Displaying high-affinity ligands on adeno-associated viral vectors enables tumor cell-specific and safe gene transfer. - Wikidata - wikimedia - TriplyDB

Displaying high-affinity ligands on adeno-associated viral vectors enables tumor cell-specific and safe gene transfer.

Displaying high-affinity ligands on adeno-associated viral vectors enables tumor cell-specific and safe gene transfer.

http://www.wikidata.org/entity/Q42541148

about

Adeno-associated Virus as a Mammalian DNA Vector Gene transfer to the CNS using recombinant adeno-associated virus Selective DNA delivery to tumor cells using an oligoarginine-LTVSPWY peptide Synthetic virology: engineering viruses for gene delivery Treatment of multifocal breast cancer by systemic delivery of dual-targeted adeno-associated viral vectors.Pulmonary Targeting of Adeno-associated Viral Vectors by Next-generation Sequencing-guided Screening of Random Capsid Displayed Peptide Libraries.A brain microvasculature endothelial cell-specific viral vector with the potential to treat neurovascular and neurological diseases.Beyond Antibodies as Binding Partners: The Role of Antibody Mimetics in Bioanalysis.Recent advances in RNA interference therapeutics for CNS diseases.CRISPR-Cas9 for in vivo Gene Therapy: Promise and Hurdles Protein engineering for cardiovascular therapeutics: untapped potential for cardiac repair.Engineering adeno-associated viruses for clinical gene therapy.CRISPR-Cas9 systems: versatile cancer modelling platforms and promising therapeutic strategies.Advances in treatment of achondroplasia and osteoarthritis.CRISPR-Cas9 for medical genetic screens: applications and future perspectives.Adeno-associated virus (AAV) vectors in cancer gene therapy.Structural Insights into Human Bocaparvoviruses.Adeno-Associated Virus Gene Therapy for Liver Disease.A chemical switch for controlling viral infectivity.Enzyme/Prodrug Systems for Cancer Gene Therapy.Seek and destroy: targeted adeno-associated viruses for gene delivery to hepatocellular carcinoma.Adeno-Associated Virus (AAV) as a Vector for Gene Therapy.Off-target-free gene delivery by affinity-purified receptor-targeted viral vectors.Incorporation of antigens into viral capsids augments immunogenicity of adeno-associated virus vector-based vaccines.Modular adeno-associated virus (rAAV) vectors used for cellular virus-directed enzyme prodrug therapy.Fusion of Anthopleurin-B to AAV2 increases specificity of cardiac gene transfer.Designed Ankyrin Repeat Proteins as Her2 Targeting Domains in Chimeric Antigen Receptor-Engineered T Cells.Oligonucleotide conjugated multi-functional adeno-associated viruses.Therapeutic applications of genetic code expansion A Library-Based Screening Strategy for the Identification of DARPins as Ligands for Receptor-Targeted AAV and Lentiviral Vectors Surface-Engineered Lentiviral Vectors for Selective Gene Transfer into Subtypes of Lymphocytes

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P2860

Displaying high-affinity ligands on adeno-associated viral vectors enables tumor cell-specific and safe gene transfer.

http://www.wikidata.org/entity/Q42541148

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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name

Displaying high-affinity ligan ...... ecific and safe gene transfer.

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Displaying high-affinity ligan ...... ecific and safe gene transfer.

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type

label

Displaying high-affinity ligan ...... ecific and safe gene transfer.

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Displaying high-affinity ligan ...... ecific and safe gene transfer.

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prefLabel

Displaying high-affinity ligan ...... ecific and safe gene transfer.

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Displaying high-affinity ligan ...... ecific and safe gene transfer.

@nl

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Molecular Therapy

P1476

Displaying high-affinity ligan ...... ecific and safe gene transfer.

@en

P2093

Anke Rasbach

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

Christian J Buchholz

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

Hanna Janicki

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

Hildegard Büning

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

Iris Völker

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

Robert C Münch

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

P2860

Mutational analysis of the adeno-associated virus type 2 (AAV2) capsid gene and construction of AAV2 vectors with altered tropism.

Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus

The atomic structure of adeno-associated virus (AAV-2), a vector for human gene therapy.

Adeno-associated virus type 2 VP2 capsid protein is nonessential and can tolerate large peptide insertions at its N terminus

Structural determinants for improved stability of designed ankyrin repeat proteins with a redesigned C-capping module

High-affinity binders selected from designed ankyrin repeat protein libraries

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

Green fluorescent protein-tagged adeno-associated virus particles allow the study of cytosolic and nuclear trafficking.

Monoclonal antibodies against the adeno-associated virus type 2 (AAV-2) capsid: epitope mapping and identification of capsid domains involved in AAV-2-cell interaction and neutralization of AAV-2 infection

Efficient selection of DARPins with sub-nanomolar affinities using SRP phage display.

P304

109-118

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scholarly article

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10.1038/MT.2012.186

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1

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21

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2012-09-11T00:00:00Z

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230832958

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22968478

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3538307

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