SAWAMURA Daisuke | Department of Dermatology, School of Medicine, Hirosaki University Hirosaki

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著作論文

Role of β-defensins in oral epithelial health and disease
ITGB4 missense mutation in a transmembrane domain causes non-lethal variant of junctional epidermolysis bullosa with pyloric atresia
Juvenile myelomonocytic leukemia presenting multiple painful erythematous lesions diagnosed as Sweet's syndrome
COL7A1 mutation G2037E causes epidermal retention of type VII collagen
In vivo transfer of TGF-α and β genes to keratinocytes
Low-grade myxofibrosarcoma invaded into the underlying skeletal muscle
Remodeling of desmosomal and hemidesmosomal adhesion systems during human hair follicle development
Possible role of 1,25-dihydroxyvitamin D_3-induced metallothionein in photoprotection against UVB injury in mouse skin and cultured rat keratinocytes
A Japanese family with dominant pretibial dystrophic epidermolysis bullosa : Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen
Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa : The splice site mutation c.6216+5G>T in the COL7A1 gene results in aberrant and normal splicings
Novel p.M1T and recurrent p.G301S mutations in cathepsin C in a Japanese patient with Papillon-Lefevre syndrome : Implications for understanding the genotype/phenotype relationship
A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjogren-Larsson syndrome
A novel Sp1-family-related cis-acting element for transcription of type VII collagen gene (COL7A1)
Expression vector with DNA of bovine papilloma virus 1 for keratinocyte gene therapy
A KERATIN K10 GENE MUTATION IN A JAPANESE PATIENT WITH EPIDERMOLYTIC HYPERKERATOSIS
Clinical and genetic analysis of Fabry disease : report of six cases including three heterozygous females
Novel mutation in a fumalate hydratase gene of a Japanese patient with multiple cutaneous and uterine leiomyomatosis
Calcineurin/NFAT-dependent regulation of 230-kDa bullous pemphigoid antigen (BPAG1) gene expression in normal human epidermal keratinocytes
Significance of sentinel node biopsy in the management of squamous cell carcinoma arising from recessive dystrophic epidermolysis bullosa
Vitamin D_3 inhibits expression of bullous pemphigoid antigen 1 through posttranscriptional mechanism without new protein synthesis
A unique monoclonal antibody 29A stains the cytoplasm of amniotic epithelia and cutaneous basement membrane
Possible role of endoplasmic reticulum stress in the pathogenesis of Darier's disease
Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism
Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa
The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa
Coexistence of Generalized Morphea with Histological Changes in Lichen Sclerosus et Atrophicus and Lichen Planus
Depigmented Macula as an Initial Manifestation of Extramammary Paget's Disease
Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid
Relation between the expression levels of the POU transcription factors Skn-1a and Skn-1n and keratinocyte differentiation
Raf kinase inhibitor protein expression correlates with differentiation but not with ERK phosphorylation in cutaneous squamous cell carcinoma
Lymphoscintigraphy for sentinel lymph node mapping in Japanese patients with malignant skin neoplasms of the lower extremities : comparison with previously investigated Japanese lymphatic anatomy

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