HIV Gene Therapy
HIV gene therapy is designed to remove or control HIV infection by addressing the virus's genetic material. Approaches include modifying immune cells' genes to withstand infection, adding antiviral genes, and utilizing CRISPR to remove viral DNA from infected cells. These novel techniques aim to give long-term control or even a cure for HIV, changing virus management.
Related Conference of HIV Gene Therapy
February 24-25, 2025
19th International Conference on Regenerative Repair and Medicine
Madrid, Spain
April 03-04, 2025
15th International Conference on Human Genetics and Genetic Diseases
Madrid, Spain
April 29-30, 2025
3rd International Conference on Cell Science and Molecular Biology
Barcelona, Spain
October 27-28, 2025
20th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
Madrid, Spain
HIV Gene Therapy Conference Speakers
Recommended Sessions
- Advanced Gene Therapeutics
- Cancer Therapies
- CAR T-cell Therapy
- Cell Culture and Bioprocessing
- Cell Science and Stem Cell Research
- Cellular Therapies
- Clinical Trials and Research in Cell and Gene Therapies
- Diabetes Gene Therapy
- Genetic Vaccines
- HIV Gene Therapy
- Human Gene Therapy
- Molecular Epigenetics
- Nano-Therapy
- Nanotechnology in Stem Cell
- Novel Stem Cell Therapy
- Skin Cell Therapy
- Stem Cell Engineering
- Stem Cell in Cardiovascular Disease
- Stem Cell in Drug Development
- Stem Cell Therapies
- Viral Gene Therapy
Related Journals
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- Stem Cell Research: - Human Genetics 2025 (Spain)
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