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Masahiro Hayashi

TitleAffiliate
InstitutionUniversity of Colorado Denver - Anschutz Medical Campus
DepartmentSOM-HMGP
Phone303.724.3111

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Okamura K, Konno T, Onami K, Nikaido M, Okazaki N, Abe Y, Hayashi M, Yaguchi Y, Sato H, Konta T, Suzuki T. A case of primarily facial pyoderma gangrenosum associated with Takayasu arteritis. JAAD Case Rep. 2017 Mar; 3(2):124-126. PMID: 28331898.
      View in: PubMed
    2. Okamura K, Hayashi M, Abe Y, Araki Y, Hozumi Y, Suzuki T. Microsatellite polymorphism located immediately upstream of the phosphatidylinositol glycan, class K gene (PIGK) affects its expression, which correlates with tyrosinase activity in human melanocytes. J Dermatol Sci. 2017 Feb; 85(2):131-134. PMID: 27919619.
      View in: PubMed
    3. Sato K, Watanabe O, Ohmiya S, Chiba F, Hayashi M, Suzuki T, Kawakami K, Nishimura H. Efficient isolation of human parainfluenza viruses 1 and 3 using MNT-1, a human malignant melanoma cell line system that exhibits an apparent cytopathic effect. Microbiol Immunol. 2016 Nov; 60(11):801-805. PMID: 27762443.
      View in: PubMed
    4. Hayashi M, Okamura K, Araki Y, Suzuki M, Tanaka T, Abe Y, Nakano S, Yoshizawa J, Hozumi Y, Inoie M, Suzuki T. A novel three dimensional imaging method for the measurement of area in vitiligo and chemical leukoderma. J Dermatol Sci. 2016 Nov; 84(2):219-221. PMID: 27576766.
      View in: PubMed
    5. Hayashi M, Jin Y, Yorgov D, Santorico SA, Hagman J, Ferrara TM, Jones KL, Cavalli G, Dinarello CA, Spritz RA. Autoimmune vitiligo is associated with gain-of-function by a transcriptional regulator that elevates expression of HLA-A*02:01 in vivo. Proc Natl Acad Sci U S A. 2016 Feb 02; 113(5):1357-62. PMID: 26787886.
      View in: PubMed
    6. Cavalli G, Hayashi M, Jin Y, Yorgov D, Santorico SA, Holcomb C, Rastrou M, Erlich H, Tengesdal IW, Dagna L, Neff CP, Palmer BE, Spritz RA, Dinarello CA. MHC class II super-enhancer increases surface expression of HLA-DR and HLA-DQ and affects cytokine production in autoimmune vitiligo. Proc Natl Acad Sci U S A. 2016 Feb 02; 113(5):1363-8. PMID: 26787888.
      View in: PubMed
    7. Jin Y, Hayashi M, Fain PR, Suzuki T, Fukai K, Oiso N, Tanemura A, Holcomb CL, Rastrou M, Erlich HA, Spritz RA. Major association of vitiligo with HLA-A*02:01 in Japanese. Pigment Cell Melanoma Res. 2015 May; 28(3):360-2. PMID: 25645285.
      View in: PubMed
    8. Kono M, Sugiura K, Suganuma M, Hayashi M, Takama H, Suzuki T, Matsunaga K, Tomita Y, Akiyama M. Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease. Hum Mol Genet. 2013 Sep 01; 22(17):3524-33. PMID: 23666529.
      View in: PubMed
    9. Hayashi M, Suzuki T. Dyschromatosis symmetrica hereditaria. J Dermatol. 2013 May; 40(5):336-43. PMID: 22974014.
      View in: PubMed
    10. Kawaguchi M, Hayashi M, Murata I, Hozumi Y, Suzuki N, Ishii Y, Wataya-Kaneda M, Funasaka Y, Kawakami T, Fukai K, Ochiai T, Nishigori C, Mitsuhashi Y, Suzuki T. Eleven novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria. J Dermatol Sci. 2012 Jun; 66(3):244-5. PMID: 22336994.
      View in: PubMed
    11. Yamada M, Sakai K, Hayashi M, Hozumi Y, Abe Y, Kawaguchi M, Ihn H, Suzuki T. Oculocutaneous albinism type 3: a Japanese girl with novel mutations in TYRP1 gene. J Dermatol Sci. 2011 Dec; 64(3):217-22. PMID: 21996312.
      View in: PubMed
    12. Narita T, Oiso N, Fukai K, Motokawa T, Hayashi M, Yokoyama K, Hozumi Y, Kawada A, Suzuki T. 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. Eur J Dermatol. 2011 May-Jun; 21(3):446-7. PMID: 21680281.
      View in: PubMed
    13. Hayashi M, Nakano H, Sawamura D, Suzuki T. Case of epidermolytic palmoplantar keratoderma with knuckle pads. J Dermatol. 2012 Jan; 39(1):84-7. PMID: 21463360.
      View in: PubMed
    14. Hayashi M, Suzuki T. Case of subcutaneous lobular capillary hemangioma. J Dermatol. 2011 Oct; 38(10):1003-6. PMID: 21434983.
      View in: PubMed
    15. Oiso N, Murata I, Hayashi M, Amatsu A, Yoshida M, Suzuki T, Kawada A. Dermoscopic features in a case of dyschromatosis symmetrica hereditaria. J Dermatol. 2011 Jan; 38(1):91-3. PMID: 21175763.
      View in: PubMed
    16. Hayashi M, Kawaguchi M, Hozumi Y, Nakano H, Sawamura D, Suzuki T. Dystrophic epidermolysis bullosa pruriginosa of elderly onset. J Dermatol. 2011 Feb; 38(2):173-8. PMID: 21269315.
      View in: PubMed
    17. Murata I, Hayashi M, Hozumi Y, Fujii K, Mitsuhashi Y, Oiso N, Fukai K, Kuroki N, Mori Y, Utani A, Tomita Y, Fujita Y, Suzuki T. Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene. J Dermatol Sci. 2010 Jun; 58(3):218-20. PMID: 20439151.
      View in: PubMed
    18. Hayashi M, Monma F, Katagiri Y, Kawaguchi M, Suzuki T. Linear immunoglobulin A bullous dermatosis associated with herpes simplex virus infection and Kawasaki disease. J Dermatol. 2010 Mar; 37(3):276-9. PMID: 20507395.
      View in: PubMed
    19. Hayashi M, Suzuki T. A missense mutation c.G2747A (p.R916Q) of ADAR1 gene in dyschromatosis symmetrica hereditaria is not a novel mutation. Arch Dermatol Res. 2010 Aug; 302(6):481-2. PMID: 20169444.
      View in: PubMed
    20. Hayashi M, Kawaguchi M, Mitsuhashi Y, Suzuki T. Case of hypereosinophilic syndrome with cutaneous necrotizing vasculitis. J Dermatol. 2008 Apr; 35(4):229-33. PMID: 18419681.
      View in: PubMed
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