スポンサーリンク
Department of Biochemistry Shinshu University School of Medicine | 論文
- The Common KRT9 Gene Mutation in a Japanese Patient with Epidermolytic Palmoplantar Keratoderma and Knuckle Pad-Like Keratoses
- A Case of Acquired Autoimmune Bullous Disease Associated with IgM Macroglobulinaemia
- First Synthesis of (±)-Basidifferquinone C, an Inducer for Fruiting-Body Formation in Polyporus arcularius
- Synthesis of (±)-Sundiversifolide Based on Lewis Acid-Mediated Claisen Rearrangement
- Cicatricial pemphigoid with widespread bullous eruption
- Different Suppressive Effects of Fucoidan and Lentinan on IL-8 mRNA Expression in in Vitro Gut Inflammation
- Childhood Bullous Pemphigoid Successfully Treated with Diaminodiphenyl Sulfone
- Schopf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A
- Edaravone, a Hydroxyl Radical Scavenger, Ameliorates the Severity of Pulmonary Hypertension in a Porcine Model of Neonatal Sepsis
- Complementary peptides against the major epitope in the NC16A domain of BP180 show no specificity as vaccines to bullous pemphigoid
- Human desmocollin 1a transiently expressed in COS-7 cells and NIH 3T3-3 cells is reacted by IgG4 antibodies in a pemphigus foliaceus serum
- Bullous Pemphigoid in an HB Virus Carrier : Interaction between Corticosteroids and HB Virus
- Immunoelectron Microscopic Localization of Peroxisomal Enzymes in the Fibrillar Structures of Rat Liver Peroxisomes Induced by Administration of Acetylsalicylic Acid.
- Immunoreactivity against intracellular domains of desmogleins in pemphigus
- A New Inhibitor of Mitochondrial Fatty Acid Oxidation
- INTRAMITOCHONDRIAL DISTRIBUTION OF THREE ACYL-COA DEHYDROGENASES IN RAT LIVER PARENCHYMAL CELLS REVEALED BY QUANTITATIVE IMMUNOELECTRON MICROSCOPY
- Evaluation of an Avidin-Biotin-Peroxidase Method with a Monoclonal Antibody to Type IV Collagen in the Differential Diagnosis of Bullous Pemphigoid and Epidermolysis Bullosa Acquisita
- Immunofluorescence studies using skin sections of recessive dystrophic epidermolysis bullosa patients indicated that the antigen of anti-p200 pemphigoid is not a fragment of type VII collagen
- Anti-p200 pemphigoid : A novel autoimmune subepidermal blistering disease
- Mucous membrane pemphigoid with immunoglobulin G autoantibodies against full-length and 120-kDa ectodomain of BP180