Search
for
Sort by
Research 61–90 of 83
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- The Roles of WNT Signaling Pathways in Skin Development and Mechanical-Stretch-Induced Skin Regeneration
- Multifaceted role of keratins in epithelial cell differentiation and transformation
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Alopecia in Epidermolysis Bullosa
- Dermatopathology and molecular genetics
- Towards a molecular understanding of hair loss and its treatment
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Hair Loss in Autoimmune Cutaneous Bullous Disorders
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Beyond Expectations
- Mechanical forces in skin disorders
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Skin transcriptome profiling of Changthangi goats highlights the relevance of genes involved in Pashmina production
- Structure and Function of the Skin
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Proteome Analysis of Human Hair Shaft
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- 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
- Decision letter: Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Animal models of human skin disease
- Intercellular junctions in normal epidermis
- Folliculin interacts with p0071 (plakophilin-4) and deficiency is associated with disordered RhoA signalling, epithelial polarization and cytokinesis
- 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