| scholarly article | Q13442814 |
| P2093 | author name string | W Xiao | |
| J M Wilson | |||
| S C Berta | |||
| M M Lu | |||
| A D Moscioni | |||
| J Tazelaar | |||
| P2860 | cites work | Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors | Q24683259 |
| Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis | Q24684374 | ||
| Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers | Q33782809 | ||
| Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity | Q34334817 | ||
| Adeno-associated virus 2-mediated gene transfer in vivo: organ-tropism and expression of transduced sequences in mice | Q34429058 | ||
| Use of Adeno-Associated Virus as a General Transduction Vector for Mammalian Cells | Q35228018 | ||
| Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy | Q35232341 | ||
| Efficient long-term gene transfer into muscle tissue of immunocompetent mice by adeno-associated virus vector | Q35872651 | ||
| Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic protein | Q35943644 | ||
| Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus | Q36242842 | ||
| Adeno-associated virus vector for high-frequency integration, expression, and rescue of genes in mammalian cells | Q36425596 | ||
| Adeno-associated virus general transduction vectors: analysis of proviral structures | Q36868692 | ||
| Zonation of metabolism and gene expression in liver. | Q40459673 | ||
| Lipoproteins and the liver sieve: the role of the fenestrated sinusoidal endothelium in lipoprotein metabolism, atherosclerosis, and cirrhosis | Q40604036 | ||
| Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 | ||
| Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors | Q43716886 | ||
| Real-time, noninvasive in vivo assessment of adeno-associated virus-mediated retinal transduction | Q45758768 | ||
| Recombinant adeno-associated virus for muscle directed gene therapy | Q45764433 | ||
| Prolonged metabolic correction in adult ornithine transcarbamylase-deficient mice with adenoviral vectors | Q45876696 | ||
| Adenovirus-mediated in vivo gene transfer and expression in normal rat liver | Q45878870 | ||
| Systemic Gene Expression After Intravenous DNA Delivery into Adult Mice | Q46128630 | ||
| An albumin enhancer located 10 kb upstream functions along with its promoter to direct efficient, liver-specific expression in transgenic mice. | Q52256521 | ||
| Receptor-mediated gene delivery and expression in vivo. | Q54740305 | ||
| Therapeutic serum concentrations of human alpha-1-antitrypsin after adenoviral-mediated gene transfer into mouse hepatocytes | Q64383253 | ||
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | vector-borne disease | Q2083837 |
| gene therapy | Q213901 | ||
| P304 | page(s) | 10222-10226 | |
| P577 | publication date | 1998-12-01 | |
| P1433 | published in | Journal of Virology | Q1251128 |
| P1476 | title | Adeno-associated virus as a vector for liver-directed gene therapy | |
| P478 | volume | 72 |
| Q24791008 | A bovine papillomavirus-1 based vector restores the function of the low-density lipoprotein receptor in the receptor-deficient CHO-ldlA7 cell line |
| Q34356203 | A limited number of transducible hepatocytes restricts a wide-range linear vector dose response in recombinant adeno-associated virus-mediated liver transduction |
| Q45861223 | Adeno-associated viral vector-mediated human vascular endothelial growth factor gene transfer stimulates angiogenesis and wound healing in the genetically diabetic mouse |
| Q36308321 | Adeno-associated virus mediated endostatin gene therapy in combination with topoisomerase inhibitor effectively controls liver tumor in mouse model |
| Q35573761 | Adeno-associated virus vector carrying human minidystrophin genes effectively ameliorates muscular dystrophy in mdx mouse model |
| Q39303013 | Adeno-associated virus-mediated gene transfer to nonhuman primate liver can elicit destructive transgene-specific T cell responses. |
| Q34981939 | Adenoassociated virus vectors for genetic immunization |
| Q44063015 | Adenovirus-mediated overexpression of Tcfe3 ameliorates hyperglycaemia in a mouse model of diabetes by upregulating glucokinase in the liver |
| Q33750605 | An advance in liver-specific gene delivery |
| Q34059643 | Anti-gp120 minibody gene transfer to female genital epithelial cells protects against HIV-1 virus challenge in vitro |
