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Research 91–120 of 1000+
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Exploring the Role of Tripeptides in Wound Healing and Skin Regeneration: A Comprehensive Review
- Structure-guided manipulation of the regioselectivity of the cyclosporine A hydroxylase CYP-sb21 from Sebekia benihana
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Somatic mutations distinguish melanocyte subpopulations in human skin
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Australasian Society for Dermatology Research Meeting, May 2007
- Vitamin D Receptor Gene Polymorphism In Chronic Telogen Effluvium; A Case-Control Study
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Alopecia Areata
- The Rotterdam Study: 2018 update on objectives, design and main results
- The Rotterdam Study: 2016 objectives and design update
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Acne, the Skin Microbiome, and Antibiotic Treatment
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Androgens and Female Sexual Function and Dysfunction—Findings From the Fourth International Consultation of Sexual Medicine
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- 5α-Reduced glucocorticoids: a story of natural selection
- A preliminary study of finasteride in Tourette syndrome
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders