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Research 511–540 of 826
- <i>Hoxc13</i> mutant mice lack external hair
- Timing of expression of the core clock gene <i>Bmal1</i> influences its effects on aging and survival
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- A new classification of pattern hair loss that is universal for men and women: Basic and specific (BASP) classification
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milk
- 9 Role of 5α-reductase in health and disease
- Finasteride induced depression: a prospective study
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Endocrine Influences on Hair Growth
- Hair Follicle: A Novel Source of Multipotent Stem Cells for Tissue Engineering and Regenerative Medicine
- Hirsutism and the Variable Response of the Pilosebaceous Unit to Androgen
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Compliance With Contraceptives and Other Treatments
- Hair morphogenesis<i>in vitro</i>: formation of hair structures suitable for implantation
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Congenital hypotrichosis due to short anagen
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Skin and hair: models for exploring organ regeneration
- One of These Things Is Not Like the Others: The Idea of Precedence in Health Technology Assessment and Coverage Decisions
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Congenital adrenal hyperplasia
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- A comparative analysis of immune privilege in pregnancy and cancer in the context of checkpoint blockade immunotherapy
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Postpartum Alopecia
- Discovery of Natural Steroid 5 Alpha-Reductase Inhibitors