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WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

A substance called TCQA could potentially darken hair by activating certain genes and increasing melanin.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Key genes influence melanin in chicken muscles, affecting their value.

Quiescent cells have increased mitochondrial activity and ECM gene expression, but reduced glycolysis.

MARCKSL1 is important for wound healing and could be a target to reduce scarring.

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

Overactive Wnt signaling in mouse skin stem cells causes acne-like cysts and shrinking oil glands, which some treatments can partially fix.

K6hf is found in specific parts of hair follicles, nails, and tongue, and is linked to hair growth and structure.