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The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

L-rhamnose may promote hair growth by boosting energy production in cells.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

The gene HDC is important for the development of hair follicles in newborn mice.

A unique gene mutation was found in a family with monilethrix.

The B2 genes are crucial for hair growth in rats.

Scientists discovered two versions of a new human hair keratin gene.

Potassium cyanide changes hair's disulfide bonds to monosulfide, affecting high-sulfur proteins more.

CARB is a strong barrier in human hair that prevents dye penetration.

Keratin-associated proteins are crucial for hair strength and structure.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

Keratin heterodimers are preferred for their specific and structural advantages.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Copper and iron cause keratin damage in hair by converting methionine to homocysteine.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Cathepsin L is essential for heart health and its absence causes heart problems and hair loss.

Keratin proteins in hair are complex and come from multiple gene families.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

Skin acetyl-CoA synthesis is crucial for overall lipid balance.