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The androgen receptor is a promising target for breast cancer treatment, especially in triple-negative cases, but more research is needed for personalized therapies.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Personalized treatment with inhibitors, minoxidil, and laser therapy helps hair loss.

The genes OVOL1 and OVOL2 are important for hair growth and may be involved in a type of skin tumor.

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

Lifestyle changes are the first step in treating infertility in PCOS, followed by medications like clomiphene and metformin, and then surgery if needed.

The document concludes that Functional Hypothalamic Amenorrhea should be carefully diagnosed and managed to prevent health complications, using lifestyle changes and specific medications.

The perception of excessive hair growth in women as abnormal is more influenced by cultural norms than by medical reasons.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Women with Systemic Lupus Erythematosus should have closely monitored pregnancies and avoid certain medications to improve their pregnancy outcomes.

Hair loss in autoimmune blistering skin diseases varies and may regrow with disease control.

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

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

Shrunken heads retain some facial features and hair characteristics, allowing for limited individual identification.

Finasteride reduces prostate cancer risk but may increase high-grade cancer chances.

Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Two mouse mutations cause similar hair loss despite different skin changes.

Testosterone is crucial for development, growth, and various body functions in mammals.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Chinese women with PCOS have higher androgen levels, which change with age and weight.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.