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The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Researchers found four genes that could help diagnose severe alopecia areata early.

Scientists created a new cell line from Cashmere goat hair and found that cytokeratin 13 is a unique marker for certain skin cells.

New treatments targeting specific genes show promise for treating keratin disorders.

Msx2 and Foxn1 are both crucial for hair growth and health.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.

The gelatin/β-TCP scaffold with nanoparticles improves wound healing and skin regeneration.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

Scientists made stem cells that can grow hair by adding three specific factors to them.

Scientists have found a way to create hair follicles from skin cells of newborn mice, which can grow and cycle naturally when injected into adult mouse skin.

A herbal extract may help treat certain types of hair loss by reducing a specific gene's activity.

The Siah1 and Siah2 genes are active in mouse skin development and hair growth, especially right after birth.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

Scientists can now create skin with hair by reprogramming cells in wounds.

Researchers created a cell line to study hair growth and found specific genes affected by dihydrotestosterone.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

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

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

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Scientists have made progress in understanding hair follicle stem cells, identifying specific genes and markers, and suggesting their use in treating hair and skin conditions.