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RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Four new genes related to sheep wool were discovered, showing genetic diversity.

QR678 Neo® improved seborrheic dermatitis symptoms in a small group of patients.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

People were generally happy with the home light therapy devices for hair loss.

Ritlecitinib has common side effects like headache and acne, and unexpected ones like diabetes and thyroid issues.

A mutation in the IL2RA gene increases the risk of alopecia areata.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

The new particle system could be a promising treatment for diseases related to the 5-α reductase enzyme.

miR-200c-3p could help diagnose and treat alopecia areata.

Clinical trials for hair loss in the USA show differences in participation among different races and ethnic groups.

The GG genotype of the KRT71 gene leads to longer wool in Gansu alpine fine-wool sheep.

Ritlecitinib significantly improves scalp hair regrowth in alopecia areata patients over time.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

An allele of the KRTAP13-2 gene may improve wool quality in sheep.

Increased TEMRA cells can predict treatment outcomes in rapidly progressive alopecia areata.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Liposomes can make the antiandrogen RU 58841 more effective for skin application by reducing absorption, increasing skin retention, and targeting sebaceous structures.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

A medicine called tofacitinib worked to treat a hair loss condition linked with a muscle and skin disease.

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.