Gene therapy utilizes the delivery of DNA into cells, which can be accomplished by several methods, summarized below. The two major classes of methods... 36 KB (4,918 words) - 09:36, 27 February 2024 |
This article contains a list of commercially available gene therapies. Alipogene tiparvovec (Glybera): AAV-based treatment for lipoprotein lipase deficiency... 10 KB (792 words) - 10:27, 12 December 2023 |
Gene therapy for color blindness is an experimental gene therapy of the human retina aiming to grant typical trichromatic color vision to individuals with... 18 KB (2,336 words) - 18:26, 1 May 2024 |
Cystic fibrosis (redirect from Gene therapy for cystic fibrosis) using gene therapy as routine therapy is not suggested. A small study published in 2015 found a small benefit. The focus of much CF gene therapy research... 160 KB (17,980 words) - 13:05, 5 May 2024 |
Lentiviral vectors in gene therapy is a method by which genes can be inserted, modified, or deleted in organisms using lentiviruses. Lentiviruses are... 29 KB (3,448 words) - 01:15, 19 February 2024 |
Tay–Sachs disease (redirect from Gene therapy for Tay–Sachs disease) allele in certain populations. Researchers are looking at gene therapy or enzyme replacement therapy as possible treatments. Tay–Sachs disease is typically... 58 KB (6,403 words) - 00:57, 22 March 2024 |
Thalassemia (redirect from Gene therapy for thalassemia) Emmanuel (February 2016). "Gene Therapy of the β-Hemoglobinopathies by Lentiviral Transfer of the β – Gene". Human Gene Therapy. 27 (2): 148–165. doi:10... 60 KB (6,619 words) - 17:35, 4 May 2024 |