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  1. Measuring the quality of life in pemphigus
  2. Complement-Activating Capacity of Autoantibodies Correlates With Disease Activity in Bullous Pemphigoid Patients
  3. A new clinical variant of acquired reactive perforating dermatosis-like bullous pemphigoid
  4. Molecular diagnosis of anti-laminin 332 (epiligrin) mucous membrane pemphigoid
  5. Serological diagnostics in the detection of IgG autoantibodies against human collagen VII in epidermolysis bullosa acquisita: a multicentre analysis
  6. The Syk Tyrosine Kinase Is Required for Skin Inflammation in an In Vivo Mouse Model of Epidermolysis Bullosa Acquisita
  7. Autoimmunity against laminins
  8. The Src family kinases Hck, Fgr, and Lyn are critical for the generation of the in vivo inflammatory environment without a direct role in leukocyte recruitment
  9. Blister‐inducing antibodies target multiple epitopes on collagen VII in mice
  10. BP180- and BP230-specific IgG autoantibodies in pruritic disorders of the elderly: a preclinical stage of bullous pemphigoid?
  11. IgG antibodies against immunodominant C-terminal epitopes of BP230 do not induce skin blistering in mice
  12. Faculty Opinions recommendation of A prospective study on clinical response and cell-mediated immunity of pemphigus patients treated with rituximab.
  13. The need for markers and predictors of Rituximab treatment resistance
  14. Ex Vivo Pathogenicity of Anti–Laminin γ1 Autoantibodies
  15. Molecular Diagnosis in Autoimmune Skin Blistering Conditions
  16. Faculty Opinions recommendation of Development of a quality-of-life instrument for autoimmune bullous disease: the Autoimmune Bullous Disease Quality of Life questionnaire.
  17. Faculty Opinions recommendation of Prevalence of specific anti-skin autoantibodies in a cohort of patients with inherited epidermolysis bullosa.
  18. Faculty Opinions recommendation of Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting.
  19. Faculty Opinions recommendation of Desmoglein 3 promotes cancer cell migration and invasion by regulating activator protein 1 and protein kinase C-dependent-Ezrin activation.
  20. Faculty Opinions recommendation of Mechanisms of mitochondrial damage in keratinocytes by pemphigus vulgaris antibodies.
  21. Faculty Opinions recommendation of Pemphigus vulgaris autoantibody profiling by proteomic technique.
  22. Childhood epidermolysis bullosa acquisita associated with severe dental alterations: A case presentation
  23. Faculty Opinions recommendation of Vulvo-cervico-vaginal manifestations and evaluation of Papanicolaou smears in pemphigus vulgaris and pemphigus foliaceus.
  24. Faculty Opinions recommendation of Signaling dependent and independent mechanisms in pemphigus vulgaris blister formation.
  25. Faculty Opinions recommendation of Diagnostic utility of direct immunofluorescence findings around hair follicles and sweat glands in immunobullous disease.
  26. Molecular Dermatology
  27. Passive transfer of collagen XVII-specific antibodies induces sustained blistering disease in adult mice
  28. Faculty Opinions recommendation of Enrichment of total serum IgG4 in patients with pemphigus.
  29. Faculty Opinions recommendation of Missing the target: characterization of bullous pemphigoid patients who are negative using the BP180 enzyme-linked immunosorbant assay.
  30. Molecular Dermatology Comes of Age
  31. Induction of Experimental Epidermolysis Bullosa Acquisita by Immunization with Murine Collagen VII
  32. Faculty Opinions recommendation of IgG autoantibody response against keratinocyte cadherins in endemic pemphigus foliaceus (fogo selvagem).
  33. Granulocyte-dependent Autoantibody-induced Skin Blistering
  34. Two Japanese cases of dermatitis herpetiformis associated each with lung cancer and autoimmune pancreatitis but showing no intestinal symptom or circulating immunoglobulin A antibodies to any known antigens
  35. Nonscarring skin blistering disease and mucosal lesions with IgA autoantibodies reactive with collagen VII and IgG reactivity with lamininγ2
  36. Faculty Opinions recommendation of Cutting Edge: Brazilian pemphigus foliaceus anti-desmoglein 1 autoantibodies cross-react with sand fly salivary LJM11 antigen.
