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Number of results

Journal

2007 | 3 | 33-44

Article title

AAV vectors for gene therapy

Title variants

Languages of publication

PL

Abstracts

EN
This paper reviews the principles of the AAV vectors' generation. It describes various methods for their production and purification, as well as ways for increasing the efficiency and selectivity of the transduction by means of capsid modifications and use of various AAV serotypes. The second part of the article briefs clinical trials carried out so far with the use of the AAV vectors, particularly emphasizing the differences between feasibilities of vectors based on AAV and other virus types.

Keywords

Journal

Year

Issue

3

Pages

33-44

Physical description

Contributors

author
author
author
author

References

Document Type

REVIEW

Publication order reference

Jozef Dulak, Zaklad Biotechnologii Medycznej, Wydzial Biochemii, Biofizyki i Biotechnologii, Uniwersytet Jagiellonski, ul. Gronostajowa 7, 31-271 Krakow, Poland

Identifiers

YADDA identifier

bwmeta1.element.element-from-psjc-716f4b2c-6a66-3513-92bc-369d25e950da
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