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Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

New peptides can delay aging and improve cell function.

Vaccination is crucial for public health, but anti-vaccine movements are a concern.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Cepharanthine is safe but not clearly effective in speeding up COVID-19 recovery.

Scientists can now create skin with hair by reprogramming cells in wounds.

The research found that different types of fibroblasts are involved in wound healing and that some blood cells can turn into fat cells during this process.

A new compound, BOI, can help hair grow by changing hair cycle phases and increasing certain cell contents.

EpiLife® media and younger donor age improve artificial skin model quality.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Low fucosylation boosts stem cell growth in the eye.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

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

A specific gene mutation causes Olmsted syndrome.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Research on "hair cloning" for hair loss shows potential for hair thickening but has not yet achieved new hair growth in humans.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A 90-year-old woman's hand lesion was a rare, aggressive skin cancer treated successfully with surgery.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Certain genetic variants in keratins increase the risk of tooth decay.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Four genes affect hair follicle density in goats.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Vegetable protein lowers cholesterol and protein deficiency can cause health issues.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.