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PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Mutations in the HOXC13 gene cause hair and nail development issues.

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

Reducing miR-30a-5p helps hair follicle stem cells grow and survive.

The LMNA mutation affects skin structure even in asymptomatic carriers.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Centrosomes are essential for healthy skin and hair growth, and their role is different from that of cilia.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

Mice with a specific BRCA1 mutation have a higher risk of tumors, especially in the uterus and ovaries.

The study revealed the detailed structure of a keratin dimer, aiding understanding of how intermediate filament proteins function.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

A gene mutation in mice causes skin defects and early death.

miR-218-5p helps skin and hair growth by targeting SFRP2 and activating a specific signaling pathway.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

ceRNA networks offer potential treatments for skin aging and wound healing.

CIP/KIP proteins help stop cell division and support hair growth.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

A high-fat diet may weaken tongue structure by reducing certain protein genes.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

Blocking mTORC1 reduces skin tumor growth in mice.

A new DSG4 gene mutation causes hair defects in a young girl.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

The improved genome of the African spiny mouse will help understand its tissue regeneration abilities.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.