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C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

Four children had unmanageable pale blond hair due to uncombable-hair syndrome.

Activating β-catenin and inactivating PTEN cause follicular tumors, not papillomas, similar to those in Cowden’s Disease.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

FOXO3 is essential for proper feather development in goose embryos.

The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

Mutations in specific llama genes may affect fiber quality for textiles.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

The flaky skin mouse mutation is a natural model for studying human psoriasis.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

Machine learning can effectively identify genes to improve wool quality in sheep.

A mutation in the KRT74 gene causes tightly curled hair.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Genes affecting wool fiber thickness in Angora rabbits were identified, which could help breed finer wool.

Genetic differences in sheep affect wool type, with fat and immune genes influencing hair traits.

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

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

A variant in the ADAM17 gene causes hair loss by increasing protein degradation through TRIM47.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.