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- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- The role of the androgen receptor gene CAG repeat polymorphism and X-chromosome inactivation pattern in postmenopausal female pattern hair loss
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Immune mechanisms associated with sex-based differences in severe COVID-19 clinical outcomes
- Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- British Society for Dermatopathology
- Androgenetic Alopecia in Men: An Update On Genetics
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- SEXUAL DIMORPHISM IN MAMMALS
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Androgen receptors and their biology
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Molecular basis of androgen insensitivity
- Sex- or Gender-specific Differences in the Clinical Presentation, Outcome, and Treatment of SARS-CoV-2
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Xenobiotica-metabolizing enzymes in the skin of rat, mouse, pig, guinea pig, man, and in human skin models
- Krt6a-Cre Transgenic Mice Direct LoxP-Mediated Recombination to the Companion Cell Layer of the Hair Follicle and Following Induction by Retinoic Acid to the Interfollicular Epidermis
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Steroid Biomarkers and Genetic Studies Reveal Inactivating Mutations in Hexose-6-Phosphate Dehydrogenase in Patients with Cortisone Reductase Deficiency
- Roles of steroid sulfatase in brain and other tissues
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese