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Research 541–570 of 1000+
- An Integrated Transcriptome Atlas of Embryonic Hair Follicle Progenitors, Their Niche, and the Developing Skin
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Advances in the human skin microbiota and its roles in cutaneous diseases
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Metabolites from Macroalgae and Its Applications in the Cosmetic Industry: A Circular Economy Approach
- Pharmacologic interventions in aging hair
- Aging of the hair follicle pigmentation system
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Therapeutic strategy for hair regeneration: hair cycle activation, niche environment modulation, wound-induced follicle neogenesis, and stem cell engineering
- Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- Metal-Chelation-Assisted Deposition of Polydopamine on Human Hair: A Ready-to-Use Eumelanin-Based Hair Dyeing Methodology
- Notch Signaling Regulates Late-Stage Epidermal Differentiation and Maintains Postnatal Hair Cycle Homeostasis
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Comparative Anatomy of Mouse and Human Nail Units
- Skin Structure, Physiology, and Pathology in Topical and Transdermal Drug Delivery
- Hair care and hair care products
- S100A6: molecular function and biomarker role
- Vibrissa hair bulge houses two populations of skin epithelial stem cells distinct by their keratin profile
- Modulation of the differentiated phenotype of keratinocytes of the hair follicle and from epidermis
- Demodicosis in Different Age Groups and Alternative Treatment Options—A Review
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Current Advances of Nanocarrier Technology-Based Active Cosmetic Ingredients for Beauty Applications
- A systematic summary of survival and death signalling during the life of hair follicle stem cells
- Optimal processing for proteomic genotyping of single human hairs
- Gata6 promotes hair follicle progenitor cell renewal by genome maintenance during proliferation
- Expression and Function of Group IIE Phospholipase A2 in Mouse Skin
- Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration