SHIMIZU Norikazu 清水教一

… Alternative Names

清水教一シミズノリカズ

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Researcher Number	60256740
Other IDs
External Links
Affiliation (Current)	2025: 東邦大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2009: 東邦大学, 医学部・第二小児科, 講師 2007: 東邦大学, 医学部第二小児科, 講師 1997 – 2001: 東邦大学, 医学部, 講師 1997: Toho Univ., 2nd Dept.of Pediatrics, Assistant professor, 医学部・第2小児科学教室, 講師 1996: 東邦大学, 医学部・第二小児科学教室, 講師 … More 1996: Toho Univ., 2nd Dept.of Pediatrics, Assistant professor, 第二小児科学教室, 講師 1995: 東邦大学, 医学部・第2小児科学教室, 講師 1993 – 1994: 東邦大学, 医学部, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics Except Principal Investigator Pediatrics / Digestive surgery / Public health/Health science
Keywords	Principal Investigator 遺伝子解析 / Wilson病 / ATP7B / genotype-phenotype correlation / Menkes disease / Wilson disease / Menkes病 / 銅輸送P-type ATPase / 先天性銅代謝異常症 / P-type ATPase … More / copper induced ATPase activity / molecular analysis / ATP7A / inborn error of copper metabolism / 銅輸送P-type ATRase / ATPase活性 / 血清セルロプラスミン値 / 遺伝子変異と病型 / 遣伝子解析 / 銅特異的ATPase活性 / 遺伝子診断 / intracellular localization / gene analysis / copper transporting P-type A Tpase / Inborn error of copper metabolism / 細胞内局在 / PCR-SSCP法 … More Except Principal Investigator Wilson disease / P-type ATPase / Wilson病 / ATP7B / in vivo footprinting / gel shift assay / reporter gene assay / ATP7A / inborn error of copper metabolism / 遺伝子解析 / Menkes病 / 遺伝性銅代謝異常症 / ceruloplasmin / 遺伝子診断 / transcription factor / transcription regulatory region / colorectal cancer / hMLH1 gene / mismatch repair gene / hypermethylation / CpG island / microsatellite instability / 発現抑制 / 転写因子 / 転写調節領域 / 大腸癌 / hMLH1遺伝子 / ミスマッチ修復遺伝子 / presymptomatic diagnosis / tetrathiomolybdate (TTM) / molecular diagnosis / gene analysis / Tetrathiomolybdate (TTM) / 銅輸送P-type ATPase / 遺伝性銅代謝異常 / テトラチオモリブデン(TTM) / 銅特異的ATPase活性 / 発症前診断 / テトラチオモリブテン(TTM) / phenotype / genotype / Menkes disease / genotypeとphenotype / Phenotype / Genotype / Anti-holoceruloplasmin monoclonal antibody / p-type ATPase / Copper metabolism / セルロプラスミン / Long-Evans Cinnamon(LEC)ラット / 抗ヒト・ホルセルロプラスミン・モノクローナル抗体 / 抗ヒト・ホロセルロプラスミン・モノクローナル抗体 / 銅代謝異常 / ウィルソン病 / 臨床検査 / 予防医学 / プロテオーム解析 / 銅代謝異常症 / ウイルソン病 / 分子予防医学 / 母子保健 Less

Preventive medical screening involving familial genetic testing of ATP7B in order to discover presymptomatic patients in families with Wilson's disease patients.
- Principal Investigator
  
  NAKAYAMA Kenji
- Project Period (FY)
  2007 – 2009
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Public health/Health science
- Research Institution
  Hokkaido Institute of Public Health
Strategy of ATP7B gene analysis for Japanese patients with Wilson disease, using ARMS method. ..................................Principal Investigator
- Principal Investigator
  
  SHIMIZU Norikazu
- Project Period (FY)
  1998 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Toho Unversity School of Medicine
Mechanism of no gene expression of hMLH1 in sporadic colorectal cancers : Identification of transcription factors and its establishment of detection method.
- Principal Investigator
  
  HEMMI Hiromichi
- Project Period (FY)
  1998 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Digestive surgery
- Research Institution
  TOHO UNIVERSITY
The etiology of inborn error of copper metabolism, new method of treatment, and function of P-type copper transporting ATPase
- Principal Investigator
  
  AOKI Tugutoshi
- Project Period (FY)
  1997 – 1999
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University School of Medicine
The structural and functional analysis of copper transporting P-type ATPase in inborn error of copper metabolismPrincipal Investigator
- Principal Investigator
  
