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Activating cannabinoid receptor 1 reduces certain keratin levels, potentially aiding psoriasis treatment.

Overexpression of R-spondin 3 leads to sparse hair and impaired hair regeneration.

The gene HDC is important for the development of hair follicles in newborn mice.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

The ventral matrix is the main source of the nail plate.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

The Paxbp1 gene is crucial for healthy hair follicles.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

CRH causes hair loss by reducing cell survival in hair follicles.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

Rac1 is vital for hair follicle health but not needed for skin maintenance.

Keratin 17 is important for skin development and may help define skin cell types.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

FTase and GGTase-I are essential for skin keratinocyte health.

Specific gene variants affect wool traits in Chinese Tan sheep.

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

Lysosomal proteases and cytoplasmic enzymes help hair follicle cells develop and differentiate.

Keratin gene regulation is similar across mammals, affecting hair follicle differentiation.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

Researchers created five new human scalp cell lines that could be useful for hair growth and loss research.

S100A3 protein is crucial for hair shaft formation in mice.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

A new DSG4 gene mutation causes hair defects in a young girl.