• Thumbnail for Lentiviral vector in gene therapy
    Lentiviral vectors in gene therapy is a method by which genes can be inserted, modified, or deleted in organisms using lentiviruses. Lentiviruses are a...
    29 KB (3,448 words) - 01:15, 19 February 2024
  • Thumbnail for Gene therapy
    used in clinical and research settings, pioneering lentivirals vector in gene therapy. Jesse Gelsinger's death in 1999 impeded gene therapy research in the...
    172 KB (17,769 words) - 04:04, 1 April 2024
  • Thumbnail for Viral vector
    onset of tumors in a mouse strain prone to tumors. Moreover, clinical trials that utilized lentiviral vectors to deliver gene therapy for the treatment...
    32 KB (3,573 words) - 14:14, 24 January 2024
  • 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...
    11 KB (1,503 words) - 22:06, 10 December 2023
  • express a specific CAR, using a vector derived from an engineered lentivirus such as HIV (see Lentiviral vector in gene therapy). The CAR programs the T cells...
    76 KB (8,019 words) - 21:29, 13 April 2024
  • hosts, and extended gene expression. Lentiviral vectors have also shown promise. Among challenges to clinical translation of gene therapy are possible immune...
    24 KB (2,918 words) - 05:14, 18 December 2023
  • (2014). "Long-term safety and tolerability of Pro Savin, a lentiviral vector-based gene therapy for Parkinson's disease: A dose escalation, open-label, phase...
    14 KB (1,819 words) - 05:17, 18 December 2023
  • Thumbnail for Gene delivery
    organism. Gene delivery is a necessary step in gene therapy for the introduction or silencing of a gene to promote a therapeutic outcome in patients and...
    24 KB (2,869 words) - 16:15, 28 August 2023
  • Lentivirus (redirect from Lentiviral)
    platelet-factor VIII, the gene that is mutated in human hemophilia. Lentiviral infection has advantages over other gene-therapy methods including high-efficiency...
    15 KB (1,711 words) - 12:25, 11 December 2023
  • "Inhibition of HIV-1 infection by lentiviral vectors expressing Pol III-promoted anti-HIV RNAs". Molecular Therapy. 8 (2): 196–206. doi:10.1016/s1525-0016(03)00165-5...
    48 KB (5,608 words) - 02:20, 6 February 2024
  • Thumbnail for Retrovirus
    ancestor at > 450 million years ago. Gammaretroviral and lentiviral vectors for gene therapy have been developed that mediate stable genetic modification...
    41 KB (4,727 words) - 15:08, 23 April 2024
  • Thumbnail 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) - 13:28, 21 April 2024
  • mutagenesis Poletti, Valentina; Mavilio, Fulvio (2021). "Designing Lentiviral Vectors for Gene Therapy of Genetic Diseases". Viruses. 13 (8): 5. doi:10.3390/v13081526...
    8 KB (1,037 words) - 11:48, 10 August 2023
  • Thumbnail for CRISPR gene editing
    regulation of disease-related genes may enable novel therapies for many diseases, especially in cases where adequate gene therapies are not yet developed or...
    151 KB (17,540 words) - 20:41, 26 April 2024
  • Thumbnail for Heparin
    Heparin (category Multiple chemicals in Infobox drug)
    retroviral and lentiviral vectors for gene therapy, allows it to be used for downstream purification of viral vectors. Heparin is being trialed in a nasal spray...
    77 KB (7,861 words) - 06:21, 9 April 2024
  • Thumbnail for Sickle cell disease
    therapy for sickle cell disease in humans were started in 2014. The clinical trials assessed the safety of lentiviral vector-modified bone marrow for adults...
    139 KB (14,950 words) - 06:30, 20 April 2024
  • Thumbnail for Short hairpin RNA
    Naldini L (November 2007). "Gene editing in human stem cells using zinc finger nucleases and integrase-defective lentiviral vector delivery". Nature Biotechnology...
    10 KB (1,259 words) - 12:22, 22 February 2024
  • Thumbnail for Didier Trono
    development of lentiviral vectors for gene therapy. Trono obtained an M.D. from the University of Geneva in 1982 and completed a clinical training in internal...
    11 KB (990 words) - 15:29, 31 January 2024
  • Thumbnail for Genome-wide CRISPR-Cas9 knockout screens
    2009). "State-of-the-art lentiviral vectors for research use: risk assessment and biosafety recommendations". Current Gene Therapy. 9 (6): 459–74. doi:10...
    55 KB (6,164 words) - 23:47, 3 December 2023
  • acknowledged specialist in HIV, lentiviral gene transfer vectors, and their medical applications. His discovery of the central DNA-flap structure in the HIV genome...
    9 KB (860 words) - 03:11, 29 March 2024
  • Thumbnail for Transduction (genetics)
    virus or viral vector. An example is the viral transfer of DNA from one bacterium to another and hence an example of horizontal gene transfer. Transduction...
    12 KB (1,392 words) - 09:01, 5 January 2024
  • Thumbnail for Michel Sadelain
    named icasM28z. In 2013, Sadelain co-founded Juno Therapeutics Inc. Sadelain also designed lentiviral vectors encoding the β-globin gene for the treatment...
    26 KB (2,399 words) - 09:23, 14 April 2024
  • Thumbnail for Severe combined immunodeficiency
    Morton J.; Sorrentino, Brian P. (18 April 2019). "Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1". New England Journal of...
    34 KB (3,231 words) - 09:48, 18 March 2024
  • Thumbnail for Marina Cavazzana
    and gene therapy. She has designed clinical trials based on lentiviral vector in gene therapy and pioneered the use of haematopoietic stem cell gene therapy...
    10 KB (1,027 words) - 10:58, 11 February 2024
  • Thumbnail for Feline immunodeficiency virus
    HIV-1, FIV has been engineered into a viral vector for gene therapy. Like other lentiviral vectors, FIV vectors integrate into the chromosome of the host...
    42 KB (4,960 words) - 06:25, 4 April 2024
  • Thumbnail for RNA interference
    Interfering RNA Delivery". Nonviral Vectors for Gene Therapy - Lipid- and Polymer-based Gene Transfer. Advances in Genetics. Vol. 88. pp. 71–110. doi:10...
    141 KB (15,437 words) - 06:13, 22 April 2024
  • Thumbnail for Small interfering RNA
    Morris KV, Rossi JJ (March 2006). "Lentiviral-mediated delivery of siRNAs for antiviral therapy". Gene Therapy. 13 (6): 553–8. doi:10.1038/sj.gt.3302688...
    55 KB (6,760 words) - 18:46, 18 April 2024
  • methods because they can transfer genes into a wide variety of human cells and have high transfer rates. Lentiviral vectors are also helpful due to their...
    34 KB (4,154 words) - 15:10, 6 April 2024
  • Betibeglogene autotemcel (category Approved gene therapies)
    safety of an improved lentiviral vector for the treatment of β-thalassemia and sickle cell disease" (PDF). Current Gene Therapy. 15 (1): 64–81. doi:10...
    20 KB (1,435 words) - 21:35, 26 January 2024
  • Thumbnail for Wiskott–Aldrich syndrome
    "Improved lentiviral vectors for Wiskott–Aldrich syndrome gene therapy mimic endogenous expression profiles throughout haematopoiesis". Gene Therapy. 15 (12):...
    37 KB (3,794 words) - 17:22, 24 January 2024