Pages that link to "Q36728109"
The following pages link to Synthetic intron improves transduction efficiency of trans-splicing adeno-associated viral vectors. (Q36728109):
Displaying 20 items.
- Scaling-up recombinant plasmid DNA for clinical trial: current concern, solution and status (Q26850997) (← links)
- A hybrid vector system expands adeno-associated viral vector packaging capacity in a transgene-independent manner (Q28256353) (← links)
- Systemic Trans-splicing adeno-associated viral delivery efficiently transduces the heart of adult mdx mouse, a model for duchenne muscular dystrophy (Q33691883) (← links)
- Full-length dystrophin reconstitution with adeno-associated viral vectors (Q33782799) (← links)
- Efficient production of dual recombinant adeno-associated viral vectors for factor VIII delivery (Q34082003) (← links)
- Meganucleases can restore the reading frame of a mutated dystrophin (Q34110253) (← links)
- Expressing Transgenes That Exceed the Packaging Capacity of Adeno-Associated Virus Capsids (Q36601946) (← links)
- Emerging strategies for cell and gene therapy of the muscular dystrophies (Q36960845) (← links)
- Efficient whole-body transduction with trans-splicing adeno-associated viral vectors (Q36968872) (← links)
- Cancer-associated SF3B1 mutants recognize otherwise inaccessible cryptic 3' splice sites within RNA secondary structures (Q37643870) (← links)
- Dual adeno-associated virus vectors result in efficient in vitro and in vivo expression of an oversized gene, MYO7A. (Q37710671) (← links)
- Gene therapy to treat cardiac arrhythmias (Q38444909) (← links)
- Functional cystic fibrosis transmembrane conductance regulator expression in cystic fibrosis airway epithelial cells by AAV6.2-mediated segmental trans-splicing (Q39877658) (← links)
- Adeno-Associated Virus (AAV) gene therapy for cystic fibrosis: current barriers and recent developments (Q40142907) (← links)
- A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence (Q40884119) (← links)
- Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors (Q41093443) (← links)
- Adeno-associated Virus (AAV) Dual Vector Strategies for Gene Therapy Encoding Large Transgenes. (Q52743732) (← links)
- Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model (Q64253691) (← links)
- Adeno-Associated Viral Vectors as a Tool for Large Gene Delivery to the Retina (Q93005504) (← links)
- Wikidata:Database reports/Constraint violations/P356 (← links | edit)