Gene Therapy for Rare Diseases

Gene Therapy mainly involves the introduction or alteration of genetic material within a cell or organism with an intention of curing the disease. Both gene therapy and cell therapy are overlapping fields of biomedical research with the goals of repairing the direct cause of Genetic diseases in DNA or cellular population respectively, the discovery of recombinant DNA technology in the 1970s provided tools to develop gene therapy efficiently. Scientists use these techniques to readily manipulate viral genomes, isolate genes and identify mutations involved in human diseases, characterize and regulate gene expressions, and engineer various non- viral and viral vectors. Various long-term treatments for anaemia, 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.

 

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

Related Conference of Gene Therapy for Rare Diseases

January 27-28, 2020

3rd Global Experts Meeting on Infectious Diseases

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2nd Global Experts Meet on STD-AIDS and Infectious Diseases

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13thWorld Congress on Virology and Infectious Diseases

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7th International Congress on Infectious Diseases

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8th International Conference on HIV AIDS STD & STIs

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7th Global Congress on Rare Diseases & Orphan Drug

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10th World Congress on Rare Diseases and Orphan Drugs

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European Summit on HIV, STD and STIs

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September 28-29, 2020

13th Global Infections Conference

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12th Euro-Global Conference on Infectious Diseases

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Intercontinental Conference on Infectious Diseases

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