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Dutasteride is more effective for male pattern baldness than finasteride, and black cohosh extract BNO 1055 is as effective as conjugated estrogens in treating postmenopausal symptoms, with added benefits in reducing sweating and mental symptoms.

The study created a new method to test drugs that affect hormone processing in skin.

Dihydrotestosterone gel improved well-being and sexual function in older men without negatively affecting prostate health.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

Loop diuretics may double bone loss in elderly men, finasteride lowers prostate cancer risk but may increase high-grade tumors, abarelix reduces testosterone quickly, and transdermal testosterone offers minimal sexual benefit for women.

RU58841, a substance from France, can potentially block the effects of hormones that cause hair loss and excessive hair growth, performing better than a similar substance, cyproterone acetate.

Dutasteride is becoming a popular hair loss treatment, proving more effective than finasteride with similar side effects.

The study created a model to help design new inhibitors for steroidal 5α-reductase enzymes.

Dutasteride helps hair growth in those unresponsive to finasteride, but may cause more sexual dysfunction.

Cyproterone acetate is used to treat conditions like prostate cancer, early puberty, excessive sexual drive, and female androgenization by affecting androgen functions and suppressing certain hormones.

Low-dose DMSO may help treat castration-resistant prostate cancer by reducing key cancer cell receptors.

Dihydrotestosterone specifically binds to hamster sebaceous glands, with a higher affinity than testosterone.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Both birth control pills improved hormone levels and skin conditions in women with hyperandrogenism, but the one with drospirenone was more effective.

A rigid compound with a common structural motif was successfully synthesized.

Anti-androgen drugs can treat conditions like prostate cancer and male pattern baldness by blocking effects of testosterone and DHT.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Finger length ratios are not linked to the number of specific gene repeats affecting testosterone sensitivity.

Manipulating 5α-reductase type 2 can affect liver fat production and glucocorticoid effects.

Neurosteroids are crucial for stress response, and targeting specific receptors may help treat certain disorders.

The nature of the side chain in RU 58841 derivatives greatly affects its AR affinity, with the N-(iodopropenyl) derivative 13 showing the highest AR binding affinity, suggesting its potential for developing high-affinity radioiodinated AR radioligands.

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

The treatment improved acne, seborrhoea, and hirsutism, with some side effects like spotting and nervousness.

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 compounds were made that block an enzyme linked to breast cancer better than existing treatments.