  37. Blocking Fc  Receptor I on Granulocytes Prevents Tissue Damage Induced by IgA Autoantibodies
  38. Faculty Opinions recommendation of Cre-mediated cell ablation contests mast cell contribution in models of antibody- and T cell-mediated autoimmunity.
  39. Faculty Opinions recommendation of Desmoglein 3-specific CD4+ T cells induce pemphigus vulgaris and interface dermatitis in mice.
  40. Prevalence of collagen VII-specific autoantibodies in patients with autoimmune and inflammatory diseases
  41. Faculty Opinions recommendation of Black patients of African descent and HLA-DRB1*15:03 frequency overrepresented in epidermolysis bullosa acquisita.
  42. Why human pemphigoid autoantibodies do not trigger disease by the passive transfer into mice?
  43. The Flavonoid Luteolin Inhibits Fcγ-Dependent Respiratory Burst in Granulocytes, but Not Skin Blistering in a New Model of Pemphigoid in Adult Mice
  44. Faculty Opinions recommendation of Cardiac autoantibodies from patients affected by a new variant of endemic pemphigus foliaceus in Colombia, South America.
  45. Faculty Opinions recommendation of An adult passive transfer mouse model to study desmoglein 3 signaling in pemphigus vulgaris.
  46. Faculty Opinions recommendation of Activation of coagulation in bullous pemphigoid and other eosinophil-related inflammatory skin diseases.
  47. Faculty Opinions recommendation of Pathogenic relevance of IgG and IgM antibodies against desmoglein 3 in blister formation in pemphigus vulgaris.
  48. Faculty Opinions recommendation of Aire-dependent thymic expression of desmoglein 3, the autoantigen in pemphigus vulgaris, and its role in T-cell tolerance.
  49. Development of an ELISA for sensitive and specific detection of IgA autoantibodies against BP180 in pemphigoid diseases
  50. Faculty Opinions recommendation of The C5a receptor on mast cells is critical for the autoimmune skin-blistering disease bullous pemphigoid.
  51. PI3K  Plays a Critical Role in Neutrophil Activation by Immune Complexes
  52. Faculty Opinions recommendation of Dermatitis herpetiformis sera or goat anti-transglutaminase-3 transferred to human skin-grafted mice mimics dermatitis herpetiformis immunopathology.
  53. Faculty Opinions recommendation of p38 MAPK activation is downstream of the loss of intercellular adhesion in pemphigus vulgaris.
  54. Faculty Opinions recommendation of Autoimmunity to desmocollin 3 in pemphigus vulgaris.
  55. Faculty Opinions recommendation of Identification of periplakin as a new target for autoreactivity in idiopathic pulmonary fibrosis.
  56. Faculty Opinions recommendation of Human IgG1 monoclonal antibody against human collagen 17 noncollagenous 16A domain induces blisters via complement activation in experimental bullous pemphigoid model.
  57. Faculty Opinions recommendation of Congenital epidermolysis bullosa acquisita: vertical transfer of maternal autoantibody from mother to infant.
  58. Faculty Opinions recommendation of False-positive intercellular cement substance antibodies due to group A/B red cell antibodies: frequency and approach.
  59. Faculty Opinions recommendation of The protease inhibitor alpha-2-macroglobulin-like-1 is the p170 antigen recognized by paraneoplastic pemphigus autoantibodies in human.
  60. Ectodomain Shedding Generates Neoepitopes on Collagen XVII, the Major Autoantigen for Bullous Pemphigoid
  61. Faculty Opinions recommendation of Actin reorganization contributes to loss of cell adhesion in pemphigus vulgaris.
  62. Faculty Opinions recommendation of Serum anti-BPAG1 auto-antibody is a novel marker for human melanoma.
  63. Pemphigus vulgaris is the most common autoimmune bullous disease in Northwestern Romania
  64. Faculty Opinions recommendation of Binding of pemphigus vulgaris IgG to antigens in desmosome core domains excludes immune complexes rather than directly splitting desmosomes.
