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Overexpressing PKCα in mice skin increases inflammation but doesn't affect tumor growth.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Collagen XXII is a marker for tissue junctions, aiding in structural integrity and found in muscles, heart, skin, and arthritic joints.

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

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

BLMP-1 is important for regular molting and gene expression cycles in worms.

Different fish use the same genes to regrow teeth.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

A KRT32 gene variant causes loose anagen hair syndrome.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

RNase L suppresses regeneration in mammals.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Activating β-catenin in certain skin cells speeds up hair growth in mice.

Wnt signaling affects the development and growth of Langerhans cells in mice.

Krox20 is important for cell differentiation in the brain and hair follicles.

Basonuclin helps keratinocytes multiply and prevents them from fully maturing.

The 4C32 gene may help in mouse skin development and differentiation.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Sostdc1 controls the size and number of hair and mammary gland structures.

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

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Trps1 is essential for proper hair follicle development.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Losing both ERBB2 and ERBB3 receptors in mice causes significant skin problems and inflammation.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.