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Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

MT-DADMe-ImmA can selectively kill head and neck cancer cells without harming normal cells.

A new gene variant causes curly coats in some dog breeds.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

AMPK activation may reduce melanoma risk in red-haired individuals.

Mutations in the SNRPE gene cause hereditary hair loss.

Mutation in hairless gene may increase hair loss risk.

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

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

The PML protein helps prevent skin cancer in mice.

Using special RNA to target a mutant gene fixed hair problems in mice.

The Shaven mutation in mice affects hair growth and causes a greasy coat due to abnormal lipid content.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Mutation in hairless gene may increase hair loss risk.

Progerin affects cell shape but not hair or skin in mice.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Vitamin D receptor gene changes don't affect alopecia areata risk.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.