Gene Therapy

Technique that uses genes to treat or prevent human disease by normal Genes into cells in place of missing or defective ones in order to correct genetic disorders is commonly known as Gene therapy. To treat a disorder by inserting a gene into a patient's cells instead of using drugs or surgery. Gene therapy is designed to introduce genetic material into cells to compensate for abnormal genes or to make a beneficial protein. If a mutated gene causes a necessary protein to be faulty or missing, gene therapy may be able to introduce a normal copy of the Gene to restore the function of the protein.

  • Track 1-1 Hepatitis
  • Track 2-2 ZFNs
  • Track 3-3 TALENs
  • Track 4-4 Muscular dystropy
  • Track 5-5 cystic fibrosis
  • Track 6-6 Somatic gene therapy
  • Track 7-7 Germline gene therapy
  • Track 8-8 Gene augmentation therapy
  • Track 9-9 Gene inhibition therapy
  • Track 10-10 Prolotherapy

Related Conference of Genetics & Molecular Biology