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The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Keratin from hair binds well to gold and BMP-2, useful for bone repair.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The B2C promoter works in sheep cells but not in mouse embryos.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.