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Gene differences affect finasteride side effects in men with hair loss.

DNA methylation of miR-365-1 causes hair follicle stem cell death by affecting DAP3.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Specific genes influence hair and cashmere growth in Laiwu black goats.

Arab APS1 patients have unique and recurrent AIRE gene mutations.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

miR-200c-3p could help diagnose and treat alopecia areata.

Understanding the APCDD1 gene can lead to new hair loss treatments.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Selecting specific KRTAP26-1 gene variants can improve wool quality in sheep.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

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

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

Tofacitinib effectively improved severe skin symptoms in a patient with Hypohidrotic Ectodermal Dysplasia.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Researchers found two new genetic variants linked to Alzheimer's disease.

High Geh gene expression in Staphylococcus aureus contributes to acne.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

A specific genetic deletion in goats affects cashmere yield and thickness.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

A new therapy for a skin blistering condition has not been developed yet.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

Genetic testing can diagnose hair loss linked to DSG4 gene variants.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.