| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0031-3955(05)70468-5 |
| P698 | PubMed publication ID | 9057789 |
| P2093 | author name string | Flotte TR | |
| Ferkol TW | |||
| P2860 | cites work | Site-specific integration by adeno-associated virus | Q24558738 |
| Adeno-associated virus (AAV) Rep proteins mediate complex formation between AAV DNA and its integration site in human DNA | Q24562760 | ||
| Lipofection: a highly efficient, lipid-mediated DNA-transfection procedure | Q24634002 | ||
| Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis | Q24684374 | ||
| A new technique for the assay of infectivity of human adenovirus 5 DNA | Q27860797 | ||
| Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy | Q28297851 | ||
| In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector | Q29547503 | ||
| Characteristics of a human cell line transformed by DNA from human adenovirus type 5 | Q29547863 | ||
| Integrins alpha v beta 3 and alpha v beta 5 promote adenovirus internalization but not virus attachment | Q29615852 | ||
| Transferrin-polycation conjugates as carriers for DNA uptake into cells | Q33562690 | ||
| Retrovirus-mediated transduction of adult hepatocytes | Q33570031 | ||
| An alternative approach to somatic cell gene therapy | Q33571138 | ||
| Correction of the genetic defect in hepatocytes from the Watanabe heritable hyperlipidemic rabbit. | Q33582226 | ||
| Transferrin-polycation-mediated introduction of DNA into human leukemic cells: stimulation by agents that affect the survival of transfected DNA or modulate transferrin receptor levels | Q33600489 | ||
| Safe and efficient generation of recombinant retroviruses with amphotropic and ecotropic host ranges | Q33644899 | ||
| Liposome formulations with prolonged circulation time in blood and enhanced uptake by tumors | Q33649082 | ||
| Phenotypic correction of factor IX deficiency in skin fibroblasts of hemophilic dogs | Q33671665 | ||
| Gene transfer into respiratory epithelial cells by targeting the polymeric immunoglobulin receptor | Q33908256 | ||
| Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: biological efficacy study. | Q45866166 | ||
| Cationic liposome-mediated intravenous gene delivery | Q45866771 | ||
| Gene therapy for the treatment of malignant brain tumors with in vivo tumor transduction with the herpes simplex thymidine kinase gene/ganciclovir system | Q45871669 | ||
| Gene therapy for vascular smooth muscle cell proliferation after arterial injury | Q45871893 | ||
| Successful ex vivo gene therapy directed to liver in a patient with familial hypercholesterolaemia | Q45871954 | ||
| Safety and short-term toxicity of a novel cationic lipid formulation for human gene therapy | Q45873048 | ||
| Aerosol and intravenous transfection of human alpha 1-antitrypsin gene to lungs of rabbits | Q45873756 | ||
| Regulation of the phosphoenolpyruvate carboxykinase/human factor IX gene introduced into the livers of adult rats by receptor-mediated gene transfer. | Q45874237 | ||
| An adenovirus vector for gene transfer into neurons and glia in the brain | Q45874317 | ||
| Direct in vivo gene transfer to airway epithelium employing adenovirus-polylysine-DNA complexes. | Q45874912 | ||
| Potentiation of cationic liposome-mediated gene delivery by polycations | Q45875849 | ||
| Adenovirus-mediated in vivo gene transfer and expression in normal rat liver | Q45878870 | ||
| Cationic liposome-mediated transfection. | Q45997090 | ||
| Systemic Gene Expression After Intravenous DNA Delivery into Adult Mice | Q46128630 | ||
| Gene-marking to trace origin of relapse after autologous bone-marrow transplantation | Q49158499 | ||
| In vivo transfection of murine lungs with a functioning prokaryotic gene using a liposome vehicle. | Q53957280 | ||
| Gene transfer by lipofection in rabbit and human secretory epithelial cells. | Q54341936 | ||
| Transfer of condensed viral DNA into eukaryotic cells using proteoliposomes. | Q54386892 | ||
| Heterologous and homologous protection against influenza A by DNA vaccination: optimization of DNA vectors. | Q54649033 | ||
| Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis | Q57416213 | ||
| Enzyme-containing Liposomes alleviate a Model for Storage Disease | Q59065869 | ||
| Human dystrophin expression in mdx mice after intramuscular injection of DNA constructs | Q59080986 | ||
| Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice | Q64377665 | ||
| Immunotherapy of malignancy by in vivo gene transfer into tumors | Q68044883 | ||
| Site-specific gene expression in vivo by direct gene transfer into the arterial wall | Q68354939 | ||
| Construction of transferrin-coated liposomes for in vivo transport of exogenous DNA to bone marrow erythroblasts in rabbits | Q68725264 | ||
| Liposome-mediated delivery of pteridine antifolates to cells in vitro: potency of methotrexate, and its alpha and gamma substituents | Q69637108 | ||
| Increased expression of DNA cointroduced with nuclear protein in adult rat liver | Q69937795 | ||
| DNAase I encapsulated in liposomes can induce neoplastic transformation of Syrian hamster embryo cells in culture | Q70705695 | ||
| In vivo gene transfer and expression in rat stomach by submucosal injection of plasmid DNA | Q71624174 | ||
| Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis | Q71660966 | ||
| Cytokine gene expression in epidermis with biological effects following injection of naked DNA | Q71708643 | ||
| Small liposomes are better than large liposomes for specific drug delivery in vitro | Q71731495 | ||
| Expression of Human Growth Hormone Fusion Genes in Cultured Lung Endothelial Cells and in the Lungs of Mice | Q72068935 | ||
| Treatment of severe combined immunodeficiency disease (SCID) due to adenosine deaminase deficiency with CD34+ selected autologous peripheral blood cells transduced with a human ADA gene. Amendment to clinical research project, Project 90-C-195, Janu | Q72096512 | ||
| Arterial gene transfer using pure DNA applied directly to a hydrogel-coated angioplasty balloon | Q72426890 | ||
| In vivo gene transfer into rabbit thyroid follicular cells by direct DNA injection | Q72858932 | ||
| In vivo and in vitro gene transfer to mammalian somatic cells by particle bombardment | Q33923219 | ||
| Protection of rabbit lungs from endotoxin injury by in vivo hyperexpression of the prostaglandin G/H synthase gene | Q34141454 | ||
| Gene transfer into the airway epithelium of animals by targeting the polymeric immunoglobulin receptor | Q34199152 | ||
| High efficiency transformation by direct microinjection of DNA into cultured mammalian cells | Q34252096 | ||
| Vaccination with irradiated tumor cells engineered to secrete murine granulocyte-macrophage colony-stimulating factor stimulates potent, specific, and long-lasting anti-tumor immunity | Q34334817 | ||
| In vitro evidence that metabolic cooperation is responsible for the bystander effect observed with HSV tk retroviral gene therapy | Q34341355 | ||
| Gene transfer into humans--immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction | Q34354588 | ||
| Expression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer | Q35072251 | ||
| Gene transfer in vivo: sustained expression and regulation of genes introduced into the liver by receptor-targeted uptake | Q35214917 | ||
| Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy | Q35232341 | ||
| Adeno-associated virus vectors | Q35305418 | ||
| Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver | Q35559973 | ||
| Retrovirus-mediated transfer of human adenosine deaminase gene sequences into cells in culture and into murine hematopoietic cells in vivo | Q35600024 | ||
| Targeted integration of adeno-associated virus (AAV) into human chromosome 19 | Q35936149 | ||
| An approach for treating the hepatobiliary disease of cystic fibrosis by somatic gene transfer | Q36307329 | ||
| Suppression of human alpha-globin gene expression mediated by the recombinant adeno-associated virus 2-based antisense vectors | Q36362722 | ||
| Adeno-associated virus vector for high-frequency integration, expression, and rescue of genes in mammalian cells | Q36425596 | ||
| Efficient gene transfer into nondividing cells by adeno-associated virus-based vectors. | Q36634983 | ||
| Efficient and sustained gene expression in primary T lymphocytes and primary and cultured tumor cells mediated by adeno-associated virus plasmid DNA complexed to cationic liposomes | Q36649855 | ||
| Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector | Q36663364 | ||
| Direct transfer of transforming growth factor beta 1 gene into arteries stimulates fibrocellular hyperplasia | Q36671684 | ||
| Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection | Q36720691 | ||
| Rescue of type I collagen-deficient phenotype by retroviral-vector-mediated transfer of human pro alpha 1(I) collagen gene into Mov-13 cells | Q36916742 | ||
| High-efficiency receptor-mediated delivery of small and large (48 kilobase gene constructs using the endosome-disruption activity of defective or chemically inactivated adenovirus particles. | Q37093747 | ||
| Adenovirus-mediated transfer of a recombinant human alpha 1-antitrypsin cDNA to human endothelial cells | Q37111501 | ||
| Factors influencing the enhancement of the infectivity of poliovirus ribonucleic acid by diethylaminoethyl-dextran | Q37122167 | ||
| Regulated high level expression of a human gamma-globin gene introduced into erythroid cells by an adeno-associated virus vector | Q37142195 | ||
| Influenza virus hemagglutinin HA-2 N-terminal fusogenic peptides augment gene transfer by transferrin-polylysine-DNA complexes: toward a synthetic virus-like gene-transfer vehicle | Q37171224 | ||
| Liposomes for the transformation of eukaryotic cells | Q37206319 | ||
| Aerosol gene delivery in vivo | Q37316567 | ||
| Introduction of foreign genes into tissues of living mice by DNA-coated microprojectiles | Q37459455 | ||
| Lymphocytes as cellular vehicles for gene therapy in mouse and man. | Q37478517 | ||
| Transferrin-polycation-DNA complexes: the effect of polycations on the structure of the complex and DNA delivery to cells | Q37511436 | ||
| Insertion of the bacterial gpt gene into the germ line of mice by retroviral infection | Q37536018 | ||
| High-efficiency gene transfer into mammalian cells: generation of helper-free recombinant retrovirus with broad mammalian host range | Q37572832 | ||
| Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells | Q37573696 | ||
| Introduction of a selectable gene into different animal tissue by a retrovirus recombinant vector | Q37577456 | ||
| Adenovirus enhancement of transferrin-polylysine-mediated gene delivery | Q37603166 | ||
| Sterically stabilized liposomes: improvements in pharmacokinetics and antitumor therapeutic efficacy | Q37650345 | ||
| Regulation of insulin-gene expression. Implications for gene therapy | Q39670848 | ||
| In vivo model of adeno-associated virus vector persistence and rescue | Q39874425 | ||
| Targeted vectors for gene therapy. | Q40545377 | ||
| High-efficiency gene transfer mediated by adenovirus-polylysine-DNA complexes | Q40624055 | ||
| Retroviral vectors for use in human gene therapy for cancer, Gaucher disease, and arthritis | Q40624060 | ||
| Direct gene transfer for the understanding and treatment of human disease | Q40667880 | ||
| Cationic liposomes for direct gene transfer in therapy of cancer and other diseases. | Q40667906 | ||
| Development and application of herpes simplex virus vectors for human gene therapy | Q40945227 | ||
| Multicompartment, numerical model of cellular events in the pharmacokinetics of gene therapies | Q41032449 | ||
| Gene transfer of drug resistance genes. Implications for cancer therapy | Q41033065 | ||
| Vaccination against tuberculosis by DNA injection | Q41182163 | ||
| Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis | Q41226051 | ||
| Tissue-specific targeting of retroviral vectors through ligand-receptor interactions | Q41428152 | ||
| Adeno-associated virus vector gene expression occurs in nondividing cells in the absence of vector DNA integration | Q41431346 | ||
| Retrovirus-mediated gene transfer of the human gamma-IFN gene: a therapy for cancer | Q41466648 | ||
| Both CFTR and outwardly rectifying chloride channels contribute to cAMP-stimulated whole cell chloride currents | Q41472192 | ||
| Receptor-mediated gene transfer to airway epithelial cells in primary culture | Q41522568 | ||
| In vivo gene therapy of hemophilia B: sustained partial correction in factor IX-deficient dogs | Q41524708 | ||
| Dual-target inhibition of HIV-1 in vitro by means of an adeno-associated virus antisense vector | Q41590056 | ||
| Gene expression from adeno-associated virus vectors in airway epithelial cells | Q41606833 | ||
| Defective regulation of outwardly rectifying Cl- channels by protein kinase A corrected by insertion of CFTR | Q41608893 | ||
| Gene transfer to respiratory epithelial cells via the receptor-mediated endocytosis pathway | Q41637324 | ||
| In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium | Q41644008 | ||
| Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill. | Q41662563 | ||
| Mapping and direct visualization of a region-specific viral DNA integration site on chromosome 19q13-qter | Q41678112 | ||
| Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer | Q41721279 | ||
| Interleukin-2 production by tumor cells bypasses T helper function in the generation of an antitumor response | Q41744259 | ||
| Development of a high-titer retrovirus producer cell line and strategies for retrovirus-mediated gene transfer into rhesus monkey hematopoietic stem cells | Q41751063 | ||
| Retroviral gene transfer using safe and efficient packaging cell lines | Q41751072 | ||
| Adenovirus-mediated transfer of a recombinant alpha 1-antitrypsin gene to the lung epithelium in vivo | Q41894646 | ||
| Transferrinfection: a highly efficient way to express gene constructs in eukaryotic cells | Q41939333 | ||
| Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 | ||
| Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. | Q42483788 | ||
| Construction of a retrovirus packaging mutant and its use to produce helper-free defective retrovirus | Q42798600 | ||
| In Vivo Gene Transfer with Retroviral Vector-Producer Cells for Treatment of Experimental Brain Tumors | Q42818740 | ||
| Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis. | Q43535009 | ||
| Localization and Induced Expression of Fusion Genes in the Rat Lung | Q43845860 | ||
| Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: toxicity study | Q44202627 | ||
| Direct gene transfer into mouse muscle in vivo | Q44656494 | ||
| Ex vivo gene therapy of familial hypercholesterolemia. | Q45083040 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 153-178 | |
| P577 | publication date | 1997-02-01 | |
| P1433 | published in | Pediatric Clinics of North America | Q7159204 |
| P1476 | title | Genetic therapy. Past, present, and future | |
| P478 | volume | 44 |
| Q40734130 | A surgical approach appropriate for targeted cochlear gene therapy in the mouse |
| Q41614363 | Cationic liposome mediated transgene expression in the guinea pig cochlea |
| Q35054512 | Effect of DNA-dependent protein kinase on the molecular fate of the rAAV2 genome in skeletal muscle |
| Q34590957 | Gene therapy and reproductive medicine |
| Q24791052 | Size does matter: overcoming the adeno-associated virus packaging limit |
| Q40858335 | Somatic gene transfer to salivary glands. |
| Q37135427 | Therapeutic strategies for Parkinson's disease: the ancient meets the future--traditional Chinese herbal medicine, electroacupuncture, gene therapy and stem cells |
Search more.