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Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The new Hairless R/J mice model improves imaging for tumor monitoring and cancer therapy evaluation.

The peptide GPIGS helps hair cells grow and speeds up hair regrowth in mice.

A 195 bp duplication in the HOXC10 gene causes crests in domestic chickens.

Hair testing can detect a single GHB exposure, useful for documenting sexual assault.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

MJ04, a new compound, effectively promotes hair growth and is a potential topical treatment for hair loss.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Hair follicle samples effectively show how well the drug MK-0752 targets and engages with the Notch pathway.

The method safely and efficiently delivers genes to the skin but may not work for conditions needing high levels of gene products.

SGK3 is essential for proper hair growth and health.

Different forms of FGF5 either promote or inhibit hair growth.

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

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Editing the FGF5 gene in sheep increases fine wool growth.

Researchers created a new mouse model for studying scleroderma.

AQB reduces harmful skin changes in systemic sclerosis.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Dsg1 is essential for maintaining a healthy skin barrier in mice.