HAYASHI MASAHIRO 林昌浩

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HAYASHI Masahiro 林昌浩

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Researcher Number	30396569
Other IDs
Affiliation (Current)	2023: 山形大学, 医学部, 講師
Affiliation (based on the past Project Information) *help	2017 – 2019: 山形大学, 医学部, 講師 2011 – 2012: 山形大学, 医学部, 助教
Review Section/Research Field	Principal Investigator Dermatology
Keywords	Principal Investigator 色素細胞 / 遺伝子変異 / ウイルス感染 / RNA 編集 / 色素異常症 / RNA編集 / メラノサイト / 遺伝性対側性色素異常症 / 遺伝子診断 / 安定ノックダウン … More / 悪性黒色腫細胞 / HLA-A / 白斑 / 発症リスク / 一塩基多型 / eQTL / 尋常性白斑 Less

Investigation of the role of HLA-A in the pathogenesis of autoimmune vitiligo and regulatory mechanism of HLA-A expressionPrincipal Investigator
- Principal Investigator
  
  HAYASHI MASAHIRO
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University
Investigation on failures of RNA editing and immune system againstviral infection in dyschromatosis symmetrica hereditariaPrincipal Investigator
- Principal Investigator
  
  HAYASHI Masahiro
- Project Period (FY)
  2011 – 2012
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Dermatology
- Research Institution
  Yamagata University

All 2019 2018 2013 2012 2011

All Journal Article Presentation Book

[Book] 伝えておきたい外用療法のコツ・色素異常症2012
- Author(s)
  林　昌浩
- Publisher
  全日本病院出版会
- Data Source
  KAKENHI-PROJECT-23791252
[Journal Article] Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mouse model of rhododendrol-induced vitiligo.2019
- Author(s)
  Hayashi M, Okamura K, Abe Y, Hozumi Y, Suzuki T
- Journal Title
  
  J Dermatol
  
  Volume: 46 Pages: 548-550
- DOI
  10.1111/1346-8138.14879
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K10228
[Journal Article] Dyschromatosis symmetrica hereditaria2013
- Author(s)
  Hayashi M, Suzuki T
- Journal Title
  
  J Dermatol
  
  Volume: 40 Pages: 336-343
- DOI
  10.1111/j.1346-8138.2012.01661.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791252
[Journal Article] Case of epidermolytic palmoplantar keratoderma with knuckle pads2012
- Author(s)
  Hayashi M, et al.
- Journal Title
  
  J Dermatol
  
  Volume: 38 Pages: 173-178
- DOI
  10.1111/j.1346-8138.2010.00953.x
- NAID
  10029330373
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23659540, KAKENHI-PROJECT-23791252
[Journal Article] Case of epidermolytic palmoplantar keratoderma with knuckle pads2012
- Author(s)
  Hayashi M
- Journal Title
  
  J Dermatol
  
  Volume: 39 Pages: 84-87
- DOI
  10.1111/j.1346-8138.2011.01226.x
- NAID
  10031184833
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791252
[Journal Article] Eleven novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria.2012
- Author(s)
  Kawaguchi M, Hayashi M, Suzuki T et al.
- Journal Title
  
  J Dermatol Sci
  
  Volume: 66 Pages: 244-245
- DOI
  10.1016/j.jdermsci.2012.01.009
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] A case of subcutaneous lobular capillary hemangioma2011
- Author(s)
  Hayashi M, Suzuki T
- Journal Title
  
  J Dermatol
  
  Volume: 38 Pages: 1003-1006
- DOI
  10.1111/j.1346-8138.2010.01163.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23791252
[Journal Article] Oculocutaneous Albinism Type 3 : a Japanese Girl With Novel Mutations in TYRP1 gene2011
- Author(s)
  Yamada M, Hayashi M, Suzuki T et al.
- Journal Title
  
  J Dermatol Sci 64
  
  Volume: 64 Pages: 217-222
- DOI
  10.1016/j.jdermsci.2011.09.005
- NAID
  10030893699
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] Dermoscopic features in a case of dyschromatosis symmetrica hereditaria.2011
- Author(s)
  Oiso N, Murata I, Suzuki T,et al.
- Journal Title
  
  J Dermatol
  
  Volume: 38 Pages: 91-93
- DOI
  10.1111/j.1346-8138.2010.01110.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Journal Article] Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT.2011
- Author(s)
  Narita T, Oiso N, Suzuki T et al.
- Journal Title
  
