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The document concludes that future heart disease research should account for sex-specific differences to improve diagnosis, treatment, and outcomes.

Polyamines help fix DNA damage accurately in cells.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

Hair loss in balding individuals is linked to changes in specific hair growth-related genes.

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

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

New genes found linked to balding, may help develop future treatments.

Plant steroid hormones show growth, health, and medicinal benefits in various organisms, including potential for treating diseases.

Female pattern hair loss diagnosed by scalp appearance, treated with combined therapies and targeted approaches.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

Assessing newborn scalp hair can reveal important health information.

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

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

High levels of androgens during early development may cause PCOS-like symptoms.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

Longer CAG repeat lengths in the androgen receptor gene are linked to higher testosterone levels in women with PCOS.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

Lifestyle changes are the main treatment for PCOS, which is a complex condition requiring early management to reduce its health impacts.

Genetic variations affecting skin structure play a key role in severe acne.

Hoxc genes control hair growth through Wnt signaling.

Female pattern hair loss has unclear causes, possibly involving genetics, hormones, and environment, and needs better treatments.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Certain metabolites are lower in women with PCOS and could be potential markers for the condition.

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

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Women with PCOS often have mood disorders and a lower quality of life, and treatment should focus on both physical and mental health.