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A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

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

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

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JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

The prototype for analyzing skin aging works technically and clinically.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

MK-0773 is a moderate inhibitor of the SRD5A2 enzyme.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Modified rat hair follicle stem cells can help create artificial hair follicles, blood vessels, and skin.

Lactobacillus paracasei HY7015 helps hair grow in mice.

Canine hair follicle cells show stem cell properties, aiding hair growth.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A genetic marker linked to a type of hair loss was found in most patients studied.

K6hf is a unique protein found only in a specific layer of hair follicles.

A new therapy for a skin blistering condition has not been developed yet.

KF19418 promotes hair growth similarly to minoxidil but is not better in live mice.

Mutations in the KRT16 gene can cause skin and nail disorders.

Loss of COL17A1 causes hair follicle stem cells to age and leads to hair loss.