Maeda Yasushi 前田寧

… Alternative Names

MAEDA Yasushi 前田寧

Less

Researcher Number	60346997
Other IDs
Affiliation (Current)	2025: 独立行政法人国立病院機構熊本再春荘病院(臨床研究部), 臨床研究部, 臨床研究部長
Affiliation (based on the past Project Information) *help	2009 – 2010: Kumamoto University, 医学部附属病院, 講師 2008: Kumamoto University, 医学部・附属病院, 講師 2006 – 2007: 熊本大学, 医学部附属病院, 講師 2002 – 2004: Department of Neurology, Kumamoto University Hospital, assistant, 医学部附属病院, 助手
Review Section/Research Field	Principal Investigator Neurophysiology and muscle physiology Except Principal Investigator Neurology / Neurology
Keywords	Principal Investigator 骨髄間質細胞 / ウイルスベクター / 遺伝子 / 移植・再生医療 / 間葉系幹細胞 / 遺伝子操作 / 細胞治療 / 筋ジストロフィー Except Principal Investigator gene therapy / dystrophin … More / helper-dependent / attachment receptor / muscular dystrophy / adenovirus vector / mdxマウス / CAR / ジストロフィン / ヘルパーウイルス依存型アデノウイルスベクター / 筋ジストロフィー / アデノウイルスベクター / 遺伝子治療 / nNOS / sleeping beautv-transoosone system / dko mouse / mdx mouse / Duchenne muscular dystrophy / full-length dystrophin / helper-dependent adenovirus vector / hleper-dependent adenovirs / Sleeping Beauty transposon / multiple muscle injection / dkoマウス / helper-dependent adenovirus / ヌードmdxマウス / 反復投与 / 接着受容体 / ヘルパー依存性 / RGD / tropism / ジストロフイン / アタッチメントレセプター / ヘルパーウイルス依存型 Less

ex vivo gene manipulation of mesenchymal stem cell and application to cell therapyPrincipal Investigator
- Principal Investigator
  
  MAEDA Yasushi
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research on Innovative Areas (Research a proposed research project)
- Research Field
  
  Neurophysiology and muscle physiology
- Research Institution
  Kumamoto University
Gene therapy for progressive muscular dystrophy using a new generation adenovirus vector and transposase
- Principal Investigator
  
  UCHINO Makoto
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kumamoto University
Gene therapy for progressive muscular dystrophy using a new generation adenovirus vector (gutless adenovirus)
- Principal Investigator
  
  UCHIN Makoto
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kumamoto University
Study on the gene therapy using a new generation adenovirus vector (gutless adenovirus)
- Principal Investigator
  
  UCHINO Makoto
- Project Period (FY)
  2001 – 2002
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Neurology
- Research Institution
  Kumamoto University

All 2011 2009 2008 2007 2006 2005 2004 Other

All Journal Article Presentation

[Journal Article] Rescue From Respiratory Dysfunction by transduction of Full-length Dystrophin to Diaphragm via the Peritoneal Cavity in Utrophn/Dystrophin Double Knockout Mice2011
- Author(s)
  Ishizaki M, Maeda Y, Kawano R, Suga T, Uchida Y, Uchino K, Yamashita S, Kimura E, Uchino M
- Journal Title
  
  Molecular Therapy
  
  Volume: 19(7) Pages: 1230-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20200013
[Journal Article] Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse2011
- Author(s)
  Suga T, Kimura E, Morioka Y, Ikawa M, Li S, Uchino K, Uchida Y, Yamashita S, Maeda Y, Chamberlain JS, Uchino M
- Journal Title
  
  PLoS One.
  
  Volume: 6(3)
- NAID
  120006957404
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20200013
[Journal Article] Mdx respiratory impairment following fibrosis of the diaphragm. Neuromuscul disord2008
- Author(s)
  Ishizaki, M., Suga, T., Kimura, E., Shiota, T., Kawano, R., Uchida, U., Uchino, K., Yamashita, S., Maeda, Y., Uchino, M.
- Journal Title
  
  (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/dystrophin double knockout mice2008
- Author(s)
  Kawano R., Ishizaki M, Maeda Y., Uchida Y., Kimura E., Uchino M.
- Journal Title
  
  Mol Ther (in press)
- NAID
  120002468583
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/ dystrophin double knockout mice. Mol Ther2008
- Author(s)
  Kawano, R., Ishizaki, M., Maeda, Y., Uchida, Y., Kimura, E., Uchino, M.
- Journal Title
  
  (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Mdx respiratory impairment following fibrosis of the diaphragm2008
- Author(s)
  Ishizaki M, Suga T, Kimura E, Shiota T, Kawano R, Uchida U, Uchino K, Yamashita S, Maeda Y, Uchino M.
- Journal Title
  
