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

The protein EZH2 blocks microRNA-22, increasing STK40 protein, which helps hair follicle stem cells change and grow hair.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A genetic hair protein variant is more common in Japanese people and is inherited.

A unique gene mutation was found in a family with monilethrix.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

ARTS helps stop tumors by promoting cell death.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

The method effectively analyzes human hair proteins, especially nonfilamentous ones.

IL-26 has antimicrobial and pro-inflammatory effects in the chronic skin condition Hidradenitis Suppurativa.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

Loss of COL17A1 causes hair follicle stem cells to age and leads to hair loss.

The polyG fragment in Hoxc13 protein helps evolve mammalian skin and hair by enhancing gene interactions.

Glypicans help hair follicle stem cells differentiate by interacting with specific receptors, influencing hair growth.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

HAPLN1 can promote hair growth and may help treat hair loss.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

The technology can help diagnose and subtype autoimmune diseases by identifying specific autoantibodies.

p63 is essential for controlling epithelial stem cells and tissue health.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

The hedgehog signalling pathway is key in skin development and basal cell carcinoma, offering insights for prevention and treatment.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.