MIRI Masato 森雅人

… Alternative Names

MORI Masato 森雅人

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Researcher Number	10337347
Affiliation (based on the past Project Information) *help	2013: 自治医科大学, 医学部, 講師 2010 – 2011: 自治医科大学, 医学部, 講師 2003 – 2008: 自治医科大学, 医学部, 講師 2002: 自治医科大学, 医学部, 助手
Review Section/Research Field	Principal Investigator Pediatrics Except Principal Investigator Pediatrics / Pediatrics
Keywords	Principal Investigator マイクロアレイ / Fmr2ノックアウトマウス / FMR2遺伝子 / 知的障害 / 脆弱X症候群 / fmr2 Except Principal Investigator MBD1 / 自閉症 / FOXP2 / 自閉性障害 … More / セクレチン受容体 / セクレチン / CADM1 / WNT signal / methyl-CpG binding protein / autism / GPR85 / 染色体7q31 / 広汎性発達障害 / WNT16 / WNT2 / 7q31-34 / 自閉症障害 / WNTシグナル / メチル化部位結合蛋白 / Knockout mouse / secretin receptor / secretin / Autism / セクレチン受容体ノックアウトマウス / ノックアウトマウス / モデルマウス / 候補遺伝子解析 / CNV / 病因遺伝子 / シナプス足場蛋白 / コピー数多型（CNV) / マイクロアレーCGH / G蛋白結合型受容体 / シナプス / LIN7 / 足場蛋白 / 遺伝子変異 / コピー数多型 / 自閉症スペクトラム障害 / ERストレス / 自閉性障害関連遺伝子 / 小児科学 / 内科系臨床医学 / Rett症候群 / DLX6 / DLX5 / MECP2 / エピジェネティクス / WNT / 発現アレイ解析 / 遺伝子発現解析 / ノックインマウス / secretin受容体 / シナプス形成 Less

Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules
- Principal Investigator
  
  YAMAGATA Takanori
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
Activation of ER stress as the major molecular pathology in autism spectrum disorder and the animal model for intervention study
- Principal Investigator
  
  MOMOI Mariko
- Project Period (FY)
  2010 – 2011
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
Research on the common molecular pathology for autism
- Principal Investigator
  
  MOMOI Mariko
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
candidate gene analysis for autism focusing on the epigenetic mechanism
- Principal Investigator
  
  YAMAGATA Takanori
- Project Period (FY)
  2006 – 2008
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
知的障害の分子遺伝学的検討:FMR2遺伝子の機能の検索Principal Investigator
- Principal Investigator
  
  森雅人
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University
Molecular and genetic analysis for autism
- Principal Investigator
  
  MOMOI Mariko Y.
- Project Period (FY)
  2003 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  JICHI MEDICAL UNIVERSITY
Identification for the genes of autism by the analysis of neuronal peptides and linkage analysis.
- Principal Investigator
  
  YAMAGATA Takanori
- Project Period (FY)
  2002 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Jichi Medical University

All 2013 2012 2009 2007 2006 2005 2004 Other

All Journal Article Presentation

[Journal Article] Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers2013
- Author(s)
  Monden Y, Mori M, Kuwajima M, Goto T, Yamagata T, Momoi MY
- Journal Title
  
  Brain Dev
  
  Volume: 35 Issue: 6 Pages: 582-585
- DOI
  10.1016/j.braindev.2012.08.006
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder.2012
- Author(s)
  2. Fujita-Jimbo E, Yu ZL, Li H, Yamagata T, Mori M, Momoi T, Momoi MY
- Journal Title
  
  PLoS One
  
  Volume: 7 Issue: 12 Pages: e51155-e51155
- DOI
  10.1371/journal.pone.0051155
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination2012
- Author(s)
  Shimojima K, Okamoto N, Suzuki Y, Saito M, Mori M, Yamagata T, Momoi MY, Hattori H, Okano Y, Hisata K, Okumura A, Yamamoto T
- Journal Title
  
  J Hum Genet
  
  Volume: 57 Issue: 9 Pages: 593-600
- DOI
  10.1038/jhg.2012.77
- NAID
  10031057000
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] Mutation in Parkinson disease-associated, G-protein coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder2012
- Author(s)
  Fujita-Jimbo E, Yu ZL, Li H, Yamagata T, Mori M, Momoi T, Momoi MY
- Journal Title
  
