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A protein called CBP is found in prostate cancer and can increase the effectiveness of certain prostate cancer treatments.

The equine epididymis mainly uses type 1 5α-reductase, and both finasteride and dutasteride can inhibit its activity.

Finasteride and dutasteride's effects are mainly due to target binding saturation and slow enzyme turnover.

Different types of PPARγ are found in varying amounts in human skin and its parts, which could affect how skin treatments work.

Some prostate cancers have gene changes that may affect treatment with certain drugs.

Two finasteride preparations are bioequivalent.

Transcutol P best increases Finasteride absorption for hair loss treatment.

A new method was developed to measure and assess the activity and inhibition of the enzyme steroid 5α-reductase.

The market for these drugs is expected to grow.

The conclusion is that a new test was created to find substances that affect specific ion channels, and it works well for drug discovery.

The research found enzymes in Stephania epigaea that help make cepharanthine.

Prostaglandins and the enzyme AKR1C3 could play a role in skin cancer and hair loss, and further research is needed to understand these mechanisms.

C60 fullerenes can alter protein function and may help develop new disease inhibitors.

Human liver enzyme DHEA ST helps process minoxidil.

New tests detect finasteride and dutasteride in urine quickly and easily.

Clove oil and grape seed extract increase finasteride skin absorption, while urea decreases it.

Different PADI isoforms help cells develop diverse functions.

Combining ciprofloxacin with other treatments may improve its effectiveness against resistant bacteria.

Regulatory challenges make developing combination therapies in urology difficult and costly.

Certain enzymes react strongly with some hormones in rat skin during hair growth, mainly in sebaceous glands and hair sheaths.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

FCE 28260 is a stronger and longer-lasting inhibitor of 5α-reductase than finasteride, which may make it a better treatment for certain medical conditions.

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.

Lack of cystatin M/E causes thin hair and dry skin.

The study developed accurate, precise, and environmentally friendly methods to measure Finasteride and Tadalafil in a new FDA-approved combination.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

New research is needed to create better drugs that block the enzyme responsible for conditions like male baldness and prostate enlargement.

Certain inhibitors applied to the skin can promote hair growth by maintaining a key hair growth signal.

We need to learn more about 5α-reductases and neuroactive steroids to safely make drugs targeting these enzymes.