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Mesenchymal stem cells may help treat hair loss by improving hair cell growth and reducing inflammation.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Hidradenitis suppurativa is linked to various diseases like obesity, depression, arthritis, and Crohn's disease, but often occurs alone.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Higher Galectin-3 levels are linked to insulin resistance and may predict androgenetic alopecia severity.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Matriptase is crucial for skin, hair, and immune cell health, and its imbalance can lead to cancer.

Hidradenitis Suppurativa is likely an autoinflammatory disease, and better understanding its causes could improve treatments.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

SIRT7 protein is crucial for starting hair growth in mice.

Two new mutations in the AR gene linked to severe androgen insensitivity were found.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

ECM1-modified stem cells can effectively treat liver cirrhosis.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

MicroRNAs are important for skin health and could be targets for new skin disorder treatments.

A new genetic mutation in mice causes permanent hair loss and skin wrinkling.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

High levels of HSP70 and IL-15 are linked to more severe alopecia areata.

The exact cause of increased 5α-reductase activity leading to hirsutism in women is still unknown.

High levels of 3 alpha-diol glucuronide in the blood are a marker of increased androgen action in women with excessive hair growth of unknown cause.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.