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A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Toy poodles may develop harmless mineral deposits around hair follicles as they age.

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

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

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

Biotin deficiency in pigs causes hair loss, skin issues, and weak claws.

BAF200 is essential for proper heart and coronary artery formation.

Vitamin B6 helps increase hair growth and density in rabbits by affecting certain cell signaling pathways.

A mutation in the KRT25 gene causes woolly hair and hair loss.

A child with a rare vitamin D-resistant condition improved with treatment.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

Chesapeake Bay retrievers' hair loss is likely a breed-specific, hereditary condition linked to abnormal steroid levels and distinct skin changes.

Epidermolysis bullosa in calves was not caused by mutations in the keratin genes bKRT5 and bKRT14.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

A new genetic mutation was found causing hair and eye issues in a boy.

Cows in El-Behera have nutritional deficiencies causing health issues like anemia and poor reproduction.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

ILC1-like cells can cause alopecia areata by themselves.

Blocking the JAK/STAT pathway may help reduce skin sensitivity in Xeroderma pigmentosum.

Vitamin C deficiency causes severe skin problems in newborn dairy calves.

Msx2 deficiency in mice leads to bone growth and organ development problems.

A Doberman Pinscher had a rare form of autoimmune disease causing hair loss and other severe symptoms.

A specific gene mutation causes a severe skin disorder in a family.

A blue Staffordshire Bull Terrier had hair loss due to color dilution alopecia, confirmed by tests, but no treatment was pursued.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Some young Angus cattle had skin problems due to not enough vitamin A, which got better after they were given more vitamin A.