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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

A gene mutation in mice causes skin defects and early death.

In situ DNA labeling in hair can help predict forensic DNA analysis success.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

A new method can detect mutations in mice by observing changes in hair follicle cells.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Ribonucleotide excision repair is crucial to prevent skin cancer.

Altering SSAT affects fat metabolism and body fat in mice.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

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

Loss of TET2 increases the risk of skin and oral cancer.

Two new gene mutations cause a rare hair disorder.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Overexpressing SSAT enzyme reduces prostate tumor growth in mice.

Imaging intestinal stem cells might help detect early signs of colorectal cancer.

SQSTM1 is linked to increased risk of alopecia areata.

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

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.