Persistence in muscle of an adenoviral vector that lacks all viral genes

Genetic correction of inherited muscle diseases, such as Duchenne muscular dystrophy, will require long term expression of the recombinant protein following gene transfer. We have shown previously that a new adenoviral vector that lacks all viral genes expressed both full-length dystrophin and β-gal...

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Библиографические подробности
Главные авторы: Chen, Hsiao-Huei, Mack, Lisa M., Kelly, Robert, Ontell, Marcia, Kochanek, Stefan, Clemens, Paula R.
Формат: Artigo
Язык:Inglês
Опубликовано: The National Academy of Sciences of the USA 1997
Предметы:
Biological Sciences
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC19970/
https://ncbi.nlm.nih.gov/pubmed/9050832
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