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Research 871–900 of 1000+
- LPA-producing enzyme PA-PLA<sub>1</sub>α regulates hair follicle development by modulating EGFR signalling
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Advances in the human skin microbiota and its roles in cutaneous diseases
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Insulin-like growth factor 1 and hair growth
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Dermal papilla-induced hair differentiation of adult epithelial stem cells from human skin
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Metabolites from Macroalgae and Its Applications in the Cosmetic Industry: A Circular Economy Approach
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Pharmacologic interventions in aging hair
- Aging of the hair follicle pigmentation system
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- Progressive Alopecia Reveals Decreasing Stem Cell Activation Probability during Aging of Mice with Epidermal Deletion of DNA Methyltransferase 1
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Nanocarriers as Active Ingredients Enhancers in the Cosmetic Industry—The European and North America Regulation Challenges
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Augmenting Endogenous Wnt Signaling Improves Skin Wound Healing
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Cylindroma as Tumor of Hair Follicle Origin
- Comparative Anatomy of Mouse and Human Nail Units
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Endogenous retinoids in the hair follicle and sebaceous gland
- Defining Hair Follicles in the Age of Stem Cell Bioengineering
- Changing the shape of hair with keratin peptides
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality