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Research 631–660 of 1000+
- Nanomaterials in hair care and treatment
- Alopecia areata is driven by cytotoxic T lymphocytes and is reversed by JAK inhibition
- Directed elimination of senescent cells by inhibition of BCL-W and BCL-XL
- Long-term renewal of hair follicles from clonogenic multipotent stem cells
- Hair follicle–derived IL-7 and IL-15 mediate skin-resident memory T cell homeostasis and lymphoma
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Homeostatic Control of Sebaceous Glands by Innate Lymphoid Cells Regulates Commensal Bacteria Equilibrium
- Androgen Signaling Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- FGF5 is a crucial regulator of hair length in humans
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Ultrasound-assisted extraction and analysis of maidenhairtree polysaccharides
- Ontogenetic Transition in Fetal Wound Transforming Growth Factor-β Regulation Correlates with Collagen Organization
- Androgen receptor–mediated inhibition of cutaneous wound healing
- A slow-cycling LGR5 tumour population mediates basal cell carcinoma relapse after therapy
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Genetic Ablation of the <i>CDP/Cux</i> Protein C Terminus Results in Hair Cycle Defects and Reduced Male Fertility
- Hypothalamic–Pituitary–Thyroid Axis Hormones Stimulate Mitochondrial Function and Biogenesis in Human Hair Follicles
- Visualising Androgen Receptor Activity in Male and Female Mice
- Syndecan-1 Is Required to Maintain Intradermal Fat and Prevent Cold Stress
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- The Cutaneous Inflammatory Response to Thermal Burn Injury in a Murine Model
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis