal Investigator
  
  Ishino Fumitoshi
- Project Period (FY)
  2019 – 2023
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 44:Biology at cellular to organismal levels, and related fields
- Research Institution
  Tokyo Medical and Dental University

All 2023 2021 2020 2019

All Journal Article Presentation

[Journal Article] Roles of retrovirus-derived PEG10 and PEG11/RTL1 in mammalian development and evolution and their involvement in human disease2023
- Author(s)
  Shiura Hirosuke、Kitazawa Moe、Ishino Fumitoshi、Kaneko-Ishino Tomoko
- Journal Title
  
  Frontiers in Cell and Developmental Biology
  
  Volume: 11 Pages: 1273638-1273638
- DOI
  10.3389/fcell.2023.1273638
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K20584, KAKENHI-PROJECT-21K06127, KAKENHI-PROJECT-23K05588, KAKENHI-PROJECT-19KK0182
[Journal Article] The role of eutherian-specific RTL1 in the nervous system and its implications for the Kagami- Ogata and Temple syndromes.2021
- Author(s)
  Kitazawa M, Sutani A, Kaneko-Ishino T, Ishino F
- Journal Title
  
  Genes Cells
  
  Volume: 26 Issue: 3 Pages: 165-179
- DOI
  10.1111/gtc.12830
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K20584, KAKENHI-PROJECT-19KK0182, KAKENHI-PROJECT-19H00978, KAKENHI-PROJECT-17K07498, KAKENHI-PROJECT-19K23744
[Journal Article] Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to the Temple and Kagami-Ogata syndromes.2020
- Author(s)
  Kitazawa M, Hayashi S, Imamura H, Takeda S, Oishi Y, Kaneko-Ishino T, Ishino F
- Journal Title
  
  Development
  
  Volume: 147 Issue: 21 Pages: 147-147
- DOI
  10.1242/dev.185918
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20K20584, KAKENHI-PROJECT-19KK0182, KAKENHI-PUBLICLY-20H04956, KAKENHI-PROJECT-19H00978, KAKENHI-PROJECT-17K07498, KAKENHI-PROJECT-18K07082, KAKENHI-PROJECT-19K23744
[Presentation] マウスにおけるPeg11/Rtl1の欠損と過剰発現はTemple症候群とKagami-Ogata症候群に関連した異なる筋肉異常を引き起こす2020
- Author(s)
  北澤萌恵、金児-石野知子、石野史敏
- Organizer
  第43回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-19K23744
[Presentation] マウスにおけるPeg11/Rtl1の欠損と過剰発現はTemple症候群と鏡-緒方症候群に関連した異なる筋肉異常を引き起こす2020
- Author(s)
  北澤萌恵、林晋一郎、今村道博、武田伸一、大石由美子、金児ー石野知子、石野史敏
- Organizer
  日本分子生物学会年会(MBSJ 2020)
- Data Source
  KAKENHI-PROJECT-19KK0182
[Presentation] Peg11/Rtl1は哺乳類の胎児・新生児期の骨格筋発生に関与する鏡―緒方症候群・テンプル症候群の主要原因遺伝子である2019
- Author(s)
  石野史敏、北澤萌恵、金児―石野知子
- Organizer
  第42回日本分子生物学学会年会(MBSJ2019)ワークショップ
- Data Source
  KAKENHI-PROJECT-19KK0182
[Presentation] Peg11/Rtl1は哺乳類の胎児・新生児の骨格筋発生に関与する鏡-緒方症候群・テンプル症候群の主要原因遺伝子である2019
- Author(s)
  石野史敏、北澤萌恵、金児-石野知子
- Organizer
  第41回日本分子生物学会年会
- Data Source
  KAKENHI-PROJECT-19K23744

1. Ishino Fumitoshi (60159754)

# of Collaborated Projects: 1 results

# of Collaborated Products: 5 results
2. 志浦寛相 (10451907)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. 石野知子 (20221757)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
4. 鈴木俊介 (30431951)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. 石野知子(金児知子)

# of Collaborated Projects: 0 results

# of Collaborated Products: 5 results

Kitazawa Moe 北澤 萌恵

KITAZAWA Moe 北澤 萌恵

Research Projects

Research Products

Co-Researchers

真獣類特異的獲得遺伝子Peg11/Rtl1の脳構造形成における機能解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of in vivo knockdown treatment for PEG11 in Kagami-Ogata syndromePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Functional analysis of PEG10 in marsupial placenta formation

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

[Journal Article] Roles of retrovirus-derived PEG10 and PEG11/RTL1 in mammalian development and evolution and their involvement in human disease2023

Author(s)

Journal Title

DOI

Data Source

[Journal Article] The role of eutherian-specific RTL1 in the nervous system and its implications for the Kagami- Ogata and Temple syndromes.2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Deficiency and overexpression of Rtl1 in the mouse cause distinct muscle abnormalities related to the Temple and Kagami-Ogata syndromes.2020

Author(s)

Journal Title

DOI

Data Source

[Presentation] マウスにおけるPeg11/Rtl1の欠損と過剰発現はTemple症候群とKagami-Ogata症候群に関連した異なる筋肉異常を引き起こす2020

Author(s)

Organizer

Data Source

[Presentation] マウスにおけるPeg11/Rtl1の欠損と過剰発現はTemple症候群と鏡-緒方症候群に関連した異なる筋肉異常を引き起こす2020

Author(s)

Organizer

Data Source

[Presentation] Peg11/Rtl1は哺乳類の胎児・新生児期の骨格筋発生に関与する鏡―緒方症候群・テンプル症候群の主要原因遺伝子である2019

Author(s)

Organizer

Data Source

[Presentation] Peg11/Rtl1は哺乳類の胎児・新生児の骨格筋発生に関与する鏡-緒方症候群・テンプル症候群の主要原因遺伝子である2019

Author(s)

Organizer

Data Source

Kitazawa Moe 北澤萌恵

KITAZAWA Moe 北澤萌恵