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Terbinafine is more effective than itraconazole for toenail fungus, especially in older patients, and debridement improves its effectiveness.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Both Ayurvedic treatments improved hair fall, with Shirodhara being especially effective.

Boswellia may improve skin inflammation symptoms and positively influence hair growth in mice.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

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

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

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

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

The research identified genes and pathways important for sheep wool growth and shedding.

Found key genes affecting hair loss, immune response, and skin development; more research needed for better treatments.

CD2 might be a new treatment target for patchy alopecia areata.

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

HOXC13 is essential for hair and nail development by regulating Foxn1.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

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

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

Hair follicles have a more inactive cell cycle than other skin cells, which may help develop targeted therapies for skin diseases and cancer.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

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