Gene Therapy
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 misfunctioned, 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.
- Vectors : Viral and Non-viral
- Therapeutic Gene Modulation
- Delivery System of Genes
- Molecular Genetics
- Clinical Genetics
Related Conference of Gene Therapy
March 25-26, 2024
14th International Conference on Human Genetics and Genetic Diseases
Montreal, Canada
Gene Therapy Conference Speakers
Recommended Sessions
- Cell Therapy
- Anti-Aging and Regenerative Medicine
- Biobanking
- Biological Tissue Substitutes
- Biomaterials and Bioengineering
- Bone and Cartilage Tissue Engineering
- Cancer Cell Biology
- Cell & Organ Regeneration
- Cell Engineering
- Dental Stem Cells and Tooth Regeneration
- Epigenome and Epigenetic Analysis
- Future of Cancer Care
- Gene Therapy
- Immunology
- Novel Approaches in Guided Tissue Regeneration
- Organ Engineering
- Personalized Medicine
- Stem cells
- Tissue Culture & Preservation
- Tissue Engineering
- Tissue Repair And Regeneration
- Translational Medicine
- Vitrification
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