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Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

MPZL3 protein helps keep sebaceous gland size and cell growth in check.

Gene expression in wool follicles changes with growth cycles, offering insights into wool and human hair growth.

p2y5, now called LPA6, is a receptor important for human hair growth.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

Wnt ligands are crucial for hair growth and repair.

Two children with lysinuric protein intolerance showed symptoms similar to lupus.

Mice with human-like EGFR had growth issues, skin defects, heart problems, and unusual bone development.

Lack of Evi in skin causes psoriasis-like symptoms in mice.

A common mutation in the hHb6 gene is linked to monilethrix, but other factors may also play a role.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The PP2A-B55α protein is essential for brain and skin development in embryos.

SPT6 prevents excessive skin inflammation by blocking a feedback loop.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Lipase H is important for hair follicle function and shaping hair fibers.

Tectoridin helps human hair cells grow and makes mouse hair longer, suggesting it could treat hair loss.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Interleukin-1 increases keratin K6 production in skin cells.

PrPC is important for neural differentiation in cattle and mouse embryonic stem cells.

Progerin affects cell shape but not hair or skin in mice.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Two new proteins, hKAP1.6 and hKAP1.7, are found in the hair follicle cortex.

A specific genetic deletion in goats affects cashmere yield and thickness.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

A genetic variant in the KRT25 gene causes tightly curled hair.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.