Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation method.
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Intermedin is a new angiogenic growth factorProduction of viral vectors using recombinase-mediated cassette exchangeA trial of somatic gene targeting in vivo with an adenovirus vector.Methods and clinical development of adenovirus-vectored vaccines against mucosal pathogensPre-existing vector immunity does not prevent replication deficient adenovirus from inducing efficient CD8 T-cell memory and recall responsesInhibition of angiogenesis by a mouse sprouty protein.Efficient gene transfer into human CD34(+) cells by a retargeted adenovirus vectorOncogenic LMO3 collaborates with HEN2 to enhance neuroblastoma cell growth through transactivation of Mash1A mammalian mirtron miR-1224 promotes tube-formation of human primary endothelial cells by targeting anti-angiogenic factor epsin2Targeting of p53-transcriptional dysfunction by conditionally replicating adenovirus is not limited by p53-homologues.Efficient and directive generation of two distinct endoderm lineages from human ESCs and iPSCs by differentiation stage-specific SOX17 transduction.High expression level of soluble SARS spike protein mediated by adenovirus in HEK293 cellsReduction of natural adenovirus tropism to mouse liver by fiber-shaft exchange in combination with both CAR- and alphav integrin-binding ablation.Autoinhibitory regulation of p73 by Delta Np73 to modulate cell survival and death through a p73-specific target element within the Delta Np73 promoterEfficient generation of hepatoblasts from human ES cells and iPS cells by transient overexpression of homeobox gene HEX.Recombinant adenovirus-mediated intestinal trefoil factor gene therapy for burn-induced intestinal mucosal injuryThe overexpression of Twinkle helicase ameliorates the progression of cardiac fibrosis and heart failure in pressure overload model in mice.Vaccination with Human Induced Pluripotent Stem Cells Creates an Antigen-Specific Immune Response Against HIV-1 gp160.An attempt to induce "Graves' disease of the gonads" by immunizing mice with the luteinizing hormone receptor provides insight into breaking tolerance to self-antigens.The thyrotropin receptor autoantigen in Graves disease is the culprit as well as the victim.Suppression of leaky expression of adenovirus genes by insertion of microRNA-targeted sequences in the replication-incompetent adenovirus vector genome.Tumor vascular targeted delivery of polymer-conjugated adenovirus vector for cancer gene therapyRecombinant adeno-vaccine expressing enterovirus 71-like particles against hand, foot, and mouth diseaseA novel and simple method for rapid generation of recombinant porcine adenoviral vectors for transgene expressionEvaluation of transduction properties of an adenovirus vector in neonatal mice.Efficient generation of functional hepatocytes from human embryonic stem cells and induced pluripotent stem cells by HNF4α transduction.NF-κB promotes leaky expression of adenovirus genes in a replication-incompetent adenovirus vector.Immune cell recruitment and cell-based system for cancer therapy.A novel adenovirus vector for easy cloning in the E3 region downstream of the CMV promoterQualitative and quantitative analysis of adenovirus type 5 vector-induced memory CD8 T cells: not as bad as their reputation.Dicer functions as an antiviral system against human adenoviruses via cleavage of adenovirus-encoded noncoding RNAIntermedin ameliorates vascular and renal injury by inhibition of oxidative stressAdenovirus vector-based incorporation of a photo-cross-linkable amino acid into proteins in human primary cells and cancerous cell lines.Adenovirus-mediated delivery of the human IFN-γ gene potentiates the cytotoxicity of daunorubicin against leukemic cells through downregulation of the α4β1 integrin/ILK/apoptosis pathway.Coating with spermine-pullulan polymer enhances adenoviral transduction of mesenchymal stem cells.Using viral vectors as gene transfer tools (Cell Biology and Toxicology Special Issue: ETCS-UK 1 day meeting on genetic manipulation of cells).An efficient method of directly cloning chimpanzee adenovirus as a vaccine vector.Type I Interferons Impede Short Hairpin RNA-Mediated RNAi via Inhibition of Dicer-Mediated Processing to Small Interfering RNA.Human induced-pluripotent stem cell-derived hepatocyte-like cells as an in vitro model of human hepatitis B virus infection.Cloning and Large-Scale Production of High-Capacity Adenoviral Vectors Based on the Human Adenovirus Type 5.
P2860
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P2860
Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation method.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Efficient construction of a re ...... oved in vitro ligation method.
@en
type
label
Efficient construction of a re ...... oved in vitro ligation method.
@en
prefLabel
Efficient construction of a re ...... oved in vitro ligation method.
@en
P1433
P1476
Efficient construction of a re ...... oved in vitro ligation method.
@en
P2093
P304
P356
10.1089/10430349850019418
P577
1998-11-01T00:00:00Z