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Publications in Pharmacology

545. Highly Efficient Tumor Transduction and Antitumor Efficacy in Experimental Human Malignant Mesothelioma Using Replicating Gibbon Ape Leukemia Virus

Molecular Therapy

English

Dual-Regulated Lentiviral Vector for Gene Therapy of X-Linked Chronic Granulomatosis

English

124. AAV-Mediated Antisense Oligonucleotide-Based Therapy for CEP290-Associated LCA

English

137. Viral Hitchhiking to Increase Therapeutic Potential: Autonomously Packaged Elements (APEs)

English

635. Development of Plasmid-Lipoparticle Systemic Delivery System That Overcome the Paradox of PEG-Stabilization While Maintaining High Transfection Potency

English

481. Analysis of Host Cell and Viral Transcriptomes During Infection by Wild-Type Species C Ad6 and Species D Ad26

English

325. A Novel Utrophin-Based Genome Engineering Strategy for Duchenne Muscular Dystrophy Utilizing Recombinases and CRISPR/Cas9

English

330. Comparing Dual AAV Vector Strategy Efficiencies for Gene Therapy in Vitro and in Vivo

English

Research Highlights

English

640. AdCD40L Immunostimulatory Gene Therapy in Combination With Cyclophosphamide Prolongs 6-Months Survival in a Phase I/Ii Trial for Malignant Melanoma

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications in Pharmacology

545. Highly Efficient Tumor Transduction and Antitumor Efficacy in Experimental Human Malignant Mesothelioma Using Replicating Gibbon Ape Leukemia Virus

Dual-Regulated Lentiviral Vector for Gene Therapy of X-Linked Chronic Granulomatosis

124. AAV-Mediated Antisense Oligonucleotide-Based Therapy for CEP290-Associated LCA

137. Viral Hitchhiking to Increase Therapeutic Potential: Autonomously Packaged Elements (APEs)

635. Development of Plasmid-Lipoparticle Systemic Delivery System That Overcome the Paradox of PEG-Stabilization While Maintaining High Transfection Potency

481. Analysis of Host Cell and Viral Transcriptomes During Infection by Wild-Type Species C Ad6 and Species D Ad26

325. A Novel Utrophin-Based Genome Engineering Strategy for Duchenne Muscular Dystrophy Utilizing Recombinases and CRISPR/Cas9

330. Comparing Dual AAV Vector Strategy Efficiencies for Gene Therapy in Vitro and in Vivo

Research Highlights

640. AdCD40L Immunostimulatory Gene Therapy in Combination With Cyclophosphamide Prolongs 6-Months Survival in a Phase I/Ii Trial for Malignant Melanoma