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Research 991–1000 of 1000+
- Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Venus trap in the mouse embryo reveals distinct molecular dynamics underlying specification of first embryonic lineages
- Genetic and molecular aspects of androgenetic alopecia
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Restoration of Spermatogenesis and Male Fertility Using an Androgen Receptor Transgene
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Efficacy of metformin therapy in adolescent girls with androgen excess: relation to sex hormone–binding globulin and androgen receptor polymorphisms
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome