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Zfp157 is active in many mouse tissues during development and in specific adult cells.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

A specific DNA region controls skin cell gene expression by working with certain proteins.

The agouti gene may help understand and treat obesity.

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

A20 protein is crucial for normal skin and hair development.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Ambras syndrome's genetic cause is unknown, as it isn't linked to androgen levels.

Targeting cholesterol, fatty acids, fibrosis, and mast cells may help treat CCCA.

The scraggly mutation causes hair loss and skin defects in mice.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

Alopecia areata involves specific immune cells, offering potential treatment targets.

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

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

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A specific gene change is linked to severe hair loss.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

The FRZB gene slows hair growth in rabbits.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

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

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.

Researchers found certain genes are overactive and others are underactive in men with early balding, which could help create new treatments.