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Finasteride use is linked to a lower risk of bladder cancer, especially in Caucasians and Hispanics.

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

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Auranofin shows promise as a cancer treatment, especially when combined with other therapies.

Blocking IL-17 can reduce joint inflammation in Ross River Virus infections.

Some men's prostate tissues have low enzyme levels due to genetic changes, possibly affecting treatment for prostate enlargement.

Patients with advanced breast cancer prioritize quality of life, overall survival, and progression-free survival in treatment decisions.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The rib-sparing technique in breast reconstruction may lead to more complications without reducing the need for further surgery.

PH-762 shows promise in treating skin cancer by effectively targeting and silencing PD-1 in tumors with minimal side effects.

Two specific genetic markers increase the risk of hair loss in Asian populations.

Quality of life, overall survival, and progression-free survival should be equally prioritized in advanced breast cancer treatment decisions.

Dalpiciclib is the safest and most satisfying CDK4/6 inhibitor for advanced breast cancer patients in China.

Certain blood markers can help predict and manage chemotherapy side effects in older cancer patients.

Certain genetic variants increase the risk of aggressive prostate cancer.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Vemurafenib causes skin side effects similar to RASopathies, requiring regular skin checks and UVA protection.

Finasteride side effects in young men may be linked to specific gene variations.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

Asiasari radix extract may be a potential treatment for melanoma because it selectively triggers cell death in melanoma cells by affecting p53 regulation.

PROTACs show promise in cancer treatment by effectively degrading specific harmful proteins.

5-Alpha-Reductase Inhibitors can cause negative side effects.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Ritlecitinib may cause severe musculoskeletal pain in some alopecia universalis patients.

The compounds tested could potentially treat hair loss and alopecia.