about
The SET domain protein Metnase mediates foreign DNA integration and links integration to nonhomologous end-joining repairThe use of retroviral vectors for gene therapy-what are the risks? A review of retroviral pathogenesis and its relevance to retroviral vector-mediated gene deliveryEffective suppression of Dengue fever virus in mosquito cell cultures using retroviral transduction of hammerhead ribozymes targeting the viral genomeRetroviral vectors for clinical immunogene therapy are stable for up to 9 years.DNA as therapeutics; an update.The role of hydrophobic amino acid grafts in the enhancement of membrane-disruptive activity of pH-responsive pseudo-peptides.High-titre retroviral vector system for efficient gene delivery into human and mouse cells of haematopoietic and lymphocytic lineages.Live bacterial vaccines--a review and identification of potential hazards.Optimised concentration and purification of retroviruses using membrane chromatographyDNA-based therapeutics and DNA delivery systems: a comprehensive review.Angiogenic and antiangiogenic gene therapy.Incorporation of quantum dots on virus in polycationic solution.Effect of fetal bovine serum on foamy and lentiviral vector production.Viral vectors: from virology to transgene expressionTransduction of Schistosoma japonicum schistosomules with vesicular stomatitis virus glycoprotein pseudotyped murine leukemia retrovirus and expression of reporter human telomerase reverse transcriptase in the transgenic schistosomesGelatin-based delivery systems for cancer gene therapy.Vector-mediated Tum-5 expression in neovascular endothelial cells for treating hepatocellular carcinoma.Mesenchymal stem cells as novel micro-ribonucleic acid delivery vehicles in kidney disease.A Lentiviral Vector Expressing Desired Gene Only in Transduced Cells: An Approach for Suicide Gene Therapy.Engineered retroviral virus-like particles for receptor targeting.Biodegradable cross-linked poly(amino alcohol esters) based on LMW PEI for gene delivery.Using intron splicing trick for preferential gene expression in transduced cells: an approach for suicide gene therapy.Cell culture processes for the production of viral vectors for gene therapy purposes.A preliminary step of a novel strategy in suicide gene therapy with lentiviral vector.Expression of YB-1 enhances production of murine leukemia virus vectors by stabilizing genomic viral RNA.Design of pH-responsive gold nanoparticles in oncologyTargeted nonviral gene therapy in prostate cancer
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
2002年论文
@zh
2002年论文
@zh-cn
name
Retroviral vectors for human gene delivery.
@ast
Retroviral vectors for human gene delivery.
@en
type
label
Retroviral vectors for human gene delivery.
@ast
Retroviral vectors for human gene delivery.
@en
prefLabel
Retroviral vectors for human gene delivery.
@ast
Retroviral vectors for human gene delivery.
@en
P1476
Retroviral vectors for human gene delivery.
@en
P2093
Mohamed Al-Rubeai
Sally McTaggart
P356
10.1016/S0734-9750(01)00087-8
P577
2002-04-01T00:00:00Z