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Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Elongating cilia boosts SKP stem cell renewal, especially with PDGF.

A method was found to select hair follicle stem cells, and beta-catenin helps them grow and change.

A KRT32 gene variant causes loose anagen hair syndrome.

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

Human cathepsin V can replace mouse cathepsin L to maintain normal skin and hair in mice.

Dynlt3 is important for melanosome transport and skin coloration.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Some people have a genetic variation that makes them less effective at breaking down drugs.

A gene mutation in mice causes skin defects and early death.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

A specific gene mutation (Y449H in K10) was found in a patient with severe skin disorder.

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

Some women with PCOS have CYP21 mutations and IRS1 variants, but these genetic factors are not major contributors to PCOS.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

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

Pygo2 is important for early growth and progression of intestinal tumors, and could be a target for treating cancers with certain mutations.

The B2 genes are crucial for hair growth in rats.

A specific gene mutation causes woolly hair and hair loss.

aPKCλ is essential for hair follicle stem cell maintenance and wound healing.

KRT72 gene helps form hair.

Cystic fibrosis can cause unusual symptoms like hair color changes, which can improve with proper treatment.

miR-195-5p reduces hair growth ability in cells by blocking a specific growth signal.

Diphencyprone initially increases mouse hair growth, then slows it, possibly due to changes in specific protein levels.

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

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