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Research 391–420 of 1000+
- Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Effects of KRTAP20-1 Gene Variation on Wool Traits in Chinese Tan Sheep
- Alopecia areata
- Clinical Snippets
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Is polycystic ovary syndrome a sexual conflict? A review
- The endocrinology of baldness
- Ovarian Hypertension: Polycystic Ovary Syndrome
- Temporal triangular alopecia and a review of 52 past cases
- Male fertility and skin diseases
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- INNOVATIVE APPROACH TO CRC PREVENTION: THE ROLE OF LOW-PENETRATION GENES
- Cardiovascular risk in patients with selected cutaneous diseases
- This Month in the Journal
- Exploring climate adaptation in European Merino sheep: a landscape genomics approach
- The role of CYP19A1 and ESR2 gene polymorphisms in female androgenetic alopecia in the Polish population
- Cosmeceutical Treatments for Androgenetic Alopecia
- Does zinc have a role in alopecia areata? A clinic-biochemical study
- A meta-analysis of the relationship between vitamin D receptor gene ApaI polymorphisms and polycystic ovary syndrome
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Sex hormones and acne
- Pathophysiology of vitiligo
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- A Pharmacogenetic Survey of Androgen Receptor (CAG)N and (GGN)N Polymorphisms in Patients Experiencing Long Term Side Effects after Finasteride Discontinuation
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Risk of autoimmune thyroid diseases in individuals with alopecia areata: A nationwide case‐control study