  65. Pathogenicity of IgG subclass autoantibodies to type VII collagen: Induction of dermal–epidermal separation
  66. Faculty Opinions recommendation of Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen.
  67. Faculty Opinions recommendation of IgA anti-epidermal transglutaminase antibodies in dermatitis herpetiformis and pediatric celiac disease.
  68. The neonatal Fc receptor as therapeutic target in IgG-mediated autoimmune diseases
  69. Faculty Opinions recommendation of Desmocollin 3-mediated binding is crucial for keratinocyte cohesion and is impaired in pemphigus.
  70. Metal sensitization precipitates skin blistering in epidermolysis bullosa acquisita
  71. Faculty Opinions recommendation of Antimitochondrial autoantibodies in pemphigus vulgaris: a missing link in disease pathophysiology.
  72. Faculty Opinions recommendation of p38MAPK signaling and desmoglein-3 internalization are linked events in pemphigus acantholysis.
  73. Faculty Opinions recommendation of A novel active mouse model for bullous pemphigoid targeting humanized pathogenic antigen.
  74. Cross-reactivity of autoantibodies from patients with epidermolysis bullosa acquisita with murine collagen VII
  75. Faculty Opinions recommendation of Desmosomal interactome in keratinocytes: a systems biology approach leading to an understanding of the pathogenesis of skin disease.
  76. T Cells Are Required for the Production of Blister-Inducing Autoantibodies in Experimental Epidermolysis Bullosa Acquisita
  77. Faculty Opinions recommendation of Antibodies to the desmoglein 1 precursor proprotein but not to the mature cell surface protein cloned from individuals without pemphigus.
  78. Faculty Opinions recommendation of Loss of the desmosomal protein perp enhances the phenotypic effects of pemphigus vulgaris autoantibodies.
  79. Faculty Opinions recommendation of Sequential intramolecular epitope spreading of humoral responses to human BPAG2 in a transgenic model.
  80. Autoimmunity against type VII collagen in inflammatory bowel disease
  81. Faculty Opinions recommendation of Pathogenic epitopes of autoantibodies in pemphigus reside in the amino-terminal adhesive region of desmogleins which are unmasked by proteolytic processing of prosequence.
  82. Faculty Opinions recommendation of A novel humanized neonatal autoimmune blistering skin disease model induced by maternally transferred antibodies.
  83. Faculty Opinions recommendation of Intravenous immunoglobulin selectively decreases circulating autoantibodies in pemphigus.
  84. Transition from pemphigus foliaceus to bullous pemphigoid: Intermolecular B-cell epitope spreading without IgG subclass shifting
  85. Faculty Opinions recommendation of Collagen XVII participates in keratinocyte adhesion to collagen IV, and in p38MAPK-dependent migration and cell signaling.
  86. Faculty Opinions recommendation of IgG from patients with bullous pemphigoid depletes cultured keratinocytes of the 180-kDa bullous pemphigoid antigen (type XVII collagen) and weakens cell attachment.
  87. Bullous Pemphigoid: A Prototypical Antibody-Mediated Organ-Specific Autoimmune Disease
  88. Faculty Opinions recommendation of Biphasic activation of p38MAPK suggests that apoptosis is a downstream event in pemphigus acantholysis.
  89. Faculty Opinions recommendation of A single helper T cell clone is sufficient to commit polyclonal naive B cells to produce pathogenic IgG in experimental pemphigus vulgaris.
  90. IgE autoantibodies against the intracellular domain of BP180
  91. Subepidermal blistering induced by human autoantibodies to BP180 requires innate immune players in a humanized bullous pemphigoid mouse model
  92. Faculty Opinions recommendation of Pemphigus vulgaris IgG directly inhibit desmoglein 3-mediated transinteraction.
  93. Bullous Pemphigoid Autoantibodies Preferentially Recognize Phosphoepitopes in Collagen XVII
  94. Cicatrising conjunctivitis with anti-basement membrane autoantibodies in ectodermal dysplasia
  95. Faculty Opinions recommendation of T helper type 2-biased natural killer cell phenotype in patients with pemphigus vulgaris.
