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Some hair proteins are specific to hair, while others are also found in skin cells.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A mutation in the KRT74 gene causes woolly hair by affecting hair texture.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

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

A genetic hair protein variant is more common in Japanese people and is inherited.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

RNA editing significantly affects hair growth and follicle cycling in the Tianzhu white yak.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

High levels of human keratin 16 in mice cause skin lesions and abnormal skin development.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

Higher childhood DHEAS levels are linked to advanced puberty and DNA changes.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

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

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Solid-state NMR can effectively study keratin structure and treatment effects in fur.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

p63 controls Satb1 to help skin develop properly.

Gene regulation evolved differently in mouse and chicken skin, but remained stable in their trunks.

A gene mutation in mice causes skin defects and early death.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A specific gene mutation causes congenital hair loss.