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PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Deleting part of a gene in mice causes wavy hair and high pup loss.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The research found that the molecule lncRNA-H19 helps hair follicle cells grow by affecting certain cell pathways in cashmere goats.

Higher levels of certain DNAs in blood may indicate hair follicle damage in alopecia areata patients.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

A new mutation in mice causes crooked whiskers and messy hair.

circRNA-1926 helps goat stem cells turn into hair follicles by affecting miR-148a/b-3p and CDK19.

Two new gene clusters important for hair formation were found on human chromosome 11.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

KRT72 gene helps form hair.

A KRT32 gene variant causes loose anagen hair syndrome.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

miR-200c-3p could help diagnose and treat alopecia areata.

Engineered bacteria can deliver antioxidants to protect skin.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The KRTAP27-1 gene variations in sheep may affect wool length and weight.

A gene mutation causes monilethrix in a Chinese family.

CD44 variant changes start alopecia areata, but don't maintain it.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

MAD2B slows down the growth of skin cells that are important for hair development by interacting with TCF4.

The mutation causes hairless mice due to mislocalized and dysfunctional HR protein.