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ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

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

The RAS pathway affects hair growth differently in CFCS and CS.

Cystatin M/E helps in the final stages of hair and nail formation by controlling certain enzymes.

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

Lysosomal proteases and cytoplasmic enzymes help hair follicle cells develop and differentiate.

Recessive X-linked ichthyosis involves a less efficient enzyme in hair follicles, suggesting two distinct enzymes.

Heparanase is essential for hair follicle health and inner root sheath differentiation.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

CARASIL can cause different symptoms even with the same genetic mutation.

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

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Keratin heterodimers are preferred for their specific and structural advantages.

A specific DNA region controls skin cell gene expression by working with certain proteins.

Stabilizing HIF1A in hair follicles may boost hair growth by enhancing energy production and blood vessel formation.

Increasing calcium sensing receptor speeds up skin and hair development in mice.

Enzyme presence in hair sheath cells decreases over time, affecting forensic analysis.

A specific chemical change in the S100A3 protein leads to the formation of a four-part structure important for hair formation.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

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

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

INT effectively shows enzyme activity and protein groups in wool and hair follicles.

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

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

The hair follicle's connective tissue is a key source of a certain collagen in human scalp skin.

The study concluded that three enzymes are important for plant development by affecting sugar composition and calcium binding in plants.