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Molecular Therapy: At the Cutting Edge of Methodology and Clinical Development.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 409, doi. 10.1038/mt.2015.23
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In This Issue.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 412, doi. 10.1038/mt.2015.24
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Research Highlights.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 413, doi. 10.1038/mt.2015.25
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Long-Term Correction of Sandhoff Disease Following Intravenous Delivery of rAAV9 to Mouse Neonates.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 414, doi. 10.1038/mt.2014.240
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Let-7 microRNAs Regenerate Peripheral Nerve Regeneration by Targeting Nerve Growth Factor.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 423, doi. 10.1038/mt.2014.220
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Development of Novel Activin-Targeted Therapeutics.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 434, doi. 10.1038/mt.2014.221
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In Vivo AAV1 Transduction With hRheb(S16H) Protects Hippocampal Neurons by BDNF Production.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 445, doi. 10.1038/mt.2014.241
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Enzyme Enhancers for the Treatment of Fabry and Pompe Disease.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 456, doi. 10.1038/mt.2014.224
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A New Cell-penetrating Peptide That Blocks the Autoinhibitory XIP Domain of NCX1 and Enhances Antiporter Activity.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 465, doi. 10.1038/mt.2014.231
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Improving Single Injection CSF Delivery of AAV9-mediated Gene Therapy for SMA: A Dose-response Study in Mice and Nonhuman Primates.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 477, doi. 10.1038/mt.2014.210
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Targeted Gene Delivery to the Enteric Nervous System Using AAV: A Comparison Across Serotypes and Capsid Mutants.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 488, doi. 10.1038/mt.2015.7
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Biological Ablation of Sentinel Lymph Node Metastasis in Submucosally Invaded Early Gastrointestinal Cancer.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 501, doi. 10.1038/mt.2014.244
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Sourcing of an Alternative Pericyte-Like Cell Type from Peripheral Blood in Clinically Relevant Numbers for Therapeutic Angiogenic Applications.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 510, doi. 10.1038/mt.2014.232
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Correction of Dystrophin Expression in Cells From Duchenne Muscular Dystrophy Patients Through Genomic Excision of Exon 51 by Zinc Finger Nucleases.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 523, doi. 10.1038/mt.2014.234
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Transplantation of Glial Progenitors That Overexpress Glutamate Transporter GLT1 Preserves Diaphragm Function Following Cervical SCI.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 533, doi. 10.1038/mt.2014.236
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Mesenchymal Stem Cells Correct Inappropriate Epithelial-mesenchyme Relation in Pulmonary Fibrosis Using Stanniocalcin-1.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 549, doi. 10.1038/mt.2014.217
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Depletion of Bone Marrow CCSP-Expressing Cells Delays Airway Regeneration.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 561, doi. 10.1038/mt.2014.223
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Efficient and Allele-Specific Genome Editing of Disease Loci in Human iPSCs.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 570, doi. 10.1038/mt.2014.226
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Functional Aspects of Intrahepatic Hepatitis B Virus-specific T Cells Induced by Therapeutic DNA Vaccination.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 578, doi. 10.1038/mt.2014.233
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Synthetic Consensus HIV-1 DNA Induces Potent Cellular Immune Responses and Synthesis of Granzyme B, Perforin in HIV Infected Individuals.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 591, doi. 10.1038/mt.2014.245
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Phase 1 Study of Intratumoral Pexa-Vec (JX-594), an Oncolytic and Immunotherapeutic Vaccinia Virus, in Pediatric Cancer Patients.
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- Molecular Therapy, 2015, v. 23, n. 3, p. 602, doi. 10.1038/mt.2014.243
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