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A standardized patch test for hair cosmetics is needed in Europe to prevent allergies, especially for hairdressers.

Genetic testing is crucial for diagnosing and managing non-Herlitz junctional epidermolysis bullosa.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

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LIPH mutations cause woolly hair in some Chinese people.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

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KRTAP28-1 gene can help breed sheep with finer wool.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

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Using both TGA and DTDG in hair straightening reduces hair damage compared to using TGA alone.

In 2013, the FTC settled with hair company Bosley over claims it illegally shared business information with a competitor.

TTD symptoms vary widely, requiring thorough evaluations.

A new antiandrogen compound was made and its detailed three-dimensional shape was described.

New mutations in the DSG4 gene cause a rare hair condition.

Skin side effects from CDK4/6 inhibitors in breast cancer patients are generally mild and treatable, allowing most patients to continue treatment.

FERONIA regulates plant growth, pollen interactions, and sugar signaling.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

Cassia HPTC is an effective hair conditioner, better than some traditional formulas.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

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LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.