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Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

GATA6 is important for maintaining and differentiating cells in a key area of human skin.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

IL-25 helps heal diabetic wounds by improving blood vessel and skin cell functions.

Blocking IL-12/IL-23 does not help with hair loss in alopecia areata for mice or humans.

Blocking LFA-1 prevents hair loss in mice.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

A specific genetic deletion in goats affects cashmere yield and thickness.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

IL-9/IL-9R signaling can negatively affect human hair growth and may be a target for treating hair loss conditions.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

ASLNC168501 may help treat hair loss by boosting hair follicle stem cell activity.

Targeting the IL-23/IL-17 pathway effectively treats several inflammatory skin diseases.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Higher Interleukin 17A levels may indicate more severe alopecia areata.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Patients with alopecia areata have higher levels of certain immune markers, suggesting new treatment targets.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

Certain gene variations may increase the risk and severity of alopecia areata.

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