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A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Psoriasis patients' immune response to a hair protein depends on their specific gene type.

New genetic mutations causing hair loss were found in a Chinese family.

A specific mutation in PA-PLA1α causes abnormal hair growth.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Scientists identified a unique type of human skin stem cell that could help with tissue repair.

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Inhibiting HSP90 increases cell adaptability and survival under stress.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

HSPGs help control stem cell behavior, affecting hair growth and offering a target for hair loss treatments.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

New mutations in the hairless gene may cause hair loss and affect bone development.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Keratin 75 might be important in oral cancer progression.

The hairless protein is important for skin, hair, and may influence cancer development.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

The HPV type 11 region activates hair-specific gene expression in mice.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Hutchinson-Gilford Progeria Syndrome causes rapid aging due to a gene mutation, with no cure yet, but research may lead to better treatments.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

The hr gene is linked to hair loss in Valle del Belice sheep.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

HPV16 oncogenes disrupt the normal activity of hair follicle stem cells.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.