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Research 31–60 of 1000+
- A temperature-sensitive <i>FERONIA</i> mutant allele that alters root hair growth
- AtCSLD3 and GhCSLD3 mediate root growth and cell elongation downstream of the ethylene response pathway in Arabidopsis
- Overview of Caffeine Effects on Human Health and Emerging Delivery Strategies
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Coffea arabica: An Emerging Active Ingredient in Dermato-Cosmetic Applications
- Exploring the Versatility of Microemulsions in Cutaneous Drug Delivery: Opportunities and Challenges
- Diseases of Hair
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Diseases of Hair
- Human hair regeneration using organoids and hair-on-chip technologies
- Microneedle-Based Technologies for Long-Acting Transdermal Drug Delivery in Wearable Devices
- Exosome-based Therapies for Androgenetic Alopecia: Mechanisms, MicroRNAs, and Clinical Prospects
- Research Progress of Extracellular Vesicles-Loaded Microneedle Technology
- HairSentinel: a time-aware anomaly detection framework for forecasting hairfall trends using temporal fusion transformers
- Multiphoton microscopic imaging of <i>in vivo</i> hair mouse skin based on two‐photon excited fluorescence and second harmonic generation
- Biology of the Hair Follicle: The Basics
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- 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
- Towards Defining the Pathogenesis of the Hairless Phenotype
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- 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