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Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

The new near-infrared LED device improves skin and hair with no side effects.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The study mapped genetic variations in sheep, linking them to traits like milk production and growth.

RTA 408 cream protects mice from radiation skin damage.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

New therapy helps treat hair loss.

Disruptions in sleep-wake cycles can cause health problems like mental, metabolic, and heart diseases, and cancer.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.

The IRE gene is important for normal root hair growth in Arabidopsis plants.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Rare genetic variants in 125 genes are linked to male-pattern hair loss.

SNP rs2479106 in the DENND1A gene may increase PCOS risk in Saudi Arabian females.

TH07 is a topical combination of finasteride, latanoprost, and minoxidil, and shows promise.

A specific gene mutation causes woolly hair and hair loss.

The ZmNF-YC1–ZmAPRG pathway in maize improves phosphorus efficiency and grain yield, suggesting it as a target for breeding better crops.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

The combination of Rhynchosia nulubilis and Polygonum multiflorum extracts may effectively promote hair growth and reduce hair loss.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

K14 expression in young rats differs from adults.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.