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Loss of Dnmt3a and Dnmt3b leads to more aggressive skin tumors, but blocking PPAR-γ can reduce this effect.

Inherited color dilution in Rex rabbits is linked to DNA methylation changes in hair follicles.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Increasing SSAT makes skin more prone to cancer.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Sgk3 is essential for normal hair follicle growth and maintenance.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Keratin proteins in hair are complex and come from multiple gene families.

Key genes linked to hair growth and cancer were identified in hairless mice.

Removing HIF-P4H-2 from certain skin cells in mice causes hair loss on the body but not the head.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

HuR is essential for Treg function and preventing autoimmunity.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Early involution in Hirosaki hairless rats' mammary glands is linked to a unique modification of STAT5A.