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Reply to: NGS library preparation may generate artifactual integration sites of AAV vectors.
- Published in:
- Nature Medicine, 2014, v. 20, n. 6, p. 578, doi. 10.1038/nm.3584
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- Article
A largely random AAV integration profile after LPLD gene therapy.
- Published in:
- Nature Medicine, 2013, v. 19, n. 7, p. 889, doi. 10.1038/nm.3230
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- Article
Transient and intensive pharmacological immunosuppression fails to improve AAV-based liver gene transfer in non-human primates.
- Published in:
- Journal of Translational Medicine, 2012, v. 10, n. 1, p. 122, doi. 10.1186/1479-5876-10-122
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- Article
AAV gene therapy as a means to increase apolipoprotein (Apo) A-I and high-density lipoprotein-cholesterol levels: correction of murine ApoA-I deficiency.
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- Journal of Gene Medicine, 2009, v. 11, n. 8, p. 697, doi. 10.1002/jgm.1344
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- Article
Recombinant adeno-associated virus-mediated gene delivery of long chain acyl coenzyme A dehydrogenase (LCAD) into LCAD-deficient mice.
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- Journal of Gene Medicine, 2008, v. 10, n. 10, p. 1113, doi. 10.1002/jgm.1242
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- Article
Development of a Liver-specific Tet-On Inducible System for AAV Vectors and Its Application in the Treatment of Liver Cancer.
- Published in:
- Molecular Therapy, 2011, v. 19, n. 7, p. 1245, doi. 10.1038/mt.2011.37
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- Article
Phenotypic Correction of a Mouse Model for Primary Hyperoxaluria With Adeno-associated Virus Gene Transfer.
- Published in:
- Molecular Therapy, 2011, v. 19, n. 5, p. 870, doi. 10.1038/mt.2010.270
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- Article
Sustained Enzymatic Correction by rAAV-Mediated Liver Gene Therapy Protects Against Induced Motor Neuropathy in Acute Porphyria Mice.
- Published in:
- Molecular Therapy, 2011, v. 19, n. 2, p. 243, doi. 10.1038/mt.2010.210
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- Article