Gene therapy is designed to introduce genetic material into cells to compensate for abnormal genes or to produce a beneficial protein. If a mutated gene results in the failure or disappearance of a necessary protein, gene therapy may be able to introduce a normal copy of the gene to restore the function of the protein.
A gene that is inserted directly into a cell usually doesn't work. Instead, a carrier called a vector is genetically engineered to deliver the gene. Some viruses are often used as vectors because they can transmit the new gene by infecting the cell. Viruses are modified to not cause disease when used in humans. Certain types of viruses, such as retroviruses, integrate their genetic material (including the new gene) into a chromosome in the human cell. Other viruses, such as adenoviruses.
Posters & Accepted Abstracts: Molecular and Genetic Medicine
Posters & Accepted Abstracts: Molecular and Genetic Medicine
Posters & Accepted Abstracts: Molecular and Genetic Medicine
Posters & Accepted Abstracts: Molecular and Genetic Medicine
Posters & Accepted Abstracts: Molecular and Genetic Medicine
Posters & Accepted Abstracts: Molecular and Genetic Medicine
Scientific Tracks Abstracts: Journal of Molecular Biomarkers & Diagnosis
Scientific Tracks Abstracts: Molecular Biomarkers & Diagnosis
Scientific Tracks Abstracts: Journal of Tissue Science and Engineering
Scientific Tracks Abstracts: Journal of Tissue Science and Engineering
Posters-Accepted Abstracts: Journal of Tissue Science and Engineering
Posters-Accepted Abstracts: Journal of Tissue Science and Engineering
Posters & Accepted Abstracts: Molecular Biology: Open Access
Posters & Accepted Abstracts: Molecular Biology: Open Access
Journal of Genetics and Genomes received 65 citations as per Google Scholar report