All Stories

  1. Two cases of erosive oral lichen planus with autoantibodies to desmoglein 3
  2. Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A gene
  3. Autoantibody profile differentiates between inflammatory and non-inflammatory bullous pemphigoid
  4. Galectin-6 is a novel skin anti-microbial peptide that is modulated by the skin barrier and microbiome
  5. Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Bullous Pemphigoid Autoantigen Collagen XVII/BP180
  6. Pyoderma Gangrenosum Associated with Acute Respiratory Distress Syndrome
  7. Increased Bacterial Load and Expression of Antimicrobial Peptides in Skin of Barrier-Deficient Mice with Reduced Cancer Susceptibility
  8. Epidermolysis Bullosa Acquisita Develops in Dominant Dystrophic Epidermolysis Bullosa
  9. Anti-laminin-gamma 1 Pemphigoid with Generalized Pustular Psoriasis and Psoriasis Vulgaris
  10. Extracellular cleavage of collagen XVII is essential for correct cutaneous basement membrane formation
  11. Mucocutaneous pyoderma gangrenosum due to trisomy 8 neutrophilic infiltrates in a patient with myelodysplastic syndrome
  12. Concomitant neoplasms in the skin and stomach unveil the role of type IV collagen and E-cadherin in mucin core protein 5AC expression in vivo
  13. Generalized acute subcutaneous edema as a rare cutaneous manifestation of severe dermatomyositis
  14. Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Pemphigoid Autoantigen, BP180
  15. Plasma cell cheilitis extending beyond vermillion border
  16. Context-Dependent Regulation of Collagen XVII Ectodomain Shedding in Skin
  17. mTOR expression correlates with invasiveness and progression of extramammary Paget's disease
  18. In vivo analysis of IgE autoantibodies in bullous pemphigoid: A study of 100 cases
  19. Plectin-related skin diseases
  20. Skipped exon inCOL7A1determines the clinical phenotypes of dystrophic epidermolysis bullosa
  21. Verrucous hyperplasia associated with neuropathy from schistorrhachis
  22. Mucosal hyperpigmentation from prophylactic minocycline for EGFR inhibitor
  23. Bowen's disease on the palm presents refractory skin erosion without erythematous plaque
  24. Metal implant-induced skin ulcer mimicking scrofuloderma
  25. Anti-BP180-type mucous membrane pemphigoid: report of two cases
  26. BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
  27. Bullous Pemphigoid Autoantibodies Directly Induce Blister Formation without Complement Activation
  28. A recurrent ‘hot spot’ glycine substitution mutation, G2043R in COL7A1, induces dominant dystrophic epidermolysis bullosa associated with intracytoplasmic accumulation of pro-collagen VII
  29. Solitary fibrous tumour fluctuating in size with menstrual cycle
  30. Epidermal barrier defects link atopic dermatitis with altered skin cancer susceptibility
  31. Paper-Based ELISA for the Detection of Autoimmune Antibodies in Body Fluid—The Case of Bullous Pemphigoid
  32. Ultrasound B-mode and elastographic findings of angiomatoid fibrous histiocytoma
  33. Epidermal Barriers
  34. Epidermal Wnt/β-catenin signaling regulates adipocyte differentiation via secretion of adipogenic factors
  35. Dermoscopic Features of Plasma Cell Cheilitis and Actinic Cheilitis
  36. Extensive Erythema and Hyperkeratosis on the Extremities and Lumbar Area as an Unusual Mani-festation of Nagashima-type Palmoplantar Keratosis
  37. Epidermolysis Bullosa Simplex
  38. c-MYC-Induced Sebaceous Gland Differentiation Is Controlled by an Androgen Receptor/p53 Axis
  39. Antibodies to epitopes on collagen XVII (COL17) induce skin fragility in COL17-humanized mice in a complement-dependent and -independent way
  40. Epidermal Wnt/beta-catenin signalling promotes dermal adipocyte differentiation during hair follicle morphogenesis and regeneration
  41. A Novel Keratin 5 Mutation in an African Family with Epidermolysis Bullosa Simplex Indicates the Importance of the Amino Acid Located at the Boundary Site Between the H1 and Coil 1A Domains
  42. The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
  43. 716 Chemical Carcinogenesis in Mice With a Defective Epidermal Barrier – Exploring the Connection Between Skin Barrier and Cancer Susceptibility
  44. Antibodies to Pathogenic Epitopes on Type XVII Collagen Cause Skin Fragility in a Complement-Dependent and -Independent Manner
