Lentiviral vectors in gene therapy is a method by which genes can be inserted, modified, or deleted in organisms using lentiviruses. Lentiviruses are a...

Gene therapy using lentiviral vectors was being explored in early stage trials as of 2009.[needs update] In a Phase I clinical trial of three patients...

a lentiviral vector administered in a US human clinical trial. In May 2007, researchers announced the first gene therapy trial for inherited retinal disease...

patients using CRISPR-Cas9 technology have shown promising results. Nevertheless, there remains a few limitations of the technology's use in gene therapy: the...

Fondation pour la Recherche Médicale Retinal gene therapy using lentiviral vectors Viral vector Lentiviral vector in gene therapy Chimeric antigen receptor Charneau...

cMyc, using a retroviral system, while Thomson and colleagues used a different set of factors, Oct4, Sox2, Nanog, and Lin28, using a lentiviral system...

reportedly had been successfully treated in mice using gene therapy. The researchers used a viral vector to make the mice—which have essentially the same...

Stargardt disease is the most common inherited single-gene retinal disease. In terms of the first description of the disease, it follows an autosomal recessive...

of the IVF and ICSI procedure. HSC-based gene therapies prepared with gamma retroviral and lentiviral vectors have in some cases shown an increased risk...