Pages that link to "Q33815070"

The following pages link to Isolation of recombinant adeno-associated virus vector-cellular DNA junctions from mouse liver (Q33815070):

Displayed 50 items.

• Novel adeno-associated viruses from rhesus monkeys as vectors for human gene therapy (Q24535690) ‎ (← links)
• Adeno-associated virus vector integration (Q24624120) ‎ (← links)
• The gene therapy journey for hemophilia: are we there yet? (Q26823818) ‎ (← links)
• Genetic fate of recombinant adeno-associated virus vector genomes in muscle (Q33186207) ‎ (← links)
• Characterization of genome integrity for oversized recombinant AAV vector (Q33576852) ‎ (← links)
• Integration preferences of wildtype AAV-2 for consensus rep-binding sites at numerous loci in the human genome (Q33632181) ‎ (← links)
• Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver (Q33737640) ‎ (← links)
• Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy (Q33793572) ‎ (← links)
• An adeno-associated virus (AAV) initiator protein, Rep78, catalyzes the cleavage and ligation of single-stranded AAV ori DNA. (Q33801126) ‎ (← links)
• Kinetics of recombinant adeno-associated virus-mediated gene transfer (Q33802149) ‎ (← links)
• Nonrandom transduction of recombinant adeno-associated virus vectors in mouse hepatocytes in vivo: cell cycling does not influence hepatocyte transduction (Q33802664) ‎ (← links)
• Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo (Q33811409) ‎ (← links)
• Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo (Q33844362) ‎ (← links)
• Involvement of cellular double-stranded DNA break binding proteins in processing of the recombinant adeno-associated virus genome. (Q33870310) ‎ (← links)
• Large-scale analysis of adeno-associated virus vector integration sites in normal human cells (Q33930318) ‎ (← links)
• Formation of AAV single stranded DNA genome from a circular plasmid in Saccharomyces cerevisiae (Q33997202) ‎ (← links)
• Liver-directed gene therapy for dyslipidemia and diabetes (Q34016399) ‎ (← links)
• Vectors for gene therapy of cardiovascular disease (Q34027386) ‎ (← links)
• Chromosomal integration and homologous gene targeting by replication-incompetent vectors based on the autonomous parvovirus minute virus of mice (Q34226663) ‎ (← links)
• Improved hepatic gene transfer by using an adeno-associated virus serotype 5 vector (Q34348760) ‎ (← links)
• Efficient generation and amplification of high-capacity adeno-associated virus/adenovirus hybrid vectors. (Q34349393) ‎ (← links)
• A limited number of transducible hepatocytes restricts a wide-range linear vector dose response in recombinant adeno-associated virus-mediated liver transduction (Q34356203) ‎ (← links)
• Hot topics in adeno-associated virus as a gene transfer vector (Q34447817) ‎ (← links)
• High-efficiency transduction of primary human hematopoietic stem cells and erythroid lineage-restricted expression by optimized AAV6 serotype vectors in vitro and in a murine xenograft model in vivo (Q34629995) ‎ (← links)
• Assessing the potential for AAV vector genotoxicity in a murine model (Q34754355) ‎ (← links)
• Consequences of DNA-dependent protein kinase catalytic subunit deficiency on recombinant adeno-associated virus genome circularization and heterodimerization in muscle tissue (Q34857785) ‎ (← links)
• Adeno-associated viruses undergo substantial evolution in primates during natural infections (Q35022838) ‎ (← links)
• Robust systemic transduction with AAV9 vectors in mice: efficient global cardiac gene transfer superior to that of AAV8. (Q35025591) ‎ (← links)
• Effect of DNA-dependent protein kinase on the molecular fate of the rAAV2 genome in skeletal muscle (Q35054512) ‎ (← 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)
• Treatment of human disease by adeno-associated viral gene transfer (Q36448393) ‎ (← links)
• Rapid uncoating of vector genomes is the key to efficient liver transduction with pseudotyped adeno-associated virus vectors (Q36509889) ‎ (← links)
• Feline immunodeficiency virus vectors persistently transduce nondividing airway epithelia and correct the cystic fibrosis defect (Q36807130) ‎ (← links)
• Adeno-associated virus vector genomes persist as episomal chromatin in primate muscle (Q36845715) ‎ (← 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)
• Progress and problems when considering gene therapy for GSD-II. (Q36960374) ‎ (← links)
• Long-term correction of inhibitor-prone hemophilia B dogs treated with liver-directed AAV2-mediated factor IX gene therapy (Q37071092) ‎ (← links)
• Unrestricted hepatocyte transduction with adeno-associated virus serotype 8 vectors in mice (Q37747148) ‎ (← links)
• Targeting the central nervous system with herpes simplex virus / Sleeping Beauty hybrid amplicon vectors (Q37895283) ‎ (← links)
• RD2-MolPack-Chim3, a packaging cell line for stable production of lentiviral vectors for anti-HIV gene therapy (Q39139624) ‎ (← links)
• Gene therapy using a liver-targeted AAV vector restores nucleoside and nucleotide homeostasis in a murine model of MNGIE. (Q39413079) ‎ (← links)
• Liver-Directed Adeno-Associated Viral Gene Therapy for Hemophilia (Q39553052) ‎ (← links)
• Integrating adenovirus-adeno-associated virus hybrid vectors devoid of all viral genes. (Q39596516) ‎ (← links)
• Chromosomal integration of transduced recombinant baculovirus DNA in mammalian cells (Q39601566) ‎ (← links)
• Adeno-associated virus site-specific integration is mediated by proteins of the nonhomologous end-joining pathway (Q39798744) ‎ (← links)
• Non-clinical Safety and Efficacy of an AAV2/8 Vector Administered Intravenously for Treatment of Mucopolysaccharidosis Type VI. (Q41347222) ‎ (← links)
• Gene therapy, early promises, subsequent problems, and recent breakthroughs. (Q41807910) ‎ (← links)
• Reprogramming adipose tissue-derived mesenchymal stem cells into pluripotent stem cells by a mutant adeno-associated viral vector (Q41896060) ‎ (← links)