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Research 61–90 of 1000+
- Topical Delivery of Protein and Peptide Using Novel Cell Penetrating Peptide IMT-P8
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Protein Kinase C<i>ε</i>, Which Is Linked to Ultraviolet Radiation-Induced Development of Squamous Cell Carcinomas, Stimulates Rapid Turnover of Adult Hair Follicle Stem Cells
- Protein kinase C is a key target for attenuation of Leigh syndrome by rapamycin
- Evaluation and formulation of Spirulina platensis proteins for potential applications in hair care products
- A Review: Proteins Involved in the Major Symptoms of Polycystic Ovarian Syndrome
- Ginsenoside F2 Reduces Hair Loss by Controlling Apoptosis through the Sterol Regulatory Element-Binding Protein Cleavage Activating Protein and Transforming Growth Factor-β Pathways in a Dihydrotestosterone-Induced Mouse Model
- Paracrine Secreted Frizzled-Related Protein 4 Inhibits Melanocytes Differentiation in Hair Follicle
- Advances in Aesthetic Therapies: Plasma-Rich Protein Procedure for the Treatment of Alopecia
- Combination of media, biomaterials and extracellular matrix proteins to enhance the differentiation of neural stem/precursor cells into neurons
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- Variation in the Exon 3–4 Region of Ovine KRT85 and Its Effect on Wool Traits
- Biology and Genetics of Hair
- Congenital hair loss disorders: Rare, but not too rare
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Molecular Genetics of Alopecias
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Wnt signaling in skin organogenesis
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Morphological Approach to Hair Disorders
- Expression of an Olfactomedin-Related Gene in Rat Hair Follicular Papilla Cells
- Ultrastructural localization of hair keratins, high sulfur keratin-associated proteins and sulfhydryl oxidase in the human hair
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Disease causing homozygous variants in the human hairless gene
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions