Efficient and Targeted Transduction of Nonhuman Primate Liver With Systemically Delivered Optimized AAV3B Vectors. - Wikidata - wikimedia - TriplyDB

Efficient and Targeted Transduction of Nonhuman Primate Liver With Systemically Delivered Optimized AAV3B Vectors.

Efficient and Targeted Transduction of Nonhuman Primate Liver With Systemically Delivered Optimized AAV3B Vectors.

http://www.wikidata.org/entity/Q36427096

about

Evaluation of engineered AAV capsids for hepatic factor IX gene transfer in murine and canine models Adeno-Associated Virus: The Naturally Occurring Virus Versus the Recombinant Vector.Strategies to generate high-titer, high-potency recombinant AAV3 serotype vectors Superior In vivo Transduction of Human Hepatocytes Using Engineered AAV3 Capsid.Humanized Mouse Models of Clinical Disease.Low-Dose Liver-Targeted Gene Therapy for Pompe Disease Enhances Therapeutic Efficacy of ERT via Immune Tolerance Induction.In vivo tissue-tropism of adeno-associated viral vectors.State of the art: gene therapy of haemophilia.Systemic delivery of adeno-associated viral vectors.Potential for cellular stress response to hepatic factor VIII expression from AAV vector Adeno-Associated Virus Type 2 and Hepatocellular Carcinoma?Efficient Gene Delivery and Expression in Pancreas and Pancreatic Tumors by Capsid-Optimized AAV8 Vectors.Selecting the Best AAV Capsid for Human Studies.Survival Advantage of Both Human Hepatocyte Xenografts and Genome-Edited Hepatocytes for Treatment of α-1 Antitrypsin Deficiency.Bioengineered AAV Capsids with Combined High Human Liver Transduction In Vivo and Unique Humoral Seroreactivity.Viral Vectors, Engineered Cells and the CRISPR Revolution.Rescue of Pompe disease in mice by AAV-mediated liver delivery of secretable acid α-glucosidase.Gene Therapy for Hemophilia.

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P2860

Efficient and Targeted Transduction of Nonhuman Primate Liver With Systemically Delivered Optimized AAV3B Vectors.

http://www.wikidata.org/entity/Q36427096

description

2015 nî lūn-bûn

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2015年の論文

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年学术文章

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2015年學術文章

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2015年學術文章

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2015年學術文章

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Efficient and Targeted Transdu ...... vered Optimized AAV3B Vectors.

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Efficient and Targeted Transdu ...... vered Optimized AAV3B Vectors.

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Efficient and Targeted Transdu ...... vered Optimized AAV3B Vectors.

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Efficient and Targeted Transdu ...... vered Optimized AAV3B Vectors.

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Efficient and Targeted Transdu ...... vered Optimized AAV3B Vectors.

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Molecular Therapy

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Efficient and Targeted Transdu ...... ivered Optimized AAV3B Vectors

@en

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Arun Srivastava

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

Christian Mueller

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

Dale L Greiner

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

Guangping Gao

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

Leonard D Shultz

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

Li Zhong

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

Mengxin Li

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

Michael A Brehm

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

Qin Su

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

Qiushi Tang

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

P2860

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

Structure, tissue-specific expression, and transforming activity of the mouse met protooncogene.

Establishment of an AAV reverse infection-based array.

The pleiotropic effects of natural AAV infections on liver-directed gene transfer in macaques

Gene transfer in the liver using recombinant adeno-associated virus

High-efficiency transduction and correction of murine hemophilia B using AAV2 vectors devoid of multiple surface-exposed tyrosines.

Human hepatocyte growth factor receptor is a cellular coreceptor for adeno-associated virus serotype 3

Successful anti-scavenger receptor class B type I (SR-BI) monoclonal antibody therapy in humanized mice after challenge with HCV variants with in vitro resistance to SR-BI-targeting agents

Adeno-associated virus 2-mediated gene transfer in vivo: organ-tropism and expression of transduced sequences in mice.

Endosomal processing limits gene transfer to polarized airway epithelia by adeno-associated virus.

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10.1038/MT.2015.174

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12

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26403887

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