1.0CTGCThttps://ctgct.si/en/Rodrigo Ortizhttps://ctgct.si/en/author/rodrigoctgct/Duško Lainšček interviewed by Svet24 - CTGCTrich600338<blockquote class="wp-embedded-content" data-secret="Qa090xnHSx"><a href="https://ctgct.si/en/objave/dusko-lainscek-interviewed-by-svet24/">Duško Lainšček interviewed by Svet24</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://ctgct.si/en/objave/dusko-lainscek-interviewed-by-svet24/embed/#?secret=Qa090xnHSx" width="600" height="338" title="“Duško Lainšček interviewed by Svet24” — CTGCT" data-secret="Qa090xnHSx" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript">
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https://ctgct.si/wp-content/uploads/2026/07/Dusko-interview.jpg29442273How does a breakthrough gene therapy begin? What does it take to turn a scientific idea into a treatment that can reach a patient?In this interview, Duško Lainšček, researcher at the Institute of Chemistry of Slovenia and member of the Centre for the Technologies of Gene and Cell Therapy (CTGCT), shares his journey from veterinary medicine to the forefront of genome editing and gene therapy development. He discusses the promise of CRISPR-based technologies, the challenges of translating research into clinical applications, and the remarkable story behind the development of a pioneering therapy for CTNNB1 syndrome.