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A new topical treatment may prevent hair loss from cancer therapy by adjusting cell death processes in hair follicles.

Activating TRPA1 reduces scarring and promotes tissue regeneration.

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

TCDD reduces EGF receptors in the liver, affecting growth and development.

Specific gene variants affect wool traits in Chinese Tan sheep.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

The treatment was not recommended due to limited effectiveness and significant side effects.

Targeting androgen receptors shows promise for treating triple-negative breast cancer, but more research is needed.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Tight hairstyles can cause a rare scalp condition with thick skin folds.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

High TSPEAR levels in colorectal cancer predict worse outcomes.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

The vitamin D receptor can regulate genes and affect hair and hormone levels without its usual activator.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Blocking IL-17 can reduce joint inflammation in Ross River Virus infections.

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

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Accurate diagnosis of rare scalp cancer requires combining clinical and radiological information.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

A gene variant causes a skin and hair disorder by disrupting protein balance.

New mutations in the hairless gene may cause hair loss and affect bone development.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.