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A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Noncoding dsRNA boosts hair growth by activating TLR3 and increasing retinoic acid.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Bcl-2 overexpression protects against UVB damage but worsens hair loss from chemotherapy.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

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

Researchers developed a 3D model of human hair follicle cells that can help understand hair growth and test new hair loss treatments.