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Research 301–330 of 1000+
- Assessment of the usefulness of dihydrotestosterone in the diagnostics of patients with androgenetic alopecia
- The Basic Science of Hair Biology
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Cicatricial Alopecia Research Foundation meeting, May 2016: Progress towards the diagnosis, treatment and cure of primary cicatricial alopecias
- Genetic basis of polycystic ovary syndrome
- Hirsutism in the Adolescent Female
- Dermatologic manifestations of endocrine disorders
- Inherited Disorders of the Hair
- A Review and Meta-Analysis of the Prevalence and Health Impact of Polycystic Ovary Syndrome Among Medical and Dental Students
- Primary cicatricial alopecias
- Premature Hair Graying: Underlying Contributors and Management Approaches - An Updated Literature Review
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Hair Loss in Children
- Syndromes of Severe Insulin Resistance (SSIRs)
- Insulin Resistance and Polycystic Ovary Syndrome
- Disorders of hair in children
- Cutaneous signals of immune system disease
- Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study
- Polycystic ovary syndrome
- Transforming growth factor-β in stem cells and tissue homeostasis
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A matter of life and death: self‐renewal in stem cells
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Ferreting out stem cells from their niches
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Female Pattern Hair Loss
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- The Polycystic Ovary Syndrome Evolutionary Paradox: a Genome-Wide Association Studies–Based, in silico, Evolutionary Explanation