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Research 91–120 of 1000+
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Semidominant Inheritance in Epidermolytic Ichthyosis
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- 545 Skin Organoids derived from NCSTN mutated patient-induced pluripotent stem cells recapitulate Hidradenitis Suppurativa pathogenic hallmarks
- Gsdma3 is required for hair follicle differentiation in mice
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- Chromosomal Localization of Mouse Hair Keratin Genes<sup>a</sup>
- A newborn presenting with congenital blistering
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Painful thickened skin on the soles of the feet
- Congenital atrichia with papular lesions
- Papular atrichia
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Keratin 17 in disease pathogenesis: from cancer to dermatoses
- Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay
- Keratins: Dynamic, flexible structural proteins of epithelial cells
- ‘Hard’ and ‘soft’ principles defining the structure, function and regulation of keratin intermediate filaments
- Keratins: the hair shaft's backbone revealed
- The role of keratin proteins and their genes in the growth, structure and properties of hair
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Decay of Skin-Specific Gene Modules in Pangolins
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Convergent Decay of Skin-specific Gene Modules in Pangolins
- Clinical Snippets
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice