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Research 31–60 of 83
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Inherited Epidermolysis Bullosa: A Clinical Case
- An Investigation of Hair and its Keratin Associated Proteins using Advanced Light Microscopy
- 1314 Advanced age impairs self-renewal and biases fate choice of hair follicle dermal stem cells
- 1315 An Integrated model of alopecia areata biomarkers highlights both Th1/Th2 upregulation, with stronger correlations between Th2 activation and disease severity
- 1312 Nrf2 activation enhances the healing of cutaneous wounds through the activation of hair follicle stem cells
- 1311 Efficacy of topical tofacitinib in promoting hair growth in non-scarring alopecia
- Epithelial–mesenchymal transition in cutaneous fibrosis disease: from mechanisms to therapy
- LITERATURE REVIEW
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Bidirectional binding property of high glycine–tyrosine keratin-associated protein contributes to the mechanical strength and shape of hair
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Birt–Hogg–Dubé syndrome
- Dysfunction of keratinocyte adhesion
- A desmosomal cadherin controls multipotent hair follicle stem cell quiescence and orchestrates regeneration through adhesion signaling
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Cell death by cornification
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Proteome Analysis of Human Hair Shaft
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Pemphigus Vulgaris IgG and Methylprednisolone Exhibit Reciprocal Effects on Keratinocytes
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Multifaceted role of keratins in epithelial cell differentiation and transformation
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis