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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Janus kinase inhibitors are promising treatments for autoimmune skin diseases like eczema and psoriasis.

ILC1-like cells can cause alopecia areata by themselves.

JAK inhibitors show promise for treating skin conditions like eczema, hair loss, and psoriasis.

Baricitinib successfully regrew hair in an 8-year-old boy with alopecia totalis linked to a KRT74 gene variant.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Targeting mitophagy may help treat alopecia areata by reducing inflammasome activation.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Ritlecitinib effectively treats severe Alopecia Areata by reducing harmful immune activity in the skin.

Double-stranded RNA causes inflammation in hair follicle cells, which may help understand and treat alopecia areata.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

People with Alopecia areata have higher levels of certain T regulatory cells in their blood.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

IL-1β inhibits human hair follicle growth.

KRT80 may worsen cancer by increasing growth and spread, but its full effects on treatment and outcomes need more research.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

AGD1's PH domain is essential for its role in root hair growth and polarity.

A gene mutation causes curly hair and hair loss in rats.

Caspase-1 helps hair stem cells move to heal wounded or inflamed skin.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

A gene mutation in mice causes skin defects and early death.

Two drugs, ritlecitinib and brepocitinib, improved scalp hair loss condition markers.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.