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Alopecia areata involves persistent gene abnormalities and immune activity, even in regrown hair, suggesting a risk of relapse.

Researchers found four genes that could help diagnose severe alopecia areata early.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The ASIP gene is crucial for determining cattle coat color.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

The PP2A-B55α protein is essential for brain and skin development in embryos.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

The 4C32 gene may help in mouse skin development and differentiation.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

The fuzzy gene is crucial for controlling hair growth cycles.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The protein CTCF is essential for skin development, maintaining hair follicles, and preventing inflammation.

Two gene areas linked to male pattern baldness found, more research needed.

Certain gene variations increase the risk of alopecia areata in Koreans.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

DNAJB9 cfRNA could help diagnose and treat female hair loss.