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Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A mother and daughter with similar hair loss conditions and identical HLA types suggest a genetic link between the conditions.

New genetic locations explain much of hair color variation in Europeans.

A new tool allows easier long-term imaging of live skin cells, helping study diseases like skin cancer.

Chemotherapy caused nail grooves and separation, but they healed after treatment stopped.

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

OCIAD2 and DCN genes affect hair growth in goats by having opposite effects on a growth signaling pathway and inhibiting each other.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Fluphenazine and iloprost can induce hair growth.

Only skin melanocytes, not other types, can color hair in mice.

Combining cell conditioning with mild protease digestion effectively shows versican mRNA in mouse skin sections.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Genetically modified cells improved skin wound healing in rats.

Researchers created five new human scalp cell lines that could be useful for hair growth and loss research.

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

A new mutation in mice causes crooked whiskers and messy hair.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Hoxc13 and hair keratin are needed for forming rough skin on frog mating pads.

Activating the sonic hedgehog pathway in chicken embryos can permanently change scales to feathers.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.