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Research 571–600 of 1000+
- The proteomics of keratin proteins
- Application of PCR Technique to Detect Polymorphism of the KRTAP1.1 Gene in Three Sheep Breeds - A Review
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Keratin 6A promotes skin inflammation through JAK1-STAT3 activation in keratinocytes
- Comparative Gene Expression Profiling of Senescent and Androgenetic Alopecia Using Microarray Analysis
- Co-option of Hair Follicle Keratins into Amelogenesis Is Associated with the Evolution of Prismatic Enamel: A Hypothesis
- Characterisation of Three Ovine KRTAP13 Family Genes and Their Association with Wool Traits in Chinese Tan Sheep
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Bioinformatic analysis of gene expression data reveals Src family protein tyrosine kinases as key players in androgenetic alopecia
- Ultrastructural localization of hair keratins, high sulfur keratin-associated proteins and sulfhydryl oxidase in the human hair
- Biochemical and immunohistochemical analyses of keratin expression in basal cell carcinoma
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Adsorption of Diclofenac and PFBS on a Hair Keratin Dimer
- The molecular basis of human keratin disorders
- Vibrissa hair bulge houses two populations of skin epithelial stem cells distinct by their keratin profile
- Hard Keratin IF and Associated Proteins
- Structural Hierarchy of Trichocyte Keratin Intermediate Filaments
- Construction of a cDNA library and identification of genes from Liaoning cashmere goat
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Type XVII collagen coordinates proliferation in the interfollicular epidermis
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Control of hair follicle cell fate by underlying mesenchyme through a CSL–Wnt5a–FoxN1 regulatory axis
- Cell Type-specific Functions of the Lysosomal Protease Cathepsin L in the Heart
- Localization of Plasminogen Activator Inhibitor Type 2 (PAI-2) in Hair and Nail: Implications for Terminal Differentiation
- The nude gene and the skin