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Finasteride effectively treats hair loss and enlarged prostate in men, with mild side effects.

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

Researchers developed a quick and sensitive way to measure finasteride in blood using a small sample size.

Dutasteride effectively treats benign prostatic obstruction, improves urinary flow, reduces prostate size, and may prevent prostate cancer, but can cause sexual side effects.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Finasteride, a drug used for certain conditions, can cause serious side effects like sexual dysfunction, suicidal thoughts, and increased diabetes risk, and there's a need for more awareness and research about these effects.

Gene variant linked to prostate cancer, hormone levels, and hair loss.

Finasteride effectively treats BPH but may increase sexual dysfunction risk.

The European Society of Endocrinology advises individualized long-term management for PCOS, focusing on lifestyle changes, accurate diagnosis, and treatments for associated health risks and symptoms.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Finasteride doesn't effectively treat hair loss in postmenopausal women.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.

Sebocytes play a key role in controlling androgen levels in human skin.

Different animals have unique versions of the enzyme that changes testosterone into another hormone, which is important for creating effective treatments for prostate and hair loss conditions.

Testosterone's muscle-building effects do not require its conversion to DHT.

Finasteride effectively inhibits 5α reductase, while plant extracts like Permixon and Bazoton don't show significant results.

Finasteride and minoxidil are effective for hair regrowth, while treatments for alopecia areata have varying success and continuous treatment is necessary.

Inhibiting 5α-reductase can help reduce prostate cancer risk and improve treatment.

Finasteride, CPA, and flutamide are all equally effective in reducing excessive hair growth in women.

The conclusion is that hair growth can be improved by activating hair cycles, changing the surrounding environment, healing wounds to create new hair follicles, and using stem cell technology.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Both drugs lower DHT levels, with GI198745 being more effective.

Spironolactone can reduce hair growth in women with hirsutism.

Dihydrotestosterone increases the activity of an enzyme in pubic skin cells that converts testosterone to dihydrotestosterone.

Finasteride reduces hair loss and treats BPH without major hormone changes, but may cause sexual dysfunction.

Androgen conjugates might be better indicators of skin sensitivity to hormones in women with excessive hair growth.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Diane 35 plus finasteride is more effective in reducing hair growth and androgen levels, but may decrease libido.

Use "female pattern hair loss" term, assess androgen excess, treat with minoxidil and other medications if needed.