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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.

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

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

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

A gene mutation causes woolly hair in a Syrian patient.

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.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

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

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

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

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

Ion-paired risedronate significantly increases skin penetration without irritation compared to risedronate alone.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

Eyelashes protect the eyes, but more research is needed to understand how.

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

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

Lysophosphatidic acid is important for skin health and disease, and could be a target for new skin disorder treatments.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

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.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.