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A new genetic tool improves the study of hair growth and potential hair disorder treatments.

ERULUS is crucial for root hair growth by controlling calcium levels.

Clinicians should consider individual factors and communicate risks and benefits when prescribing ritlecitinib for adolescent alopecia areata.

Ritlecitinib effectively promotes hair regrowth in severe and very severe alopecia areata.

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

QR678 treatments were more effective and comfortable for male hair loss than PRP treatments.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

Botryococcus braunii's three chemical races should be reclassified as separate species.

B-type hairs on female butterfly legs help them choose where to lay eggs.

The study found that urine metabolites M1b or M4 are the best indicators of ATD use in horses, with detection possible up to 77 hours in urine and 28 hours in blood.

Ginsenoside Rb1 slows down aging in mice by affecting cell growth, cell death, and metabolism.

A new test helps find drugs to treat head and neck cancer by targeting c-Rel.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Recipient site necrosis is a rare but serious complication of hair transplants, often linked to smoking, diabetes, and hypertension.

Rac1 is vital for hair follicle health but not needed for skin maintenance.

PRX102 is essential for rice root hair growth by helping transport substances to the tips.

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

HPV8 causes skin cancer by expanding specific skin stem cells.

Orai1 protein is crucial for tooth development and affects enamel thickness and mineralization.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with less inflammation.

TRPS1 is crucial for bone, kidney, and hair follicle development.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.