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The study found that balding scalps have more thin hairs and larger oil glands, which might contribute to skin conditions related to hair loss.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

A woman's diabetes improved after removing ovarian tumors that caused high testosterone levels.

Artemis protein may help control hair growth and health by influencing cell processes.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Blocking JAK/STAT pathways can help treat hair loss from alopecia areata.

Latanoprost, a glaucoma drug, showed potential for promoting hair growth in bald monkeys, especially at higher doses.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

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

The study found average numbers for different types of hair follicles in the scalp and observed differences between men and women, suggesting reasons for more common hair shedding in women.

Metabolic syndrome reduces effectiveness of hair loss treatment.

Cosmeceuticals may benefit skin health but need more research for efficacy and safety confirmation.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

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

Pannexin 3 is important for bone formation and the development of bone cells.

Modified pep7, named EPM peptide, effectively promotes hair growth at low concentrations and works well with minoxidil.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Certain genetic mutations can lower bad cholesterol and reduce heart disease risk, leading to effective cholesterol-lowering drugs.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Notch signalling helps skin cells differentiate and prevents tumors.

Platycladus orientalis leaf extract helps hair grow by activating certain proteins.

Special astrocytes improved learning and memory in rats after a stroke.