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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Sox9 levels in brain stem cells affect whether they stay as stem cells or become neurons.

Piezo1 helps skin grow by managing metabolism and inflammation.

AP-1 controls tumor cell type by affecting key signaling pathways.

Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

Researchers found 15 new genetic links to skin traits in Japanese women.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Low oxygen levels affect the behavior of certain proteins in human skin cells.

Meis2 is essential for whisker development, independent of nerve involvement.

The hairless gene in Kunming mice is important for hair and skin, and shows genetic variations.

Protein Kinase Cε increases skin sensitivity to UV damage and skin cancer risk.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Blocking TGFβ-RI signaling enhances surface ectoderm differentiation from human stem cells.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

The fuzzy gene is crucial for controlling hair growth cycles.

ISX-9 helps stem cells heal lung injury better by boosting growth factor secretion.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Ectodysplasin-A1 is crucial for developing hair, teeth, and glands.

A new genetic mutation was found causing hair and eye issues in a boy.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Targeting the p63 gene could help treat skin diseases.