  45. Mucous membrane pemphigoid with generalized blisters: IgA and IgG autoantibodies target both laminin‐332 and type XVII collagen
  46. Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome
  47. Subepidermal blistering disease with 3 distinct autoantibodies: Anti-BP230, anti-laminin gamma-1, and anti-laminin-332
  48. Consequences of Two Different Amino-Acid Substitutions at the Same Codon in KRT14 Indicate Definitive Roles of Structural Distortion in Epidermolysis Bullosa Simplex Pathogenesis
  49. Malignant skin tumours in patients with inherited ichthyosis
  50. DNA‐based prenatal diagnosis of plectin‐deficient epidermolysis bullosa simplex associated with pyloric atresia
  51. Type XVII collagen ELISA indices significantly decreased after bullous pemphigoid remission
  52. Childhood subepidermal blistering disease with autoantibodies to type VII collagen and laminin-332
  53. Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome
  54. Spontaneous Remission of Solitary-Type Infantile Myofibromatosis
  55. Human IgG1 Monoclonal Antibody against Human Collagen 17 Noncollagenous 16A Domain Induces Blisters via Complement Activation in Experimental Bullous Pemphigoid Model
  56. Complete Paternal Isodisomy of Chromosome 17 in Junctional Epidermolysis Bullosa with Pyloric Atresia
  57. A founder effect of c.1938delC in ITGB4 underlies junctional epidermolysis bullosa and its application for prenatal testing
  58. Plectin deficiency leads to both muscular dystrophy and pyloric atresia in epidermolysis bullosa simplex
  59. Bone marrow transplantation restores epidermal basement membrane protein expression and rescues epidermolysis bullosa model mice
  60. Epidermolysis Bullosa in Japan
  61. Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex
  62. Animal Models of Epidermolysis Bullosa
  63. PrevalentLIPHfounder mutations lead to loss of P2Y5 activation ability of PA-PLA1α in autosomal recessive hypotrichosis
  64. Localized Linear IgA/IgG Bullous Dermatosis
  65. Response of Intractable Skin Ulcers in Recessive Dystrophic Epidermolysis Bullosa Patients to an Allogeneic Cultured Dermal Substitute
  66. Keratinocyte-/Fibroblast-Targeted Rescue of Col7a1-Disrupted Mice and Generation of an Exact Dystrophic Epidermolysis Bullosa Model Using a Human COL7A1 Mutation
  67. Secondary syphilis mimicking warts in an HIV-positive patient
  68. Circulating IgA and IgE autoantibodies in antilaminin-332 mucous membrane pemphigoid
  69. A Novel Humanized Neonatal Autoimmune Blistering Skin Disease Model Induced by Maternally Transferred Antibodies
  70. Widespread keratosis follicularis squamosa
  71. Pemphigus foliaceus associated with oesophageal cancer
  72. Autoantibodies against type XVII collagen C-terminal domain in a patient with bullous pemphigoid associated with psoriasis vulgaris
  73. Morphological and genetic analysis of steatocystoma multiplex in an Asian family with pachyonychia congenita type 2 harbouring aKRT17missense mutation
  74. Type XVII Collagen is a Key Player in Tooth Enamel Formation
  75. Usefulness of thermography techniques for evaluating the disease activity in Kimura’s disease
  76. Cutaneous pemphigus vulgaris with skin features similar to the classic mucocutaneous type: a case report and review of the literature
  77. Acquired perforating dermatosis appearing as elastosis perforans serpiginosa and perforating folliculitis
  78. Leukaemic dissemination of Merkel cell carcinoma in a patient with systemic lupus erythematosus
  79. Precursor B-cell lymphoblastic lymphoma presented with intraocular involvement and unusual skin manifestations
  80. Novel ABCA12 Mutations Identified in Two Cases of Non-Bullous Congenital Ichthyosiform Erythroderma Associated with Multiple Skin Malignant Neoplasia
  81. Amicrobial pustulosis associated with IgA nephropathy and Sjögren's syndrome
  82. Non‐Hodgkin lymphoma preceded by recalcitrant eczema
  83. Keratoacanthoma developing on nevus sebaceous in a child
  84. Mycosis Fungoides Bullosa
  85. Severe cholinergic urticaria successfully treated with scopolamine butylbromide in addition to antihistamines
  86. Two cases of atypical melanocytic lesions in recessive dystrophic epidermolysis bullosa infants
  87. Ultrastructural Features of Trafficking Defects Are Pronounced in Melanocytic Nevus in Hermansky–Pudlak Syndrome Type 1