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Research 211–240 of 1000+
- Defining a Region of the Human Keratin 6a Gene That Confers Inducible Expression in Stratified Epithelia of Transgenic Mice
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- The extraction and characterization of human nail keratin
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- “Structural imprinting” of the cutaneous immune effector function
- Comparative aspects of the inner root sheath in adult and developing hairs of mammals in relation to the evolution of hairs
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- Immunohistochemical Expression of Keratins in Normal Ovine Skin and in Chronic Dermatitis due to Sarcoptes scabiei
- Immunohistochemical demonstration of keratins 8 and 14 in benign tumours of the skin appendage
- Keratins and disease at a glance
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Development of a mechanically stable human hair keratin film for cell culture
- Effects of hyperbaric oxygen therapy on rat facial skin
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Emerging interactions between skin stem cells and their niches
- Organogenesis From Dissociated Cells: Generation of Mature Cycling Hair Follicles From Skin-Derived Cells
- Human Peptidylarginine Deiminase Type III: Molecular Cloning and Nucleotide Sequence of the cDNA, Properties of the Recombinant Enzyme, and Immunohistochemical Localization in Human Skin
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- The Two Functional Keratin 6 Genes of Mouse Are Differentially Regulated and Evolved Independently from Their Human Orthologs
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Stem cells in embryonic skin development
- Multi-potentiality of a new immortalized epithelial stem cell line derived from human hair follicles
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells