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- The role of mutations on gene AR, in androgenetic alopecia syndrome
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- Sequence of the intron/exon junctions of the coding region of the human androgen receptor gene and identification of a point mutation in a family with complete androgen insensitivity.
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- The Molecular Basis of Androgen Insensitivity
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Modulation of Androgen Receptor Transcriptional Activity
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.
- Novel Missense Mutation in the P-Box of Androgen Receptor in a Patient with Androgen Insensitivity Syndrome
- A Theoretical Model for the Treatment of Androgenetic Alopecia Using the STEAP3 Protein, and the Genetic Challenges of Treating AGA
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- This Month in the Journal
- Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer
- Finding bald spots on chromosome 20p11
- Molecular mechanisms of androgen receptor functions
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Disorders linked to insufficient androgen action in male children
- Disorders linked to insufficient androgen action in male children
- Skin Development and Disease: A Molecular Perspective
- Non-canonical dimerization of the androgen receptor and other nuclear receptors: implications for human disease
- Androgen receptors and their biology