Curing Genetic Diseases through Genome Reprogramming, Volume 182 captures an historic moment in the field of gene therapy―the dawn of a new age in which the dream of curing genetic diseases has become realizable. The volume presents the most clinically advanced gene therapy and genome editing approaches for the treatment of genetic diseases in specific organs, including difficult therapeutic targets, futuristic ideas of genetic interventions, and large scale human genome repair. An initial chapter addresses the complex ethical aspects involved in the very idea of modifying the human genome.
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Gianluca Petris is currently a Marie Skłodowska-Curie European Fellow and Investigator Scientist developing synthetic genomics tools at the Medical Research Council (MRC) Laboratory of Molecular Biology, Cambridge, United Kingdom. Prior to that, as a postdoctoral fellow at the Department of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Italy, he developed and applied CRISPR technologies and delivery vehicles for the correction of genetic diseases. Dr. Petris published several papers in the field of CRISPR-therapeutics and CRISPR applications, filed four patent families and co-founded a company for the development of gene therapies for genetic diseases. He was awarded a MSc Degree in Medical Biotechnology working on antibody engineering and rotavirus at the University of Trieste, Italy, and a PhD in Life Sciences (Open University, United Kingdom) in recognition of his research on protein folding and protein quality control carried out at the International Centre for Genetic Engineering and Biotechnology (ICGEB), Trieste, Italy.
Curing Genetic Diseases through Genome Reprogramming captures an historic moment in the field of gene therapy: the dawn of a new age in which the dream of curing genetic diseases has become realisable. The volume develops from the most clinically advanced gene therapy and genome editing approaches, for the treatment of genetic diseases in specific organs, towards the most difficult therapeutic targets and futuristic ideas of genetic interventions and large scale human genome repair. A specific initial chapter is dedicated to address the complex ethical aspects involved in the very idea of modifying the human genome.
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