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

c-Kit is important for heart regeneration and cancer development.

A KRT32 gene variant causes loose anagen hair syndrome.

K15 and Id3 are important in hair follicle regeneration, with K15 increasing in early stages and Id3 responding later.

Canine hair follicles have stem cells in the bulge region.

p63 controls Satb1 to help skin develop properly.

Keratin 17 is modified by RSK1 in response to growth and stress, affecting skin growth and stress response.

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

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

MEF2C is crucial for normal hair cycle progression.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

Frog skin cells need the protein desmoplakin for proper development and cell layer formation.

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

TRF1 is crucial for creating and maintaining stem cells and marks both pluripotent and adult stem cells.

Basal cell carcinoma shows keratin patterns similar to undifferentiated hair follicle cells.

Clim proteins are essential for maintaining healthy corneas and hair follicles.

Tmem50b and 2610305D13Rik genes play key roles in early mouse embryo development.

Basal cell carcinomas and squamous cell carcinomas have different gene activity patterns, suggesting unique treatment approaches.

Type XVII collagen helps control skin cell growth and could be a target for anti-aging treatments.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Complex basal cell carcinomas need personalized treatment due to unique genetic mutations.

Stress in hair follicle stem cells causes inflammation in a chronic skin condition through a specific immune response pathway.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

ROR2 is crucial for hair follicle stem cell maintenance and self-renewal.

Keratin 19 helps identify skin stem cells, with its presence varying by body location, age, and culture stage.

KLHL24-mutant stem cells help understand skin and heart disease.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.