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Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

ILC1-like cells can independently cause alopecia areata.

Interleukin‐1 α reduces androgen receptor levels and increases certain cytokines in human scalp cells.

A humanized IL-2 fusion protein boosts T regulatory cells and helps control hair loss in Alopecia Areata.

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

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Monilethrix is linked to a gene cluster on chromosome 12.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

The study suggested certain immune cells might cause alopecia areata, but it was retracted.

Expressing the human vitamin D receptor in skin cells prevents hair loss in certain mice.

Chronic graft-versus-host disease in the skin shows strong Th1 immune response and unique barrier issues.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Asthma may increase the risk of alopecia areata.

ILC1-like cells may contribute to hair loss in alopecia areata and could be new treatment targets.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Certain RNAs may help diagnose alopecia areata by affecting keratin genes.

Higher levels of CCL7 are linked to more severe hair loss in alopecia areata patients.

A genetic defect in vitamin D receptors causes severe rickets and hair loss in children, but some heal as they age.

The hedgehog signaling pathway is crucial for hair growth but not for the initial creation of hair follicles.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

ILC1-like cells may contribute to hair loss in alopecia areata.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

Oleanolic acid improved hair growth in mice by affecting hair growth pathways and reducing inflammation.

The hairless protein is important for skin, hair, and may influence cancer development.

Blocking LFA-1 prevents hair loss in mice.