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Collagen XVIII and Bmx tyrosine kinase are important for hair growth and skin cancer development.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

A truncated protein linked to breast cancer may change cell adhesion.

SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

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

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

COX2 and ATP synthase control the size of hedgehog spines.

The research identified six functional hair keratin genes and four pseudogenes, providing insights into hair formation and gene organization.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Early over-expression of FoxN1 harms immune and skin development.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Calcium signals and SHH guide the direction of feather growth in chicken skin.

Lack of vitamin D receptor increases skin tumor risk by boosting hedgehog signaling.

FOXN1 gene variants cause low T cells and immune issues from birth.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Activating the sonic hedgehog pathway in chicken embryos can permanently change scales to feathers.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Foxn1 is essential for hair pigmentation by directing pigment transfer to hair cells.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Foxn1 helps skin cells mature by controlling a specific protein's activity.