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The first Japanese case of a genetic hair disorder caused by specific mutations in the LIPH gene was identified.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Hormone replacement therapy may improve hair growth in the frontal hairline of postmenopausal women with hair loss.

A genetic variant linked to hair thinning in Japanese women was found.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

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

Higher cortisol levels are linked to poor coping, while higher DHEA levels are linked to job confidence.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

5% minoxidil works better for hair growth than 1% minoxidil.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

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

Epigenetic differences affect hair loss in identical Japanese male twins.

1% topical minoxidil solution significantly improved hair growth in Japanese women with androgenetic alopecia, with no major side effects.

Finasteride is effective and safe for long-term use in treating hair loss in Japanese men.

The emulgel with Saw Palmetto and Sophora Japonica shows promise for treating hair loss.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Dr. Shoji Okuda was a pioneer in hair transplant surgery, but his work was initially overlooked and is now recognized alongside Dr. Norman Orentreich.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

Japanese researchers created new hair follicles from human cells that grew hair when put into mice, and other findings showed a link between eye disease severity and corneal thickness, gene mutations affecting hearing and touch, and the safety of the shingles vaccine for adults over 50.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Longer CAG repeats in gene linked to more severe hair loss in females.

An 82-year-old man's white hair regained color after taking etretinate for psoriasis.

A man got heart infection from scalp infection caused by artificial hair implants.

Hair loss in a drug reaction case involved both a common shedding phase and an immune attack on hair follicle stem cells.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Hair loss is due to thinner hairs, not less hairs; hair diameter indicates balding progression and treatment effectiveness.

A gene variation is linked to hair thickness in Asians.

Human hair contains various lipids that vary among individuals and help protect the hair.

Older people's hair becomes less shiny because it gets more uneven and curved.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.