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NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

IL-1α levels are higher in alopecia areata patients, suggesting a role in the disease.

New mutations in the hairless gene may cause hair loss and affect bone development.

Blocking TYK2 might be a new way to treat hair loss from alopecia areata.

Blocking IL-17a can improve age-related smell loss in mice.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

IGN genes may regulate hair growth and could be targeted for hair-loss treatments.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

A KRT32 gene variant causes loose anagen hair syndrome.

People with alopecia areata have fewer IL-10 producing immune cells, which might contribute to the condition.

Two new gene mutations cause a rare hair disorder.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The conclusion is that the IL-6/STAT3 activation affects p63 expression in healing wounds, which may help in hair follicle regeneration.

A vitamin D receptor mutation causes rickets and affects immune responses.

The androgen receptor gene doesn't affect women with recurrent spontaneous abortions, but having a mutant genotype might protect against it.

Certain immune cells are linked to non-scarring hair loss, suggesting potential for immune-targeted treatments.

Tocilizumab therapy may cause skin and hair conditions like halo naevi, vitiligo, and alopecia areata.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Targeting Interleukin-13 could help treat alopecia areata linked with atopic dermatitis.