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Research 61–90 of 1000+
- Transcriptomics analysis reveals molecular alterations underpinning spaceflight dermatology
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Detecting the Mechanism behind the Transition from Fixed Two-Dimensional Patterned Sika Deer (Cervus nippon) Dermal Papilla Cells to Three-Dimensional Pattern
- Clinical, Dermoscopic and In-Vivo Reflectance Confocal Microscopy Evaluation of a Case of Graham Little-Piccardi-Lassueur Syndrome Successfully Treated with Narrowband-UVB Phototherapy
- Causality of Aging Hallmarks
- Androgenic Alopecia: Cross-Talk Between Cell Signal Transduction Pathways
- IL-17a induces age-related olfactory dysfunction by impairing regeneration and promoting respiratory metaplasia in mice
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Evidence-Based and Potential Benefits of Metformin in the Polycystic Ovary Syndrome: A Comprehensive Review
- Health and fertility in World Health Organization group 2 anovulatory women
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- KIF18B is a cell-type specific regulator of spindle orientation in the epidermis
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- 9 Role of 5α-reductase in health and disease
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Biology and Genetics of Hair
- Physiologic functions of PP2A: Lessons from genetically modified mice
- Trans‐species hair growth induction by human hair follicle dermal papillae
- COVID-19: Understanding Inter-Individual Variability and Implications for Precision Medicine
- 46,XY DSD due to impaired androgen production
- Genome-wide association study of skin complex diseases
- The Genetics of Human Skin Disease
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Epigenetic regulation in adult stem cells and cancers
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence