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A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Researchers found a genetic region that influences the number of coat layers in dogs.

New treatments targeting specific genes show promise for treating keratin disorders.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

PLIN2 affects hair growth in cashmere goats, potentially improving cashmere quality.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Higher expression of the keratin-associated protein 8.1 gene in Liaoning cashmere goats is linked to finer cashmere fibers.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

pCLCA2 protein may help maintain skin structure and function.

Autosomal recessive woolly hair is rare and involves tightly coiled hair without other health issues.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

GhPLDα1 helps thicken cotton fiber walls by boosting cellulose production.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

The gene GJA1 is important for regulating coarse hair density in goats.

Sheep cells were successfully modified to include a spider silk protein gene.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Glycogen helps E. coli cells divide unevenly and organize their contents.

New pyridine compounds effectively inhibit GSK3, a diabetes treatment target.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

Glycosaminoglycan levels peak early in hair growth and decrease as the cycle progresses.

The enzyme from human skin can cross-link proteins and needs calcium to work.

A specific gene variant may increase the risk of developing Alopecia Areata.

TRα and CRABPII genes change their activity levels during goat fetal skin development.