  PLoS One
  
  Volume: 7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23390275
[Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009
- Author(s)
  Nakashima, N, Yamagata, T, Mori M, Kuwajima M, Suwa K, MOMOI MY.
- Journal Title
  
  Brain & Development Feb3 (E-pub)
- NAID
  10027212757
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390301
[Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009
- Author(s)
  Nakashima N, Yamagata T, Mori M, Kuwajima M, Suwa K, Momoi MY.
- Journal Title
  
  Brain Dev. In press
- NAID
  10027212757
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591165
[Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009
- Author(s)
  Nakajima N, Yamagata T, MoriM, Kuwajima M, Suwa K, Momoi MY.
- Journal Title
  
  Brain Dev doi:10
  
  Pages: 1016-1016
- NAID
  10027212757
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18390301
[Journal Article] Evidence supporting WNT16 as autism susceptible gene.2006
- Author(s)
  Imai M, Yamagata T, Mori M, Momoi MY.
- Journal Title
  
  Am J Genet (In press)
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Two new XPD patients compound heterozygotes for the same mutation demonstrate diverse clinical features.2005
- Author(s)
  Fujimoto M, Leech SN, Theron T, Mori M, Fawcett H, Botta E, Nozaki Y, Yamagata T, Moriwaki S, StefaniniM, Momoi MY, Nakagawa H, Shuster S, Moss C, Lehmann AR.
- Journal Title
  
  J Invest Dermatol 25:86-92-3250 (BBRC-06-6032)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients.2005
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY
- Journal Title
  
  Brain & Dev 27
  
  Pages: 321-325
- NAID
  10019356605
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.2005
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY
- Journal Title
  
  Brain Dev 27
  
  Pages: 207-210
- NAID
  10015453725
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14570766
[Journal Article] Absence of causative mutation and presence of autism-related allele in FOXP in Japanese autistic population2005
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY
- Journal Title
  
  Brain & Dev 27
  
  Pages: 207-210
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.2005
- Author(s)
  L Li H, Yamagata T, Mori M, Momoi MY
- Journal Title
  
  Brain and Development 27
  
  Pages: 207-210
- NAID
  10015453725
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14570766
[Journal Article] RSK2 gene mutations in Coffin-Lowry syndrome with drop episodes.2005
- Author(s)
  Nakamura M, Yamagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain Dev 27
  
  Pages: 114-117
- NAID
  10015453219
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes I autistic spectrum disorders.2005
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain & Development (In press)
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.2005
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain & Development 27
  
  Pages: 207-210
- NAID
  10015453725
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Absence of caisative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.2005
- Author(s)
  Li H, Yamagta T, Mori M, Momoi MY.
- Journal Title
  
  Brain ＆ Dev 27
  
  Pages: 207-210
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] RSK2 gene mutation in Coffinn-Lowy syndrome with erop episodes.2005
- Author(s)
  Nakamura M, Yamagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain ＆ Dev 27
  
  Pages: 114-117
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients.2005
- Author(s)
  Li H, Yamagata T, Mori M, Yasuhara A, Momoi MY
- Journal Title
  
  Brain Dev. 27
  
  Pages: 321-325
- NAID
  10019356605
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-14570766
[Journal Article] Two new XPD patients counopund heterozygotes for the same mutation demonstrate diverse clinical features.2005
- Author(s)
  Fijimoto M, Leech SN, Theron T, Mori M, _nozaki Y, Momoi MY. et al.
- Journal Title
  
  J Invest Dermatol 25
  
  Pages: 86-92
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients.2005
- Author(s)
  Li H, Yamagata T, Mori M, Yasuhara A, Momoi MY
- Journal Title
  
  Brain and Development 27
  
  Pages: 321-325
- NAID
  10019356605
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-14570766
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes in auistic patients.2005
- Author(s)
  Li H, Yamagta T, Mori M, Yasuhara A, Momoi MY.
- Journal Title
  
  Brain ＆ Dev 27
  
  Pages: 321-325
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese aitistic patients.2005
- Author(s)
  Li H, Yaqmagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain Dev 27
  
  Pages: 207-210
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients.2005
- Author(s)
  Li H, Yamagata T, Mori M, Yasuhara A, Momoi MY.
- Journal Title
  
