AYA Kunihiko 綾邦彦

… Alternative Names

綾邦彦アヤクニヒコ

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Researcher Number	20379762
Affiliation (Current)	2025: 岡山大学, 医学部, 客員研究員
Affiliation (based on the past Project Information) *help	2021 – 2023: 岡山大学, 医学部, 客員研究員 2013 – 2017: 岡山大学, 医学部, 客員研究員 2011 – 2012: 岡山大学, 大学病院, 講師 2011: 岡山大学, 岡山大学病院, 講師 2010: 岡山大学, 病院, 講師 … More 2009: Okayama University, 大学病院, 助教 2008: Okayama University, 医学部・歯学部附属病院, 助教 2007: Okayama University, 医学部歯学部・附属病院, 助教 2006: 岡山大学, 医学部・歯学部附属病院, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator ポドシン / 輸送蛋白 / 蛋白尿 / ネフリン / ネフローゼ / 細胞内輸送 / 先天性 / nephrin / ネフローゼ症候群 / 細胞・組織 … More / 遺伝子 / 小児腎・泌尿器学 / MCLMR症候群 / 体重増加不良 / 消化管 / 異形腺管 / 尿細管 / ポドサイト / 腎炎 / 質量分析 / ホドシン / シグナル伝達 Less

MCLMR症候群における輸送蛋白の役割Principal Investigator
- Principal Investigator
  
  綾邦彦
- Project Period (FY)
  2021 – 2024
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Okayama University
clarification of the mechanism of proteinuria related with tranport proteinPrincipal Investigator
- Principal Investigator
  
  AYA KUNIHIKO
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
clarification of the mechanism of proteinuria with conditional knockout micePrincipal Investigator
- Principal Investigator
  
  KUNIHIKO AYA
- Project Period (FY)
  2012
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
identification of proteins interacting with causative molecules for hereditary nephrotic syndrome and analysis of pathogenesis of it.Principal Investigator
- Principal Investigator
  
  AYA Kunihiko
- Project Period (FY)
  2009 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University
The clarification of pathgenesis of Japanese congenital nephrotic syndrome and the search for molecule to ameriorate proteinuriaPrincipal Investigator
- Principal Investigator
  
  AYA Kunihiko
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Okayama University

All 2014 2013 2012 2011 2010 2009 2008 2007

All Journal Article Presentation Book Patent

[Book] 臨床腎臓内科学2013
- Author(s)
  綾邦彦ら
- Total Pages
  1051
- Publisher
  南山堂
- Data Source
  KAKENHI-PROJECT-24659499
[Book] 臨床腎臓内科学を分担執筆2013
- Author(s)
  綾邦彦
- Publisher
  南山堂
- Data Source
  KAKENHI-PROJECT-24659499
[Book] 小児腎臓病学先天性ネフローゼ症候群2012
- Author(s)
  綾邦彦
- Total Pages
  460
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-21591387
[Book] 小児腎臓病学先天性ネフローゼ症候群を分担執筆2012
- Author(s)
  綾邦彦
- Total Pages
  460
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-21591387
[Book] 腎疾患・透析最新の治療 2011-2013 紫斑病性腎炎小児を分担執筆2011
- Author(s)
  綾邦彦
- Total Pages
  454
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-21591387
[Book] 腎疾患・透析最新の治療2011-2013紫斑病性腎炎小児2011
- Author(s)
  綾邦彦
- Total Pages
  454
- Publisher
  南江堂
- Data Source
  KAKENHI-PROJECT-21591387
[Book] 小児科臨床ピクシス小児のネフローゼと腎炎先天性ネフローゼ症候群2011
- Author(s)
  綾邦彦
- Total Pages
  222
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-21591387
[Book] 小児科臨床ピクシス小児のネフローゼと腎炎先天性ネフローゼ症候群を分担執筆2010
- Author(s)
  綾邦彦
- Total Pages
  222
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-21591387
[Journal Article] Functional analysis of NPHS1 mutations in Japanese patients2014
- Author(s)
  Miyai T Aya K et al.
- Journal Title
  
  Histol Histopathol
  
  Volume: 29(2) Pages: 279-284
- NAID
  120005468266
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659499
[Journal Article] 遺伝性ネフローゼ症候群原因分子の解析2013
- Author(s)
  綾邦彦宮井貴之
- Journal Title
  
  annual review腎臓
  
  Volume: 2013巻 Pages: 118-124
- Data Source
  KAKENHI-PROJECT-24659499
[Journal Article] 遺伝性ネフローゼ症候群原因分子の解析2013
- Author(s)
  綾邦彦他
- Journal Title
  
  annual review　腎臓
  
  Volume: 2013巻 Pages: 118-124
- Data Source
  KAKENHI-PROJECT-24659499
[Journal Article] 先天性ネフローゼ症候群2012
- Author(s)
  綾邦彦
- Journal Title
  
