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Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

Machine learning can predict how well patients with alopecia areata will respond to certain treatments.

CD4 T cells can cause alopecia areata by activating CD8 T cells to attack hair follicles.

Hair follicles help attract immune cells to minor skin injuries.

Alopecia areata involves immune system changes, especially in severe cases, with potential new treatment targets identified.

An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

A mutation in the human hairless gene causes alopecia universalis.

Hair testing is crucial for forensic science and public health.

Human hair keratins were cataloged, showing their roles in hair differentiation stages.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.

Topical immunotherapy for alopecia areata may work by creating immune cell clusters in the skin.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

Recent selection on immune response genes was identified across seven ethnicities.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

Alopecia areata involves unique activation of certain immune cells.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Human TMEM2 does not break down hyaluronan but helps control its metabolism.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

CD4 T cells need IFN-γ to cause hair loss in alopecia areata.

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

Alopecia areata severity is linked to increased TH1 and TH2 activity.

Different keratins have unique expression patterns in mouse skin cells.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.