Gene Therapy

Gene therapy primarily involves the introduction or alteration of genetic material within a cell  or organism with an intention of curing the disease. Both cell therapy and gene therapy are overlapping fields of biomedical analysis with the goals of repairing the direct cause of genetic diseases in dna or cellular population respectively. The invention of recombinant dna technology within the 1970s provided tools to efficiently develop gene therapy. Scientists use these techniques to promptly manipulate viral genomes, isolate genes and determine mutations concerned in human disease, characterize and regulate gene expressions, and engineer numerous viral and non-viral vectors. Numerous long term treatments for anemia, haemophilia, cystic fibrosis, muscular dystrophy, Gauscher’s disease, lysosomal storage diseases, cardiovascular diseases, diabetes and diseases of bones and joints are resolved through successful gene therapy and are elusive these days.

 

    Related Conference of Gene Therapy

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