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Research 301–330 of 1000+
- Lymphoid Enhancer-binding Factor-1 (LEF1) Interacts with the DNA-binding Domain of the Vitamin D Receptor
- Aromatase deficiency in a male patient - Case report and review of the literature.
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Systematic Analysis of Non-coding RNAs Involved in the Angora Rabbit (Oryctolagus cuniculus) Hair Follicle Cycle by RNA Sequencing
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Androgen Receptor Accelerates Premature Senescence of Human Dermal Papilla Cells in Association with DNA Damage
- Hairless is a nuclear receptor corepressor essential for skin function
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Genetic Fate Mapping Using Site-Specific Recombinases
- Parkinson's disease and skin
- The ITGB6 gene: its role in experimental and clinical biology
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Field Cancerization: From Molecular Basis to Selective Field-Directed Management of Actinic Keratosis
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Activation of β-Catenin Signaling in CD133-Positive Dermal Papilla Cells Drives Postnatal Hair Growth
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Biochemistry of epidermal stem cells
- Congenital adrenal hyperplasia
- The hair follicle enigma
- Stem cells and aberrant signaling of molecular systems in skin aging
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Comparative transcriptomic analysis of dermal wound healing reveals de novo skeletal muscle regeneration in Acomys cahirinus
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The Genetics of Human Skin Disease
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep