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Androgen receptor inactivation delays skin cancer onset and reduces incidence in mice, with gender differences in susceptibility.

Dermal EZH2 controls skin cell development and hair growth in mice.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

HDAC1 is crucial for skin development and preventing tumors.

The HIF-2α/ARNT complex is important for hair follicle development by controlling cell growth.

Increasing miR-149 reduces hair follicle stem cell growth and hair development by affecting certain cell growth pathways.

Certain skin proteins can form anchoring structures without the protein AMACO.

Alopecia areata is caused by an immune response, and targeting immune cells might help treat it.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

The study suggests that the arrector pili muscle is important for hair health and its damage might contribute to hair loss.

Mutations in the androgen receptor gene cause androgen insensitivity, leading to female traits in genetically male individuals.

Targeting amphiregulin may improve treatment for fibrosis and cancer.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

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

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

KAP8.2 gene variations affect cashmere quality in goats.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

DNA methylation changes in Tan sheep affect growth and fur traits.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Acne patients have higher mTOR gene expression.

Researchers found four genes that could help diagnose severe alopecia areata early.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

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

The G(S) alpha subunit gene may help start hair follicle growth in newborn mice.