スポンサーリンク
Department of Dermatology, Hirosaki University School of Medicine | 論文
- A Study of Atopic Dermatitis in Elementary School Children in Hirosaki City, Aomori Prefecture, Japan
- Amicrobial pustulosis associated with IgA nephropathy and Sjögren's syndrome
- 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
- Cytokine modulation of retinoic acid-inducible gene-I (RIG-I) expression in human epidermal keratinocytes
- 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
- Effect of Helicobacter pylori eradication in the treatment of Japanese patients with chronic idiopathic urticaria
- 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
- Dominant dystrophic epidermolysis bullosa caused by a novel G2037R mutation and by a known G2028R mutation in the type VII collagen gene (COL7A1)
- 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
- The study of ultraviolet B-induced apoptosis in cultured mouse keratinocytes and in mouse skin
- Successful Treatment of Mucosal Melanosis of the Lip with Normal Pulsed Ruby Laser
- Successful Treatment of Dark-colored Epidermal Nevus with Ruby Laser
- 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