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Certain gene variations might increase the risk of a hair loss condition in Koreans.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Mouse keratin 6 isoforms have different expression patterns in various tissues.

DKK-1 gene linked to hair loss in AGA and AA patients; more research needed for potential therapy.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

The hairless (hr) gene is essential for normal hair follicle function and its mutation leads to hair loss.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

HPV8 E6 gene causes growth of certain skin stem cells.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

CAP1/Prss8 does not activate PAR2 or inhibit PN-1.

The Apc gene is crucial for normal skin and thymus development.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Gene expression regulates keratin production for normal hair growth.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

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

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Keratin 10 end domains may increase skin cancer risk by reducing cell death.

Keratin gene clusters in humans and marsupials are similarly organized.

A gene mutation causes monilethrix in a Chinese family.

K42 and K124 keratins are only found in horse hoof lamellae.

YAP1 is important for skin regeneration and may affect skin disorder treatments.