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Determination of Specific CD4 and CD8 T Cell Epitopes after AAV2- and AAV8-hF.IX Gene Therapy.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 260, doi. 10.1016/j.ymthe.2005.10.006
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- Article
Exosomes Derived from Genetically Modified DC Expressing FasL Are Anti-inflammatory and Immunosuppressive.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 289, doi. 10.1016/j.ymthe.2005.09.015
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- Article
Recombinant Adenovirus Vaccines Can Successfully Elicit CD8<sup>+</sup> T Cell Immunity under Conditions of Extreme Leukopenia.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 270, doi. 10.1016/j.ymthe.2005.09.018
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Enhancement of Cellular Immune Response to a Prostate Cancer DNA Vaccine by Intradermal Electroporation.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 320, doi. 10.1016/j.ymthe.2005.08.005
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- Article
Overcoming Diabetes-Induced Hyperglycemia through Inhibition of Hepatic Phosphoenolpyruvate Carboxykinase (GTP) with RNAi.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 401, doi. 10.1016/j.ymthe.2005.08.026
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The End of the Beginning: OncolyticVirotherapy Achieves Clinical Proof-of-Concept.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 237, doi. 10.1016/j.ymthe.2005.12.005
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Inside This Month.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 239, doi. 10.1016/j.ymthe.2005.12.006
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- Article
Research Update.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 240, doi. 10.1016/j.ymthe.2005.12.004
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- Article
Gene Therapy Strategies for Duchenne Muscular Dystrophy Utilizing Recombinant Adeno-associated Virus Vectors.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 241, doi. 10.1016/j.ymthe.2005.11.001
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- Article
Safety and Efficacy of AAV-Mediated Calpain 3 Gene Transfer in a Mouse Model of Limb-Girdle Muscular Dystrophy Type 2A.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 250, doi. 10.1016/j.ymthe.2005.09.017
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Immunization with a Lentiviral Vector Stimulates both CD4 and CD8 T Cell Responses to an Ovalbumin Transgene.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 310, doi. 10.1016/j.ymthe.2005.08.025
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- Article
Potent Vaccine Therapy with Dendritic Cells Genetically Modified by the Gene-Silencing-Resistant Retroviral Vector GCDNsap.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 301, doi. 10.1016/j.ymthe.2005.09.021
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- Article
Transfection of Dendritic Cells with in Vitro-Transcribed CMV RNA Induces Polyclonal CD8<sup>+</sup>- and CD4<sup>+</sup>-Mediated CMV-Specific T Cell Responses.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 280, doi. 10.1016/j.ymthe.2005.08.019
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- Article
Hypersensitivity and Loss of Disease Site Targeting Caused by Antibody Responses to PEGylated Liposomes.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 328, doi. 10.1016/j.ymthe.2005.09.014
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- Article
Activation of Refractory T Cell Responses against Hepatitis C Virus Core Protein by Ablation of Interfering Hydrophobic Domains.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 338, doi. 10.1016/j.ymthe.2005.09.005
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- Article
Second-Generation Replication-Competent Oncolytic Adenovirus Armed with Improved Suicide Genes and ADP Gene Demonstrates Greater Efficacy without Increased Toxicity.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 347, doi. 10.1016/j.ymthe.2005.10.005
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- Article
Bystander Effect Contributes to the Antitumor Efficacy of CaSm Antisense Gene Therapy in a Preclinical Model of Advanced Pancreatic Cancer.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 357, doi. 10.1016/j.ymthe.2005.06.485
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- Article
Integration Site Selection by HIV-Based Vectors in Dividing and Growth-Arrested IMR-90 Lung Fibroblasts.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 366, doi. 10.1016/j.ymthe.2005.10.009
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- Article
Successful Treatment of UGT1A1 Deficiency in a Rat Model of Crigler–Najjar Disease by Intravenous Administration of a Liver-Specific Lentiviral Vector.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 374, doi. 10.1016/j.ymthe.2005.09.022
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Efficient control of gene expression in the hematopoietic system using a single Tet-on inducible lentiviral vector.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 382, doi. 10.1016/j.ymthe.2005.09.012
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Equal Potency of Gammaretroviral and Lentiviral SIN Vectors for Expression of O<sup>6</sup>-Methylguanine–DNA Methyltransferase in Hematopoietic cells.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 391, doi. 10.1016/j.ymthe.2005.08.012
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Effective Inhibition of HBV Replication in Vivo by Anti-HBx Short Hairpin RNAs.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 411, doi. 10.1016/j.ymthe.2005.10.013
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Intracellular Trafficking of Plasmids during Transfection Is Mediated by Microtubules.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 422, doi. 10.1016/j.ymthe.2005.10.004
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Mechanistic Studies of Sequential Injection of Cationic Liposome and Plasmid DNA.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 429, doi. 10.1016/j.ymthe.2005.08.021
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Mammalian Gene Targeting with Designed Zinc Finger Nucleases.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 438, doi. 10.1016/j.ymthe.2005.08.003
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Inducing Tolerance to a Soluble Foreign Antigen by Encapsulated Cell Transplants.
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- Molecular Therapy, 2006, v. 13, n. 2, p. 447, doi. 10.1016/j.ymthe.2005.08.010
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