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The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

Reducing SFRP1 can promote hair growth and may help treat hair loss.

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

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

The hairless protein is important for skin, hair, and may influence cancer development.

EDA2R gene linked to hair loss.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

p53 protein may help protect or kill neurons under stress.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

The B2C promoter works in sheep cells but not in mouse embryos.

TCDD reduces EGF receptors in the liver, affecting growth and development.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Two new gene clusters important for hair formation were found on human chromosome 11.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

PRIDE syndrome includes skin and hair issues from cancer treatment with EGFR inhibitors.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

A newly found RNA in Cashmere goats may play a role in hair growth and development.

GFP transgenic mice help study cell origins in skin grafts.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

Targeting amphiregulin may improve treatment for fibrosis and cancer.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

A specific gene mutation causes Olmsted syndrome.

A new neural network helps identify key regulators in cell changes, aiding in understanding diseases and finding new treatments.