  96. Faculty Opinions recommendation of Evidence of key role of Cdk2 overexpression in pemphigus vulgaris.
  97. Neonatal Fc receptor deficiency protects from tissue injury in experimental epidermolysis bullosa acquisita
  98. Faculty Opinions recommendation of Serum levels of BAFF are increased in bullous pemphigoid but not in pemphigus vulgaris.
  99. Faculty Opinions recommendation of Correlation of IgE autoantibody to BP180 with a severe form of bullous pemphigoid.
  100. Faculty Opinions recommendation of Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) associated with pemphigoid nodularis: a case report and review of the literature.
  101. Binding of avian IgY to type VII collagen does not activate complement and leucocytes and fails to induce subepidermal blistering in mice
  102. Faculty Opinions recommendation of Endemic pemphigus vulgaris.
  103. Faculty Opinions recommendation of The IgM anti-desmoglein 1 response distinguishes Brazilian pemphigus foliaceus (fogo selvagem) from other forms of pemphigus.
  104. Faculty Opinions recommendation of Human bullous pemphigoid antigen 2 transgenic skin elicits specific IgG in wild-type mice.
  105. Faculty Opinions recommendation of A new model for dermatitis herpetiformis that uses HLA-DQ8 transgenic NOD mice.
  106. Faculty Opinions recommendation of Anti-desmoglein 3 (Dsg3) monoclonal antibodies deplete desmosomes of Dsg3 and differ in their Dsg3-depleting activities related to pathogenicity.
  107. IgG4 autoantibodies induce dermal–epidermal separation
  108. The alternative pathway of complement activation is critical for blister induction in experimental autoimmune epidermolysis bullosa
  109. Enzyme‐linked immunosorbent assay using multimers of the 16th non‐collagenous domain of the BP180 antigen for sensitive and specific detection of pemphigoid autoantibodies
  110. Faculty Opinions recommendation of IgE basement membrane zone antibodies induce eosinophil infiltration and histological blisters in engrafted human skin on SCID mice.
  111. Faculty Opinions recommendation of Dissecting the anti-desmoglein autoreactive B cell repertoire in pemphigus vulgaris patients.
  112. Experimental models of epidermolysis bullosa acquisita
  113. Immunopathology and molecular diagnosis of autoimmune bullous diseases
  114. NADPH oxidase is required for neutrophil-dependent autoantibody-induced tissue damage
  115. Faculty of 1000 evaluation for The Cartilage Matrix Protein Subdomain of Type VII Collagen Is Pathogenic for Epidermolysis Bullosa Acquisita.
  116. Faculty Opinions recommendation of Involvement of a tissue-specific autoantibody in skin disorders of murine systemic lupus erythematosus and autoinflammatory diseases.
  117. Faculty Opinions recommendation of Humanization of autoantigen.
  118. Erythema gyratum repens-like eruption in a patient with epidermolysis bullosa acquisita associated with ulcerative colitis
  119. The relevance of the IgG subclass of autoantibodies for blister induction in autoimmune bullous skin diseases
  120. Spatiotemporal distribution of Fras1/Frem proteins during mouse embryonic development
  121. IgA‐Pemphigus – Vorkommen von Anti‐Desmocollin‐1‐und Anti‐Desmoglein‐1‐Antikörpern bei einem Patienten
  122. IgA pemphigus – Occurrence of anti‐Desmocollin 1 and anti‐Desmoglein 1 antibody reactivity in an individual patient
  123. Autoantibodies From Patients With BSLE Inducing Recruitment of Leukocytes to the Dermoepidermal Junction and Subepidermal Splits in Cryosections of Human Skin
  124. Localisation of bullous pemphigoid antigen 180 (BP180) in cultured human keratinocytes: functionally relevant modification by calcium
  125. Generation and Characterization of Monoclonal Antibodies Against the Intracellular Domain of Hemidesmosomal Type XVII Collagen
  126. Immunoadsorption against two distinct epitopes on human type XVII collagen abolishes dermal‐epidermal separation induced in vitro by autoantibodies from pemphigoid gestationis patients
