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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.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

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.

Lung repair involves both dedicated and flexible stem cells, important for developing new treatments.

New genes found linked to balding, may help develop future treatments.

Plant steroid hormones show growth, health, and medicinal benefits in various organisms, including potential for treating diseases.

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.

FLRG and follistatin have different roles in wound healing.

Some natural compounds may help overcome drug resistance in certain cancers, but more research is needed.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

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

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Genetic variations affecting skin structure play a key role in severe acne.

Hoxc genes control hair growth through Wnt signaling.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Certain metabolites are lower in women with PCOS and could be potential markers for the condition.

A blood pressure drug, diltiazem, may also help treat influenza.

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Damaging mitochondrial DNA in mice speeds up aging due to increased reactive oxygen species, not through the p53/p21 pathway.

FGF5s can block the effects of FGF5, which may help control hair growth in cashmere goats.