NOZAKI Yasuyuki 野崎靖之

Researcher Number	90281295
Other IDs
Affiliation (based on the past Project Information) *help	2013: 自治医科大学, 医学部, 助教 2007 – 2008: 自治医科大学, 医学部, 助教 2006: 自治医科大学, 医学部, 助手 1996 – 2001: 自治医科大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Pediatrics Except Principal Investigator Pediatrics / Pediatrics
Keywords	Principal Investigator 発達障害 / 家族性精神遅滞 / 脆弱X症候群 / トリプレットリピート / ヒルシュスプルング病 / RET / ET3 / EDNRB / Mash1 / MITF / Hoxa-4 … More Except Principal Investigator … More 脆弱X症候群 / 自閉性障害 / 自閉症 / セクレチン / G蛋白結合型受容体 / セクレチン受容体 / EXT1 / GRPR / トリプレットリピート / 精神遅滞 / トリプレットリピート伸展疾患 / 家族性精神遅滞 / シナプス形成 / CADM1 / FOXP2 / secretin受容体 / ノックインマウス / 遺伝子発現解析 / 発現アレイ解析 / WNT / 自閉症スペクトラム障害 / コピー数多型 / 遺伝子変異 / 足場蛋白 / LIN7 / シナプス / マイクロアレーCGH / コピー数多型（CNV) / シナプス足場蛋白 / 病因遺伝子 / CNV / 候補遺伝子解析 / モデルマウス / 筋強直性ジストロフィー症 / トリプレットリピート疾患 / 片麻痺性片頭痛 / 脊髄小脳失調症 / 遅発性小脳失調症 / カスパーゼ8 / カスパーゼ12 / 先天性筋ジストロフィー / 細胞死 / caspase-3 / 三塩基対リピート疾患 / Pfu polymerase ポリメラーゼ / 毛根 / 遺伝子診断 / 筋強直性ジストロフィー / MT-PK遺伝子 / DMAHP遺伝子 / myotonic dystrophy / trinucleotide repeat disorder / hemiplegic migraine / spinocerebellar degeneration / late-onset cerebellar ataxia / caspase-8 / caspase-12 / 遺伝子解析 / GRRP / 家族性多発性外骨腫 / ノックアウトマウス / autism / mutation analysis / secretin / secretin receptor / G-protein coupled receptor / Hereditary Multiple Exostosis Less

Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules
- Principal Investigator
  
  YAMAGATA Takanori
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
Research on the common molecular pathology for autism
- Principal Investigator
  
  MOMOI Mariko
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
Analysis of G-protein coupled receptors as candidate genes for autism
- Principal Investigator
  
  YAMAGATA Takanori
- Project Period (FY)
  2000 – 2001
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical School
日本におけるヒルシュスプルング病の病型と遺伝子変異の相関、新しい原因遺伝子の同定Principal Investigator
- Principal Investigator
  
  野崎靖之
- Project Period (FY)
  1998 – 1999
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
Studies on the molecular genetics and diagnostic and therapeutic procedures for myotonic dystrophy and allied disorders
- Principal Investigator
  
  MOMOI Mariko
- Project Period (FY)
  1998 – 2000
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  JICHI MEDICAL SCHOOL
トリプレットリピート伸展疾患の遺伝子診断法の確立、病態解析、新たな疾患遺伝子同定
- Principal Investigator
  
  MOMOI Mariko
- Project Period (FY)
  1996 – 1997
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
発達障害に関する遺伝子の同定、染色体座位の決定Principal Investigator
- Principal Investigator
  
  野崎靖之
- Project Period (FY)
  1996
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University

All 2014 2013 2012 2011

All Journal Article Presentation

[Journal Article] LIN7A depletion disrupts cerebral cortex development contributing to intellectual disability in 12q21-deletion syndrome2014
- Author(s)
  Matsumoto A, Mizuno M, Hamada N, Nozaki Y, Jimbo E, Momoi M, Nagata K, Yamagata T
- Journal Title
  
  PLoS One.
  
