Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors. - Wikidata - wikimedia - TriplyDB

Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

http://www.wikidata.org/entity/Q41093443

about

Gene therapy for monogenic liver diseases: clinical successes, current challenges and future prospects.Correction of Monogenic and Common Retinal Disorders with Gene Therapy.Dual AAV gene therapy for Duchenne muscular dystrophy with a 7-kb mini-dystrophin gene in the canine model.Viral vector-based tools advance knowledge of basal ganglia anatomy and physiology.Systemic delivery of adeno-associated viral vectors.Nanotherapy for Duchenne muscular dystrophy.Going non-viral: the Sleeping Beauty transposon system breaks on through to the clinical side.Advancements in the design and scalable production of viral gene transfer vectors.Methods and Applications of CRISPR-Mediated Base Editing in Eukaryotic Genomes.Genome Surgery and Gene Therapy in Retinal Disorders.Target-Cell-Directed Bioengineering Approaches for Gene Therapy of Hemophilia A.Adeno-associated Virus (AAV) Dual Vector Strategies for Gene Therapy Encoding Large Transgenes.Recent progress and considerations for AAV gene therapies targeting the central nervous system.Foamy Virus Vectors Transduce Visceral Organs and Hippocampal Structures following In Vivo Delivery to Neonatal Mice

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P2860

Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

http://www.wikidata.org/entity/Q41093443

description

2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

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type

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Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

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prefLabel

Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

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978-1-4939-3271-9_2

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Methods in Molecular Biology

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Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.

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P2093

Matthew L Hirsch

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R J Samulski

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Sonya J Wolf

http://www.w3.org/2001/XMLSchema#string

P2860

Circular intermediates of recombinant adeno-associated virus have defined structural characteristics responsible for long-term episomal persistence in muscle tissue.

Homologous recombination mediates functional recovery of dysferlin deficiency following AAV5 gene transfer

A hybrid vector system expands adeno-associated viral vector packaging capacity in a transgene-independent manner

Successful transduction of liver in hemophilia by AAV-Factor IX and limitations imposed by the host immune response

AAV recombineering with single strand oligonucleotides.

Characterization of genome integrity for oversized recombinant AAV vector.

AAV's anatomy: roadmap for optimizing vectors for translational success

Systemic Trans-splicing adeno-associated viral delivery efficiently transduces the heart of adult mdx mouse, a model for duchenne muscular dystrophy

Effect of genome size on AAV vector packaging.

Evidence for the failure of adeno-associated virus serotype 5 to package a viral genome > or = 8.2 kb.

P304

21-39

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scholarly article

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10.1007/978-1-4939-3271-9_2

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1382

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2016-01-01T00:00:00Z

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26611576

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4971574

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