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Publications by Vidyullatha Vasireddy

556. Comparative in Vitro Transduction Efficiency of AAV Vector Serotypes 1-9 in Different Cellular Models

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2016English

Elovl4 5-Bp Deletion Knock-In Mouse Model for Stargardt-Like Macular Degeneration Demonstrates Accumulation of ELOVL4 and Lipofuscin

Experimental Eye Research
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2009English

Related publications

677. Stabilizing the rAAV Vector Genome Increases AAV Vector Transduction Efficiency

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2015English

High AAV Vector Purity Results in Serotype- And Tissue-Independent Enhancement of Transduction Efficiency

Gene Therapy
Molecular MedicineGeneticsMolecular Biology
2009English

CFTR Gene Transduction in Neonatal Rabbits Using Anadeno-Associated Virus (AAV) Vector

Gene Therapy
Molecular MedicineGeneticsMolecular Biology
1997English

307. Rational Development of 12 Different AAV Serotypes as Scaffolds for Peptide Display

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2015English

AAV Natural Infection Induces Broad Cross-Neutralizing Antibody Responses to Multiple AAV Serotypes in Chimpanzees

Human gene therapy. Clinical development
Genetics
2016English

Trans-Ocular Electric Current in Vivo Enhances AAV-mediated Retinal Gene Transduction After Intravitreal Vector Administration

Molecular Therapy - Methods and Clinical Development
Molecular MedicineGeneticsMolecular Biology
2019English

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

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2013English

CNS-restricted Transduction and CRISPR/Cas9-mediated Gene Deletion With an Engineered AAV Vector

Molecular Therapy - Nucleic Acids
Drug DiscoveryMolecular Medicine
2016English

High-Throughput Screening Identifies Kinase Inhibitors That Increase Dual AAV Vectors Transduction in Vitro and in Mouse Retina

Human Gene Therapy
Molecular MedicineGeneticsMolecular Biology
2018English

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