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Research 241–270 of 541
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- The Skin Microbiome: Current Landscape and Future Opportunities
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Expression of Desmoglein 1 Compensates for Genetic Loss of Desmoglein 3 in Keratinocyte Adhesion
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Recently Identified Forms of Epidermolysis Bullosa
- Developing stratified epithelia: lessons from the epidermis and thymus
- Anatomy and Physiology of the Skin
- Reduced cell cohesiveness of outgrowths from eccrine sweat glands delays wound closure in elderly skin
- Skin Development and Disease: A Molecular Perspective
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- Characterization of the Promoter Regions of Two Sheep Keratin-Associated Protein Genes for Hair Cortex-Specific Expression
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- The expression of equine keratins K42 and K124 is restricted to the hoof epidermal lamellae of Equus caballus
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Characters of KRT80 and its roles in neoplasms diseases
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Impact of constant light exposure during pregnancy on skin of neonatal New Zealand rabbits: structural and ultrastructural study
- A 4kb Fragment of the Desmocollin 3 Promoter Directs Reporter Gene Expression to Parakeratotic Epidermis and Primary Hair Follicles
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- 169 TEDAR, a skin-specific long non-coding RNA, orchestrates the late epidermal differentiation program in the human epidermis
- Prediction of cell states and key transcription factors of the human cornea through integrated single-cell omics analyses