Human autoantibodies against the 230-kD bullous pemphigoid antigen (BPAG1) bind only to the intracellular domain of the hemidesmosome, whereas those against the 180-kD bullous pemphigoid antigen (BPAG2) bind along the plasma membrane of the hemidesm
about
Neutrophil elastase cleaves the murine hemidesmosomal protein BP180/type XVII collagen and generates degradation products that modulate experimental bullous pemphigoidAssessment of splice variant-specific functions of desmocollin 1 in the skinCompound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis bullosa and abnormal dentitionThree novel homozygous point mutations and a new polymorphism in the COL17A1 gene: relation to biological and clinical phenotypes of junctional epidermolysis bullosaTwo forms of collagen XVII in keratinocytes. A full-length transmembrane protein and a soluble ectodomainDetection of antigens by immunofluorescence on ultrathin cryosections of skin.Application of confocal laser scanning microscopy to differential diagnosis of bullous pemphigoid and epidermolysis bullosa acquisita.Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigenInduction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagen.Experimental models for the autoimmune and inflammatory blistering disease, Bullous pemphigoid.180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa.The role of T cells in cutaneous autoimmune disease.Autoantibodies against adhesion molecules and structures in blistering skin diseasesEpidermal basement membrane: its molecular organization and blistering disorders.Passive transfer of collagen XVII-specific antibodies induces sustained blistering disease in adult miceOne gene but different proteins and diseases: the complexity of dystonin and bullous pemphigoid antigen 1.Cellular mechanosensitivity to substrate stiffness decreases with increasing dissimilarity to cell stiffness.Epidermal and dermal integration into sphere-templated porous poly(2-hydroxyethyl methacrylate) implants in mice.Precise ultrastructural localization of in vivo deposited IgG antibodies in fresh perilesional skin of patients with bullous pemphigoid.Immunoglobulin G deposition to nonhemidesmosomal lamina lucida and early neutrophil involvement are characteristic features in a case of anti-p200 pemphigoid.Evidence for a role of eosinophils in blister formation in bullous pemphigoid.180-kDa bullous pemphigoid antigen defective generalized atrophic benign epidermolysis bullosa: report of four cases with an unusually mild phenotype.Discovery of a patient with strongly suspected bullous pemphigoid in a ward by oral health care providers.Structural Analysis of the Predicted Coiled-coil Rod Domain of the Cytoplasmic Bullous Pemphigoid Antigen (BPAG1)
P2860
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P2860
Human autoantibodies against the 230-kD bullous pemphigoid antigen (BPAG1) bind only to the intracellular domain of the hemidesmosome, whereas those against the 180-kD bullous pemphigoid antigen (BPAG2) bind along the plasma membrane of the hemidesm
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Human autoantibodies against t ...... lasma membrane of the hemidesm
@en
type
label
Human autoantibodies against t ...... lasma membrane of the hemidesm
@en
prefLabel
Human autoantibodies against t ...... lasma membrane of the hemidesm
@en
P2093
P2860
P356
P1476
Human autoantibodies against t ...... lasma membrane of the hemidesm
@en
P2093
P2860
P304
P356
10.1172/JCI116368
P407
P577
1993-04-01T00:00:00Z