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Research 331–360 of 1000+
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Biology and Genetics of Hair
- SOX11 and SOX4 drive the reactivation of an embryonic gene program during murine wound repair
- Physiologic functions of PP2A: Lessons from genetically modified mice
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Inhibition of β-catenin signalling in dermal fibroblasts enhances hair follicle regeneration during wound healing
- FOXO1, TGF-β Regulation and Wound Healing
- Flares of systemic lupus erythematosus during pregnancy and the puerperium: prevention, diagnosis and management
- Female pattern hair loss
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- PAK4 signaling in health and disease: defining the PAK4–CREB axis
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Effects of 5-alpha reductase inhibitors on erectile function, sexual desire and ejaculation
- Beyond Expectations
- Replicative stress, stem cells and aging
- Prostaglandin D2 Inhibits Wound-Induced Hair Follicle Neogenesis through the Receptor, Gpr44
- Dermatoscopy of hair shaft disorders
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- The Paradox of p53: What, How, and Why?
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- The Inflammatory Caspases-1 and -11 Mediate the Pathogenesis of Dermatitis in Sharpin-Deficient Mice