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The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Hoxc13 is essential for hair growth and follicle development.

Mutations in the HOXC13 gene cause hair and nail development issues.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

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

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

HEM-13HDC, a mix of 8 herbal extracts, helps hair grow and affects hair growth at a molecular level.

HLD10 can include increased body hair and Mongolian spots.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Hoxc13 gene is essential for hair, nail, and papilla development.

A specific gene mutation causes sparse, brittle hair in a family.

TCDD changes skin cell growth and keratin production in mice.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

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

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

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

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.