  腎と透析
  
  Volume: 72巻増刊 Pages: 271-274
- Data Source
  KAKENHI-PROJECT-24659499
[Journal Article] NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome2009
- Author(s)
  Aya K et al.
- Journal Title
  
  Nephrol Dial Transplant
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790721
[Journal Article] NPHS 1 gene mutation in Japanese patients with congenital nephrotic syndrome2009
- Author(s)
  Aya K, et.al.
- Journal Title
  
  Nephrol Dial Transplant
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18790721
[Journal Article] 先天性・乳児ネフローゼ症候群2008
- Author(s)
  綾邦彦
- Journal Title
  
  小児内科 40巻増刊
  
  Pages: 845-849
- Data Source
  KAKENHI-PROJECT-18790721
[Journal Article] 先天性ネフローゼ症候群2007
- Author(s)
  綾邦彦ら
- Journal Title
  
  腎と透析 62巻
  
  Pages: 60-64
- Data Source
  KAKENHI-PROJECT-18790721
[Journal Article] 先天性ネフローゼ症候群2007
- Author(s)
  綾邦彦、清水純也、高岩正典、宮井貴之、田中弘之
- Journal Title
  
  腎と透析 62
  
  Pages: 60-64
- Data Source
  KAKENHI-PROJECT-18790721
[Patent] 腎障害の新規マーカー2010
- Inventor(s)
  綾邦彦, 大内田守
- Industrial Property Rights Holder
  岡山大学
- Industrial Property Number
  2010-216786
- Filing Date
  2010-09-28
- Data Source
  KAKENHI-PROJECT-21591387
[Patent] 腎障害の新規マーカー2010
- Inventor(s)
  綾邦彦,大内田守
- Industrial Property Rights Holder
  岡山大学
- Filing Date
  2010-09-28
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] ポドシン輸送システムの探索2012
- Author(s)
  宮原宏幸　綾邦彦他
- Organizer
  日本小児腎臓病学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24659499
[Presentation] ポドシン細胞内輸送システムの探索2012
- Author(s)
  綾邦彦, 他
- Organizer
  日本腎臓病学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-24659499
[Presentation] ポドシンの輸送システムの探索2012
- Author(s)
  宮原宏幸, 綾邦彦, 他
- Organizer
  日本小児腎臓病学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-24659499
[Presentation] ポドシンの輸送システムの探索2012
- Author(s)
  宮原宏幸, 綾邦彦
- Organizer
  分子腎臓フォーラム
- Place of Presentation
  京都
- Year and Date
  2012-01-21
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 日本人先天性ネフローゼ症候群患者が持つNPHS1遺伝子変異の機能解析2011
- Author(s)
  宮井貴之, 綾邦彦
- Organizer
  日本腎臓学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] NPHS2 gene mutations in a Japanese patient with steroid resistant nephrotic syndrome2011
- Author(s)
  Aya K, et al
- Organizer
  アジア小児腎臓病学会ACPN
- Place of Presentation
  Fukuoka
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 日本人先天性ネフローゼ症候群患者が持つNPHS1遺伝子変異の機能解析2011
- Author(s)
  宮井貴之, 綾邦彦
- Organizer
  日本小児科学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 日本人先天性ネフローゼ症候群(先天ネ症)患者が持つNPHS1遺伝子変異の機能解析2010
- Author(s)
  宮井貴之, 綾邦彦
- Organizer
  日本小児腎臓病学会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 治療に反応し寛解に至ったび漫性糸球体硬化(DMS)例2010
- Author(s)
  宮井貴之, 綾邦彦
- Organizer
  日本腎臓学会
- Place of Presentation
  神戸
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 日本人先天性ネフローゼ患者遺伝子異常の創始者効果2010
- Author(s)
  綾邦彦
- Organizer
  日本小児科学会
- Place of Presentation
  盛岡
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 先天性ネフローゼ症候群の発症機序2010
- Author(s)
  綾邦彦
- Organizer
  山陰腎疾患研究会
- Place of Presentation
  米子
- Year and Date
  2010-03-20
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] Functional analysis of NPHS1 gene mutations with Japanese congenital nephrotic syndrome patients2010
- Author(s)
  Miyai T, Aya K, et al.
- Organizer
  国際腎臓病学会IPNA
- Place of Presentation
  ニューヨーク
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] Functional analysis of NPHS1 gene mutations with Japanese congenital nephrot ic syndrome patients2010
- Author(s)
  Miyai T, Aya K, et al
- Organizer
  国際腎臓病学会IPNA
- Place of Presentation
  ニューヨーク
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] 日本人先天性ネフローゼ患者遺伝子異常の創始者効果についての検討2009
- Author(s)
  綾邦彦
- Organizer
  日本小児腎臓病学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] NPHS1遺伝子異常nt2515(delC)の創始者効果についての検討2009
- Author(s)
  綾邦彦
- Organizer
  日本腎臓学会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-21591387
[Presentation] NPHS 2(ポドシン)異常を有したステロイド抵抗性ネフローゼ症候群(SRNS)の一例2008
- Author(s)
  綾邦彦ら
- Organizer
  日本小児科学会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] NPHS2(ポドシン)異常を有したステロイド抵抗性ネフローゼ症候群(SRNS)の一例2008
- Author(s)
  綾邦彦
- Organizer
  日本小児科学会
- Place of Presentation
  東京
- Year and Date
  2008-04-01
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] NPHS 2異常を有した日本人SRNS例2008
- Author(s)
  綾邦彦ら
- Organizer
  日本腎臓学会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] NPHS2異常を有した日本人SRNS例2008
- Author(s)
  綾邦彦
- Organizer
  日本腎臓学会
- Place of Presentation
  福岡
- Year and Date
  2008-05-01
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] Genetic analysis of Japanese patients with congenital nephrotic syndrome(CNS)2007
- Author(s)
  Aya K et al.
- Organizer
  14th Congress of the International Pediatric Nephrology Assocation
- Place of Presentation
  Budapest, Hungary
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] 著名な頭蓋骨離開を認めたタステロイド抵抗性ネフローゼ症候群(SRMS)の一例2007
- Author(s)
  綾邦彦、山下美保、二宮伸介、宮井貴之、高岩正典、田中弘之、森島恒雄
- Organizer
  第42回日本小児腎臓病学会学術集会
- Place of Presentation
  横浜市
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] 著名な頭蓋骨離開を認めたステロイド抵抗性ネフローゼ症候群(SRNS)の一例2007
- Author(s)
  綾邦彦
- Organizer
  第42回日本小児腎臓病学会学術集会
- Place of Presentation
  横浜市
- Data Source
  KAKENHI-PROJECT-18790721
[Presentation] Genetic analysis of Japanese patients with congenital nephrotic syndrome(CNS).2007
- Author(s)
  Aya K.
- Organizer
  14th Congress of the International Pediatric Nephrology Assocation.
- Place of Presentation
  Budapest, Hungary
- Data Source
  KAKENHI-PROJECT-18790721

