Cell & Gene Therapy
Gene therapy aims to transfer genetic material into cells to provide them with new functions. A gene transfer agent has to be safe, capable of expressing the desired gene for a sustained period of time in a sufficiently large population of cells to produce a biological effect. Identifying a gene transfer tool that meets all of these criteria has proven to be a difficult objective. Viral and nonviral vectors, in vivo, ex vivo and in situ strategies co-exist at present, although ex vivo lenti-or retroviral vectors are presently the most popular.Natural stem cells (from embryonic, hematopoietic, mesenchymal, or adult tissues) or induced progenitor stem (iPS) cells can be modified by gene therapy for use in regenerative medicine.
- In-vivo gene transfer
- Ex-vivo gene transfer
- Gene doping
- Application of gene therapy
- Allogeneic Cell Therapy
- Human embryonic stem cells
- Mesenchymal Stem Cell Therapy
Related Conference of Cell & Gene Therapy
March 09-10, 2026
21th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
Singapore City, Singapore
June 18-19, 2026
16th International Conference on Human Genetics and Genetic Diseases
Singapore City, Singapore
June 18-19, 2026
19th International Conference on Genomics & Pharmacogenomics
Singapore City, Singapore
Cell & Gene Therapy Conference Speakers
Recommended Sessions
- Advances in Stem Cell
- Biobanking
- Biomaterials and Bioengineering
- Bone and Cartilage Tissue Engineering
- Cancer Therapy
- Cell & Gene Therapy
- Cell and Organ Regeneration
- Cell Engineering
- Ethical and Legal Issues
- Immunotherapy
- Market Analysis
- Organ & Tissue Transplantation
- Regenerative Medicine
- Rejuvenation- Fight Aging
- Scaffolds for Tissue Engineering
- Stem Cell Therapy
- Tissue Culture & Preservation
- Tissue Repair and Regeneration
- Tissue Science & Engineering
- Translational Medicine
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