  SHIMIZU Norikazu
- Project Period (FY)
  1996 – 1997
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University School of Medicine
Correlation between genotype and phenotype of inborn error of copper metabolism
- Principal Investigator
  
  AOKI Tsugutoshi
- Project Period (FY)
  1995 – 1996
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University
Wilson病患者における遺伝子構造異常の解析Principal Investigator
- Principal Investigator
  
  清水教一
- Project Period (FY)
  1994
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University
Molecular analysis for the etiology of Wilson disease
- Principal Investigator
  
  AOKI Tsugutoshi
- Project Period (FY)
  1993 – 1994
- Research Category
  
  Grant-in-Aid for General Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University

All 2009

All Presentation

[Presentation] RT-PCR法によるウイルソン病簡易診断の可能性-モデル動物を用いた試み-2009
- Author(s)
  中山憲司, 加藤芳伸, 清水教一, 奥井登代, 澤田幸治, 青木継稔
- Organizer
  第13回ウイルソン病研究会学術集会
- Place of Presentation
  東邦大学大森病院(東京都大田区)
- Year and Date
  2009-05-13
- Data Source
  KAKENHI-PROJECT-19590658
[Presentation] LECラットを用いたウイルソン病簡易診断法の探索2009
- Author(s)
  中山憲司, 加藤芳伸, 清水教一, 奥井登代, 松本耕三, 澤田幸治, 青木継稔
- Organizer
  第19回LECラット研究会
- Place of Presentation
  帝京大学医学部付属病院(東京都板橋区)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-19590658
[Presentation] RT-PCR法によるウイルソン病簡易診断の可能性-モデル動物を用いた試み-2009
- Author(s)
  中山憲司, 加藤芳伸, 清水教一, 奥井登代, 澤田幸治, 青木継稔
- Organizer
  第13回ウイルソン病研究会学術集会
- Place of Presentation
  東京都(東邦大学医療センター大森病院)
- Year and Date
  2009-05-13
- Data Source
  KAKENHI-PROJECT-19590658
[Presentation] LECラットを用いたウイルソン病簡易診断法の探索2009
- Author(s)
  中山憲司, 加藤芳伸, 清水教一, 奥井登代, 松本耕三, 澤田幸治, 青木継稔
- Organizer
  第19回LECラット研究会学術集会
- Place of Presentation
  東京都(帝京大学附属病院)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-19590658

1. HEMMI Hiromichi (90165514)

# of Collaborated Projects: 5 results

# of Collaborated Products: 0 results
2. YAMAGUCHI Yukitoshi (30277339)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
3. AOKI Tsugutoshi (50057585)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
4. FUJIOKA Yoshimi (30256739)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
5. UCHIYAMA Toshimitu (50057709)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. SUZUKI Tomohiro (10414327)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
7. SAWADA Yukiharu (80111128)

# of Collaborated Projects: 2 results

# of Collaborated Products: 4 results
8. SHIMATAKE Hiroyuki (40010110)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
9. NAKAYAMA Kenji (30442594)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
10. KATOH Yoshinobu (00414326)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
11. TAMURA Mamoru (80089888)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. INOUE Akira (10151599)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. KAZAMA Hiromi (90224386)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. TSUJITA Kazunori (60130374)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

SHIMIZU Norikazu 清水 教一

清水 教一 シミズ ノリカズ

Research Projects

Research Products

Co-Researchers

Preventive medical screening involving familial genetic testing of ATP7B in order to discover presymptomatic patients in families with Wilson's disease patients.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Strategy of ATP7B gene analysis for Japanese patients with Wilson disease, using ARMS method. ..................................Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Mechanism of no gene expression of hMLH1 in sporadic colorectal cancers : Identification of transcription factors and its establishment of detection method.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The etiology of inborn error of copper metabolism, new method of treatment, and function of P-type copper transporting ATPase

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The structural and functional analysis of copper transporting P-type ATPase in inborn error of copper metabolismPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Correlation between genotype and phenotype of inborn error of copper metabolism

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Wilson病患者における遺伝子構造異常の解析Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular analysis for the etiology of Wilson disease

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Presentation] RT-PCR法によるウイルソン病簡易診断の可能性-モデル動物を用いた試み-2009

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] LECラットを用いたウイルソン病簡易診断法の探索2009

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] RT-PCR法によるウイルソン病簡易診断の可能性-モデル動物を用いた試み-2009

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] LECラットを用いたウイルソン病簡易診断法の探索2009

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

SHIMIZU Norikazu 清水教一

清水教一シミズノリカズ