Gene Therapy

Gene therapy essentially involves the introduction or alteration of genetic material among the cell or organism with associate intention of curing of the sickness. The individual cell therapy and gene therapy uses overlapping fields of medical analysis with the goals of repairing the direct  Genetic diseases in polymer or cellular population respectively, the invention of DNA technology within the 1970’s provided tools with efficiency develop gene theraphy. Scientists use these techniques to promptly manipulate infective agent genomes, isolate genes and establish mutations concerned in human sickness, characterize and regulate sequence expressions, and engineer numerous infective agent and non-viral vectors. Numerous long-term treatments for anemia, hemophilia, mucoviscidosis, genetic defect, Gauscher’s sickness, lysosomal storage diseases, vas diseases, polygenic disease and diseases of bones and joints are resolved through successful gene therapy.

 

  • Process of gene therapy
  • Gene therapy products
  • Different vectors for gene therapy
  • Gene therapy for malignant melanoma
  • Gene therapy for sickle-cell disease
  • Development of regenerative treatment models

Related Conference of Gene Therapy

August 25-25, 2022

7th International Conference on Molecular Medicine and Diagnostics

Singapore City, Singapore
September 19-20, 2022

International Summit on Genomics and Proteomics

Dublin, Ireland
September 19-20, 2022

15th World Congress on Stem Cell Research

Dublin, Ireland
October 17-18, 2022

21st International Conference on Structural Biology

Barcelona, Spain
November 21-22, 2022

4th Annual summit on Cell Signaling and Cancer Therapy

Montreal, Canada

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