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New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

CD28 is a promising target for treating alopecia areata with belatacept.

CD28 is a promising target for treating alopecia areata with belatacept.

CD98hc's role in skin health decreases with age.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

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

New mutations in the hairless gene may cause hair loss and affect bone development.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

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

HLA-DRB5 and other genes may be linked to alopecia universalis.

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

MOF controls skin development by regulating genes for mitochondria and cilia.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

FGF13 gene changes cause excessive hair growth in a rare condition.

Three genes linked to the development of trichilemmal cysts were found.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

A truncated protein linked to breast cancer may change cell adhesion.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The ABCG2 gene variant increases the risk of high uric acid and cholesterol, especially in overweight or obese young Mexican males.

Certain genes are linked to the risk of developing Alopecia Areata.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Researchers found a new mutation causing total hair loss from birth.

Hair shaft changes may be linked to CCCA, but their role is unclear.