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Camellia oleifera seed shell polyphenols and 1,3,6-tri-O-galloylglucose can help treat hair loss by reducing certain hormones and promoting hair growth.

Too much AKR1C3 enzyme causes resistance to finasteride by increasing testosterone.

Flutamide caused damage to male rat reproductive organs and may affect fertility.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

Asian hair loss differs from Europeans; consider individual needs and psychological well-being for treatment.

Avicennia Marina extract and avicequinone C can reduce hair loss hormone production and increase hair growth factors, suggesting they could be used to treat androgenic alopecia.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Hormones and metabolism play a complex role in prostate enlargement, and more research is needed to improve diagnosis and treatment.

Bolandiol, a synthetic steroid, builds muscle and bone without greatly affecting sex glands, and works differently from other hormones.

Normal levels of DHT can reduce belly fat and increase muscle, but too much can lead to hair loss, prostate issues, and possibly heart disease.

New regenerative therapies show promise for treating hair loss.

Adenosine helps human hair grow and prevents hair loss by targeting specific cells.

AR polyglycine repeat doesn't cause baldness.

Mice with human gene experienced hair loss when treated with DHT.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

New compounds were made that are promising for prostate cancer therapy.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

A substance called Cell-free fat extract can effectively treat common hair loss by increasing hair growth and density.

Testosterone affects androgen receptors and lipid storage in cells, while DHEA does not convert to testosterone or affect these receptors in the same way.

Enobosarm may effectively treat androgen receptor-positive breast cancer with fewer side effects.

A three-month treatment with a GnRH agonist significantly lowered androgen levels and 5α-reductase activity in men with benign prostatic hyperplasia.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Dutasteride and finasteride affect different cell types differently.

A gene called BMAL1 plays a role in controlling hair growth.

Androgen receptors are active in many tissues of both male and female mice, not just reproductive organs.

Male children's genital development issues can be caused by genetic mutations or environmental factors affecting hormone action.

Prostate cancer cells can make their own androgens to activate the androgen receptor, and treatments like abiraterone may increase this ability, suggesting new therapies should target the entire steroid-making pathway.

Androgens may cause hair loss by increasing TGF-beta1 from scalp cells, which inhibits hair cell growth.