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The document concludes that for hair and feather growth, it's better to target the environment around stem cells than the cells themselves.

Wnt signaling may be linked to heart diseases in aging and could be a target for future treatments.

Skin stem cells maintain and repair the outer layer of skin, with some types being essential for healing wounds.

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

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

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

Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

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.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Platelet-rich plasma may help hair follicle cells grow by affecting certain genes and pathways.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The document concludes that managing female hyperandrogenism requires a combination of identifying the cause, lifestyle changes, medication, and cosmetic treatments.

Trichoepitheliomas can be hard to distinguish from other skin conditions and often start in teenage years.

SA linked to mitochondrial issues and oxidative stress, while AGA involves disrupted hair growth genes.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Tiny RNA molecules help control the growth of plant hairs.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Forensic medicine is crucial for justice and needs continuous innovation and technology integration.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.