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CD28 is a promising target for treating alopecia areata with belatacept.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

People with rheumatoid arthritis have a higher risk of developing alopecia areata.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

Certain gene variations may increase the risk of hair loss in Egyptians.

Donor lymphocyte infusions effectively treated leukemia relapse but caused vitiligo and alopecia areata.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

CD25+ CD4+ Tregs and certain plasma proteins are linked to hair loss.

Higher PD-1 levels mean fewer CD8+ T cells in alopecia areata hair follicles.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Researchers found a genetic region that influences the number of coat layers in dogs.

Mutations in the LIPH gene cause woolly hair in a child.

A specific gene mutation causes a severe skin disorder in a family.

A mouse gene mutation increases the risk of skin cancer.

Higher PD-1 levels are linked to fewer immune cells in hair follicles in alopecia areata.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

CD2 might be a new treatment target for patchy alopecia areata.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Atopic dermatitis increases the risk of some autoimmune diseases.

Higher levels of PD-L1 are linked to more severe hair loss in people with Alopecia Areata.