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Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

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

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Deleting TNFα gene reduces skin cancer risk in certain mice.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

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

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

A specific gene mutation causes severe skin and nail issues and hair loss.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

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

A specific gene mutation causes woolly hair and hair loss.

A one-year-old cat had multiple benign skin tumors similar to those known in humans.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

TTD hair brittleness is caused by multiple structural abnormalities.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

A mutation in mice causes hair loss and immune problems.

New genetic mutations causing hair loss were found in a Chinese family.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.