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A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

Hoxc13 gene is essential for hair, nail, and papilla development.

The cancer gene c-Myc increases harmful chemicals that damage DNA and can lead to cancer, but antioxidants can reduce this damage.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

TCDD reduces EGF receptors in the liver, affecting growth and development.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

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

Targeting ornithine decarboxylase can help prevent skin cancer.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

CD80CD86 deficiency causes hair loss by disrupting regulatory T cells.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

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

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

A gene mutation in mice causes severe skin disorder similar to a human condition.

Egfl6 is not needed for zebrafish face development.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Mutations in the HOXC13 gene cause hair and nail development issues.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.