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High-throughput LC-MS screening is effective for finding new autotaxin inhibitors for asthma treatment.

Diagonal earlobe crease and lipoprotein(a) together help diagnose coronary heart disease.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Ginseng may improve skin health and anti-aging, but how it works is still unclear.

Mutations in the LIPH gene cause woolly hair in a child.

Lactobacillus plantarum hydrolysates may help increase hair growth by boosting VEGF production.

Higher levels of small, dense LDL cholesterol are linked to a greater risk of heart attack in young adults.

Fat tissue stem cells may help increase hair growth.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Finasteride causes temporary cell death in BPH tissues.

Hair loss improved with treatment and successful transplant.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Gintonin-enriched fraction promotes hair growth and could be a potential alopecia treatment.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

A woman's hair turned gray and fell out after starting a cancer drug called imatinib mesylate.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

LIPH mutations cause woolly hair in some Chinese people.

Clinics using lasers should have trained laser safety supervisors to reduce accidents and possibly lower insurance costs.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Young Indian women with PCOS have a higher risk of heart disease, not linked to thyroid function but to higher levels of certain fats and homocysteine.

Hair loss in young men in Central India is linked to severe heart disease.

Baldness may indicate higher heart disease risk in men.

LiPADI is a useful tool for monitoring the severity and treatment of lichen planus.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.