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Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The research identified genes and pathways important for sheep wool growth and shedding.

Mutations in the SNRPE gene cause hereditary hair loss.

Enzyme presence in hair sheath cells decreases over time, affecting forensic analysis.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

The research suggests immune system changes and specific gene expression may contribute to male hair loss, proposing potential new treatments.