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Some African American women's central scalp hair loss is linked to genetics and past fungal scalp infections, with more research needed on other causes.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

Nonionic liposomes are the best for delivering genes to skin cells.

Noggin overexpression delays eyelid opening by affecting cell death and skin cell development.

Polycystic Ovary Syndrome is linked to higher risk of hypertension and heart disease.

There are still challenges in diagnosing and treating chronic skin diseases, but there is hope for future improvements.

The conclusion is that individual differences in COVID-19 severity are influenced by factors like age, sex, race, and genetics, which are important for personalized medicine.

The extracellular matrix is crucial for controlling skin stem cell behavior and health.

Prostaglandin D₂ might be targeted for new male pattern baldness treatments.

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

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

Some skin conditions may indicate metabolic syndrome, which could help with early detection and management of related health issues.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

Wnt signaling is important for development and cell regulation but can cause diseases like cancer when not working properly.

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Panax ginseng extract helps mice grow hair.

Hormones during pregnancy and lactation keep skin stem cells inactive, preventing hair growth.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

Adrenal disorders can cause lasting brain and behavior issues in children.

Skin and hair can regenerate after injury due to changes in gene activity, with potential links to how cancer spreads. Future research should focus on how new hair follicles form and the processes that trigger their creation.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Skin organoids are a promising new model for studying human skin development and testing treatments.

Girls with PCOS during adolescence have a higher risk of developing type 2 diabetes, and early treatment can help manage this risk.

Gene therapy, especially using atoh1, shows promise for creating functional sensory hair cells in the inner ear, but dosing and side effects need to be managed for clinical application.

Further research is needed to improve hair regeneration using stem cells and nanomaterials.

The study suggests that acne keloidalis nuchae is linked to conditions like pseudofolliculitis barbae, scalp infections, metabolic syndrome, and is more common in males with an average onset age of 25.4 years.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.