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Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

The Bsk mutation doesn't involve keratin gene recombination and its cause is unknown.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Somatic BHD mutations are rare in Japanese renal tumors.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.