Persistent transgene expression in mouse liver following in vivo gene transfer with a delta E1/delta E4 adenovirus vector.
about
Adenovector-mediated hair cell regeneration is affected by promoter type.Increased revascularization efficacy after administration of an adenovirus encoding VEGF(121).In vitro and in vivo biology of recombinant adenovirus vectors with E1, E1/E2A, or E1/E4 deleted.Transient inhibition of CD28 and CD40 ligand interactions prolongs adenovirus-mediated transgene expression in the lung and facilitates expression after secondary vector administrationThe E4-6/7 protein functionally compensates for the loss of E1A expression in adenovirus infectionGeneration of an adenovirus vector lacking E1, e2a, E3, and all of E4 except open reading frame 3.Regulation of adenovirus-mediated transgene expression by the viral E4 gene products: requirement for E4 ORF3.Gene therapy in the CNS.A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus.Helper-Dependent Adenoviral Vectors.Adenoviral producer cellsAdenovirus-mediated persistent cystic fibrosis transmembrane conductance regulator expression in mouse airway epithelium.Role of E4 in eliciting CD4 T-cell and B-cell responses to adenovirus vectors delivered to murine and nonhuman primate lungs.Efficient, repeated adenovirus-mediated gene transfer in mice lacking both tumor necrosis factor alpha and lymphotoxin alpha.Adenovirus vectors with the 100K gene deleted and their potential for multiple gene therapy applicationsRole for the adenovirus IVa2 protein in packaging of viral DNAReplication-defective vector based on a chimpanzee adenovirus.Human adenovirus type 35: nucleotide sequence and vector development.Multiply deleted [E1, polymerase-, and pTP-] adenovirus vector persists despite deletion of the preterminal protein.Persistent hepatic expression of human apo A-I after transfer with a helper-virus independent adenoviral vector.Reversal of hypopigmentation in phenylketonuria mice by adenovirus-mediated gene transfer.Adenoviral vectors: prospects for gene delivery to the central nervous system.Variation in the immune response to adenoviral vectors in the brain: influence of mouse strain, environmental conditions and priming.Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration.Transient cyclophosphamide treatment before intraportal readministration of an adenoviral vector can induce re-expression of the original gene construct in rat liver.Next-generation adenoviral vectors: new and improved.Cotransfection of heme oxygenase-1 prevents the acute inflammation elicited by a second adenovirus.Regulated hepatic insulin gene therapy of STZ-diabetic rats.Non-invasive observation of repeated adenoviral GFP gene delivery to the anterior segment of the monkey eye in vivo.
P2860
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P2860
Persistent transgene expression in mouse liver following in vivo gene transfer with a delta E1/delta E4 adenovirus vector.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年学术文章
@wuu
1997年学术文章
@zh
1997年学术文章
@zh-cn
1997年学术文章
@zh-hans
1997年学术文章
@zh-my
1997年学术文章
@zh-sg
1997年學術文章
@yue
1997年學術文章
@zh-hant
name
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@en
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@nl
type
label
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@en
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@nl
prefLabel
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@en
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@nl
P2093
P356
P1433
P1476
Persistent transgene expressio ...... E1/delta E4 adenovirus vector.
@en
P2093
P2888
P304
P356
10.1038/SJ.GT.3300404
P577
1997-05-01T00:00:00Z
P5875
P6179
1026353996