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Research 151–180 of 1000+
- Main Plenary Sessions: Summaries of Papers
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Oncogenes and morphogens: intricacies of targeted therapy in cutaneous basal cell carcinoma
- Harmless Herbs? A Review of the Recent Literature
- Development of a Chitosan Nanofibrillar Scaffold for Skin Repair and Regeneration
- Antioxidants in dermatology
- Plasticity and Cytokinetic Dynamics of the Hair Follicle Mesenchyme During the Hair Growth Cycle: Implications for Growth Control and Hair Follicle Transformations
- Prevalence of Skin Conditions Among Pediatric Patients in the Region of Istanbul
- Modulating testosterone pathway: a new strategy to tackle male skin aging?
- Clinical Management in Psychodermatology
- British Society for Dermatopathology: Summaries of Papers
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Learning from nudity: lessons from the nude phenotype
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Alopecia areata: An update
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- 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
- Autoimmunity and autoimmune co-morbidities in psoriasis
- 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
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- 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
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- The Clinical Presentation of Systemic Lupus Erythematosus