Nishizaki Yuriko 西崎有利子

… Alternative Names

Researcher Number	90378901
Affiliation (Current)	2020: 横浜薬科大学, 薬学部, 講師
Affiliation (based on the past Project Information) *help	2017: 横浜薬科大学, 薬学部, 講師 2014 – 2015: 愛知県心身障害者コロニー発達障害研究所, 周生期学部, 研究員 2011 – 2014: 愛知県心身障害者コロニー発達障害研究所, 周生期学部, リサーチレジデント 2010: 京都大学, 再生医科学研究所, 研究員 2008: 京都大学, 再生医科学研究所, 研究員(学術研究奨励) 2007: 京都大学, 再生医科学研究所, 研究員(科学研究)
Review Section/Research Field	Principal Investigator Pediatrics / Orthopaedic surgery Except Principal Investigator Developmental biology / Pediatrics
Keywords	Principal Investigator Sip1 / SIP1 / 神経管閉鎖 / 二分脊椎症 / BMP / Wnt-PCPパスウェー / 細胞極性 / 縫線核 / セロトニン / 神経 … More Except Principal Investigator 細胞分化 / 腱 / 靱帯 / 強靱結合組織 / Tenomodulin / Chondromodulin-I / 腱細胞 / tenomodulin / chondromodulin-I / SIP1 / zeb2 / zfhx1b / モワットウィルソン症候群 / ノックアウトマウス / ZFHX1転写因子ファミリー / 脳の構造と機能 / 脳 / 精神遅滞 / 転写因子 / 遺伝・先天異常学 / モワット-ウィルソン症候群 / SIP1ノックアウトマウス / SIP1ヘテロ欠損マウス Less

The role of Sip1 gene for development of the serotonergic neurons of the raphePrincipal Investigator
- Principal Investigator
  
  NISHIZAKI Yuriko
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Yokohama College of Pharmacy
  Institute for Developmental Research, Aichi Human Service Center
The study on the role of SIP1, the causative gene for Mowat-Wilson syndrome in human, in structural and functional development of brain using mouse system
- Principal Investigator
  
  HIGASHI Yujiro
- Project Period (FY)
  2011 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Institute for Developmental Research, Aichi Human Service Center
An analysis of mechanism of neural tube closure using the SIP1 knock-out mice as a spina bifida modelPrincipal Investigator
- Principal Investigator
  
  NISHIZAKI Yuriko
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Institute for Developmental Research, Aichi Human Service Center
椎間板形成における転写制御因子Pax1の機能解析Principal Investigator
- Principal Investigator
  
  西崎有利子
- Project Period (FY)
  2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Orthopaedic surgery
- Research Institution
  Kyoto University
Molecular analysis of tendon and ligament formation
- Principal Investigator
  
  SHUKUNAMI Chisa
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Developmental biology
- Research Institution
  Kyoto University

All 2015 2014 2013 2012 2008 Other

All Journal Article Presentation

[Journal Article] De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.2015
- Author(s)
  51.Takagi T, Nishizaki Y, Matsui F, Wakamatsu N, Higashi Y.
- Journal Title
  
  Hum Mol Genet
  
  Volume: 24 Pages: 6390-6402
- DOI
  10.1093/hmg/ddv350
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461539, KAKENHI-PROJECT-26461557, KAKENHI-PROJECT-26462225
[Journal Article] SIP1 expression pattern in brain investigated by generating a SIP1-EGFP reporter knock-in mouse2014
- Author(s)
  Nishizaki, Y., Takagi, T., Matsui, F. and Higashi, Y.
- Journal Title
  
  Genesis
  
  Volume: 52 Pages: 56-57
- DOI
  10.1002/dvg.22726
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591525, KAKENHI-PROJECT-23791215, KAKENHI-PROJECT-25461399
[Journal Article] Chondromodulin-I and tenomodulin are differentially expressed in the avascular mesenchyme during mouse and chick development2008
- Author(s)
  C. Shukunami, A. Takimoto, S. Miura, Y. Nishizaki, Y. Hiraki
- Journal Title
  
  Cell Tissue Res. 332
  
  Pages: 111-122
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19570205
[Presentation] モデルマウスを用いたモワット・ウィルソン症候群の病態形成の解析2013
- Author(s)
  高木豪、西崎有利子、松井ふみ子、東雄二郎
- Organizer
  第36回日本分子生物学会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-23791215
[Presentation] モデルマウスを用いたモワット・ウィルソン症候群の病態形成の解析2013
- Author(s)
  高木豪, 西崎有利子, 松井ふみ子, 東雄二郎
- Organizer
  第36回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド
- Data Source
  KAKENHI-PROJECT-23791215
[Presentation] レポーターノックインマウスを用いたモワット- ウィルソン症候群の原因遺伝子SIP1の発現解析2013
- Author(s)
  西崎有利子，高木豪，松井ふみ子，東雄二郎
- Organizer
  第３６回日本分子生物学会年会
- Place of Presentation
  神戸ポートアイランド
- Data Source
  KAKENHI-PROJECT-23791215
[Presentation] レポーターノックインマウスを用いたモワット・ウィルソン症候群の原因遺伝子SIP1の発現解析2013
- Author(s)
  西崎有利子、高木豪、松井ふみ子、東雄二郎
- Organizer
  第36回日本分子生物学会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-23791215
[Presentation] δEF1/zeb1は下垂体後葉の形成に必須である (δEF1/zeb1 is Essential for Development of the Posterior Lobe of Pituitary)2012
- Author(s)
  東雄二郎,高木豪,西崎有利子,松井ふみ子,中西圭子,時田義人
- Organizer
  第35回日本分子生物学会年会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23791215
[Presentation] deltaEF1/zeb1 is Essential for Development of the Posterior Lobe of Pituitary2012
- Author(s)
  Yujiro HIgashi, Tsuyoshi Takagi, Yuriko Nishizaki, Fumiko Matsui, Keiko Nakanishi, Yoshihito Tokita
- Organizer
  第３５回日本分子生物学会年会
- Place of Presentation
  福岡国際会議場、マリンメッセ福岡（福岡）
- Data Source
  KAKENHI-PROJECT-23791215
[Presentation] Tenomodulin遺伝子の腱・靱帯特異的な転写制御領域の解析2008
- Author(s)
  西崎有利子
- Organizer
  第40回日本結合組織学会学術大会・第55回マトリックス研究会大会合同学術集会
- Place of Presentation
  東京
- Year and Date
  2008-05-30
- Data Source
  KAKENHI-PROJECT-19570205
[Presentation] Tenomodulin遺伝子の腱・靭帯特異的な転写制御領域の解析2008
- Author(s)
  西崎有利子, 杉本由紀, 開祐司, 宿南知佐
- Organizer
  第40回日本結合組織学会学術大会・第55回マトリックス研究会大会合同学術集会
- Place of Presentation
  東京
- Year and Date
  2008-05-30
- Data Source
  KAKENHI-PROJECT-19570205
[Presentation] モデルマウスを用いたモワット・ウィルソン症候群の病態形成の解析
- Author(s)
  高木豪、西崎有利子、松井ふみ子、東雄二郎
- Organizer
  第36回日本分子生物学会
- Place of Presentation
  神戸国際会議場（神戸）
- Data Source
  KAKENHI-PROJECT-23591525
[Presentation] レポーターノックインマウスを用いたモワット-ウィルソン症候群の原因遺伝子SIP1の発現解析
- Author(s)
  西崎有利子、高木豪、松井ふみ子、東雄二郎
- Organizer
  第36回日本分子生物学会
- Place of Presentation
  神戸国際会議場（神戸）
- Data Source
  KAKENHI-PROJECT-23591525
[Presentation] Loss of Zeb2 Causes Glomerulocystic Kidney Disease in Mice.
- Author(s)
  Rasouly M.H., Chan S., Pisarek-Horowitz A., Nishizaki Y., Higashi Y., Lu W.
- Organizer
  Annual meeting of the American Society of Nephrology
- Place of Presentation
  Philadelphia, PA
- Year and Date
  2014-11-13 – 2014-11-16
- Data Source
  KAKENHI-PROJECT-26461557

1. HIGASHI Yujiro (30181069)

# of Collaborated Projects: 2 results

# of Collaborated Products: 5 results
2. SHUKUNAMI Chisa (60303905)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
3. 若松延昭

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Nishizaki Yuriko 西崎 有利子

NISHIZAKI Yuriko 西崎 有利子

Research Projects

Research Products

Co-Researchers

The role of Sip1 gene for development of the serotonergic neurons of the raphePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The study on the role of SIP1, the causative gene for Mowat-Wilson syndrome in human, in structural and functional development of brain using mouse system

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

An analysis of mechanism of neural tube closure using the SIP1 knock-out mice as a spina bifida modelPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

椎間板形成における転写制御因子Pax1の機能解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular analysis of tendon and ligament formation

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] De novo inbred heterozygous Zeb2/Sip1 mutant mice uniquely generated by germ-line conditional knockout exhibit craniofacial, callosal and behavioral defects associated with Mowat-Wilson syndrome.2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] SIP1 expression pattern in brain investigated by generating a SIP1-EGFP reporter knock-in mouse2014

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Chondromodulin-I and tenomodulin are differentially expressed in the avascular mesenchyme during mouse and chick development2008

Author(s)

Journal Title

Data Source

[Presentation] モデルマウスを用いたモワット・ウィルソン症候群の病態形成の解析2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] モデルマウスを用いたモワット・ウィルソン症候群の病態形成の解析2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] レポーターノックインマウスを用いたモワット- ウィルソン症候群の原因遺伝子SIP1の発現解析2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] レポーターノックインマウスを用いたモワット・ウィルソン症候群の原因遺伝子SIP1の発現解析2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] δEF1/zeb1は下垂体後葉の形成に必須である (δEF1/zeb1 is Essential for Development of the Posterior Lobe of Pituitary)2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] deltaEF1/zeb1 is Essential for Development of the Posterior Lobe of Pituitary2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Tenomodulin遺伝子の腱・靱帯特異的な転写制御領域の解析2008

Nishizaki Yuriko 西崎有利子

NISHIZAKI Yuriko 西崎有利子