Stem Cell and Genetic Clinical Research

A novel treatment area of contemporary medicine is gene therapy. Its development is a natural outcome of the revolution ushered in by the development of recombinant DNA technology in the 1970s. Although gene therapy is still very experimental, it has the potential to be a significant therapeutic approach. In theory, it permits the introduction of genetic material into the tissues and organs of patients. As a result, damaged genes can be removed or have their normal functions restored. Additionally, the process enables cells to acquire new capabilities, such as the ability to produce immune system mediator proteins that aid in the fight against cancer and other disorders. Monogenic hereditary illnesses like cystic fibrosis were formerly thought to be the main targets for gene therapy.

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