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Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

WWOX deficiency in mice causes skin and fat tissue problems due to disrupted cell survival signals.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Cyclosporin promotes hair growth by boosting cell growth and reducing cell death.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

AP-2α and AP-2β are crucial for healthy skin and hair.

CCCA is a common scarring hair loss in African descent women, possibly linked to genetics, hair care practices, and health issues like diabetes.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

FGF20 is essential for hair follicle stem cell growth and development in fine-wool sheep.

N-WASP is essential for normal hair growth in mice.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

Biglycan helps regulate hair growth and regeneration.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

A cat's poor wound healing was linked to a genetic deletion in the COL5A1 gene.

Inhibiting AP-1 changes skin tumor types and affects tumor cell identity.

Skin needs dermal β-catenin activity for hair growth and skin cell multiplication.

Basal cell carcinomas in mice can start from hair follicle stem cells and other skin cell types, depending on signaling levels.

Lower SMAD2/3 activation predicts more severe skin cancer.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

Nε-(carboxymethyl) lysine delays hair growth by blocking a key protein.

Krox20 is important for maintaining stem cells in the skin and affects hair growth and color.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

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.

CCCA is a hair loss type affecting African women, possibly caused by grooming and chemicals, with various treatments and needing more research.