  Neuromuscular disorders (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Regions downstream from the WW domain of dystrophin are impotant for binding to postsynaptic densities in the brain2008
- Author(s)
  Sakamoto T, Arima T, Ishizaki M, Kawano R, Koide T, Uchida Y, Ymashita S, Kimura E, Hirano T, Maeda Y, Uchino M.
- Journal Title
  
  Neuromuscular disorders (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/dystrophin double knockout mice.2008
- Author(s)
  Kawano R., Ishizaki M, Maeda Y., Uchida Y., Kimura E., Uchino M.
- Journal Title
  
  Mol Ther (in press)
- NAID
  120002468583
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Regions Downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain. Neuromuscul Disord2008
- Author(s)
  Sakamoto, T., Arima, T., Ishizaki, M., Kawano, R., Koide, T., Uchida, Y., Yamashita, S., Kimura, E., Hirano, T., Maeda, Y., Uchino, M.
- Journal Title
  
  (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Journal Article] Myopathy phenotype in transgenic mice expressing mutated PABPN1 as a model of oculopharyngeal muscular dystrophy.2004
- Author(s)
  Hino H., Araki K., Uyama E., Takeya M., Araki M., Yoshinobu K., Miike K., Kawazoe Y., Maeda Y., Uchino M., Yamamura K.
- Journal Title
  
  Hum.Mol.Genet. 13
  
  Pages: 181-190
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590897
[Journal Article] Targeted conversion of the transthyretin gene in vitro and in vivo.2004
- Author(s)
  Nakamura M., Ando Y., Nagahara S., Sano A., Ochiya T., Maeda S., Kawaji T., Ogawa M., Hirata A., Terazaki H., Haraoka K., Tanihara H., Ueda M., Uchino M., Yamamura K., Yamashita T.
- Journal Title
  
  Gene Therapy 11
  
  Pages: 838-846
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590897
[Journal Article] Myopathy phenotype in transgenic mice expressing mutated PABPN1 as a model of oculopharyngeal muscular dystrophy2004
- Author(s)
  Hino H., Araki K., Uyama E., Takeya M., Araki M., Yoshinobu K., Miike K., Kawazoe Y., Maeda Y., Uchino M., Yamamura K.
- Journal Title
  
  Hum.Mol.Genet. 13
  
  Pages: 181-190
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590897
[Journal Article] Effective repetitive dystrophin gene transfer into skeletal muscle of adult mdx mice using a helper-dependent adenovirus vector expressing the Coxsackievirus and adenovirus receptor(CAR) and dystrophin.
- Author(s)
  Uchida Y., Maeda Y, Kimura E, Yamashita S, Nishida Y, Arima T, Hirano T, Uyama E, Mita S., Uchino M.
- Journal Title
  
  J Gene Med (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15590897
[Journal Article] Effective repetitive dystrophin gene transfer into skeletal muscle of adult mdx mice using a helper-dependent adenovirus vector expressing the Coxsackie-virus and adenovirus receptor (CAR) and dystrophin.
- Author(s)
  Uchida Y., Maeda Y, Kimura E, Yamashita S, Nishida Y, Arima T, Hirano T, Uyama E, Mita S., Uchino M.
- Journal Title
  
  J Gene Med (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15590897
[Journal Article] Effective repetitive dystrophin gene transfer into skeletal muscle of adult mdx mice using a helper-dependent adenovirus vector expressing the Coxsackie-virus and adenovirus receptor (CAR) and dystrophin.
- Author(s)
  Uchida Y., Maeda Y, Kimura E, Yamashita S, Nishida Y, Arima T, Hirano T, Uyama E, Mita S., Uchino M.
- Journal Title
  
