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The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

UVB radiation changes the levels of certain microRNAs in skin cells, which may affect cell survival and hair growth.

Intense Pulsed Light is an effective and safe hair removal method for people with excessive hair growth.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

Eruptive vellus hair cysts likely originate from the infrainfundibulum and sebaceous duct.

Finasteride helps female-pattern hair loss.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Keratin 17 is important for hair and nail structure and affects pachyonychia congenita symptoms.

A 15-year-old girl has a benign skin tumor on her neck.

Two new gene clusters important for hair formation were found on human chromosome 11.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

The document concludes that reactivation of herpesviruses, especially HHV-6, is linked to severe symptoms and complications in drug-induced hypersensitivity syndrome.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

A rare skin reaction from cancer treatment was successfully managed with topical treatments and antihistamines.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Two new gene clusters important for hair formation were found on human chromosome 11.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.