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Christine L. Halbert

Fred Hutchinson Cancer Research Center

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398. Sustained Expression of a Canine Micro-Dystrophin Lead To Improvement of Limb Muscle Function in Dystrophic Dogs Following Large Scale AAV-Mediated Treatment

2015 Molecular Therapy
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smooth muscle cells in vivo Adeno-associated virus vector transduction of vascular

2015
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Elimination of contaminating cap genes in AAV vector virions reduces immune responses and improves transgene expression in a canine gene therapy model

2014 Gene Therapy
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Successful Regional Delivery and Long-term Expression of a Dystrophin Gene in Canine Muscular Dystrophy: A Preclinical Model for Human Therapies

2012 Molecular Therapy
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Original ArticleSuccessful Regional Delivery and Long-term Expression of a Dystrophin Gene in Canine Muscular Dystrophy: A Preclinical Model for Human Therapies

2012
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Capsid-expressing DNA in AAV vectors and its elimination by use of an oversize capsid gene for vector production

2011 Gene Therapy
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Jaagsiekte Sheep Retrovirus and Enzootic Nasal Tumor Virus Promoters Drive Gene Expression in All Airway Epithelial Cells of Mice but Only Induce Tumors in the Alveolar Region of the Lungs

2011 Journal of Virology
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Lung Cancer in Mice Induced by the Jaagsiekte Sheep Retrovirus Envelope Protein Is Not Maintained by Rare Cancer Stem Cells, but Tumorigenicity Does Correlate with Wnt Pathway Activation

2011 Molecular Cancer Research
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Expression of human α1-antitrypsin in mice and dogs following AAV6 vector-mediated gene transfer to the lungs

2010 Molecular Therapy
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Efficient Transduction of Skeletal Muscle Using Vectors Based on Adeno-associated Virus Serotype 6 (vol 10, pg 671, 2004)

2009 Molecular Therapy
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