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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

A man had two rare autoimmune diseases that might be connected.

Two genetic variations in Moa buffalo help them adapt to heat.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

A rare gene variant causes hair and nail issues in a family.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Certain gene variations are linked to a higher risk of severe acne, suggesting a genetic influence on the condition.

Blocking a protein called prostaglandin D2 might help treat hair loss.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Lack of vitamin D receptor increases skin tumor risk by boosting hedgehog signaling.

H3K4me3 helps control RSPO3 to influence hair growth and development.

Mice with the ab gene have abnormal sebaceous gland development, affecting sebum production.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

The development of breeding tubercles in male zebrafish relies on a specific enzyme that processes hormones.

Blocking BMP signaling causes hair loss and disrupts hair growth cycles.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

New genes and pathways are important for testosterone production and male sexual development.