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Research 481–510 of 1000+
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- The cutaneous serotoninergic/melatoninergic system: securing a place under the sun
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- The Catalog of Human Hair Keratins
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Biotin and biotinidase deficiency
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Learning from nudity: lessons from the nude phenotype
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Dermatologic Manifestations of Polycystic Ovary Syndrome
- Androgens and Female Sexual Function and Dysfunction—Findings From the Fourth International Consultation of Sexual Medicine
- 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
- New clinico‐genetic classification of trichothiodystrophy
- Nonclassic adrenal hyperplasia
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Characteristics of Men Who Report Persistent Sexual Symptoms After Finasteride Use for Hair Loss
- Newly Developed Targeted Therapies Against the Androgen Receptor in Triple-Negative Breast Cancer: A Review
- CRISPR/Cas9‐mediated loss of FGF5 function increases wool staple length in sheep
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Androgen modulation of Wnt/β-catenin signaling in androgenetic alopecia
- Identification of the Key Genes Associated with Different Hair Types in the Inner Mongolia Cashmere Goat
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype