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Research 61–90 of 1000+
- The Mean Staple Length of Wool Fibre Is Associated with Variation in the Ovine Keratin-Associated Protein 21-2 Gene
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Current Genetics in Hair Diseases
- 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
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Gsdma3 is required for hair follicle differentiation in mice
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Papular atrichia
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- Genetics of Structural Hair Disorders
- Keratins: the hair shaft's backbone revealed
- Painful thickened skin on the soles of the feet
- Decay of Skin-Specific Gene Modules in Pangolins
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Biology and Genetics of Hair
- The hair shaft: normality, abnormality, and genetics
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Steatocystoma Multiplex
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Atrichia with papular lesions
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation