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Overexpression of PKCepsilon leads to increased TNFalpha, promoting metastatic squamous cell carcinoma in mice.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A new gene mutation linked to a skin condition was found in a Spanish family.

ILC1-like cells can cause alopecia areata by themselves.

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.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Mouse skin cells can become sperm-like cells in the lab.

A specific genetic deletion in goats affects cashmere yield and thickness.

A gene mutation causes curly hair and hair loss in rats.

Sox10 is important for hair follicle development and hair growth cycles.

The FOS gene helps hair growth in Tan sheep.

Plerixafor may help restore skin pigmentation safely.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

Trps1 is essential for proper hair follicle development.

Different fish use the same genes to regrow teeth.

The osteopontin gene is active in a specific part of rat hair follicles during a certain hair growth phase and might affect hair cycle and diseases.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

CUX1 boosts sheep hair cell growth and affects curl patterns.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

miR-129-5p affects hair growth by targeting the HOXC13 gene.

PTEN helps control the number and health of skin stem cells by working with the protein BMAL1.

Removing Gsdma1/2/3 genes reduces skin cell overgrowth by blocking a specific cell pathway.

The Apc gene is crucial for normal skin and thymus development.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

ICP5249 helps hair grow by activating a specific cell pathway.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.