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A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

Alkaline ceramidase 1 is crucial for healthy skin and energy balance.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Women with hyperandrogenism have higher androgen levels and lower SHBG, which may contribute to conditions like excessive hair growth and early puberty.

Phospholipase A2 enzymes play key roles in skin health and disease.

CYP11A1 is crucial for skin health and disease by producing important steroids.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

LHX2 and SOX9 identify unique hair follicle cell groups, crucial for hair maintenance.

A specific gene mutation causes congenital hair loss.

Overexpressing SSAT in mice makes them highly sensitive to polyamine analogues, causing liver damage and high mortality.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

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

Dermal EZH2 controls skin cell growth and differentiation in mice.

Sheep hair follicle transglutaminases are calcium-dependent.

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

A substance called compound-1 could help increase hair growth by maintaining prostaglandin levels in hair follicles.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Changing YBX1 protein activity affects skin stem cell function and aging.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.