  Volume: 9
- DOI
  10.1371/journal.pone.0092695
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-13J40147, KAKENHI-PROJECT-23390275, KAKENHI-PROJECT-24390271, KAKENHI-PROJECT-24500386, KAKENHI-PROJECT-25670488
[Presentation] 発達障害患者CNV領域におけるシナプス関連分子の解析.2013
- Author(s)
  松本歩、山形崇倫、野崎靖之、神保恵理子、永田浩一、桃井真里子
- Organizer
  第55回日本小児神経学会
- Place of Presentation
  大分
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] 発達障害患者 CNV領域におけるシナプス関連分子の解析2013
- Author(s)
  松本歩, 山形崇倫, 野崎靖之, 神保恵理子, 永田浩一, 桃井真里子
- Organizer
  第55回日本小児神経学会
- Place of Presentation
  大分
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Mental Retardation2012
- Author(s)
  Matsumoto A, Yamagata T, Nozaki Y, Jimbo EF, Momoi MY
- Organizer
  The 62rd Annual Meeting for the American Society of Human Genetics
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Menta Retardation2012
- Author(s)
  Matsumoto A, Yamagata T, Nozaki Y, Jimbo E, Momoi MY
- Organizer
  The 62th Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  San Francisco
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Duplication of GPC3 in the boy with growth retardation and developmental delay2011
- Author(s)
  Nakashima N, Yamamgata T, Saito M, Nozaki Y, Momoi MY
- Organizer
  The 61st Annual Meeting of the American Society of Human Genetics
- Place of Presentation
  Montreal, Canada
- Year and Date
  2011-11-14
- Data Source
  KAKENHI-PROJECT-23390275

1. YAMAGATA Takanori (00239857)

# of Collaborated Projects: 4 results

# of Collaborated Products: 5 results
2. MOMOI Mariko (90166348)

# of Collaborated Projects: 3 results

# of Collaborated Products: 0 results
3. MORI Masato (10337347)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. 斉藤茂子 (00260836)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. NAKAMURA Miki (20296114)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. GOTO Tamako (40364509)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. KUWAJIMA Mari (30398515)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. NAGATA Kouichi (50252143)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
9. NAKASHIMA Naomi (20337330)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
10. MONDEN Yukifumi (80382951)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. NAGASHIMA Masako (70438662)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. JINBO Eriko (20291651)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. TSURU Tomohiko (90296111)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. SUWA Kiyotaka (30285796)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 小黒範子 (10214107)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 小林葉子 (20245046)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. FUJITA Eriko

# of Collaborated Projects: 0 results

# of Collaborated Products: 5 results
18. 桃井隆

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

NOZAKI Yasuyuki 野崎 靖之

Research Projects

Research Products

Co-Researchers

Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Research on the common molecular pathology for autism

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Analysis of G-protein coupled receptors as candidate genes for autism

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

日本におけるヒルシュスプルング病の病型と遺伝子変異の相関、新しい原因遺伝子の同定Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Studies on the molecular genetics and diagnostic and therapeutic procedures for myotonic dystrophy and allied disorders

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

トリプレットリピート伸展疾患の遺伝子診断法の確立、病態解析、新たな疾患遺伝子同定

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

発達障害に関する遺伝子の同定、染色体座位の決定Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] LIN7A depletion disrupts cerebral cortex development contributing to intellectual disability in 12q21-deletion syndrome2014

Author(s)

Journal Title

DOI

Data Source

[Presentation] 発達障害患者CNV領域におけるシナプス関連分子の解析.2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 発達障害患者 CNV領域におけるシナプス関連分子の解析2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Mental Retardation2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Interstitial Deletion 12(q21.2-q21.33) in a Boy with Facial Dysmorphism and Menta Retardation2012

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Duplication of GPC3 in the boy with growth retardation and developmental delay2011

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

NOZAKI Yasuyuki 野崎靖之