| Q39504973 | Biochemical correction of very long-chain acyl-CoA dehydrogenase deficiency following adeno-associated virus gene therapy. |
| Q35496476 | Characterization of anti-HIV activity mediated by R88-APOBEC3G mutant fusion proteins in CD4+ T cells, peripheral blood mononuclear cells, and macrophages |
| Q64977765 | Circumventing cellular immunity by miR142-mediated regulation sufficiently supports rAAV-delivered OVA expression without activating humoral immunity. |
| Q48269203 | Clinical response to persistent, low-level beta-glucuronidase expression in the murine model of mucopolysaccharidosis type VII. |
| Q92017672 | Curing hemophilia A by NHEJ-mediated ectopic F8 insertion in the mouse |
| Q34433170 | Endosomal processing limits gene transfer to polarized airway epithelia by adeno-associated virus. |
| Q42099566 | Enhanced gene transfer to arthritic joints using adeno-associated virus type 5: implications for intra-articular gene therapy |
| Q33782319 | Evaluation of a rapamycin-regulated serotype 2 adeno-associated viral vector in macaque parotid glands |
| Q35928797 | Existence of transient functional double-stranded DNA intermediates during recombinant AAV transduction |
| Q39682511 | Feasibility of generating adeno-associated virus packaging cell lines containing inducible adenovirus helper genes |
| Q38937862 | Gene Therapy for Alpha-1 Antitrypsin Deficiency Lung Disease |
| Q33831193 | Gene and cell-mediated therapies for muscular dystrophy. |
| Q34107177 | Gene therapy for dyslipidemia: clinical prospects |
| Q24792755 | Gene therapy for lipid disorders |
| Q39550492 | Gene therapy vectors based on adeno-associated virus type 1. |
| Q41869331 | Generation and characterization of chimeric recombinant AAV vectors |
| Q45731966 | Hepatitis B virus vector carries a foreign gene into liver cells in vitro |
| Q39593544 | High-titer, wild-type free recombinant adeno-associated virus vector production using intron-containing helper plasmids |
| Q34447817 | Hot topics in adeno-associated virus as a gene transfer vector |
| Q27307010 | Impact of age at administration, lysosomal storage, and transgene regulatory elements on AAV2/8-mediated rat liver transduction |
| Q35085243 | Improved survival of ischemic cutaneous and musculocutaneous flaps after vascular endothelial growth factor gene transfer using adeno-associated virus vectors |
| Q34197559 | Intraarticular factor IX protein or gene replacement protects against development of hemophilic synovitis in the absence of circulating factor IX. |
| Q64964706 | Intrapleural Gene Therapy for Alpha-1 Antitrypsin Deficiency-Related Lung Disease. |
| Q33870310 | Involvement of cellular double-stranded DNA break binding proteins in processing of the recombinant adeno-associated virus genome. |
| Q33815070 | Isolation of recombinant adeno-associated virus vector-cellular DNA junctions from mouse liver |
| Q30496514 | Liver-directed recombinant adeno-associated viral gene delivery rescues a lethal mouse model of methylmalonic acidemia and provides long-term phenotypic correction |
| Q34254706 | Oligonucleotide-mediated gene targeting in human hepatocytes: implications of mismatch repair |
| Q42170619 | Optimized human factor IX expression cassettes for hepatic-directed gene therapy of hemophilia B. |
| Q36509889 | Rapid uncoating of vector genomes is the key to efficient liver transduction with pseudotyped adeno-associated virus vectors |
| Q36953325 | Recombinant adeno-associated virus transduction and integration |
| Q33811409 | Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo |
| Q92987777 | Regulated hAAT Expression from a Novel rAAV Vector and Its Application in the Prevention of Type 1 Diabetes |
| Q36144795 | Retargeting transposon insertions by the adeno-associated virus Rep protein. |
| Q36454880 | Sustained correction of bleeding disorder in hemophilia B mice by gene therapy |
| Q37814051 | The complex and evolving story of T cell activation to AAV vector-encoded transgene products |
| Q39594915 | Transduction of well-differentiated airway epithelium by recombinant adeno-associated virus is limited by vector entry. |
| Q37747148 | Unrestricted hepatocyte transduction with adeno-associated virus serotype 8 vectors in mice |
| Q35847178 | Viral-mediated gene therapy for the muscular dystrophies: successes, limitations and recent advances |
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