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NKIRAS2 can suppress certain skin tumors but its effect on cancer varies with context and expression level.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

Skin cells and immune cells change in a skin condition called hidradenitis suppurativa, and a certain treatment can improve these changes.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

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

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Researchers found that certain miRNAs, which affect immune system regulation, are differently expressed in mice with a hair loss condition compared to healthy mice.

S100A4 promotes aggressive ovarian cancer and is a potential treatment target.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

MicroRNA-205 helps hair grow by changing the stiffness and contraction of hair follicle cells.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

HPH-15, a new compound, effectively reduces skin fibrosis in experiments without causing harm.

Blocking miR-27a increases sheep hair follicle stem cell growth and decreases cell death, which could help improve wool quality and treat hair loss.

High insulin levels may increase the risk of pilonidal sinus disease in female teens.

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.

Human adrenals and gonads have a unique enzyme for steroid hormone production.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

SQSTM1 is linked to increased risk of alopecia areata.

miR-486 may help prevent hair loss in alopecia areata.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Mutations in the hairless protein gene cause hair loss.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.