Gene Therapies

Gene therapy is designed to introduce genetic material into cells to compensate for abnormal genes and to form a beneficial protein. If a mutated gene causes a necessary protein to be faulty or missing or misfunctional, gene therapy could also be introduced with a normal copy of the gene to restore the function of the protein. Researchers usually do that employing a virus to hold the genetic cargo into cells, as a result of that’s what viruses evolved to do with their own genetic material. In the future, this technique could permit doctors to treat a disorder by inserting a gene into a patient’s cells rather than using medicine or surgery.

7th International Conference on Tissue Engineering & Regenerative Medicine October 02-04, 2017 Barcelona, Spain; 10th World Congress and Expo on Cell & Stem Cell Research March 19-21, 2018 New York, USA;

  • Vectors : Viral and Non-viral
  • Therapeutic Gene Modulation
  • Delivery System of Genes
  • Molecular Genetics

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August 23-24 , 2017

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Gene Therapies Conference Speakers