Orii Kenji 折居建治

… Alternative Names

ORII Kenji 折居建治

折居建治オリイケンジ

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Researcher Number	30332688
Other IDs
Affiliation (Current)	2023: 岐阜大学, 医学部附属病院, 非常勤講師
Affiliation (based on the past Project Information) *help	2014 – 2016: 岐阜大学, 医学部附属病院, 准教授 2010: Gifu University, 医学部附属病院, 准教授 2008 – 2009: Gifu University, 医学部附属病院, 助教 2006: 岐阜大学, 大学院医学系研究科, 助手 2005: 岐阜大学, 医学部附属病院, 助手 2002: 岐阜大, 医学部附属病院, 助手 2001: 岐阜大学, 医学部・附属病院, 助手
Review Section/Research Field	Principal Investigator Pediatrics / Pediatrics
Keywords	Principal Investigator 神経変性 / MyD88 / 立体構造解析 / Death Domain / TIR Domain / 毛細血管拡張性運動失調症 / ATM / Mre11 / NBS1 / 小児神経学 … More / 小脳変性症 / 脳神経疾患 / 遺伝子 / 遺伝子修復 / 先天代謝異常症 / ムコ多糖症 / 新規治療薬 / 骨関節症状 / ポリ硫酸ペントサン / サイトカイン / ウロン酸 Less

Study on the safety and effect of novel therapeutic agents for mucopolysaccharidosisPrincipal Investigator
- Principal Investigator
  
  Orii Kenji
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Gifu University
The analysis of congenital DNA-repair abnormality with cerebellar degenerationPrincipal Investigator
- Principal Investigator
  
  ORII Kenji
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Gifu University
毛細血管拡張性運動失調症における神経変性機構を解明するための基礎的研究Principal Investigator
- Principal Investigator
  
  折居建治
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Gifu University
病的なサイトカイン血症を来す病因関連蛋白質の立体構造解析と新たな治療法の開発Principal Investigator
- Principal Investigator
  
  折居建治
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Gifu University

All 2016 2015 2010 2009 2006

All Journal Article Presentation

[Journal Article] STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.2010
- Author(s)
  Hirotomo Saitsu, Mitsuhiro Kato, Ippei Okada, Kenji E. Orii, Tsukasa Higuchi, Hideki Hoshino, Masaya Kubota, Hiroshi Arai, Tstsuzo Tagawa, Shigeru Kimura, Akira Sudo, Sahoko Miyama, Yuichi Takami, Toshihide Watanabe, Akira Nishimura, Kiyomi Nishimura, Noriko Miyake, Takahito Wada, Hitoshi Osaka, Naomi Kondo, Kiyoshi Hayasaka, Naomichi Matsumoto
- Journal Title
  
  Epilepsia Vol.51
  
  Pages: 1528-1168
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.2010
- Author(s)
  Hirotomo Saitsu, Mitsuhiro Kato, Ippei Okada, Kenji E. Orii, Tsukasa Higuchi, Hideki Hoshino, Masaya Kubota, Hiroshi Arai, Tstsuzo Tagawa, Shigeru Kimura, Akira Sudo, Sahoko Miyama, Yuichi Takami, Toshihide Watanabe, Akira Nishimura, Kiyomi Nishimura, Noriko Miyake, Takahito Wada, Hitoshi Osaka, Naomi Kondo, Kiyoshi Hayasaka, Naomichi Matsumoto
- Journal Title
  
  Epilepsia
  
  Volume: Vol.51(12) Pages: 1528-1167
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.2010
- Author(s)
  Zenichiro Kato, Masahiro Morimoto, Kenji E, Orii, Tomomi Kato, Naomi Kondo
- Journal Title
  
  Pediatric Radiology. Vol 40 supple
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.2010
- Author(s)
  Zenichiro Kato, Masahiri Morimoto, Kenji E, Orii, Tomomi Kato, Naomi Kondo
- Journal Title
  
  Pediatric Radiology
  
  Volume: Vol.40 Suppl1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] Structural basis for the multiple interactions of the Myd88 TIR domain in TLR4 signaling2009
- Author(s)
  Hidenori Ohnishi, Hidehiko Tochio, Zenichiro Kato, Kenji E.Orii, Ailian Li, Takeshi Kimura, Hidekazu Hiroaki, Naomi Kondo, Masahiro Shirakawa
- Journal Title
  
  PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 106 25
  
  Pages: 10260-10265
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] Masahiro Shirakawa Structural basis for the multiple interactions of the Myd88 TIR domain in TLR4 signaling2009
- Author(s)
  Hidenori Ohnishi, Hidehiko Tochio, Zenichiro Kato, Rend E.Orii, Ailian Li, Takeshi Kimura Hidekazu Hiroaki, Naomi Kondo
- Journal Title
  
  PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA Vol 106
  
  Pages: 10260-10265
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency.2009
- Author(s)
  Pierre-Olivier Frappart, Youngsoo Lee, Helen R Russell, Nader Chalhoub, Yong-Dong Wang, Kenji E.Orii Jingfeng Zhao, Naomi Kondo, Suzanne J.Baker, Peter J.McKinnon
- Journal Title
  
  PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATE S OF AMERICA Vol 106
  
  Pages: 1880-1885
- Data Source
  KAKENHI-PROJECT-20591220
[Journal Article] Acute disseminated encephalomyelitis associated with enterovirus 71.2006
- Author(s)
  Kato Z, Omoya K, Orii KE, Kondo N
- Journal Title
  
  Journal of pediatric Infectious Disease 1
  
  Pages: 115-118
- Data Source
  KAKENHI-PROJECT-17790696
[Journal Article] Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.2006
- Author(s)
  Orii KE, Lee Y, Kondo N, McKinnon PJ
- Journal Title
  
  Proceedings of National Academy of Science of the U. S. A. 103・26
  
  Pages: 10017-10022
- Data Source
  KAKENHI-PROJECT-17790696
[Presentation] Safety study of sodium pentosan polysulfate for adult patients with mucopolysaccharidosis type II2016
- Author(s)
  折居建治、戸松俊治、鈴木康之、Alexander Solyom、Edward H. Schuchman、Calogera M. Simonaro、折居忠夫、深尾敏幸
- Organizer
  12th Annual WORLD Symposium 2016
- Place of Presentation
  San Diego(アメリカ合衆国）
- Year and Date
  2016-02-29
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461523
[Presentation] ムコ多糖症II型成人患者に対するポリ硫酸ペントサン投与の検討2015
- Author(s)
  折居建治、戸松俊治、鈴木康之、折居忠夫、深尾敏幸
- Organizer
  第57回日本先天代謝異常学会
- Place of Presentation
  大阪市、大阪国際会議場
- Year and Date
  2015-11-12
- Data Source
  KAKENHI-PROJECT-26461523
[Presentation] ムコ多糖症に対するペントサンの臨床研究・臨床治験について2015
- Author(s)
  折居建治、戸松俊治
- Organizer
  第19回日本ムコ多糖症研究会
- Place of Presentation
  大阪市、ホテルアウィーナ大阪
- Year and Date
  2015-09-21
- Data Source
  KAKENHI-PROJECT-26461523

1. TOMATSU SHUNJI (70237105)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
2. SUZUKI YASUYUKI (90154559)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. 折居忠夫 (20045339)

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results

Orii Kenji 折居 建治

ORII Kenji 折居 建治

折居 建治 オリイ ケンジ

Research Projects

Research Products

Co-Researchers

Study on the safety and effect of novel therapeutic agents for mucopolysaccharidosisPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

The analysis of congenital DNA-repair abnormality with cerebellar degenerationPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

毛細血管拡張性運動失調症における神経変性機構を解明するための基礎的研究Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

病的なサイトカイン血症を来す病因関連蛋白質の立体構造解析と新たな治療法の開発Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.2010

Author(s)

Journal Title

Data Source

[Journal Article] STXBP1 mutations in early infantile epileptic encephalopathy with suppression-burst pattern.2010

Author(s)

Journal Title

Data Source

[Journal Article] Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.2010

Author(s)

Journal Title

Data Source

[Journal Article] Developmental changes of radiological findings in Fukuyama-type congenital muscular dystrophy.2010

Author(s)

Journal Title

Data Source

[Journal Article] Structural basis for the multiple interactions of the Myd88 TIR domain in TLR4 signaling2009

Author(s)

Journal Title

Data Source

[Journal Article] Masahiro Shirakawa Structural basis for the multiple interactions of the Myd88 TIR domain in TLR4 signaling2009

Author(s)

Journal Title

Data Source

[Journal Article] Recurrent genomic alterations characterize medulloblastoma arising from DNA double-strand break repair deficiency.2009

Author(s)

Journal Title

Data Source

[Journal Article] Acute disseminated encephalomyelitis associated with enterovirus 71.2006

Author(s)

Journal Title

Data Source

[Journal Article] Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.2006

Author(s)

Journal Title

Data Source

[Presentation] Safety study of sodium pentosan polysulfate for adult patients with mucopolysaccharidosis type II2016

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] ムコ多糖症II型成人患者に対するポリ硫酸ペントサン投与の検討2015

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] ムコ多糖症に対するペントサンの臨床研究・臨床治験について2015

Author(s)

Orii Kenji 折居建治

ORII Kenji 折居建治

折居建治オリイケンジ