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Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Variation in the TCHH gene affects wool curliness in sheep.

A specific gene mutation causes woolly hair and hair loss.

Spt4 and Spt6 are essential for fat cell development.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

GBP1 is a key target for treating Epstein-Barr virus-related kidney cancer, and finasteride may help.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Heat shock protein 27 is more present in the active growth phase of human scalp hair follicles.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

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

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Phospholipase Cδ1 is crucial for normal skin and hair development.

Certain gene variations may increase the risk of PCOS in South Indian women.

Genetic variants in specific genes cause a type of hair loss.

Mutations in the SNRPE gene cause hereditary hair loss.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The CTLA-4 gene change studied does not affect Polycystic Ovarian Syndrome in the women tested.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.