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An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Early diagnosis and proper treatment improve outcomes for methylmalonic acidemia.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Sex steroids affect the MafB gene differently in male and female hamsters.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Laminin-511 is essential for proper melanocyte movement and development in mice.

Gene therapy in mice increased lifespan and improved health without causing cancer.

Age-related hearing loss involves cochlear damage and metabolic changes.

Mice with human skin protein K8 had more skin problems and cancer.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

CDP is crucial for lung and hair follicle cell development.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe side effects.

Gene therapy with the Math1 gene helped regenerate balance-related cells and improve balance in mice.

Iron deficiency causes hair loss in white rats and mice.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

A new mouse model effectively mimics vitiligo for research and drug testing.

Tranexamic acid turns white hair brown in certain mice by affecting specific proteins.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Scientists identified and cloned specific keratin proteins in mouse hair.

WWP2 is crucial for tooth development in mice.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Too much Sonic Hedgehog protein stops hair growth in embryos.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Overexpressing COX-2 in mice skin reduces skin tumor development.