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The FTO gene hinders stem cells in hair follicles from becoming pigment cells.

Snail1 may contribute to fibrosis in frontal fibrosing alopecia in postmenopausal women.

Trps1 plays a key role in hair follicle development and cycling.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

miR-140-y helps control feather growth in geese by affecting the Wnt signaling pathway.

Too much Sonic Hedgehog protein stops hair growth in embryos.

A specific gene mutation causes complete hair loss without other health issues.

Fadrozole and Finasteride change frog sex ratios and cause intersex animals with altered gene expressions.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Overexpressing the MSX-2 gene in mice causes skin and hair growth issues.

A20 protein is crucial for normal skin and hair development.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Researchers developed a mouse model that tracks hair growth using bioluminescence, improving accuracy in studying hair cycles.

Runx1 affects hair growth, cancer development, and autoimmune diseases in epithelial tissues.

Deleting NIPP1 in mouse skin cells causes early aging and chronic skin issues.

Nelfb is crucial for forming skin fat tissue by regulating genes needed for fat cell development.

Folliculin helps regulate energy and nutrient sensing, impacting Birt–Hogg–Dubé syndrome.

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

Chicken feather gene mutation helps understand human hair disorders.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

Lack of certain fatty acids causes skin, immune, and fertility issues in mice.