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Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Dimethylarsinic acid speeds up skin tumor growth in certain mice.

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

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

TCDD reduces EGF receptors in the liver, affecting growth and development.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

Using 5-butylpicolinate esters improves the sensitivity and reliability of detecting testosterone and dihydrotestosterone in saliva.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Dandelion-derived carbon dots effectively kill bacteria and speed up wound healing.

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

A new gene, JMJD1C, may affect testosterone levels in men.

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

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

A reliable method was created to measure dutasteride and related molecules in capsules.

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Cats with abnormal hair had DSG4 gene changes causing hair problems.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.