1. OUCHIDA Mamoru (80213635)

# of Collaborated Projects: 4 results

# of Collaborated Products: 0 results
2. 岡剛史 (50160651)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

AYA Kunihiko 綾 邦彦

綾 邦彦 アヤ クニヒコ

Research Projects

Research Products

Co-Researchers

MCLMR症候群における輸送蛋白の役割Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

clarification of the mechanism of proteinuria related with tranport proteinPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

clarification of the mechanism of proteinuria with conditional knockout micePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

identification of proteins interacting with causative molecules for hereditary nephrotic syndrome and analysis of pathogenesis of it.Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The clarification of pathgenesis of Japanese congenital nephrotic syndrome and the search for molecule to ameriorate proteinuriaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 臨床腎臓内科学2013

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[Book] 臨床腎臓内科学を分担執筆2013

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[Book] 小児腎臓病学先天性ネフローゼ症候群2012

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[Book] 小児腎臓病学先天性ネフローゼ症候群を分担執筆2012

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[Book] 腎疾患・透析 最新の治療 2011-2013 紫斑病性腎炎 小児を分担執筆2011

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[Book] 腎疾患・透析最新の治療2011-2013紫斑病性腎炎小児2011

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[Book] 小児科臨床ピクシス小児のネフローゼと腎炎先天性ネフローゼ症候群2011

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[Book] 小児科臨床ピクシス 小児のネフローゼと腎炎先天性ネフローゼ症候群を分担執筆2010

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[Journal Article] Functional analysis of NPHS1 mutations in Japanese patients2014

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NAID

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[Journal Article] 遺伝性ネフローゼ症候群原因分子の解析2013

AYA Kunihiko 綾邦彦

綾邦彦アヤクニヒコ

[Book] 腎疾患・透析最新の治療 2011-2013 紫斑病性腎炎小児を分担執筆2011

[Book] 小児科臨床ピクシス小児のネフローゼと腎炎先天性ネフローゼ症候群を分担執筆2010