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- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Genetic, hormonal and metabolic aspects of PCOS: an update
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- The role of keratin proteins and their genes in the growth, structure and properties of hair
- Selective Modulation of Hedgehog/GLI Target Gene Expression by Epidermal Growth Factor Signaling in Human Keratinocytes
- Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Genetic Basis of Male Pattern Baldness
- Generic Development of Topical Dermatologic Products: Formulation Development, Process Development, and Testing of Topical Dermatologic Products
- Keratin gene mutations in disorders of human skin and its appendages
- Genetics of polycystic ovary syndrome: searching for the way out of the labyrinth
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Health-related quality of life in women with polycystic ovary syndrome: A comparison with the general population using the Polycystic Ovary Syndrome Questionnaire (PCOSQ) and the Short Form-36 (SF-36)
- Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair
- Genetic Disorders and Defects in Vitamin D Action
- Generalized Pustular Psoriasis
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Genetic prediction of male pattern baldness
- Genetic architecture of mouse skin inflammation and tumour susceptibility
- Vestibular Hair Cell Regeneration and Restoration of Balance Function Induced by Math1 Gene Transfer
- Genetically Altered Expression of Spermidine/Spermine N1-Acetyltransferase Affects Fat Metabolism in Mice via Acetyl-CoA
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- Gene Array Profiling and Immunomodulation Studies Define a Cell-Mediated Immune Response Underlying the Pathogenesis of Alopecia Areata in a Mouse Model and Humans
- Integument pattern formation involves genetic and epigenetic controls: feather arrays simulated by digital hormone models.
- Genetic basis of skin appendage development
- Genetically null mice reveal a central role for epidermal growth factor receptor in the differentiation of the hair follicle and normal hair development.