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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

AP-1 controls tumor cell type by affecting key signaling pathways.

K31 can identify clear secretory cells in human sweat glands.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

A specific gene mutation causes woolly hair and hair loss.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

AIMP1 can boost hair growth by increasing stem cell activity.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

Finasteride helps female-pattern hair loss.

Trps1 is essential for proper hair follicle development.

ADAM 10 and ADAM 12 proteins are involved in different stages of hair growth and could be targets for treating hair disorders.

Plet-1 protein helps hair follicle cells move and stick to tissues.

AgK114 protein helps in hamster skin injury recovery.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A peptide from hair follicle stem cells can boost hair growth.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Deleting MED1 in skin cells causes hair loss and skin changes.

YAP1 is important for skin regeneration and may affect skin disorder treatments.

Ptprq has multiple forms that change during inner ear development.

KRT72 gene helps form hair.