Found: 15
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Benzoate X receptor zinc-finger gene switches for drug-inducible regulation of transcription.
- Published in:
- Gene Therapy, 2012, v. 19, n. 4, p. 458, doi. 10.1038/gt.2011.112
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- Article
Radioiodine therapy of thyroid carcinoma following Pax-8 gene transfer.
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- Gene Therapy, 2012, v. 19, n. 4, p. 435, doi. 10.1038/gt.2011.110
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- Article
Development of optimized AAV3 serotype vectors: mechanism of high-efficiency transduction of human liver cancer cells.
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- Gene Therapy, 2012, v. 19, n. 4, p. 375, doi. 10.1038/gt.2011.105
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- Article
10-year safety follow-up in patients with local VEGF gene transfer to ischemic lower limb.
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- Gene Therapy, 2012, v. 19, n. 4, p. 392, doi. 10.1038/gt.2011.109
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- Article
A retroviral vector suitable for ultrasound image-guided gene delivery to mouse brain.
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- Gene Therapy, 2012, v. 19, n. 4, p. 396, doi. 10.1038/gt.2011.120
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- Article
Single-chain VαVβ T-cell receptors function without mispairing with endogenous TCR chains.
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- Gene Therapy, 2012, v. 19, n. 4, p. 365, doi. 10.1038/gt.2011.104
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- Publication type:
- Article
RNAi-mediated knockdown of HMG CoA reductase enhances gene expression from physiologically regulated low-density lipoprotein receptor therapeutic vectors in vivo.
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- Gene Therapy, 2012, v. 19, n. 4, p. 463, doi. 10.1038/gt.2011.103
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- Article
HPV-16 E1, E2 and E6 each complement the Ad5 helper gene set, increasing rAAV2 and wt AAV2 production.
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- Gene Therapy, 2012, v. 19, n. 4, p. 418, doi. 10.1038/gt.2011.115
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- Article
Sustained correction of OTC deficiency in spf<sup> ash</sup> mice using optimized self-complementary AAV2/8 vectors.
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- Gene Therapy, 2012, v. 19, n. 4, p. 404, doi. 10.1038/gt.2011.111
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- Publication type:
- Article
Gene therapy in a murine model of methylmalonic acidemia using rAAV9-mediated gene delivery.
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- Gene Therapy, 2012, v. 19, n. 4, p. 385, doi. 10.1038/gt.2011.108
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- Article
AAV vectors transduce hepatocytes in vivo as efficiently in cirrhotic as in healthy rat livers.
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- Gene Therapy, 2012, v. 19, n. 4, p. 411, doi. 10.1038/gt.2011.119
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- Article
Encapsulated engineered myoblasts can cure Hurler syndrome: preclinical experiments in the mouse model.
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- Gene Therapy, 2012, v. 19, n. 4, p. 355, doi. 10.1038/gt.2011.94
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- Publication type:
- Article
Rescue administration of a helper-dependent adenovirus vector with long-term efficacy in dogs with glycogen storage disease type Ia.
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- Gene Therapy, 2012, v. 19, n. 4, p. 443, doi. 10.1038/gt.2011.86
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- Publication type:
- Article
Improved systemic antitumor therapy with oncolytic adenoviruses by replacing the fiber shaft HSG-binding domain with RGD.
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- Gene Therapy, 2012, v. 19, n. 4, p. 453, doi. 10.1038/gt.2011.106
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- Publication type:
- Article
Epidermal growth factor improves lentivirus vector gene transfer into primary mouse hepatocytes.
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- Gene Therapy, 2012, v. 19, n. 4, p. 425, doi. 10.1038/gt.2011.117
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- Publication type:
- Article