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Research 181–210 of 815
- Severe cutaneous adverse reactions to drugs
- Wnt Signaling in Skin Development, Homeostasis, and Disease
- Roles for Msx and Dlx homeoproteins in vertebrate development
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- Biology and Genetics of Hair
- Learning from nudity: lessons from the nude phenotype
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- Safety of testosterone treatment in postmenopausal women
- What causes hidradenitis suppurativa ?—15 years after
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Zinc as an ambivalent but potent modulator of murine hair growth in vivo- preliminary observations
- The Inflammatory Caspases-1 and -11 Mediate the Pathogenesis of Dermatitis in Sharpin-Deficient Mice
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Nonclassic adrenal hyperplasia
- 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
- Characteristics of Men Who Report Persistent Sexual Symptoms After Finasteride Use for Hair Loss
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Primary cicatricial alopecia: Recent advances in understanding and management
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Congenital hair loss disorders: Rare, but not too rare
- Morphological Approach to Hair Disorders
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Trichoscopy in Hair Shaft Disorders