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Research 541–570 of 1000+
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Androgens/Androgen Receptor in the Management of Skin Diseases
- Adrenal and Gonadal Activity, Androgen Concentrations, and Adult Height Outcomes in Boys With Silver-Russell Syndrome
- A different approach to PCOS: evaluation of spermiogram results in male patients with a family history of PCOS
- Wokeness in Our Practice
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- The role of 5-α-reductase inhibition in supressing progression of male androgenetic alopecia − a postulate for further studies on possible application of saw palmetto extracts
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- The First Visit: Consult and Workup Before Sperm Banking
- Female Pattern Hair Loss
- Male reproductive health after 3 months from SARS-CoV-2 infection: a multicentric study
- Fertility evaluation of infertile women: a committee opinion
- A Comment on Coronavirus Disease 2019 and the Hair
- Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase
- Prioritizing susceptibility genes for the prognosis of male-pattern baldness with transcriptome-wide association study
- Hox genes in development and beyond
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Research gaps in medical treatment of transgender/nonbinary people
- Hair follicle-derived mesenchymal cells support undifferentiated growth of embryonic stem cells
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review
- Synopsis: 2005 Annual Meeting of the American Society of Andrology