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Baldness in men with prostate cancer is linked to higher levels of certain sex hormones, but chest hair density is not.

Genetic differences may affect COVID-19 deaths; anti-androgens could be potential treatment.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Nuclear hormone receptors play a significant role in skin wound healing and could lead to better treatment methods.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

Sex hormones like estrogen and testosterone may affect COVID-19 severity differently in men and women, potentially influencing prevention and treatment strategies.

Genetic factors and diet significantly increase the risk of male pattern baldness.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Aromatase gene variation may increase female hair loss risk.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

AR/EDA2R gene linked to early-onset female hair loss, but 20p11 gene not involved.

Diagnosing hyperandrogenism in women is complex and requires accurate testing methods and consideration of SHBG levels.

Blocking prolactin increases the activity of secondary hair follicles in cashmere goats.

Skin problems in COVID-19 patients are rare and may be due to the body's complex immune response or blood clotting issues.

Experts recommend using evidence-based methods to diagnose and treat hirsutism, focusing on symptoms and underlying causes.

The document concludes that more research is needed to fully understand the causes of PCOS.

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

Vitamin D deficiency is common in women with PCOS and linked to some metabolic problems, but not the main cause of their metabolic issues.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

More research is needed to understand how testosterone is maintained in adult males.

Copper deficiency may cause hair loss, and treating it could involve nutrition and hormones.