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Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

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

A gene mutation causes curly hair and hair loss in rats.

Losing eyelashes or eyebrows can be a sign of many different health problems and needs a careful approach to treat effectively.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

ULBP3 could be a marker for diagnosing alopecia areata incognita and may be linked to its cause and development.

A certain gene variant may increase the risk of polycystic ovary syndrome in Chinese women.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

The N gene affects the protein makeup of mouse hair.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

The Cyp11a1 gene variation has a weak link to PCOS, but higher di-hydro-testosterone levels are found in PCOS patients.

CT60 polymorphism might increase the risk of Alopecia Areata.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The new compound was more effective than finasteride in reducing markers of hair loss and prostate issues in cell tests.

The rs1128977 gene variant may affect cholesterol and body measurements.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Polycystic ovarian shape is a genetic sign of PCOS and its hormonal and metabolic features can be inherited.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.