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Research 331–360 of 1000+
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Learning from nudity: lessons from the nude phenotype
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Alopecia areata: An update
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic adrenal hyperplasia
- Nonclassic Congenital Adrenal Hyperplasia
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- De Novo Production of Dermal Papilla Cells during the Anagen Phase of the Hair Cycle
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Human Hair Follicle Stem/Progenitor Cells Express Hypoxia Markers
- The Clinical Presentation of Systemic Lupus Erythematosus
- Nonclassic congenital adrenal hyperplasia
- Tumor Necrosis Factor-Alpha and Polycystic Ovarian Syndrome: A Clinical, Biochemical, and Molecular Genetic Study
- Genome-wide association study of skin complex diseases
- Effect of the Polymorphisms of Keratin Associated Protein 8.2 Gene on Fibre Traits in Inner Mongolia Cashmere Goats
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation