Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Isolation of Recombinant Adeno-Associated Virus Vector-Cellular DNA Junctions from Mouse Liver

1 Jul 1999

Abstract excerpt

Recombinant adeno-associated virus (rAAV) vectors allow for sustained expression of transgene products from mouse liver following a single portal vein administration. Here a rAAV vector expressing human coagulation factor F.IX (hF.IX), AAV-EF1alpha-F.IX (hF.IX expression was controlled by the human elongation factor 1alpha [EF1alpha] enhancer-promoter) was injected into mice via the portal vein or tail vein, or...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to RNA Interference and Gene Delivery
Share to Viral Infections and Immunology Research
Share to Virus-based gene therapy research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 10364291
DOI: 10.1128/jvi.73.7.5438-5447.1999

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Isolation of Recombinant Adeno-Associated Virus Vector-Cellular DNA Junctions from Mouse LiverPMID 10364291Read ↗

Extrachromosomal Recombinant Adeno-Associated Virus Vector Genomes Are Primarily Responsible for Stable Liver Transduction In VivoSemantic proximity Read ↗

Ribosomal DNA Integrating rAAV-rDNA Vectors Allow for Stable Transgene ExpressionSemantic proximity Read ↗

Molecular analysis of AAV5-hFVIII-SQ vector-genome-processing kinetics in transduced mouse and nonhuman primate liversSemantic proximity Read ↗

CRISPR/Cas9-Mediated in vivo Genetic Correction in a Mouse Model of Hemophilia ASemantic proximity Read ↗

AAV-mediated genome editing is influenced by the formation of R-loopsSemantic proximity Read ↗

Large-Scale Analysis of Adeno-Associated Virus Vector Integration Sites in Normal Human CellsSemantic proximity Read ↗

High-Level Factor VIII Gene Expression <i>In Vivo</i> Achieved by Nonviral Liver-Specific Gene Therapy VectorsSemantic proximity Read ↗

Recombinant Adeno-Associated Viral Vectors Mediate Long-Term Transgene Expression in MuscleSemantic proximity Read ↗

Hybrid Adeno-Associated Virus Bearing Nonhomologous Inverted Terminal Repeats Enhances Dual-Vector Reconstruction of Minigenes <i>In Vivo</i>Semantic proximity Read ↗

Efficient Gene Delivery and Targeted Expression to Hepatocytes <i>In Vivo</i> by Improved Lentiviral VectorsSemantic proximity Read ↗

Efficient Gene Targeting Mediated by Adeno-Associated Virus and DNA Double-Strand BreaksSemantic proximity Read ↗

Intramolecular recombination enables the formation of hepatitis B virus (HBV) cccDNA in mice after HBV genome transfer using recombinant AAV vectors.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.