Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1-deleted adenoviruses.
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Progress towards gene therapy for cystic fibrosisSurface TRAIL decoy receptor-4 expression is correlated with TRAIL resistance in MCF7 breast cancer cellsAn adenovirus type 5 (Ad5) amplicon-based packaging cell line for production of high-capacity helper-independent deltaE1-E2-E3-E4 Ad5 vectors.Endocytosis and nuclear trafficking of adeno-associated virus type 2 are controlled by rac1 and phosphatidylinositol-3 kinase activation.Engineering viral vectors to subvert the airway defense response.Concise Review: The Potential Use of Intestinal Stem Cells to Treat Patients with Intestinal Failure.Inhibition of hepatitis B virus replication during adenovirus and cytomegalovirus infections in transgenic miceRecombinant, replication-defective adenovirus gene transfer vectors induce cell cycle dysregulation and inappropriate expression of cyclin proteins.Transfer of a cathelicidin peptide antibiotic gene restores bacterial killing in a cystic fibrosis xenograft modelUpregulation of class I major histocompatibility complex antigens by interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivoGene therapy in human cancer: report of human clinical trials.Adenoviral-mediated gene transfer in wound healing.Gene transfer into the airway epithelium of animals by targeting the polymeric immunoglobulin receptorAdenoviral-mediated gene transfer to fetal pulmonary epithelia in vitro and in vivo.Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbitCurrent status of gene therapy for inherited lung diseasesGene therapy for brain tumors: regression of experimental gliomas by adenovirus-mediated gene transfer in vivo.Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapyNormalization of raised sodium absorption and raised calcium-mediated chloride secretion by adenovirus-mediated expression of cystic fibrosis transmembrane conductance regulator in primary human cystic fibrosis airway epithelial cells.Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liverEmerging drug treatments for cystic fibrosis.Gene therapy for cystic fibrosis: challenges and future directionsGenotypic analysis of respiratory mucous sulfation defects in cystic fibrosis.Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenovirusesExpression of alpha v beta 5 integrin is necessary for efficient adenovirus-mediated gene transfer in the human airway.Efficient dual transcomplementation of adenovirus E1 and E4 regions from a 293-derived cell line expressing a minimal E4 functional unit.Adenovirus-mediated gene transfer to ciliated airway epithelia requires prolonged incubation time.Recombinant adenoviruses with large deletions generated by Cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo.Lentivirus-mediated gene transfer to the respiratory epithelium: a promising approach to gene therapy of cystic fibrosis.Adenoviral vectors: development and application.Noncytopathic clearance of lymphocytic choriomeningitis virus from the hepatocyte.Gene delivery to the airwayA novel cationic lipid greatly enhances plasmid DNA delivery and expression in mouse lung.Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosisDifferentiation of xenografted human fetal lung parenchyma.Incorporation of adenovirus in calcium phosphate precipitates enhances gene transfer to airway epithelia in vitro and in vivo.Gene therapy with helper-dependent adenoviral vectors: current advances and future perspectives.Anti-Inflammatory Effects of Modified Adenoviral Vectors for Gene Therapy: A View through Animal Models Tested.Augmentation of innate host defense by expression of a cathelicidin antimicrobial peptide.Factors influencing adeno-associated virus-mediated gene transfer to human cystic fibrosis airway epithelial cells: comparison with adenovirus vectors.
P2860
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P2860
Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1-deleted adenoviruses.
description
1993 nî lūn-bûn
@nan
1993年の論文
@ja
1993年論文
@yue
1993年論文
@zh-hant
1993年論文
@zh-hk
1993年論文
@zh-mo
1993年論文
@zh-tw
1993年论文
@wuu
1993年论文
@zh
1993年论文
@zh-cn
name
Direct gene transfer of human ...... with E1-deleted adenoviruses.
@en
Direct gene transfer of human ...... with E1-deleted adenoviruses.
@nl
type
label
Direct gene transfer of human ...... with E1-deleted adenoviruses.
@en
Direct gene transfer of human ...... with E1-deleted adenoviruses.
@nl
prefLabel
Direct gene transfer of human ...... with E1-deleted adenoviruses.
@en
Direct gene transfer of human ...... with E1-deleted adenoviruses.
@nl
P2093
P2860
P356
P1433
P1476
Direct gene transfer of human ...... s with E1-deleted adenoviruses
@en
P2093
J R Yankaskas
K Kozarsky
L D Stratford-Perricaudet
M Perricaudet
P2860
P2888
P356
10.1038/NG0593-27
P407
P577
1993-05-01T00:00:00Z
P5875
P6179
1010312039