KATO Masaaki 加藤昌昭

Researcher Number	50622479
Affiliation (based on the past Project Information) *help	2015: 東北大学, 病院, 助教 2012 – 2015: 東北大学, 大学病院, 助教 2013: 東北大学, 病院, 助教
Review Section/Research Field	Except Principal Investigator Neurology
Keywords	Except Principal Investigator プロテアソーム / 骨格筋 / 封入体筋炎 / RNA / 神経変性 / 運動ニューロン / 神経変性疾患 / ＡＬＳ / ALS / iPS細胞 … More / 筋萎縮性側索硬化症 / 封入体を伴う筋疾患 / 次世代シークエンサー / CytoplasmicBodyMyopathy / 筋疾患 / 筋萎縮 / 1 C　臨床神経分子遺伝学 Less

Genetic analysis and establishment of in vitro model for inclusion body myositis
- Principal Investigator
  
  Aoki Masashi
- Project Period (FY)
  2014 – 2015
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Neurology
- Research Institution
  Tohoku University
Elucidating the RNA pathomechanism in FUS-FALS iPS induced motor neurons
- Principal Investigator
  
  Aoki Masashi
- Project Period (FY)
  2013 – 2015
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Neurology
- Research Institution
  Tohoku University
Analysis to reveal a disease causing gene in a family with hereditary myopathy with inclusion body
- Principal Investigator
  
  AOKI Masashi
- Project Period (FY)
  2012 – 2013
- Research Category
  
  Grant-in-Aid for Challenging Exploratory Research
- Research Field
  
  Neurology
- Research Institution
  Tohoku University

All 2016 2014 2013

All Journal Article Presentation

[Journal Article] Genotype-phenotype relationships in familial ALS with FUS/TLS mutations in Japan2016
- Author(s)
  Akiyama T, Warita H, Kato M, Nishiyama A, Izumi R, Ikeda C, Kamada M, Suzuki N, Aoki M
- Journal Title
  
  Muscle Nerve
  
  Volume: Jan 28 Issue: 3 Pages: 398-404
- DOI
  10.1002/mus.25061
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461288, KAKENHI-PROJECT-15H05667, KAKENHI-PROJECT-25293199
[Journal Article] Proteasome dysfunction induces muscle growth defects and protein aggregation2014
- Author(s)
  Kitajima Y, Tashiro Y, Suzuki N, Warita H, Kato M, Tateyama M, Ando R, Izumi R, Yamazaki M, Abe M, Sakimura K, Ito H, Urushitani M, Nagatomi R, Takahashi R, and Aoki M
- Journal Title
  
  J Cell Sci
  
  Volume: 127 Pages: 5204-5217
- DOI
  10.1242/jcs.150961
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26290023, KAKENHI-PROJECT-26350979, KAKENHI-PROJECT-26670436
[Journal Article] Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure.2013
- Author(s)
  Izumi R, Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y.
- Journal Title
  
  J Hum Genet.
  
  Volume: 58(5) Pages: 259-66
- NAID
  10031177220
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24659421
[Journal Article] Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure2013
- Author(s)
  Izumi R, Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y
- Journal Title
  
  J Hum Genet
  
  Volume: 58(5) Issue: 5 Pages: 259-66
- DOI
  10.1038/jhg.2013.9
- NAID
  10031177220
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390268, KAKENHI-PROJECT-23591229, KAKENHI-PROJECT-23659513, KAKENHI-PROJECT-23791148, KAKENHI-PUBLICLY-24116503, KAKENHI-PROJECT-24659421, KAKENHI-PROJECT-24700951
[Presentation] 筋萎縮性側索硬化症モデルラット微小血管の壁細胞を標的とした運動ニューロン保護2013
- Author(s)
  割田　仁，水野秀紀，加藤昌昭，鈴木直輝，青木正志
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-25293199
[Presentation] A mutation in A-band titin is associated with hereditary myopathy with early respiratory failure in a Japanese family2013
- Author(s)
  Izumi R, Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y.
- Organizer
  the 63rd Annual Meeting of The American Society of Human Genetics
- Place of Presentation
  Boston, MA,USA
- Year and Date
  2013-10-24
- Data Source
  KAKENHI-PROJECT-24659421
[Presentation] A mutation in A-band titin is associated with hereditary myopathy with early respiratory failure in a Japanese family.2013
- Author(s)
  Izumi R,Niihori T, Aoki Y, Suzuki N, Kato M, Warita H, Takahashi T, Tateyama M, Nagashima T, Funayama R, Abe K, Nakayama K, Aoki M, Matsubara Y
- Organizer
  the 63rd Annual Meeting of The American Society of Human Genetics
- Place of Presentation
  Boston,USA
- Data Source
  KAKENHI-PROJECT-24659421
[Presentation] 東北大学における家族性ALS遺伝子検査の検討2013
- Author(s)
  加藤昌昭，割田　仁，井泉瑠美子，島倉奈緒子，安藤里紗，鈴木直輝，青木正志
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-25293199
[Presentation] Myofibrillar myopathyの大家系における次世代型シークエンサーを用いた原因遺伝子の同定2013
- Author(s)
  井泉瑠美子,鈴木直輝,加藤昌昭,割田仁,高橋俊明,竪山真規,新堀哲也,青木洋子,松原洋一,舟山亮,西田有一郎,長嶋剛史,中山啓子,青木正志
- Organizer
  第54回日本神経学会学術大会
- Place of Presentation
  東京
- Year and Date
  2013-05-29
- Data Source
  KAKENHI-PROJECT-24659421

1. AOKI Masashi (70302148)

# of Collaborated Projects: 3 results

# of Collaborated Products: 6 results
2. Naoki SUZUKI (70451599)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
3. Hitoshi WARITA (30400245)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
4. OKANO Hideyuki (60160694)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
5. NIIHORI Tetsuya

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. 漆谷真

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
7. 松原洋一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

KATO Masaaki 加藤 昌昭

Research Projects

Research Products

Co-Researchers

Genetic analysis and establishment of in vitro model for inclusion body myositis

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Elucidating the RNA pathomechanism in FUS-FALS iPS induced motor neurons

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Analysis to reveal a disease causing gene in a family with hereditary myopathy with inclusion body

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Genotype-phenotype relationships in familial ALS with FUS/TLS mutations in Japan2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Proteasome dysfunction induces muscle growth defects and protein aggregation2014

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure.2013

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure2013

Author(s)

Journal Title

DOI

NAID

Data Source

[Presentation] 筋萎縮性側索硬化症モデルラット微小血管の壁細胞を標的とした運動ニューロン保護2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] A mutation in A-band titin is associated with hereditary myopathy with early respiratory failure in a Japanese family2013

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

[Presentation] A mutation in A-band titin is associated with hereditary myopathy with early respiratory failure in a Japanese family.2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] 東北大学における家族性ALS遺伝子検査の検討2013

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] Myofibrillar myopathyの大家系における次世代型シークエンサーを用いた原因遺伝子の同定2013

Author(s)

Organizer

Place of Presentation

Year and Date

Data Source

KATO Masaaki 加藤昌昭