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Research 271–300 of 829
- Congenital and Hereditary Skin Diseases
- Recognition and management of <i>Staphylococcus aureus</i> toxin‐mediated disease
- Mechanical forces in skin disorders
- What's new in the pathogeneses and triggering factors of bullous pemphigoid
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle
- Alopecia in Epidermolysis Bullosa
- Heterogeneous disease: A child case of lichen planus pemphigoides triggered by varicella
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Alopecia developed in a transitional case from pemphigus foliaceus to pemphigus vulgaris
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Hemidesmosomes and Notch signaling regulate epidermal differentiation via delamination
- Scarring Alopecia in a 66‐Year‐Old Woman
- A Comprehensive Review on Trichogram and Trichoscopy in Dermatology
- SnapshotDx Quiz: May 2020
- Hair follicle stem cell progeny heal blisters while pausing skin development
- 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus
- The role of Kindlin-1 in skin homeostasis and tumor development
- In this Issue
- Clinical Patterns and Frequency of Dermatological Manifestations Associated with Pregnancy
- Abstracts
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)
- Case report: Pseudoporphyria in a 56-year-old man as a result of finasteride intake
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- The Case Files
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case