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DHT deficiency may disrupt rat epididymis function by affecting estrogen receptors.

Activating TLR3 helps improve skin and hair follicle regeneration after wounds.

A genetic variant in the GJB6 gene likely caused the Labrador's paw pad condition.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

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

Mutations in the hairless protein gene cause hair loss.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

EDA2R gene linked to hair loss.

Gene linked to common hair loss found, may lead to new treatments.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Three new gene mutations cause rickets and hair loss, treatable with high calcium and calcidol, but hair regrowth is rare.

Patients with Discoid Lupus Erythematosus have lower vitamin D and antioxidant levels and higher oxidative stress.

p120-catenin helps control skin inflammation by regulating cadherin levels.

AGA patients have higher heart disease risk.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Damage to skin releases dsRNA, which activates TLR3 and helps in skin and hair follicle regeneration.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

LRIG1 is linked to better survival in Merkel cell carcinoma.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.

Clq deficiency is linked to systemic lupus erythematosus symptoms.