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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 reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

Oral itraconazole effectively reaches and treats deep skin layers in guinea pigs.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Ishige sinicola extract may help prevent muscle atrophy through its antioxidant and anti-inflammatory effects.

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Four antibodies were developed to help study hair follicle cell differentiation.

The method greatly improves low-light sports images' quality and reduces artifacts.

MK-5108 is safe and shows potential against tumors, especially alone.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

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Activating liver X receptors can reduce fibrosis by stopping certain immune cells from releasing harmful proteins.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

The MIRA technique improves cellulite treatment and skin quality better than standard methods.

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The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

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AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

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Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

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Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Serum IMA levels may be linked to premature hair graying and erectile dysfunction.