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Research 30 of 83
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Immunolocalization of junctional proteins in human hairs indicates that the membrane complex stabilizes the inner root sheath while desmosomes contact the companion layer through specific keratins
- Animal models of human skin disease
- Intercellular junctions in normal epidermis
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Alopecia in Epidermolysis Bullosa
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Dermatopathology and molecular genetics
- Inherited Disorders of the Hair
- Towards a molecular understanding of hair loss and its treatment
- Biology and Genetics of Hair
- Beyond Expectations
- Mechanical forces in skin disorders
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital hair loss disorders: Rare, but not too rare
- The Genetics of Human Skin Disease
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Differential proteomics of lesional vs. non-lesional biopsies revealed non-immune mechanisms of alopecia areata
- Molecular Genetics of Alopecias
- 1310 Anti-aging effects of retinoid hydroxypinacolone retinoate on skin models
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- Structure and Function of the Skin
- DNA Methylation‐Regulated ZDHHC17 Promotes the Risk of Facial Skin Aging