Viruses naturally reproduce by transferring genetic material into cells for transcription and translation. Scientists harness this ability to introduce genetic sequences and modulate cellular function ...

Example for viral gene therapy using an Adenovirus vector. A new gene is inserted into an adenovirus vector, which is used to introduce the modified DNA into a human cell. If the treatment is ...

This combination of engineered DNA inside the AAV shell (the capsid) is called a vector ... other types of therapies. This may lead to regulators having more questions about gene therapy ...

We can prepare viral vectors to Good Laboratory Practice standards. The preclinical data generated by agents produced by the GLP practice can be valuable in the later development of clinical trials in ...

This research evaluates the effects of various gene therapy viral vectors on RPE cells to determine efficacy for therapeutic ...

Next-generation sequencing allows for critical insights into gene therapy products, which can help streamline and accelerate ...

Cyclosporin H boosts a new lentivirus-delivered gene therapy with enhanced anti-sickling properties in blood stem cells from ...