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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.

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

Fat tissue stem cells may help increase hair growth.

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.

Megestrol acetate helps fat-derived stem cells grow, move, and turn into fat cells through a specific receptor.

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

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

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.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

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

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

The research found that certain microRNAs are important for human hair growth and health.

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

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

The endocannabinoid system affects oil production and inflammation in skin cells.

Zinc deficiency disrupts hair growth and cycle, but zinc supplements can fix this.

Certain steroids in the brain affect mood and symptoms of depression, and treatments targeting these steroids show promise for improving these symptoms.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Finding functions for unknown GPCRs is hard but key for making new drugs.

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

Asia has made significant progress in tissue engineering and regenerative medicine, but wider clinical use requires more development.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

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.

Different types of fibroblasts play various roles in both healthy and diseased tissues, and understanding them better could improve treatments for fibrotic diseases.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

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

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.