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An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Different keratins have unique expression patterns in mouse skin cells.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

The MTR gene affects wool quality and production in Chinese Merino sheep.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

A new gene, JMJD1C, may affect testosterone levels in men.

Finasteride may help reduce COVID-19 infection by altering a key gene.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.

Prostaglandin D2 blocks new hair growth after skin injury through the Gpr44 receptor.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

20(S)-Protopanaxadiol-aglycone may help prevent and treat prostate cancer by reducing androgen receptor activity.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

TRPV3 gene mutations cause Olmsted syndrome symptoms, but severity varies.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Reduced AR gene methylation may cause early pubic hair growth in girls.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Human hair follicles contain a complex network of prostanoid receptors that may influence hair growth.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

SRD5A1 is crucial in advanced prostate cancer, and blocking both SRD5A1 and SRD5A2 is more effective than targeting SRD5A2 alone.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Certain gene variants are linked to severe acne, especially in males.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.