OKADA Hirokazu 岡田浩一

… Alternative Names

岡田浩一オカダヒロカズ

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Researcher Number	60233342
Other IDs
Affiliation (Current)	2025: 埼玉医科大学, 医学部, 教授
Affiliation (based on the past Project Information) *help	2013 – 2024: 埼玉医科大学, 医学部, 教授 2010 – 2012: 埼玉医科大学, 医学部, 准教授 2004: Saitama Medical School, Department of Nephrology, Associate Professor, 医学部, 助教授 2001 – 2003: 埼玉医科大学, 医学部, 講師 1993: 慶應義塾大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Kidney internal medicine / Basic Section 53040:Nephrology-related / Kidney internal medicine Except Principal Investigator Kidney internal medicine / Basic Section 53040:Nephrology-related / Kidney internal medicine / Urology / 膠原病・アレルギー・感染症内科学
Keywords	Principal Investigator 腎線維化 / 線維芽細胞 / 尿細管上皮細胞 / 線維化 / 細胞周期 / 慢性腎臓病 / 急性腎障害 / アポトーシス / CCN2 / 遺伝子改変動物 … More / 増殖因子 / 形質転換 / 慢性腎臓病(CKD) / 急性腎障害(AKI) / カスパーゼ / gene therapy / fibroblast / fibrosis / Rapidly progressive glomerulo-nephritis / gancyclovir / thymidine kinase / トランスジェニックマウス / 間質線維化 / 抗基底膜抗体腎炎 / FSP1 / 腎間質線維化 / 急速進行性糸球体腎炎 / 遺伝子治療 / 急性進行性糸球体腎炎 / ノックインマウス / CKD / 糸球体硬化 / NFkBシグナル / ポドサイト / NFkB / NFkB 経路 / 老化 / 腎臓 / サイトカイン / 拒絶反応 / 移植 … More Except Principal Investigator 慢性腎臓病 / CCN2 / 腎線維化 / focal adhesion kinase / β-catenin / FAK / 線維化 / 腎臓内科 / 内科 / インテグリン / gene transfection / promoter analysis / Osteopontin / iKB / プロモーター解析 / 遺伝子導入 / オステオポンチン / promoter / transfection / 尿細管上皮 / オステオポンチン(OPN) / 分子標的薬 / 転移性腎癌 / 進行性腎癌 / チロシンキナーゼ阻害薬 / 分子標的治療薬 / 蛋白尿 / 腎癌 / 半月体 / メサンギウム細胞 / 糸球体腎炎 / 治療薬 / TLR4 / ポドサイト / FSP1 / Jagged1 / Th17アジュバントcurdlan / Th2アジュバント / アトピー性皮膚炎 / 腎炎 / NODマウス / Jaggedl / Notch ligands / curdlan / Th17アジュバント / アジュバント / アレルギー学 Less

CCN2による線維化促進性情報伝達系を標的とした慢性腎臓病の進展抑制療法の開発Principal Investigator
- Principal Investigator
  
  岡田浩一
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Saitama Medical University
Development of a method to suppress the severity of chronic kidney disease through elucidation of mechanism of transition from acute kidney injuryPrincipal Investigator
- Principal Investigator
  
  Okada Hirokazu
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Saitama Medical University
Development of novel therapeutics for chronic and acute kidney injury through the regulation of CCN2 function
- Principal Investigator
  
  Inoue Tsutomu
- Project Period (FY)
  2019 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Saitama Medical University
Pathogenesis and treatment of tubular epithelium-mediated AKI to CKD transitionPrincipal Investigator
- Principal Investigator
  
  Okada Hirokazu
- Project Period (FY)
  2016 – 2018
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Saitama Medical University
Development of a new treatment approach for chronic kidney disease by controlling CCN2 function
- Principal Investigator
  
  Inoue Tsutomu
- Project Period (FY)
  2016 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Saitama Medical University
Clinical analysis of urinary biomarkers predictive of renal injury due to tyrosine kinase inhibitors for advanced renal cell carcinoma
- Principal Investigator
  
  oyama masafumi
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Urology
- Research Institution
  Saitama Medical University
Generation of anti-fibrotic therapy to combat progression of CKD via CCN2 blockadePrincipal Investigator
- Principal Investigator
  
  Okada Hirokazu
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Saitama Medical University
Novel strategy for the treatment of active nephritis using secreted FSP1
- Principal Investigator
  
  IWANO Masayuki
- Project Period (FY)
  2012 – 2014
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Kidney internal medicine
- Research Institution
  University of Fukui
Effects of renal tissue-specific NFkB blockade on aging kidneysPrincipal Investigator
- Principal Investigator
  
  OKADA Hirokazu
- Project Period (FY)
  2010 – 2012
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Saitama Medical University
Qualitative analysis of adjuvant activities and its application to immunity-related diseases
- Principal Investigator
  
  MATSUSHITA Sho
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  膠原病・アレルギー・感染症内科学
- Research Institution
  Saitama Medical University
Generation of an anti-fibrotic therapeutic gene using a tubular epithelium-specific expression gene casette and iKB cDNA
- Principal Investigator
  
  KANNO Yoshihiko
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Saitama Medical School, School of Medicine
Effect of fibroblast-specific suicidal-gene against rapidly progressive glomerulonephritisPrincipal Investigator
- Principal Investigator
  
  OKADA Hirokazu
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Saitama Medical School
移植腎の拒絶反応におけるサイトカインおよび細胞接着分子の遺伝子発現Principal Investigator
- Principal Investigator
  
  岡田浩一
- Project Period (FY)
  1993
- Research Category
  
  Grant-in-Aid for Encouragement of Young Scientists (A)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Keio University

All 2023 2022 2021 2020 2019 2018 2017 2016 2010 2009 2003 Other

All Journal Article Presentation

[Journal Article] Module 4-Deficient CCN2/Connective Tissue Growth Factor Attenuates the Progression of Renal Fibrosis via Suppression of Focal Adhesion Kinase Phosphorylation in Tubular Epithelial Cells2023
- Author(s)
  Amano Hiroaki、Inoue Tsutomu、Kusano Takeru、Fukaya Daichi、Kosakai Wakako、Okada Hirokazu
- Journal Title
  
  Molecular and Cellular Biology
  
  Volume: 43 Issue: 10 Pages: 515-530
- DOI
  10.1080/10985549.2023.2253130
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08731
[Journal Article] Analysis of the Function of CCN2 in Tubular Epithelium Cells with a Focus on Renal Fibrogenesis2022
- Author(s)
  Amano Hiroaki、Inoue Tsutomu、Kusano Takeru、Okada Hirokazu
- Journal Title
  
  Methods Mol Biol
  
  Volume: 13 Pages: 411-426
- DOI
  10.1007/978-1-0716-2744-0_28
- ISBN
  9781071627433, 9781071627440
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08731, KAKENHI-PROJECT-20K08614
[Journal Article] Tocilizumab-induced immunocomplex glomerulonephritis: a report of two cases2020
- Author(s)
  Fukaya Daichi、Inoue Tsutomu、Kogure Yuta、Kajiyama Hiroshi、Ishizawa Keisuke、Seto Takeru、Hasegawa Hajime、Mimura Toshihide、Okada Hirokazu
- Journal Title
  
  CEN Case Reports
  
  Volume: 9 Issue: 4 Pages: 318-325
- DOI
  10.1007/s13730-020-00478-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08731, KAKENHI-PROJECT-20K08805
[Journal Article] Glomerular solidification is associated with nephritis-related clinical parameters in IgA nephropathy2019
- Author(s)
  Inoue Tsutomu、Luo Yankun、Seto Takeru、Suzuki Hiromichi、Okada Hirokazu
- Journal Title
  
  Renal Failure
  
  Volume: 41 Issue: 1 Pages: 893-898
- DOI
  10.1080/0886022x.2019.1665545
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08731, KAKENHI-PROJECT-16K09627
[Journal Article] Cellular communication network factor 2 (CCN2) promotes the progression of acute kidney injury to chronic kidney disease2019
- Author(s)
  Inoue Tsutomu、Kusano Takeru、Amano Hiroaki、Nakamoto Hidetomo、Okada Hirokazu
- Journal Title
  
  Biochemical and Biophysical Research Communications
  
  Volume: 517 Issue: 1 Pages: 96-102
- DOI
  10.1016/j.bbrc.2019.07.024
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08731, KAKENHI-PROJECT-16K09627
[Journal Article] 【腎硬化症への対策】腎硬化症の薬物治療　糖尿病合併例、有蛋白尿例を含む2017
- Author(s)
  岡田浩一
- Journal Title
  
