Pages that link to "Q33737640"
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The following pages link to Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver (Q33737640):
Displayed 50 items.
- Gene therapy for haemophilia (Q24187977) (← links)
- Gene therapy for haemophilia (Q24202755) (← links)
- DNA ligase III and DNA ligase IV carry out genetically distinct forms of end joining in human somatic cells (Q24297891) (← links)
- Adeno-associated virus vector integration (Q24624120) (← links)
- A transposon and transposase system for human application (Q24630047) (← links)
- Adeno-associated Virus as a Mammalian DNA Vector (Q26782605) (← links)
- Perinatal systemic gene delivery using adeno-associated viral vectors (Q26852989) (← links)
- Selection of target sites for mobile DNA integration in the human genome (Q28766367) (← links)
- High-resolution genome-wide mapping of transposon integration in mammals (Q28769896) (← links)
- Gene expression omnibus: microarray data storage, submission, retrieval, and analysis (Q31057685) (← links)
- Designer gene delivery vectors: molecular engineering and evolution of adeno-associated viral vectors for enhanced gene transfer (Q33296224) (← links)
- Characterization of genome integrity for oversized recombinant AAV vector (Q33576852) (← links)
- Progress towards gene therapy for haemophilia B. (Q33844184) (← links)
- A NEW RECOMBINANT ADENO-ASSOCIATED VIRUS (AAV)-BASED RANDOM PEPTIDE DISPLAY LIBRARY SYSTEM: INFECTION-DEFECTIVE AAV1.9-3 AS A NOVEL DETARGETED PLATFORM FOR VECTOR EVOLUTION. (Q33908400) (← links)
- Large-scale analysis of adeno-associated virus vector integration sites in normal human cells (Q33930318) (← links)
- AAV-mediated liver-directed gene therapy. (Q33987462) (← links)
- Correction of chromosomal mutation and random integration in embryonic stem cells with helper-dependent adenoviral vectors (Q34016088) (← links)
- Scavenger receptors and their potential as therapeutic targets in the treatment of cardiovascular disease (Q34218552) (← links)
- Liver transduction with recombinant adeno-associated virus is primarily restricted by capsid serotype not vector genotype (Q34233154) (← links)
- Targeted integration of a rAAV vector into the AAVS1 region (Q34299854) (← links)
- rAAV-mediated tumorigenesis: still unresolved after an AAV assault (Q34310293) (← links)
- Intranasal vaccination with recombinant adeno-associated virus type 5 against human papillomavirus type 16 L1 (Q34434903) (← links)
- Assessing the potential for AAV vector genotoxicity in a murine model (Q34754355) (← links)
- Analysis of AAV serotypes 1-9 mediated gene expression and tropism in mice after systemic injection (Q34770058) (← links)
- Long-term safety and efficacy following systemic administration of a self-complementary AAV vector encoding human FIX pseudotyped with serotype 5 and 8 capsid proteins. (Q34994506) (← links)
- Hybrid adeno-associated viral vectors utilizing transposase-mediated somatic integration for stable transgene expression in human cells (Q35014865) (← links)
- Adeno-associated virus gene repair corrects a mouse model of hereditary tyrosinemia in vivo. (Q35105022) (← links)
- The mechanism of gene targeting in human somatic cells (Q35139201) (← links)
- Long-term sex-biased correction of circulating propionic acidemia disease markers by adeno-associated virus vectors (Q35199291) (← links)
- Existence of transient functional double-stranded DNA intermediates during recombinant AAV transduction (Q35928797) (← links)
- AAV-mediated gene targeting is significantly enhanced by transient inhibition of nonhomologous end joining or the proteasome in vivo (Q36084471) (← links)
- DNA palindromes with a modest arm length of greater, similar 20 base pairs are a significant target for recombinant adeno-associated virus vector integration in the liver, muscles, and heart in mice (Q36099246) (← links)
- The role of DNA-PKcs and artemis in opening viral DNA hairpin termini in various tissues in mice (Q36099356) (← links)
- Targeting site-specific chromosome integration (Q36154277) (← links)
- The threefold protrusions of adeno-associated virus type 8 are involved in cell surface targeting as well as postattachment processing (Q36155013) (← links)
- Predicting preferential DNA vector insertion sites: implications for functional genomics and gene therapy (Q36187534) (← links)
- AAV vectors containing rDNA homology display increased chromosomal integration and transgene persistence. (Q36298638) (← links)
- Ribosomal DNA integrating rAAV-rDNA vectors allow for stable transgene expression. (Q36298655) (← links)
- AAV vectors for the nucleolus (Q36298659) (← links)
- Precise hit: adeno-associated virus in gene targeting (Q36302317) (← links)
- Gene therapy progress and prospects--vectorology: design and production of expression cassettes in AAV vectors (Q36384464) (← links)
- Patterns of scAAV vector insertion associated with oncogenic events in a mouse model for genotoxicity (Q36401085) (← links)
- Treatment of human disease by adeno-associated viral gene transfer (Q36448393) (← links)
- Successful attenuation of humoral immunity to viral capsid and transgenic protein following AAV-mediated gene transfer with a non-depleting CD4 antibody and cyclosporine (Q36479748) (← links)
- Nonviral-mediated hepatic expression of IGF-I increases Treg levels and suppresses autoimmune diabetes in mice (Q36560683) (← links)
- Genome Engineering Using Adeno-associated Virus: Basic and Clinical Research Applications (Q36675277) (← links)
- Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle (Q36845715) (← links)
- RNA interference-induced hepatotoxicity results from loss of the first synthesized isoform of microRNA-122 in mice. (Q36880385) (← links)
- Frequency and spectrum of genomic integration of recombinant adeno-associated virus serotype 8 vector in neonatal mouse liver (Q36898802) (← links)
- Recombinant adeno-associated virus transduction and integration (Q36953325) (← links)