MATSUDA Mitsuhiro 松田光弘

… Alternative Names

松田光弘マツダミツヒロ

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Researcher Number	70569368
Affiliation (Current)	2025: 久留米大学, 医学部, 助教
Affiliation (based on the past Project Information) *help	2015 – 2017: 久留米大学, 医学部, 助教
Review Section/Research Field	Principal Investigator Dermatology
Keywords	Principal Investigator ゴルジ体ストレス / 小胞体ストレス / RNAi / 三次元培養 / 疾患モデル / ヘイリーヘイリー病

The study of relationship between stress response and pathogenesis of Hailey Hailey disease using cell culture modelPrincipal Investigator
- Principal Investigator
  
  MATSUDA Mitsuhiro
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Dermatology
- Research Institution
  Kurume University

All 2018 2017 2016 2015

All Journal Article

[Journal Article] Superficial epidermolytic ichthyosis concomitant with atopic dermatitis2018
- Author(s)
  Shimada H, Takeo N, Saito-Shono T, Ishikawa K, Sakai T, Goto M, Hatano Y, Fujiwara S, Matsuda M, Hamada T, Nakama T, Hashimoto T, Kono M, Akiyama M, Kitajima Y
- Journal Title
  
  Eur J Dermatol
  
  Volume: 28(1) Pages: 94-96
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19707
[Journal Article] A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene2017
- Author(s)
  Yasuda H, Kanazawa N, Matsuda M, Hamada T, Furumura M, Hashimoto T, Nakama T, Furukawa F
- Journal Title
  
  Ann Dermatol
  
  Volume: 29(5) Pages: 642-644
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19707
[Journal Article] Functional study of TGM1 missense mutations in autosomal recessive congenital ichthyosis.2016
- Author(s)
  Numata S, Teye K, Karashima T, Matsuda M, Hamada T, Hashimoto T.
- Journal Title
  
  Exp Dermatol.
  
  Volume: 25(8) Issue: 8 Pages: 657-9
- DOI
  10.1111/exd.13000
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19707
[Journal Article] Corneodesmosin gene deletion is prevalent in Japanese patients with peeling skin disease: identification of 2 new cases.2016
- Author(s)
  Teye K, Suga Y, Numata S, Ishii N, Krol RP, Ohata C, Matsuda M, Honma M, Ishida-Yamamoto A, Hamada T, Hashimoto T.
- Journal Title
  
  Journal of Dermatological Science
  
  Volume: 82 Issue: 2 Pages: 134-137
- DOI
  10.1016/j.jdermsci.2016.01.012
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K08582, KAKENHI-PROJECT-24591620, KAKENHI-PROJECT-26460894, KAKENHI-PROJECT-25460881, KAKENHI-PROJECT-15K19707
[Journal Article] Two novel missense mutations of STS gene underlie X-linked recessive ichthyosis: understanding of the mutational and structural spectrum.2016
- Author(s)
  Oyama N, Matsuda M, Hamada T, Numata S, Teye K, Hashimoto T, Hasegawa M.
- Journal Title
  
  J Eur Acad Dermatol Venereol.
  
  Volume: 30(9) Issue: 9 Pages: 1629-31
- DOI
  10.1111/jdv.13231
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K19707
[Journal Article] Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases.2016
- Author(s)
  Nishikawa R, Takahashi H, Matsuda M, Imaoka K, Ogawa M, Teye K, Tsuchisaka A, Koga H, Komorowski L, Probst C, Hachiya T, Fritzler MJ, Ishii N, Ohata C, Furumura M, Krol RP, Muro Y, Morita E, Hashimoto T
- Journal Title
  
  Exp Dermatol
  
  Volume: 25 Issue: 5 Pages: 369-371
- DOI
  10.1111/exd.12981
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09799, KAKENHI-PROJECT-26860905, KAKENHI-PROJECT-16K10180, KAKENHI-PROJECT-15K19707
[Journal Article] A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome.2016
- Author(s)
  Numata S, Teye K, Krol RP, Okamatsu Y, Hashikawa K, Matsuda M, Fortugno P, Di Zenzo G, Castiglia D, Zambruno G, Hamada T, Hashimoto T.
- Journal Title
  
  Exp Dermatol.
  
  Volume: 25(7) Issue: 7 Pages: 568-70
- DOI
  10.1111/exd.13011
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19707
[Journal Article] Loss of heterozygosity in a case of glomuvenous malformations.2015
- Author(s)
  Ohata C, Matsuda M, Hamada T, Shintani T, Muto I, Nagata H, Furumura M, Nakama T
- Journal Title
  
  J Dermatol
  
  Volume: 印刷中 Issue: 6 Pages: 646-647
- DOI
  10.1111/1346-8138.12849
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-25461678, KAKENHI-PROJECT-25860975, KAKENHI-PROJECT-15K19707
[Journal Article] Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia.2015
- Author(s)
  Numata S, Teye K, Krol RP, Karashima T, Fukuda S, Matsuda M, Ishii N, Furumura M, Ohata C, Saminathan SD, Ariffin R, Pramono ZA, Leong KF, Hamada T, Hashimoto T
- Journal Title
  
  J Dermatol Sci
  
  Volume: 78 Issue: 1 Pages: 82-85
- DOI
  10.1016/j.jdermsci.2015.02.006
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K19707, KAKENHI-PROJECT-25461678
[Journal Article] A three-dimensional in vitro culture model of Hailey-Hailey disease.2015
- Author(s)
  Matsuda M, Hamada T, Numata S, Teye K, Ishii N, Ohata C, Furumura M, Nakama T, Hashimoto T
- Journal Title
  
  Exp Dermatol
  
  Volume: 24 Issue: 10 Pages: 788-789
- DOI
  10.1111/exd.12777
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K19707, KAKENHI-PROJECT-25461678

1. HONMA Masaru

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
2. 大畑千佳

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
3. 古村南夫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
4. 石井文人

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

MATSUDA Mitsuhiro 松田 光弘

松田 光弘 マツダ ミツヒロ

Research Projects

Research Products

Co-Researchers

The study of relationship between stress response and pathogenesis of Hailey Hailey disease using cell culture modelPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] Superficial epidermolytic ichthyosis concomitant with atopic dermatitis2018

Author(s)

Journal Title

Data Source

[Journal Article] A Case of Hailey-Hailey Disease with a Novel Nonsense Mutation in the ATP2C1 Gene2017

Author(s)

Journal Title

Data Source

[Journal Article] Functional study of TGM1 missense mutations in autosomal recessive congenital ichthyosis.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Corneodesmosin gene deletion is prevalent in Japanese patients with peeling skin disease: identification of 2 new cases.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Two novel missense mutations of STS gene underlie X-linked recessive ichthyosis: understanding of the mutational and structural spectrum.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome.2016

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Loss of heterozygosity in a case of glomuvenous malformations.2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia.2015

Author(s)

Journal Title

DOI

Data Source

[Journal Article] A three-dimensional in vitro culture model of Hailey-Hailey disease.2015

Author(s)

Journal Title

DOI

Data Source

MATSUDA Mitsuhiro 松田光弘

松田光弘マツダミツヒロ