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A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Certain genes may influence hair loss differently in men and women.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

An enzyme other than TNAP might be responsible for vitamin B-6 metabolism in the skin.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Overexpressing the mineralocorticoid receptor in mouse skin causes skin thinning, early skin barrier development, eye issues, and hair loss.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

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

Low m6Ascores in melanoma predict better survival and response to immunotherapy.

Mutations in the HOXC13 gene cause hair and nail development issues.

Identified genes linked to male-pattern baldness may help develop new treatments.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

The KRTAP15-1 gene affects cashmere fiber thickness in goats.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

New mutations in the DSG4 gene cause a rare hair condition.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

A specific gene variation in goats is linked to better growth traits.

Different forms of the Vitamin D receptor can impact metabolic and hormone issues in Polycystic Ovary Syndrome.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Methotrexate for rheumatoid arthritis often causes side effects like diarrhea, fatigue, and hair loss, especially at higher doses.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.