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Research 511–540 of 1000+
- Obstructive sleep apnea, low transferrin saturation levels, and male‐pattern baldness
- Evaluation and treatment of male and female pattern hair loss
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Prediction of male-pattern baldness from genotypes
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Long-term treatment with finasteride 1 mg decreases the likelihood of developing further visible hair loss in men with androgenetic alopecia (male pattern hair loss).
- Hair regrowth in a male patient with extensive androgenetic alopecia on estrogen therapy
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- Effects of <i>In Utero</i> Exposure to D-004, a Lipid Extract from <i>Roystonea regia</i> Fruits, in the Male Rat: A Comparison with Finasteride
- HuR ablation destabilizes Foxp3 mRNA and impairs regulatory T cell function, contributing to an autoimmune phenotype
- Scalp microbiome in male androgenetic alopecia: 16S rRNA sequencing-based clinical characterization, mouse model validation, and effects on hair follicle cells
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- 643 Male pattern baldness and risk of incident skin cancer in a cohort of men
- Male pattern hair loss: Taking one for the team: The selfless gene
- Can male-pattern baldness be prevented?
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Physiological analysis of Iraqi male patients with hair loss: A cross-sectional study
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- A review of the treatment of male pattern hair loss
- Antioxidant enzyme expression of mRNA and protein in the epididymis of finasteride-treated male rat offspring during postnatal development
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Potential genetic associations of acne scar phenotypes: IL1A in fibrotic scarring and CYB5R1 in atrophic scarring
- Physiology of the Hypothalamic Pituitary Gonadal Axis in the Male
- Transient mitochondrial DNA double strand breaks in mice cause accelerated aging phenotypes in a ROS-dependent but p53/p21-independent manner