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BMP signaling helps prevent skin tumors by blocking cancer-promoting pathways.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

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

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

Mice with CBS deficiency are healthier on a low-methionine diet.

Lhx2 helps retinal cells respond to signals for eye development.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

CS12192 effectively treats alopecia areata with better safety than current options.

Id2 gene helps keep hair follicle stem cells inactive.

Alkaline Ceramidase 1 prevents early hair loss in mice by keeping hair follicle stem cells balanced.

Scube3 gene affects mouse embryo growth in multiple areas, but needs more research.

Without keratin 10, there's more growth and development of oil-producing skin cells.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

GABAergic steroid precursors reduce ethanol withdrawal symptoms in certain mice.

Lack of functional CYLD in mice leads to early aging and cancer.

Signals from skin cells controlled by Rac proteins help turn certain precursor cells into white fat cells.

Parental uveitis causes hair loss in offspring of C57BL/6J mice.

Meis2 is essential for whisker development, independent of nerve involvement.

BST2 is a key marker for hair loss disease alopecia areata.

A new mouse model helps study melanocyte cells using GFP expression.

The angora mouse mutation causes long hair and hair defects due to a gene deletion.

Too much Sonic Hedgehog protein stops hair growth in embryos.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Deleting Crif1 in mouse skin disrupts skin balance and hair growth.

EZH2 is crucial for uterine gland development and female fertility.

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

Methionine restriction works better than betaine for treating CBS deficiency symptoms in mice.

Pvalb8 is essential for zebrafish hearing and hair cell development, and its mutation causes hearing loss.