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Research 31–60 of 1000+
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Keratin expression by corneal and limbal stem cells during development
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Keratin 6A promotes skin inflammation through JAK1-STAT3 activation in keratinocytes
- Building Models for Keratin Disorders
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Keratin 15 promotes a progenitor cell state in basal keratinocytes of skin epidermis
- The genetic basis of dermatophytosis skin infection susceptibility
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Multifaceted role of keratins in epithelial cell differentiation and transformation
- Crosstalk between vimentin and keratins in viral infection: Implications across the viral life cycle
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- The molecular basis of human keratin disorders
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Human iPS Cell-Derived Cell Aggregates Exhibited Dermal Papilla Cell Properties in in vitro Three-Dimensional Assemblage Mimicking Hair Follicle Structures
- A newborn presenting with congenital blistering
- Molecular Regulation of Secondary Hair Follicle Stem Cell by S100a4 in Cashmere Goat
- Assessing protein sequencing in human single hair shafts of decreasing lengths
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures
- Single-cell transcriptomics defines keratinocyte differentiation in avian scutate scales
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation