I am a scientist, businessman, author, and philanthropist. For nearly two decades, I was a professor at Harvard Medical School and Harvard School of Public Health where I founded two academic research departments, the Division of Biochemical Pharmacology and the Division of Human Retrovirology.
This story is part of a series on the current progression in Regenerative Medicine. In 1999, I defined regenerative medicine as the collection of interventions that restore tissues and organs damaged by disease, injured by trauma, or worn by time to normal function. I include a full spectrum of chemical, gene, and protein-based medicines, cell-based therapies, and biomechanical interventions that achieve that goal.
Imagine being able to eliminate the root cause of diseases by manipulating genes. Thanks to the transformative field of gene therapy, this prospect is no longer just a far-fetched idea but an exciting reality.between 2000 and the 2010s, marking a golden era in medical history. These breakthroughs have opened up new possibilities and treatments for previously incurable genetic disorders, giving hope to millions of people around the world.
The leukemia cases in the SCID-X1 trials highlighted the importance of carefully designing gene therapy vectors to avoid unintended activation of oncogenes. This setback led to iand propelled gene therapy into a new age. The project facilitated gene therapy by identifying genes for various conditions and diseases, thus. This type of medicine uses genome sequencing and data analysis to customize diagnosis and treatment based on an individual's genetic makeup.
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