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Future efforts should focus on improving target specificity, minimizing toxicity, and exploring the dual potential of both inhibition and activation of CYP51A1 depending on disease context
MSC manufacturing for academic clinical trials: from a clinical-grade to a full GMP-compliant process
Following the final wash, the supernatant was aspirated to a final volume of 200 L
Regulatory Harmonization: Policymakers must work towards regulatory harmonization to streamline approvals across different regions
Patients on testosterone therapy who are interested in trial participation should inform their prescribing clinician and search for eligible UK studies via the NIHR 'Be Part of Research' portal
Both of these approaches are dangerous and unnecessary
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