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A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

TLR7-based compounds may help manage chemotherapy-induced hair loss.

TGF-β2 helps yak hair follicles enter the regression phase, while HSP70 tries to prevent it.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

MJ04, a new compound, effectively promotes hair growth and is a potential topical treatment for hair loss.

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

Mutations in the hairless protein gene cause hair loss.

KRTAP10 proteins help form the hair shaft's tough outer layer by interacting with specific hair keratins.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

JW0061 may be a new treatment for hair loss by promoting hair growth through WNT signaling.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Secukinumab reduces immune activity in hidradenitis suppurativa skin.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

The E2 protein affects gene activity in hair follicles of mice.

UTX is crucial for skin differentiation and health, especially in females.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The fragrance cyclohexyl salicylate helps promote hair growth and increase hair stem cell numbers.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

A new mutation in the HR gene causes hair loss in a specific family.