  J Gene Med (in press)
- Data Source
  KAKENHI-PROJECT-15590897
[Presentation] Repetitive allotransplantation of bone marrow stromal cells to muscular dystrophy model mice drastically improves the body build and life span2011
- Author(s)
  Maeda Y
- Organizer
  19th Annual Congress of the European Society of Gene and Cell Therapy(ESGCT)
- Place of Presentation
  Brighton, UK
- Data Source
  KAKENHI-PROJECT-20200013
[Presentation] 筋ジストロフィー根本治療に向けての骨髄間質間葉系幹細胞へのウイルスベクターによる遺伝子操作2009
- Author(s)
  前田寧
- Organizer
  第27回日本神経治療学会総会
- Place of Presentation
  熊本市民会館
- Data Source
  KAKENHI-PROJECT-20200013
[Presentation] 筋ジストロフィー根本治療に向けての骨髄間質間葉系幹細胞へのウイルスベクターによる遺伝子操作2009
- Author(s)
  前田寧
- Organizer
  第27 回日本神経治療学会総会
- Place of Presentation
  熊本市民会館
- Data Source
  KAKENHI-PROJECT-20200013
[Presentation] 横隔膜へのジストロフィン導入による筋ジストロフィーモデルマウスの呼吸機能改善効果2009
- Author(s)
  前田寧
- Organizer
  第50 回日本神経学会総会
- Place of Presentation
  仙台国際センター
- Data Source
  KAKENHI-PROJECT-20200013
[Presentation] 横隔膜へのジストロフィン導入による筋ジストロフィーモデルマウスの呼吸機能改善効果2009
- Author(s)
  前田寧
- Organizer
  第50回日本神経学会総会
- Place of Presentation
  仙台国際センター
- Data Source
  KAKENHI-PROJECT-20200013
[Presentation] 筋ジストロフィーモデルマウスの骨格筋への完全長dystrophin導入の効果2008
- Author(s)
  前田寧
- Organizer
  第49回日本神経学会総会
- Place of Presentation
  パシフィコ横浜
- Data Source
  KAKENHI-PROJECT-20200013
[Presentation] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/ dystrophin double knockout mice.2007
- Author(s)
  Ishizaki, M., Kawano, R., Maeda, Y., Uchida, Y., Kimura, E., Uchino, M.
- Organizer
  American Society of Gene Therapy 10th annual meeting
- Place of Presentation
  Seattle, USA
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Presentation] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/dystrophin double knockout mice2007
- Author(s)
  Ishizaki M, Kawano R., Maeda Y., Kimura E., Uchino M.
- Organizer
  American Sosiety of Gene Terapy
- Place of Presentation
  Seattle
- Year and Date
  2007-05-31
- Data Source
  KAKENHI-PROJECT-18590951
[Presentation] Restoration of physical performance in symptomatic utrophin/ dystrophin double knockout(U/D dko) mice by the helper-dependent adenovirus vector(HDAdv)-mediated full-length dystrophin expression.2006
- Author(s)
  Kawano, R., Ishizaki, M., Uchida, Y., Kimura, E., Maeda, Y., Uchino, M.
- Organizer
  11th European Society of Gene Therapy Annual meeting
- Place of Presentation
  Athens, Greece
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590951
[Presentation] Effective repetitive dystrophin gene transfer into skeletal muscle of adult mdx mice using a helper-dependent adenovirus vector expressing the coxsackievirus and adenovirus receptor(CAR) and dystrophin2005
- Author(s)
  Uchida, Y., Maeda, Y., Kimura, E., Uchino, M.
- Organizer
  American Society of Gene Therapy 9th annual meeting
- Place of Presentation
  Baltimore, USA
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18590951

1. UCHINO Makoto (20117336)

# of Collaborated Projects: 4 results

# of Collaborated Products: 19 results
2. KIMURA En (60433025)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results

Maeda Yasushi 前田 寧

MAEDA Yasushi 前田 寧

Research Projects

Research Products

Co-Researchers

ex vivo gene manipulation of mesenchymal stem cell and application to cell therapyPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Gene therapy for progressive muscular dystrophy using a new generation adenovirus vector and transposase

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Gene therapy for progressive muscular dystrophy using a new generation adenovirus vector (gutless adenovirus)

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Study on the gene therapy using a new generation adenovirus vector (gutless adenovirus)

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Rescue From Respiratory Dysfunction by transduction of Full-length Dystrophin to Diaphragm via the Peritoneal Cavity in Utrophn/Dystrophin Double Knockout Mice2011

Author(s)

Journal Title

Data Source

[Journal Article] Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse2011

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Mdx respiratory impairment following fibrosis of the diaphragm. Neuromuscul disord2008

Author(s)

Journal Title

Description

Data Source

[Journal Article] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/dystrophin double knockout mice2008

Author(s)

Journal Title

NAID

Description

Data Source

[Journal Article] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/ dystrophin double knockout mice. Mol Ther2008

Author(s)

Journal Title

Description

Data Source

[Journal Article] Mdx respiratory impairment following fibrosis of the diaphragm2008

Author(s)

Journal Title

Description

Data Source

[Journal Article] Regions downstream from the WW domain of dystrophin are impotant for binding to postsynaptic densities in the brain2008

Author(s)

Journal Title

Description

Data Source

[Journal Article] Transduction of full-length dystrophin to multiple skeletal muscles improves motor performance and lifespan in utrophin/dystrophin double knockout mice.2008

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Regions Downstream from the WW domain of dystrophin are important for binding to postsynaptic densities in the brain. Neuromuscul Disord2008

Author(s)

Journal Title

Description

Data Source

[Journal Article] Myopathy phenotype in transgenic mice expressing mutated PABPN1 as a model of oculopharyngeal muscular dystrophy.2004

Author(s)

Journal Title

Description

Data Source

[Journal Article] Targeted conversion of the transthyretin gene in vitro and in vivo.2004

Maeda Yasushi 前田寧

MAEDA Yasushi 前田寧