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Androgens play a complex role in skin conditions like acne and hair loss in women, and normal blood levels don't always show true androgen status.

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

FOXN1 gene variants cause low T cells and immune issues from birth.

Polycystic Ovary Syndrome is common but often undiagnosed, and early treatment is important to prevent health problems.

Men are more likely to get infectious skin diseases, while women are more prone to autoimmune and pigment-related skin conditions, influenced by biological and environmental factors.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

PNU157706 reduced rat sperm movement and fertility without affecting offspring health.

Type I interferons play a key role in the development of various skin diseases.

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

WNT10A mutations cause varied symptoms in patients with odonto-onycho-dermal dysplasia.

The normal human prostate does not significantly affect blood DHT levels.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

The document concludes that diagnosing PCOS in teenagers is difficult and should focus on specific hormone levels and menstrual irregularities, while also considering treatment for symptoms and related health issues.

Finasteride side effects in young men may be linked to specific gene variations.

Researchers found a gene mutation responsible for a rare hair loss condition.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Some skin diseases and their treatments can negatively affect male fertility.

Early diagnosis and treatment of PCOS in young people is important to prevent long-term health problems.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

Various treatments exist for hair loss, but more research is needed for better options.

COVID-19 may affect male fertility and women might have better outcomes due to hormonal and immune differences.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Adult stem cells with Tp63 can form hair and skin cells when placed in new skin, showing they have hidden abilities for skin repair.

Androgens can both increase body hair and cause scalp hair loss.

Androgenic Alopecia, a common hair loss condition, can be effectively treated with finasteride and other treatments.

Mercury allergy linked to specific genes may contribute to burning mouth syndrome, and silicon might play a role in maintaining healthy hair.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

The document concludes that more research is needed to create suitable diagnostic criteria and understand PCOS in Korean women, and genetics may allow for personalized treatment.