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Research 991–1000 of 1000+
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The molecular basis of human keratin disorders
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Hair Growth Promoting Effect of 4HGF Encapsulated with PGA Nanoparticles (PGA-4HGF) by β-Catenin Activation and Its Related Cell Cycle Molecules
- Construction of a cDNA library and identification of genes from Liaoning cashmere goat
- Regulation of Involucrin Gene Expression
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds