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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Shorter GGN repeats in the androgen receptor gene are linked to androgenetic alopecia.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

The rs1128977 gene variant may affect cholesterol and body measurements.

Key genes and pathways influence wool traits in Merino sheep.

SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

A new therapy for a skin blistering condition has not been developed yet.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

BMAL1 and Period1 genes can influence human hair growth.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Genetic differences affect breast cancer treatment success with tamoxifen in South African patients.

Certain genes influence immunoglobulin levels in Chinese Holstein cows, which can improve calf health.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.