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A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

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

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

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Iron supplements combined with Quilib lotion effectively treat hair loss in people with iron deficiency anemia.

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A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

TRIV-509 quickly improves skin barrier and cell health in atopic dermatitis.

LLLT devices for hair loss need more research to define proper guidelines.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

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The Thai version of the Family Dermatology Life Quality Index is a reliable and valid tool for assessing the quality of life of patients' families.

The Polish version of the Alopecia Areata Quality of Life Index is a reliable tool for assessing quality of life in Polish-speaking patients with alopecia areata.

LX-38 is a safer drug option for treating prostate issues and hair loss without hormonal side effects.

LX-38 is a safer drug option for hair loss and prostate issues without hormonal side effects.