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Research 781–810 of 1000+
- Keratin 15 Expression in Stratified Epithelia: Downregulation in Activated Keratinocytes
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Probing the Effects of Stress Mediators on the Human Hair Follicle
- Sic Transit Gloria: Farewell to the Epidermal Transit Amplifying Cell?
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Agouti and Agouti-related Protein: Analogies and Contrasts
- Insulin Sensitizers for the Treatment of Hirsutism: A Systematic Review and Metaanalyses of Randomized Controlled Trials
- Localization, Age- and Site-Dependent Expression, and Regulation of 11β-Hydroxysteroid Dehydrogenase Type 1 in Skin
- Fluorescence Microscopy—An Outline of Hardware, Biological Handling, and Fluorophore Considerations
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Minoxidil: a review of its pharmacological properties and therapeutic use.
- Physiological and biological skin changes in pregnancy
- Environmental Air Pollutants Affecting Skin Functions with Systemic Implications
- Beyond Expectations
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Causes and Management of Hypertrichosis
- Conserved γδ T cell selection by BTNL proteins limits progression of human inflammatory bowel disease
- Functional Interpretation of Genome-Wide Association Study Evidence in Alopecia Areata
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis
- SARS‐CoV‐2‐induced telogen effluvium: a multicentric study
- Genetic predictors of testosterone and their associations with cardiovascular disease and risk factors: A Mendelian randomization investigation
- BLIMP1 Is Required for Postnatal Epidermal Homeostasis but Does Not Define a Sebaceous Gland Progenitor under Steady-State Conditions
- Use of low-level laser therapy as monotherapy or concomitant therapy for male and female Androgenetic alopecia
- Combinatorial Therapy of Letrozole- and Quercetin-Loaded Spanlastics for Enhanced Cytotoxicity against MCF-7 Breast Cancer Cells
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Keratin intermediate filaments in the colon: guardians of epithelial homeostasis
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes