scholarly article | Q13442814 |
P2093 | author name string | Y Yang | |
J L Miller | |||
E F Vanin | |||
A W Nienhuis | |||
J Bertran | |||
F Rueda | |||
A Fenimore-Justman | |||
P2860 | cites work | Expression and structure of the human NGF receptor | Q24295226 |
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 | ||
Tight control of gene expression in mammalian cells by tetracycline-responsive promoters | Q24564850 | ||
Second-strand synthesis is a rate-limiting step for efficient transduction by recombinant adeno-associated virus vectors | Q24682739 | ||
Transduction with recombinant adeno-associated virus for gene therapy is limited by leading-strand synthesis | Q24684374 | ||
Selective extraction of polyoma DNA from infected mouse cell cultures | Q29547500 | ||
Recombinant adeno-associated virus-mediated gene transfer into hematopoietic progenitor cells. | Q41443981 | ||
Use of retroviral vectors for gene transfer and expression | Q41582824 | ||
Mapping and direct visualization of a region-specific viral DNA integration site on chromosome 19q13-qter | Q41678112 | ||
Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain | Q42280576 | ||
A putative murine ecotropic retrovirus receptor gene encodes a multiple membrane-spanning protein and confers susceptibility to virus infection | Q42798292 | ||
A new strategy for large-scale preparation of high-titer recombinant adeno-associated virus vectors by using packaging cell lines and sulfonated cellulose column chromatography | Q45768354 | ||
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA- immunodeficient patients | Q45866834 | ||
T lymphocyte-directed gene therapy for ADA- SCID: initial trial results after 4 years. | Q45866838 | ||
Gene-marking to trace origin of relapse after autologous bone-marrow transplantation | Q49158499 | ||
Direct demonstration that autologous bone marrow transplantation for solid tumors can return a multiplicity of tumorigenic cells. | Q54199437 | ||
A gene transfer strategy for making bone marrow cells resistant to trimetrexate | Q71078512 | ||
Detection of receptor-specific murine leukemia virus binding to cells by immunofluorescence analysis | Q33932054 | ||
Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector | Q34188887 | ||
DNA synthesis and topoisomerase inhibitors increase transduction by adeno-associated virus vectors | Q34251868 | ||
Engraftment of gene-modified umbilical cord blood cells in neonates with adenosine deaminase deficiency | Q34454454 | ||
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 | ||
Adeno-associated virus vectors preferentially transduce cells in S phase. | Q35754006 | ||
Adeno-associated virus vectors transduce primary cells much less efficiently than immortalized cells. | Q35833899 | ||
Asymmetric replication in vitro from a human sequence element is dependent on adeno-associated virus Rep protein | Q35837075 | ||
Recombinant adeno-associated virus (rAAV)-mediated expression of a human gamma-globin gene in human progenitor-derived erythroid cells | Q35837539 | ||
Targeted integration of adeno-associated virus (AAV) into human chromosome 19 | Q35936149 | ||
Cloning of adeno-associated virus into pBR322: rescue of intact virus from the recombinant plasmid in human cells | Q36288360 | ||
Adeno-associated virus 2-mediated high efficiency gene transfer into immature and mature subsets of hematopoietic progenitor cells in human umbilical cord blood | Q36363237 | ||
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 | ||
DNA-damaging agents greatly increase the transduction of nondividing cells by adeno-associated virus vectors. | Q36638167 | ||
Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector | Q36663364 | ||
Envelope-binding domain in the cationic amino acid transporter determines the host range of ecotropic murine retroviruses. | Q36686256 | ||
Retroviral infection and expression of cationic amino acid transporters in rodent hepatocytes. | Q36686283 | ||
Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection | Q36720691 | ||
A neutralizable epitope common to the envelope glycoproteins of ecotropic, polytropic, xenotropic, and amphotropic murine leukemia viruses | Q36796266 | ||
Helper-free stocks of recombinant adeno-associated viruses: normal integration does not require viral gene expression | Q36830429 | ||
A safe packaging line for gene transfer: separating viral genes on two different plasmids | Q36865708 | ||
Adeno-associated virus general transduction vectors: analysis of proviral structures | Q36868692 | ||
A recombinant plasmid from which an infectious adeno-associated virus genome can be excised in vitro and its use to study viral replication | Q36919184 | ||
Regulated high level expression of a human gamma-globin gene introduced into erythroid cells by an adeno-associated virus vector | Q37142195 | ||
