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Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

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

The condition is linked to chromosome 12, but no mutations were found in the known genes.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

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A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

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Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

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A 645-nm diode laser effectively penetrates swine soft tissues, suggesting predictable therapeutic effects.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

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

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Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

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