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The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Only one of the two K16 genes on chromosome 17 makes a functional protein for keratin filaments.

Increased Stat3 activity reduces hair follicle stem cells and boosts other stem/progenitor cells.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

A new gene mutation is linked to monilethrix in the studied family.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

p120-catenin helps control skin inflammation by regulating cadherin levels.

Stat3 activation increases hair follicle progenitors but reduces bulge region stem cells.

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

Mettl3 is essential for normal tissue development and self-renewal by regulating gene expression.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

A rabbit gene important for hair development was identified and detailed.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.

p63 controls Satb1 to help skin develop properly.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

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

Scientists discovered two versions of a new human hair keratin gene.

PSENEN gene mutations can cause both Dowling-Degos disease and acne inversa.

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

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

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

PTCH gene mutations contribute to basal cell carcinoma development.