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Loss of the p53 gene alone causes tumors, and losing both p53 and Rb genes speeds up aggressive skin cancer.

17-β estradiol and prednisolone may speed up hair regrowth after chemotherapy.

The combination of tadalafil and finasteride improves urinary symptoms and erectile function in men with enlarged prostates.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Two new gene clusters important for hair formation were found on human chromosome 11.

A gene mutation causes woolly hair in a Syrian patient.

Inhibitors of the enzyme 5 alpha-reductase could potentially treat disorders like prostate cancer and baldness.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

Encapsulating chlorogenic acid in nanoparticles boosts type 17 collagen production, potentially aiding skin care.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

A new mutation in the HR gene causes hair loss in a specific family.

Seven new genetic risk areas for prostate cancer were found.

Incidental prostate cancer was found in 4.89% of patients undergoing surgery for benign prostatic hyperplasia.

Inactivating both p53 and Rb genes in mice speeds up aggressive skin cancer development.

Steroid sex hormones activate matriptase in prostate cancer cells but not in breast cancer cells.

2-Methoxyestradiol causes cancer cell death by activating specific pathways, but androgens can block this effect.

The new delivery system improved raloxifene's skin absorption and effectiveness against cancer cells.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Different species and human skin models vary in their skin enzyme activities, with pig skin and some models closely matching human skin, useful for safety assessments and understanding the skin's protective roles.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A new therapy for a skin blistering condition has not been developed yet.