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Methyl jasmonate boosts tanshinone production in Salvia miltiorrhiza callus cultures.

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

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

A new method quickly detects alcohol use from hair in under an hour.

Testosterone treatment may change estrogen receptor methylation in AFAB individuals.

Immunofluorescence tomography is a cost-effective method for creating detailed 3-D images of tissues.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

Deleting part of a gene in mice causes wavy hair and high pup loss.

A 25-year-old man with multiple skin tumors was successfully treated with acitretin and methotrexate.

Manganese levels in hair may be linked to multiple sclerosis.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

TSC22D genes are key in metabolic diseases and cancer, offering potential as treatment targets.

PMC shows promise as a treatment for hair loss.

The study found that different genes are active in cashmere goats' hair growth stages, which can help improve cashmere production.

Cyproterone acetate is a safe treatment that causes modest feminization in transgender female adolescents, and works better with added estrogens.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Activated LEF/TCF complexes are crucial for hair development and cycling.

Bacillus sp. TC5 products help hair regrowth and improve skin drug absorption.

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

The study found markers indicating that cells responsible for hair color are differentiating in specific areas of the hair follicle.

The CTLA-4 gene polymorphism does not affect polycystic ovarian syndrome.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.