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The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Activated protein C helps protect mice from long-term radiation damage.

Miz1 is essential for proper hair structure and growth.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Truncated LTBP-1 disrupts TGF-β signaling, affecting hair growth.

The GPRC6A-Duox1 axis helps control hair growth and loss by affecting hydrogen peroxide production.

High levels of ODC and a mutant Ha-ras gene cause tumors in mice.

Overactive Wnt5a disrupts hair follicle orientation in mice.

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

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

The p75 neurotrophin receptor is important for hair follicle regression by controlling cell death.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

The gene Prss53 affects hair shape and bone development in rabbits.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Certain mice without specific receptors or mast cells don't lose hair from stress.

Sonic hedgehog signaling is needed for the development of touch-receptor cells in the skin, and the loss of Polycomb repressive complex 2 can lead to more of these cells.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Mice with human skin protein K8 had more skin problems and cancer.

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

A mutation in the KRTHB5 gene causes hair and nail issues.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Disrupted stem cell signals in hairpoor mice cause hair loss.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

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