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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

Ptch2 plays a key role in controlling stem cell function and the ability to regenerate after birth.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

The most common sign of aging at the gene level is more Ectodysplasin A2 Receptor (EDA2R) being made.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

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

Researchers found a genetic region that influences the number of coat layers in dogs.

A missing mK6irs1 gene causes hair loss in mice.

A specific mutation in PA-PLA1α causes abnormal hair growth.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

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

Recombinant keratin materials may better promote skin cell differentiation than natural keratin.

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

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Removing Mediator 1 causes teeth cells to turn into hair cells.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Ritlecitinib may help treat alopecia areata by protecting hair follicles.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Lgr5 and the vitamin D receptor are key in controlling skin inflammation and tumor risk in mice.

Malt1 protease is essential for regulatory T cell function and could be targeted to boost antitumor immunity.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

RXRα is crucial for hair growth and skin cell function.