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Adeno-associated virus serotype 9 vectors transduce murine alveolar and nasal epithelia and can be readministered

Airway-directed gene transfer has emerged as a promising approach for the treatment of the two genetic diseases of the lung, namely cystic fibrosis and α-1-antitrypsin deficiency. Herein we describe the transduction efficiency of a novel adeno-associated virus (AAV) vector, AAV2/9, across murine nas...

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Bibliografske podrobnosti
Main Authors: Limberis, Maria P., Wilson, James M.
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 2006
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1559741/
https://ncbi.nlm.nih.gov/pubmed/16938846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0601433103
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