Use of adeno-associated virus as a mammalian DNA cloning vector: transduction of neomycin resistance into mammalian tissue culture cells | Q37573696 | ||
Recombinant junctions formed by site-specific integration of adeno-associated virus into an episome | Q38290022 | ||
Adeno-associated viruses: an update. | Q39511024 | ||
Transfer of genes to humans: early lessons and obstacles to success | Q40418899 | ||
Adeno-associated virus vectors for gene therapy | Q40429008 | ||
Gene marking after bone marrow transplantation. | Q40470692 | ||
Gene transfer into hematopoietic progenitor and stem cells: progress and problems. | Q40607279 | ||
Prospects for the use of adeno-associated virus as a vector for human gene therapy | Q40643988 | ||
Adeno-associated virus: a vector system for efficient introduction and integration of DNA into a variety of mammalian cell types | Q40660263 | ||
The basic science of gene therapy | Q40907463 | ||
Inducible, high-level production of infectious murine leukemia retroviral vector particles pseudotyped with vesicular stomatitis virus G envelope protein | Q40973862 | ||
High-efficiency transfer of the T cell co-stimulatory molecule B7-2 to lymphoid cells using high-titer recombinant adeno-associated virus vectors | Q41263327 | ||
Cell lines for the production of recombinant adeno-associated virus | Q41286219 | ||
Adenovirus-mediated transfer of the amphotropic retrovirus receptor cDNA increases retroviral transduction in cultured cells | Q41397592 | ||
Adeno-associated virus vector gene expression occurs in nondividing cells in the absence of vector DNA integration | Q41431346 | ||
P433 | issue | 10 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | vector-borne disease | Q2083837 |
P304 | page(s) | 6759-6766 | |
P577 | publication date | 1996-10-01 | |
P1433 | published in | Journal of Virology | Q1251128 |
P1476 | title | Recombinant adeno-associated virus-mediated high-efficiency, transient expression of the murine cationic amino acid transporter (ecotropic retroviral receptor) permits stable transduction of human HeLa cells by ecotropic retroviral vectors | |
P478 | volume | 70 |
Q33851610 | Adaptation of chimeric retroviruses in vitro and in vivo: isolation of avian retroviral vectors with extended host range |
Q35889029 | Adeno-associated virus type 2-mediated transfer of ecotropic retrovirus receptor cDNA allows ecotropic retroviral transduction of established and primary human cells. |
Q35898429 | Adeno-associated virus vector integration junctions. |
Q33695816 | Adeno-associated virus vectors and hematology |
Q45861914 | Adenovirus-mediated expresssion of the murine ecotropic receptor facilitates transduction of human hematopoietic cells with an ecotropic retroviral vector. |
Q45888368 | Controlling mammalian gene expression with small molecules |
Q33804483 | Design and packaging of adeno-associated virus gene targeting vectors |
Q39881544 | Development of high-titer retroviral producer cell lines by using Cre-mediated recombination. |
Q45151455 | Efficient gene transfer into human cord blood CD34+ cells and the CD34+CD38- subset using highly purified recombinant adeno-associated viral vector preparations that are free of helper virus and wild-type AAV. |
Q33186207 | Genetic fate of recombinant adeno-associated virus vector genomes in muscle |
Q33649500 | High-fidelity correction of mutations at multiple chromosomal positions by adeno-associated virus vectors. |
Q41480639 | Human gene targeting by viral vectors |
Q33781976 | Infectious clones and vectors derived from adeno-associated virus (AAV) serotypes other than AAV type 2. |
Q39366416 | Long-term engraftment and angiogenic properties of lentivirally transduced adipose tissue-derived stromal cells |
Q75401742 | Model of unidirectional transluminal gene transfer |
Q37743813 | Novel adeno-associated virus vector vaccine restricts replication of simian immunodeficiency virus in macaques |
Q36302317 | Precise hit: adeno-associated virus in gene targeting |
Q39878393 | Recombinant adeno-associated virus mediates a high level of gene transfer but less efficient integration in the K562 human hematopoietic cell line |
Q36634119 | Reduction in levels of the cyclin-dependent kinase inhibitor p27(kip-1) coupled with transforming growth factor beta neutralization induces cell-cycle entry and increases retroviral transduction of primitive human hematopoietic cells |
Q45879177 | Selective transduction of HIV-1-infected cells by the combination of HIV and MMLV vectors |
Q39008906 | T-cell receptor transfer into human T cells with ecotropic retroviral vectors. |
Q39116422 | Transduction of human embryonic stem cells by ecotropic retroviral vectors. |
Q30495724 | Transduction of human primitive repopulating hematopoietic cells with lentiviral vectors pseudotyped with various envelope proteins |
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