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Research 121–150 of 1000+
- The Study on Biological Function of Keratin 26, a Novel Member of Liaoning Cashmere Goat Keratin Gene Family
- The New Keratin Nomenclature
- Advances in molecular pathogenesis of hidradenitis suppurativa: Dysregulated keratins and ECM signaling
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Co-option of Hair Follicle Keratins into Amelogenesis Is Associated with the Evolution of Prismatic Enamel: A Hypothesis
- Keratin biomaterials for wound healing and tissue regeneration: A promising approach in biomedical applications
- Human epithelial hair follicle stem cells and their progeny: Current state of knowledge, the widening gap in translational research and future challenges
- Thyroxine (T4) may promote re-epithelialisation and angiogenesis in wounded human skin ex vivo
- The remarkable legacy of the K6/ODC mouse: mechanisms of polyamine-promoted tumorigenesis revealed
- Biology and Genetics of Hair
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- 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
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Increased rate of hair keratin gene loss in the cetacean lineage
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Assessment of markers expressed in human hair follicles according to different skin regions
- K6/ODC transgenic mice as a sensitive model for carcinogen identification
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- The molecular basis of human keratin disorders
- The HOXC13-controlled expression of early hair keratin genes in the human hair follicle does not involve TALE proteins MEIS and PREP as cofactors
- Delayed epidermal permeability barrier formation and hair follicle aberrations in Inv-Cldn6 mice
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Transdifferentiation of corneal epithelium into epidermis occurs by means of a multistep process triggered by dermal developmental signals
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo
- Spermidine Promotes Human Hair Growth and Is a Novel Modulator of Human Epithelial Stem Cell Functions