Virus vector design in gene therapy

Molecular Medicine Today

Volumn 1, Issue 9, 1995, Pages 410-417

  Günzburg, Walter H ^a   Salmons, Brian ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADENO ASSOCIATED VIRUS; ADENOVIRUS; ANIMAL; GENE THERAPY; GENE TRANSFER; GENE VECTOR; GENETICS; HUMAN; METHODOLOGY; RETROVIRUS; REVIEW; VIRUS;

ADENOVIRIDAE; ANIMALS; DEPENDOVIRUS; GENE THERAPY; GENE TRANSFER TECHNIQUES; GENETIC VECTORS; HUMANS; RETROVIRIDAE; VIRUSES;

EID: 0029417969     PISSN: 13574310     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1357-4310(95)90771-8     Document Type: Review

References (31)

1. Human gene therapy
2. Gene transfer into humans — immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction
3. Human gene therapy comes of age
4. Characteristics of a human cell line transformed by DNA from human adenovirus type 5
5. Region E3 of adenovirus: a cassette of genes involved in host immunosurveillance and virus-cell interaction
6. Packaging capacity and stability of human adenovirus type 5 vectors
7. Identification of a repeated sequence element required for efficient encapsidation of the adenovirus type 5 chromosome
8. Disseminated adenoviral infection presenting as acute pancreatitis
9. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis
10. A controlled study of adenoviral-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis
11. Rescue, propagation, and partial-purification of a helper virus-dependent adenovirus vector
12. Adeno-associated virus vectors transduce primary cells much less efficiently than immortalized cells
13. Targeted integration of adeno-associated virus (AAV) into human chromosome 19
14. DNA related to the transforming gene(s) of avian sarcoma viruses is present in normal avian DNA
15. Tumorigenesis by slow-transforming retroviruses — an update
16. Concerted activation of two potential proto-oncogenes in carcinomas induced by mouse mammary tumour virus
17. Non-viral gene therapy
18. Helper virus induced T cell lymphoma in non-human primates after retroviral mediated gene transfer
19. Low-pH induced conformational changes in viral fusion proteins: implications for the fusion mechanism
20. Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells
21. The ADA human gene therapy clinical protocol
22. Successful ex vivo gene therapy directed to liver in a patient with familial hypercholestrolaemia
23. Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir
24. Targeting of retroviral vectors for gene therapy
25. Retroviral vectors related to the myeloproliferative sarcoma virus allow efficient expression in hematopoietic stem and precursor cell lines, but retroviral infection is reduced in more primitive cells
26. Construction of retroviral vectors for targeted delivery and expression of therapeutic genes