  Brain Dev 27
  
  Pages: 321-325
- NAID
  10019356605
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] RSK gene mutations in Coffin-Lowry syndrome with drop episodes.2004
- Author(s)
  Nakamura M, Yamagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain & Development 26
  
  Pages: 453-458
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Dichloroacetate treatment for mitochondrial vytopathy : ling-term egffets in MELAS.2004
- Author(s)
  Mori M, Yamagata T, Saito S, Gotou, Momoi MY.
- Journal Title
  
  Brain $ Development 26
  
  Pages: 453-458
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Non-invasive screening of fragile X syndrome using urine and hair roots.2004
- Author(s)
  Suwa T, Tamagata T, Mori M, Momoi MY.
- Journal Title
  
  Brain & Development 26
  
  Pages: 380-383
- NAID
  10020552348
- Data Source
  KAKENHI-PROJECT-15390326
[Journal Article] Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY
- Journal Title
  
  Brain and Development (In press)
- NAID
  10015453725
- Data Source
  KAKENHI-PROJECT-14570766
[Journal Article] Mutation analysis of methyl-CpG binding protein family genes in autistic patients
- Author(s)
  Li H, Yamagata T, Mori M, Momoi MY
- Journal Title
  
  Brain and Development (In press)
- NAID
  10019356605
- Data Source
  KAKENHI-PROJECT-14570766
[Presentation] A NDUFA1 mutation in a boy with mitochondrial complexIdeficiency.2013
- Author(s)
  Miyauchi A, Monden Y, Mori M, Sugie H, Osaka H, Murayama K, Ohtake A, Yamagata T
- Organizer
  The 55th Annual Meeting of The Japanese Society for Inherited Metabolic Diseases(JSIMD)
- Place of Presentation
  Tokyo
- Data Source
  KAKENHI-PROJECT-23390275
[Presentation] Genes regulated by MECP2 as candidate genes for autism2007
- Author(s)
  N.Nakashima,T.Yamagata,Z.Yu,K.Suwa,M.Mori,andM.Y.Momoi.
- Organizer
  Annual Meeting of American Society of Human Genetics
- Place of Presentation
  San Diego
- Year and Date
  2007-10-25
- Data Source
  KAKENHI-PROJECT-18591165

1. YAMAGATA Takanori (00239857)

# of Collaborated Projects: 5 results

# of Collaborated Products: 28 results
2. MOMOI Mariko (90166348)

# of Collaborated Projects: 3 results

# of Collaborated Products: 18 results
3. NAKASHIMA Naomi (20337330)

# of Collaborated Projects: 3 results

# of Collaborated Products: 2 results
4. NOZAKI Yasuyuki (90281295)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. KUWAJIMA Mari (30398515)

# of Collaborated Projects: 2 results

# of Collaborated Products: 3 results
6. SUWA Kiyotaka (30285796)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
7. GOTO Tamako (40364509)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. SAITO Mari (10424011)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
9. NAGATA Kouichi (50252143)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. MONDEN Yukifumi (80382951)

# of Collaborated Projects: 1 results

# of Collaborated Products: 2 results
11. NAGASHIMA Masako (70438662)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. JINBO Eriko (20291651)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
13. FUJITA Eriko

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results

MIRI Masato 森 雅人

MORI Masato 森 雅人

Research Projects

Research Products

Co-Researchers

Analysis for the pathogenesis and the target molecules of treatment for autism focusing on G-protein coupled receptors and synaptic molecules

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Activation of ER stress as the major molecular pathology in autism spectrum disorder and the animal model for intervention study

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Research on the common molecular pathology for autism

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

candidate gene analysis for autism focusing on the epigenetic mechanism

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

知的障害の分子遺伝学的検討:FMR2遺伝子の機能の検索Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Molecular and genetic analysis for autism

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Identification for the genes of autism by the analysis of neuronal peptides and linkage analysis.

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers2013

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Mutation in Parkinson disease-associated, G-protein-coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder.2012

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination2012

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Mutation in Parkinson disease-associated, G-protein coupled receptor 37 (GPR37/PaelR) is related to Autism spectrum disorder2012

Author(s)

Journal Title

Data Source

[Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009

Author(s)

Journal Title

NAID

Data Source

[Journal Article] Expression analysis and mutation detection of DLX5 and DLX6 in autism.2009

Author(s)

Journal Title

MIRI Masato 森雅人

MORI Masato 森雅人