  日本医事新報
  
  Volume: 4854 Pages: 34-40
- Data Source
  KAKENHI-PROJECT-16K09627
[Journal Article] 【動脈硬化up to date】腎線維化を考慮したCKD治療戦略　腎線維化はどこまで解明されたか2017
- Author(s)
  岡田浩一
- Journal Title
  
  循環plus
  
  Volume: 17 Pages: 2-6
- Data Source
  KAKENHI-PROJECT-16K09627
[Journal Article] 腎線維化を考慮したCKD治療戦略　腎線維化はどこまで解明されたか2016
- Author(s)
  岡田浩一
- Journal Title
  
  循環plus.
  
  Volume: 17 Pages: 4-6
- Data Source
  KAKENHI-PROJECT-16K09627
[Journal Article] CKDの進展抑制と治療 RA系阻害薬を中心とする薬物療法の現状と今後への期待2016
- Author(s)
  岡田浩一
- Journal Title
  
  内科
  
  Volume: 118 Pages: 83-87
- Data Source
  KAKENHI-PROJECT-16K09627
[Journal Article] 腎機能障害慢性腎臓病(CKD)2016
- Author(s)
  岡田浩一
- Journal Title
  
  臨床泌尿器科
  
  Volume: 70 Pages: 150-153
- Data Source
  KAKENHI-PROJECT-16K09627
[Journal Article] Fibroblasts stimulated via HLA-II produce PGE 2 and regulate cytokine production from Th cells.2010
- Author(s)
  Nahoko Kato-Kogoe, Hideki Ohyama, Fusanori Nishimura, Michio Meguro, Sayuri Yoshizawa, Yuka Okada, Keiji Nakasho, Koji Yamanegi, Naoko Yamada, Masaki Hata, Takehiro Higashi, Nobuyuki Terada, Sho Matsushita
- Journal Title
  
  Lab Invest 90
  
  Pages: 1747-1756
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591192
[Journal Article] Human leukocyte histocompatibility antigen class II-induced cytokines from human gingival fibroblasts promote proliferation of human umbilical vein endothelial cells : potential association with enhanced angiogenesis in chronic periodontal inflammation2009
- Author(s)
  Okada Y.
- Journal Title
  
  J Periodont Res. 44
  
  Pages: 103-109
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591192
[Journal Article] D1-Like Receptor Antagonist Inhibits IL-17 Expression and Attenuates Crescent Formation in Nephrotoxic Serum Nephritis.2009
- Author(s)
  Okada,H., Inoue T., Hashimoto K., Suzuki H., Matsushita S.
- Journal Title
  
  Am J Nephrol 30
  
  Pages: 274-279
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591192
[Journal Article] D1-Like Receptor Antagonist Inhibits IL-17 Expression and Attenuates Crescent Formation in Nephrotoxic Serum Nephritis2009
- Author(s)
  Okada, H.
- Journal Title
  
  Am J Nephrol. 30
  
  Pages: 274-279
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591192
[Journal Article] Dopamine D1-like receptor antagonist, SCH23390, exhibits a preventive effect on diabetes mellitus that occurs naturally in NOD mice2009
- Author(s)
  Hashimoto, K., Inoue, T., Higashi T., Takei S., Katayama S., Takagi, R., Okada, H., Matsushita S.
- Journal Title
  
  Biochem. Biophys. Res. Commun 383
  
  Pages: 460-463
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591192
[Journal Article] Human leukocyte histocompatibility antigen class II-induced cytokines from human gingival fibroblasts promote proliferation of human umbilical vein endothelial cells : potential association with enhanced angiogenesis in chronic periodontal inflammation.2009
- Author(s)
  Okada Y, Meguro M, Ohyama H, Yoshizawa S, Takeuchi-Hatanaka K, Kato N, Matsushita S, Takashiba S, Nishimura F.
- Journal Title
  
  J Periodont Res 44
  
  Pages: 103-109
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591192
[Journal Article] Direct contact between human peripheral blood mononuclear cells and renal fibroblasts facilitates the expression of monocyte chemoattractant protein-12003
- Author(s)
  Hao, L., H.Okada, Y.Kanno, T.Inoue, T.Kobayashi, Y.Watanabe, et al.
- Journal Title
  
