Search Results1-3 of  3

  • TOYOMAKI Yuka ID: 9000002062805

    Department of Dermatology, Hirosaki University Graduate School of Medicine (2009 from CiNii)

    Articles in CiNii:4

    • Dominant dystrophic epidermolysis bullosa caused by a novel G2037R mutation and by a known G2028R mutation in the type VII collagen gene (COL7A1) (2006)
    • Calcineurin/NFAT-dependent regulation of 230-kDa bullous pemphigoid antigen (BPAG1) gene expression in normal human epidermal keratinocytes (2008)
    • A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjogren-Larsson syndrome (2008)
  • TOYOMAKI Yuka ID: 9000018732198

    弘前大学大学院医学研究科皮膚科学講座 (2014 from CiNii)

    Articles in CiNii:3

    • Glycine-to-valine Missense Mutation in the Collagan VII Gene of a Patient with Pretibial Dystrophic Epidermolysis Bullosa (2004)
    • Buschke-Ollendorff Syndrome Pathogenetic Mutation in An Intron/Exon Boundary of the LEMD3 Gene (2011)
    • Functional Analysis of LEMD3 Mutation in Buschke-Ollendorff Syndrome (2014)
  • Toyomaki Yuka ID: 9000273027209

    Department of Dermatology, Hirosaki University School of Medicine (2004 from CiNii)

    Articles in CiNii:1

    • Glycine-to-valine Missense Mutation in the Collagen VII Gene of a Patient with Pretibial Dystrophic Epidermolysis Bullosa (2004)
Page Top