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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.

Lipase H is important for hair follicle function and shaping hair fibers.

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.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Phospholipase A2 enzymes play key roles in skin health and disease.

Botanical extracts can help treat hair loss in people with certain genetic conditions.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

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

Minoxidil can improve hair growth in some patients with woolly hair due to LIPH variants, with varying responses and mild side effects.

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

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

Minoxidil solution applied twice daily improved hair growth in patients with Woolly Hair/Hypotrichosis due to LIPH gene issues, with mild side effects.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

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

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

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Different genes are linked to various types of hair loss.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Squarticles, tiny particles made from sebum-derived lipids, can effectively deliver minoxidil, a hair growth drug, directly to hair follicles and skin cells, with less skin penetration and more tolerability.

Certain factors can start hair growth in adult skin by making cells communicate and form new hair follicles.

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