Coexistence of Generalized Morphea with Histological Changes in Lichen Sclerosus et Atrophicus and Lichen Planus
スポンサーリンク
概要
- 論文の詳細を見る
- 1998-06-01
著者
-
HASHIMOTO Isao
Department of Dermatology, Hirosaki University School of Medicine
-
SAWAMURA Daisuke
Department of Dermatology, School of Medicine, Hirosaki University Hirosaki
-
Sawamura Daisuke
Department Of Dermatology Hirosaki University Graduate School Of Medicine
-
Hashimoto Isao
Department Of Dermatology Hirosaki University School Of Medicine
-
YAGUCHI Tadashi
Department of Dermatology, Hirosaki University School of Medicine
-
NOMURA Kazuo
Division of Dermatology, Aomori Prefectural Central Hospital
-
KONTA Ritsuko
Division of Dermatology, Goshogawara City Seihoku Central Hospital
-
UMEKI Kaoru
Division of Dermatology, Goshogawara City Seihoku Central Hospital
-
Konta Ritsuko
Division Of Dermatology Goshogawara City Seihoku Central Hospital
-
Sawamura D
Kyushu Inst. Technol. Fukuoka Jpn
-
Umeki Kaoru
弘前大学 皮膚科
-
Yaguchi Tadashi
Department Of Dermatology Hirosaki University School Of Medicine
関連論文
- A Study of Atopic Dermatitis in Elementary School Children in Hirosaki City, Aomori Prefecture, Japan
- 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
- 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
- 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
- Decrease in Class Pi Glutathione Transferase mRNA Levels by Ultraviolet Irradiation of Cultured Rat Keratinocytes
- 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
- S-9. Posteromedical Hypothalamotomoy for Intractable Pain : Basic and Clinical Studies
- Depigmented Macula as an Initial Manifestation of Extramammary Paget's Disease
- A keratin K14 gene mutation in a Japanese patient with the Dowling-Meara type of epidermolysis bullosa simplex
- Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid
- Leukemia cutis is an early sign of blast transformation that may mimic a common skin disease : Sycosis-like eruptions in chronic myelomonocytic leukemia
- Thermodynamic Stability of the Spontaneous Polarization and the Space Charge Layer in Ferroelectric/Semiconductor Heterostructures
- 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
- Overview of epidermolysis bullosa
- Hailey-Hailey disease with affective disorder : Report of a case with novel ATP2C1 gene mutation
- Dystrophic epidermolysis bullosa pruriginosa of elderly onset
- Expression of Raf Kinase Inhibitor Protein in Keratinocyte Differentiation in the Mouse Epidermis
- Garlic-induced irritant contact dermatitis mimicking nail psoriasis
- The compound heterozygote for new/recurrent COL7A1 mutations in a Japanese patient with bullous dermolysis of the newborn
- On an Essentially Complete Class of the Estimators Under Certain Restrictions on Parameters
- Two cases of recessive dystrophic epidermolysis bullosa diagnosed as severe generalized
- Characterization of Stimulator of Interferon Genes (STING) Expression in Human Epidermal Keratinocytes
- Reduction in epidermal Langerhans cells in patients with necrolytic migratory erythema
- Follicular mucinosis associated with radiation therapy