CERA

About

Dr Daniel Urrutia Cabrera

Research Fellow

Dr Daniel Urrutia Cabrera’s research focuses on using cellular reprogramming and gene therapy – aiming to develop innovative treatments for retinal degenerative diseases.

Dr Daniel Urrutia Cabrera

Research Fellow

BSc, MSc, PhD

Dr Daniel Urrutia is a Research Fellow in the Cellular Reprogramming Research team at the Centre for Eye Research Australia (CERA).

He has contributed to more than 12 research projects at leading institutions in Australia, Germany and Mexico. Dr Urrutia completed his MSc at the University of Göttingen (Germany) and his PhD at CERA with the support of a Melbourne Research Scholarship.

Alongside Professor Raymond Wong, Dr Urrutia is the co-inventor of a patented technology to repair the retina through the generation of new photoreceptors using cellular reprogramming. This technology has been licensed to CERA’s biotech startup, Mirugen Pty Ltd, with the objective of accelerating its translation into the clinic.

Currently, Dr Urrutia’s research aims to bridge his technical expertise in stem cells, gene therapy and tissue engineering with research commercialisation and patient advisory groups to drive high-impact translational research.

Key research questions
  • How can we generate retinal cells in the laboratory using cellular reprogramming and stem cell technologies?
  • Can cellular reprogramming rejuvenate the retina and treat retinal degenerative diseases?
  • How can we improve the cargo capacity of viral vectors for use in retinal gene therapy?
  • What signals cause retinal diseases and ageing?

Current projects

Selected publications

Key collaborators

Funding and support

Current projects

  • Using cellular reprogramming to stimulate the production of new photoreceptors as a treatment for retinal degenerative diseases.
  • Epigenetic reprogramming as an innovative approach to rejuvenate and protect the retina from degeneration.
  • Understanding the molecular signals that define retinal cell identity, ageing and disease.
  • Optimisation of viral vectors for retinal gene therapy.

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