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Research 31–60 of 1000+
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- The Role of Histone Demethylases in Disease
- Skin Penetration and Permeation Properties of Transcutol® in Complex Formulations
- Understanding Microemulsions and Nanoemulsions in (Trans)Dermal Delivery
- 3D bioprinting of hepatocyte-derived exosome-reinforced skin organoid for efficient skin regeneration
- Molecular Genetics of Human Hair Diseases
- Topical and transdermal lipid-polymer hybrid nanoparticles (LPN): an integration in advancing dermatological treatments
- Applications of Tea (Camellia sinensis) and its Active Constituents in Cosmetics
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- Self‐organizing hair peg‐like structures from dissociated skin progenitor cells: New insights for human hair follicle organoid engineering and Turing patterning in an asymmetric morphogenetic field
- Exosomes in Aesthetic Medicine: An Overview
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- Modulation of Vitamin D Receptor Activity by the Corepressor Hairless: Differential Effects of Hairless Isoforms
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- Emulgel: A Novel Approach For Hydrophobic Drugs
- Relative uptake of minoxidil into appendages and stratum corneum and permeation through human skin in vitro
- A review on: Herbal hair gel preparation and evaluation
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Cold thermal injury from cold caps used for the prevention of chemotherapy-induced alopecia
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Prostaglandin-Induced Hair Growth
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Relation of Skin Polyamines to the Hairless Phenotype in Transgenic Mice Overexpressing Spermidine/Spermine N1-Acetyltransferase
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia