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Human hair and mouse whiskers emit similar biomagnetic fields.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

A new method accurately measures nine specific hormones in human blood.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A new tool can analyze hair to detect changes due to hormones, genetics, and aging.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

Genetic studies on hair traits can improve understanding of health and disease.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Modified β-catenin can cause different effects in mouse skin cells, leading to cysts or tumors depending on the cell type.

The MTR gene affects wool quality and production in Chinese Merino sheep.

Nanoparticle systems make cancer treatment less toxic.

The flexible fixed-sequence testing method allows for more effective evaluation of multiple goals in a clinical trial while controlling the risk of false positives.

Hair analysis can provide insights into a person's medical history and location over time.

Cell-based screening methods are useful and cost-effective for drug discovery but have pros and cons.

The study found that a one-step antibody method is better than the LSAB method for accurately studying hair follicle structures without false positives.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

Insulin resistance varies among PCOS types, and simple math tools can help identify it early.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

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

The model successfully predicted new uses for existing drugs, like using certain hormonal and heart medications for respiratory and Parkinson's diseases, and a cancer drug for diabetes.

A new method effectively measures nicotine and cotinine in blood and urine for forensic analysis.

The study maps how genes are regulated during mouse hair growth.

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

The method effectively induces skin cancer in mice for studying tumor development.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.