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CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

Claudin-1 is important for the barrier function and growth of hair.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Cronkhite-Canada syndrome can sometimes show unusual colonic adenomatous polyps.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Deleting the scd1 gene in mice prevents obesity by disrupting skin lipids and improving heat regulation.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

The HCR gene contributes to psoriasis risk.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Drospirenone can hide symptoms of certain hormonal disorders, complicating diagnosis.

A unique gene mutation was found in a family with monilethrix.

A new mouse mutation causes skin and hair issues, influenced by another gene.

Newly found stem cells in horse hooves show promise for treating a hoof disease called laminitis.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Allergic contact dermatitis may promote hair growth by activating hair follicle stem cells.

Certain genes and high cholesterol levels increase heart disease risk in Ethiopian patients with high blood pressure.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

β-catenin helps hair follicle stem cells grow by activating a specific cell pathway.

Mutations in the DSG4 gene cause specific hair and scalp issues.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.