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A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

A gene mutation in mice causes skin defects and early death.

The protein CCN2 controls hair growth by affecting hair follicle formation and stem cell activity in mice.

CI-1033 causes skin lesions in rats, similar to humans, due to EGF receptor inhibition.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

The RHC complex with nicotinamide promotes hair growth and health.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Activating TLR3 boosts autophagy gene expression in skin cells.

Adding cerium(III) chloride to Grignard reagents improves the making of compounds that could treat prostate issues and hair loss.

A preauricular crease is common in people with coronary artery disease.

MicroRNA-22-3p hinders hair regrowth in male pattern baldness by affecting a specific protein.

A new genetic mutation was found causing hair and eye issues in a boy.

Cell adhesion molecules are important in the development of certain skin diseases.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Targeting the protein Caveolin-1 might help treat a type of scarring hair loss called Frontal Fibrosing Alopecia.

Plasmalogens activate a channel in cells that may stimulate hair growth.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Aromoline and DRD4 are potential targets for osteoarthritis treatment.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.