  Am J Nephrol 23・4
  
  Pages: 208-213
- Data Source
  KAKENHI-PROJECT-14571033
[Presentation] 腎線維化の進行にはCCN2-integrinを介したFAKのリン酸化が関与する2021
- Author(s)
  深谷大地、井上勉、天野博明、岡田浩一
- Organizer
  日本CCNファミリー研究会
- Data Source
  KAKENHI-PROJECT-19K08731
[Presentation] CCN2/CTGF Causes Renal Fibrosis Progression Through the Integrin/FAK Signal Pathway2021
- Author(s)
  Daichi Fukaya, Tsutomu Inoue, Hiroaki Amano, Yusuke Watanabe, Hirokazu Okada
- Organizer
  Kidney Week 2021, Annual Meeting of American Society of Nephrology
- Data Source
  KAKENHI-PROJECT-19K08731
[Presentation] CCN2/CTGFはintegrin/FAKを介して腎線維化を進行する2021
- Author(s)
  深谷大地, 天野博明, 井上勉, 草野武, 岡田浩一
- Organizer
  第64回日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-19K08731
[Presentation] CCN2/CTGFはintegrin/FAKを介して腎線維化を進行する2021
- Author(s)
  深谷大地、井上勉、天野博明、岡田浩一
- Organizer
  日本分子腎臓フォーラム
- Data Source
  KAKENHI-PROJECT-19K08731
[Presentation] CCN2 Module IV-Derived Decoy Peptides Attenuate Renal Fibrogenesis Through Inhibition of FAK Pathway in the Tubular Epithelium2019
- Author(s)
  Hiroaki Amano, Tsutomu Inoue, Hirokazu Okada
- Organizer
  Annual Meeting of American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08731
[Presentation] CCN2 Module IV-Derived Decoy Peptides Attenuate Renal Fibrogenesis Through Inhibition of FAK Pathway in the Tubular Epithelium2019
- Author(s)
  Hiroaki Amano, Tsutomu Inoue, Hirokazu Okada
- Organizer
  Annual Meeting of American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09627
[Presentation] CCN2 module 4はFAKのリン酸化を介して腎線維化を促進する2019
- Author(s)
  天野博明、井上勉、草野武、岡田浩一
- Organizer
  日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-19K08731
[Presentation] CCN2 module 4はFAKのリン酸化を介して腎線維化を促進する2019
- Author(s)
  天野博明、井上勉、草野武、岡田浩一
- Organizer
  日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-16K09627
[Presentation] CCN2 module-IV promotes renal fibrosis through activation of the FAK pathway in the tubular epithelium2018
- Author(s)
  天野博明、井上勉、草野武、岡田浩一
- Organizer
  The annual meeting ofthe American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09626
[Presentation] CCN2 Module-IV Promotes Renal Fibrosis Through Activation of the FAK Pathway in the Tubular Epithelium2018
- Author(s)
  Hiroaki Amano, Tustomu Inoue, Hirokazu Okada
- Organizer
  Annual meeting of American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09627
[Presentation] 初代皮膚線維芽細胞におけるCCN2 module-IVの作用機序について2018
- Author(s)
  天野博明、井上勉、草野武、岡田浩一
- Organizer
  第61回日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-16K09626
[Presentation] 初代皮膚線維芽細胞におけるCCN2 module-IVの作用機序について2018
- Author(s)
  天野博明, 井上勉, 草野武, 岡田浩一
- Organizer
  日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-16K09627
[Presentation] Module IV-defected mutant CCN2 knock-in transgenic mice grow and develop normally, but fibrotic properties are attenuated in a number of kidney diseases.2017
- Author(s)
  天野博明、井上勉、草野武、岡田浩一
- Organizer
  The annual meeting ofthe American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09626
[Presentation] Module IV-defected mutant CCN2 knock-in transgenic mice grow and develop normally, but fibrotic properties are attenuated in a number of kidney diseases.2017
- Author(s)
  Tsutomu Inoue, Ono Atsushi, Hirokazu Okada.
- Organizer
  Annual Meeting of American Society of Nephrology 2018 (Kidney Week 2018)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-16K09627
[Presentation] 尿細管上皮細胞のCaspase活性とCCN2発現はAKIからCKDへの移行を修飾する2016
- Author(s)
  草野武、井上勉、中元秀友、岡田浩一
- Organizer
  第59回日本腎臓学会学術総会
- Place of Presentation
  横浜
- Year and Date
  2016-06-17
- Data Source
  KAKENHI-PROJECT-16K09626
[Presentation] 尿細管上皮細胞のCaspase活性とCCN2発現はAKIからCKDへの移行を修飾する2016
- Author(s)
  草野武, 井上勉, 中元秀友, 岡田浩一
- Organizer
  第59回日本腎臓学会学術総会
- Place of Presentation
  横浜
- Year and Date
  2016-06-17
- Data Source
  KAKENHI-PROJECT-16K09627
[Presentation] A Module IV-Defective CCN2 Mutant and Module IV-Derived Decoy Peptides Attenuate Renal Fibrogenesis
- Author(s)
  Tsutomu Inoue, MD, PhD, Takeru Kusano, MD, Hiroaki Amano, MD, Kei Sugiyama, MD, Hiromichi Suzuki, MD, PhD, Hirokazu Okada, MD, PhD
- Organizer
  Kidney Week 2014, The annual meeting of the American Society of Nephrology
- Place of Presentation
  Philadelphia Convention Center, Philadelphia, PA, USA
- Year and Date
  2014-11-13 – 2014-11-16
- Data Source
  KAKENHI-PROJECT-25461228

