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Modified rat hair follicle stem cells can help create artificial hair follicles, blood vessels, and skin.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Accurate diagnosis and early specialist referral are crucial for managing 46,XY Disorders of Sex Development.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Overexpression of IKZF1 and Ikaros causes hair loss in mice similar to alopecia areata.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Keratin genes help explain how hair and feathers develop differently in mammals and birds.

FGF signaling is crucial for starting feather development in chicken embryos.

KAP8.1 protein is crucial for hair structure and interacts with keratin 85.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

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

New mutations in the hairless gene may cause hair loss and affect bone development.

Cantú syndrome is caused by mutations in the ABCC9 gene.

VEGF165 helps hair follicle stem cells become blood vessel cells, aiding new blood vessel growth.

Activated LEF/TCF complexes are crucial for hair development and cycling.

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

Four transcription factors can convert mouse cells into hair cell-like cells, aiding hearing loss research and treatment.

The Gsdma3 gene is essential for normal hair development in mice.

Mutations in specific llama genes may affect fiber quality for textiles.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Two gene variants cause white spots in cattle.

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

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.