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Research 631–660 of 1000+
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- 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
- 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
- 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
- Clonal Growth of Dermal Papilla Cells in Hydrogels Reveals Intrinsic Differences between Sox2-Positive and -Negative Cells In Vitro and In Vivo
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- ACNE
- Bacteria induce skin regeneration via IL-1β signaling
- How to diagnose a lipodystrophy syndrome
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- High proliferation and delamination during skin epidermal stratification
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Wnt signaling: the good and the bad
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Idiopathic Hirsutism*
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Interactions of the Vitamin D Receptor with the Corepressor Hairless