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MCHR2 gene duplications may be linked to alopecia areata.

Increasing PBX1 reduces aging and cell death in hair follicle stem cells by boosting SIRT1 and lowering PARP1 activity.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Mice skin has components that could help with hair growth and might be used for diabetes treatment.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

The skin's basement membrane is specially designed to support different types of connections between skin layers and hair follicles.

A new gene mutation causes a rare type of hair loss.

Hoxc13 gene is essential for hair, nail, and papilla development.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

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

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

The Itpr3 gene causes a specific hair pattern in mice.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

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

Too much Smad7 can cause serious changes in skin tissues, including problems with hair growth, thymus shrinkage, and eye development issues.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Sinapic acid may help fight obesity and promote hair growth.

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

MicroRNAs are important for skin development and diseases and could be used for treatment and diagnosis.

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

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.