  Eur J Dermatol
  
  Volume: 21 Pages: 446-447
- DOI
  10.1684/ejd.2011.1350
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591236, KAKENHI-PROJECT-23791252
[Presentation] Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mice model of rhododendrol-induced leukoderma2018
- Author(s)
  Masahiro Hayashi, Ken Okamura, Yuko Abe, Yutaka Hozumi, Imi Saito,Tamio Suzuki
- Organizer
  International Investigative Dermatology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10228
[Presentation] A Case of epidermolytic palmoplantar keratoderma with knuckle pads2011
- Author(s)
  Hayashi M, Nakano H, Sawamura D, Suzuki T
- Organizer
  22nd World Congress of Dermatology
- Place of Presentation
  Seoul, Korea
- Data Source
  KAKENHI-PROJECT-23791252
[Presentation] リンパ節転移を伴った左腋窩のprimary mucinous carcinoma of the skinの一例2011
- Author(s)
  林　昌浩、山田真枝子、片桐美之、松永　純、水谷雅臣、鈴木民夫
- Organizer
  第110回日本皮膚科学会総会
- Place of Presentation
  震災のより紙上発表
- Data Source
  KAKENHI-PROJECT-23791252
[Presentation] A Case of epidermolytic palmoplantar keratoderma with knuckle pads2011
- Author(s)
  Hayashi M, Nakano H, Sawamura D, T. Suzuki
- Organizer
  22nd World Congress of Dermatology
- Place of Presentation
  COEX Convention and Exhibition Center, Seoul, Korea
- Data Source
  KAKENHI-PROJECT-23791252
[Presentation] Hereditary hypo-pigmentary disorders2011
- Author(s)
  T. Suzuki, M. Hayashi
- Organizer
  22nd World Congress of Dermatology
- Place of Presentation
  COEX Convention and Exhibition Center, Seoul, Korea
- Data Source
  KAKENHI-PROJECT-23791252
[Presentation] Albinochip: a universal genetic diagnosis for all known mutations associated to albinism2011
- Author(s)
  E. Molto, A. Fernandez, C. Phillips, M. Torres, O. Maronas, B. Arveiler, F. Morice-Picard, A. Taieb, R. Aquaron, V. Schiaffino, M. Hayashi, T. Suzuki, M. Martinez, M. J. Trujillo, C. Ayuso, A. Carracedo, L. Montoliu
- Organizer
  21st International Pigment Cell Conference
- Place of Presentation
  Palais des Congres of Bordeaux, Bordeaux, France
- Data Source
  KAKENHI-PROJECT-23791252

1. 鈴木民夫 (30206502)

# of Collaborated Projects: 1 results

# of Collaborated Products: 6 results
2. HOZUMI Yutaka

# of Collaborated Projects: 1 results

# of Collaborated Products: 3 results
3. 沢村大輔

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

HAYASHI MASAHIRO 林 昌浩

HAYASHI Masahiro 林 昌浩

Research Projects

Research Products

Co-Researchers

Investigation of the role of HLA-A in the pathogenesis of autoimmune vitiligo and regulatory mechanism of HLA-A expressionPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

Investigation on failures of RNA editing and immune system againstviral infection in dyschromatosis symmetrica hereditariaPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Book] 伝えておきたい外用療法のコツ・色素異常症2012

Author(s)

Publisher

Data Source

[Journal Article] Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mouse model of rhododendrol-induced vitiligo.2019

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Dyschromatosis symmetrica hereditaria2013

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Case of epidermolytic palmoplantar keratoderma with knuckle pads2012

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Case of epidermolytic palmoplantar keratoderma with knuckle pads2012

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Eleven novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria.2012

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A case of subcutaneous lobular capillary hemangioma2011

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Oculocutaneous Albinism Type 3 : a Japanese Girl With Novel Mutations in TYRP1 gene2011

Author(s)

Journal Title

DOI

NAID

Data Source

[Journal Article] Dermoscopic features in a case of dyschromatosis symmetrica hereditaria.2011

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Two children with a mild or moderate piebaldism phenotype and a father without leukoderma in a family with the same recurrent missense mutation in the kinase domain of KIT.2011

Author(s)

Journal Title

DOI

Data Source

[Presentation] Janus kinase inhibitor tofacitinib does not facilitate the repigmentation in mice model of rhododendrol-induced leukoderma2018

Author(s)

Organizer

Data Source

[Presentation] A Case of epidermolytic palmoplantar keratoderma with knuckle pads2011

Author(s)

Organizer

Place of Presentation

Data Source

[Presentation] リンパ節転移を伴った左腋窩のprimary mucinous carcinoma of the skinの一例2011

Author(s)

HAYASHI MASAHIRO 林昌浩

HAYASHI Masahiro 林昌浩