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

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.

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.

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.

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.

Birds can lose neck feathers due to a genetic change that increases a gene's activity, helping them adapt to heat.

Sensitive skin is often caused by nerve fibers and environmental factors, and can be managed with mild skincare and professional advice.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Long-term testosterone therapy can cause hormone suppression, affect prostate and heart health, and alter physical characteristics, but does not increase prostate cancer risk and needs more research for full risk assessment.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.