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Research 151–180 of 1000+
- Enhancing hair regeneration: Recent progress in tailoring nano-structured lipid carriers through surface modification strategies
- A review on follicular targeting for the treatment of hirsutism
- An Investigation of Hair and its Keratin Associated Proteins using Advanced Light Microscopy
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Neovascularization during healing of wounds treated with dermal substitutes and fibrin glue in nude mice
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- Increased dipicolinic acid production with an enhanced <i>spoVF</i> operon in <i>Bacillus subtilis</i> and medium optimization
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- Identification of the cell lineage at the origin of basal cell carcinoma
- Advances of Non-Ionic Surfactant Vesicles (Niosomes) and Their Application in Drug Delivery
- Serotoninergic and melatoninergic systems are fully expressed in human skin
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- A new look into an old problem: keratins as tools to investigate determination, morphogenesis, and differentiation in skin.
- Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
- Hairless triggers reactivation of hair growth by promoting Wnt signaling
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Tissue Engineering and Regenerative Medicine: Achievements, Future, and Sustainability in Asia
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Hair follicle stem cell differentiation is inhibited through cross‐talk between Wnt/β‐catenin and androgen signalling in dermal papilla cells from patients with androgenetic alopecia
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Inhibition of skin 5α-reductase by oral contraceptive progestins<i>in vitro</i>
- Cell Types Promoting Goosebumps Form a Niche to Regulate Hair Follicle Stem Cells
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Exosomes and Their Bioengineering Strategies in the Cutaneous Wound Healing and Related Complications: Current Knowledge and Future Perspectives
- The Transcriptional Co-Activator cAMP Response Element-Binding Protein-Binding Protein Is Expressed in Prostate Cancer and Enhances Androgen- and Anti-Androgen-Induced Androgen Receptor Function