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A new peptide from ginseng berries may help prevent hair loss by promoting cell growth and reducing stress damage.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.

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

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

New patents show progress in developing drugs targeting the Wnt pathway for diseases like cancer and hair loss.

Blocking 5α-reductase can harm memory and brain structure, and increase harmful brain changes in male mice used for Alzheimer's disease research.

Eclipta alba extract may help treat obesity by blocking fat cell formation and lowering blood lipid levels.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Certain foods and supplements can help treat skin diseases alongside medication.

TLR2 is important for hair growth and can be targeted to treat hair loss.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Targeting NETs may help reduce fibrosis in Crohn's disease.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

Certain IL-18 gene variations may increase the risk of alopecia areata.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

A mouse gene mutation increases the risk of skin cancer.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

Beta-sitosterol and stigmasterol might help prevent hair loss by blocking a specific enzyme.

Curcuma aeruginosa Roxb. may help treat hair loss by affecting specific biological pathways.

TLR2 helps control hair growth and regeneration, and its reduction with age or obesity can impair hair growth.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.