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Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

RXR agonists may promote hair growth in humans.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Rapamycin reduces skin cell growth and tumor development by affecting cell signaling in mice.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

Raltitrexed conjugates are less potent than the free drug but more effective at high concentrations.

Type XIX Collagen is present in specific skin and hair cells during development.

miR-22 helps skin cancer grow and spread by activating specific cell signals.

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

Constant-release melatonin reduces SOX21 gene expression in goats during the hair follicle resting phase.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Dermal EZH2 controls skin cell growth and differentiation in mice.

FOXC1 is essential for keeping hair follicle stem cells inactive and maintaining their environment for healthy hair growth.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Sox13 is a useful marker for early hair follicle development but not essential for hair growth.

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

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

RAGE is a potential target for melanoma treatment, but its effectiveness is uncertain due to variable expression levels.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Researchers developed a mouse model that tracks hair growth using bioluminescence, improving accuracy in studying hair cycles.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

BMI1 is essential for preventing hair greying and maintaining hair color.

The study found that the protein Dkk4 helps regulate hair growth by controlling Wnt signaling in mice.

Wnt signaling is vital for cell growth, development, and cancer research.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

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