Striving for ideal viral constructs by modifying its structure, including promoters, would make the viral gene therapy more promising. Further assessment of the promoters and their expression profiles such as those shown in Table 1 and new designs of hybrid promoters may achieve optimal expression features for ocular gene therapies. © Springer 2008.
CITATION STYLE
Hashimoto, T. (2008). Development of viral vectors with optimal transgene expression for ocular gene therapies. In Advances in Experimental Medicine and Biology (Vol. 613, pp. 113–119). https://doi.org/10.1007/978-0-387-74904-4_12
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