1. INOUE Tsutomu (30406475)

# of Collaborated Projects: 8 results

# of Collaborated Products: 22 results
2. KANNO Yoshihiko (30276232)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
3. MATSUSHITA Sho (50167649)

# of Collaborated Projects: 1 results

# of Collaborated Products: 4 results
4. HIGASHI Takehiro (00468381)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
5. AWATA Takuya (40184303)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
6. KOUSAKA Hitoshi (00251554)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. SIMOJYO Naoki (40221303)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. IWANO Masayuki (20275324)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. KIMURA Hideki (20283187)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. NAKATANI Kimihiko (80398445)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
11. oyama masafumi (70276351)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. SUZUKI Hiromichi (80129494)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. KIKUTA Tomohiro (70383239)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 城武卓 (10528805)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 天野博明 (10862675)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. MIYAWAKI Atsushi

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results

OKADA Hirokazu 岡田 浩一

岡田 浩一 オカダ ヒロカズ

Research Projects

Research Products

Co-Researchers

CCN2による線維化促進性情報伝達系を標的とした慢性腎臓病の進展抑制療法の開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of a method to suppress the severity of chronic kidney disease through elucidation of mechanism of transition from acute kidney injuryPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Development of novel therapeutics for chronic and acute kidney injury through the regulation of CCN2 function

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Pathogenesis and treatment of tubular epithelium-mediated AKI to CKD transitionPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Development of a new treatment approach for chronic kidney disease by controlling CCN2 function

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Clinical analysis of urinary biomarkers predictive of renal injury due to tyrosine kinase inhibitors for advanced renal cell carcinoma

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Generation of anti-fibrotic therapy to combat progression of CKD via CCN2 blockadePrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Novel strategy for the treatment of active nephritis using secreted FSP1

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Effects of renal tissue-specific NFkB blockade on aging kidneysPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Qualitative analysis of adjuvant activities and its application to immunity-related diseases

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Generation of an anti-fibrotic therapeutic gene using a tubular epithelium-specific expression gene casette and iKB cDNA

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Effect of fibroblast-specific suicidal-gene against rapidly progressive glomerulonephritisPrincipal Investigator

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移植腎の拒絶反応におけるサイトカインおよび細胞接着分子の遺伝子発現Principal Investigator

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OKADA Hirokazu 岡田浩一

岡田浩一オカダヒロカズ

[Journal Article] 【腎硬化症への対策】腎硬化症の薬物治療　糖尿病合併例、有蛋白尿例を含む2017

[Journal Article] 【動脈硬化up to date】腎線維化を考慮したCKD治療戦略　腎線維化はどこまで解明されたか2017

[Journal Article] 腎線維化を考慮したCKD治療戦略　腎線維化はどこまで解明されたか2016

[Journal Article] 腎機能障害慢性腎臓病(CKD)2016