  127. Scarring autoimmune bullous disease in a Ugandan patient with autoantibodies to BP180, BP230, and laminin 5
  128. Schleimhautpemphigoid mit Autoantikörpern gegen Laminin 5
  129. Anti‐laminin 5 mucous membrane pemphigoid
  130. Mechanisms of blister induction by autoantibodies
  131. IgG autoantibodies to type VII collagen and an exclusive IgG3 reactivity to the laminin α3 chain in a patient with an autoimmune subepidermal blistering disease
  132. Successful adjuvant treatment of severe bullous pemphigoid by tryptophan immunoadsorption
  133. Penfigoide de mucosas: anticuerpos IgG e IgA contra el antígeno BP180
  134. Subepidermal blistering disease with autoantibodies to both the p200 autoantigen and the α3 chain of laminin 5
  135. Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagen
  136. Induction of dermal-epidermal separation in mice by passive transfer of antibodies specific to type VII collagen
  137. Subclass distribution of type VII collagen-specific autoantibodies in patients with inflammatory bowel disease
  138. Comparative analysis of methods for detection of anti-laminin 5 autoantibodies in patients with anti-epiligrin cicatricial pemphigoid
  139. Downregulation of CXCR1 and CXCR2 Expression on Human Neutrophils by Helicobacter pylori: a New Pathomechanism in H. pylori Infection?
  140. Granulocyte‐derived elastase and gelatinase B are required for dermal–epidermal separation induced by autoantibodies from patients with epidermolysis bullosa acquisita and bullous pemphigoid
  141. Bullöse Autoimmundermatosen (II): Therapie
  142. Kongreßkalender
  143. Localized linear IgA disease induced by ampicillin/sulbactam
  144. Development of an ELISA for the detection of autoantibodies to BP230
  145. Immunoblotting and Enzyme-Linked Immunosorbent Assay for the Diagnosis of Pemphigoid Gestationis
  146. Bullöse Autoimmundermatosen (I): Pathogenese und Diagnostik
  147. The Autoantigen of Anti-p200 Pemphigoid Is an Acidic Noncollagenous N-Linked Glycoprotein of the Cutaneous Basement Membrane
  148. The 97-kDa (LABD97) and 120-kDa (LAD-1) Fragments of Bullous Pemphigoid Antigen 180/Type XVII Collagen Have Different N-Termini
  149. Successful treatment of linear IgA disease with salazosulphapyridine and intravenous immunoglobulins
  150. Pemphigoid gestationis: maternal sera recognize epitopes restricted to the N-terminal portion of the extracellular domain of BP180 not present on its shed ectodomain
  151. Protein A immunoadsorption: a novel and effective adjuvant treatment of severe pemphigus
  152. Memory B Cells Specific for the NC16A Domain of the 180kDa Bullous Pemphigoid Autoantigen Can Be Detected in Peripheral Blood of Bullous Pemphigoid Patients and Induced In Vitro to Synthesize Autoantibodies
  153. Autoreactive T cell responses in pemphigus and pemphigoid
  154. Subacute prurigo variant of bullous pemphigoid: Autoantibodies show the same specificity compared with classic bullous pemphigoid
  155. Autoantibodies to Type VII Collagen Mediate Fcγ-Dependent Neutrophil Activation and Induce Dermal-Epidermal Separation in Cryosections of Human Skin
  156. A Highly Sensitive and Simple Assay for the Detection of Circulating Autoantibodies against Full-Length Bullous Pemphigoid Antigen 180
  157. Autoantibodies to Bullous Pemphigoid Antigen 180 Induce Dermal–Epidermal Separation in Cryosections of Human Skin
  158. Vesikel, Lichtempfindlichkeit, orale Ulzerationen und Arthralgien bei einer 40-Jührigen
  159. Cicatricial pemphigoid differs from bullous pemphigoid and pemphigoid gestationis regarding the fine specificity of autoantibodies to the BP180 NC16A domain
  160. Cicatricial pemphigoid with circulating autoantibodies to beta4 integrin, bullous pemphigoid 180 and bullous pemphigoid 230
  161. Dermatology resources on the Internet: a practical guide for dermatologists