Diversity of airway epithelial cell targets for in vivo recombinant adenovirus-mediated gene transfer.
about
Fatty acid modification of the coxsackievirus and adenovirus receptor.Variability of human systemic humoral immune responses to adenovirus gene transfer vectors administered to different organsCAR-dependent and CAR-independent pathways of adenovirus vector-mediated gene transfer and expression in human fibroblasts.Augmentation of pulmonary host defense against Pseudomonas by FcgammaRIIA cDNA transfer to the respiratory epithelium.Nonneurotropic adenovirus: a vector for gene transfer to the brain and gene therapy of neurological disordersVulnerability of the human airway epithelium to hyperoxia. Constitutive expression of the catalase gene in human bronchial epithelial cells despite oxidant stressAdenoviral-mediated gene transfer to fetal pulmonary epithelia in vitro and in vivo.Low-efficiency of percutaneous adenovirus-mediated arterial gene transfer in the atherosclerotic rabbitMyotubes from transgenic mdx mice expressing full-length dystrophin show normal calcium regulation.Transient gene expression from yeast artificial chromosome DNA in mammalian cells is enhanced by adenovirus.Developing cell therapy techniques for respiratory disease: intratracheal delivery of genetically engineered stem cells in a murine model of airway injury.Gene therapy for cystic fibrosis: challenges and future directionsIn vivo suppression of injury-induced vascular smooth muscle cell accumulation using adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene.Therapeutic antitumor response after immunization with a recombinant adenovirus encoding a model tumor-associated antigenTargeting gene expression to specific cells of kidney tubules in vivo, using adenoviral promoter fragments.Immunizing patients with metastatic melanoma using recombinant adenoviruses encoding MART-1 or gp100 melanoma antigensPackaging capacity and stability of human adenovirus type 5 vectors.Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapiesElevated expression of NEU1 sialidase in idiopathic pulmonary fibrosis provokes pulmonary collagen deposition, lymphocytosis, and fibrosis.Adenoviral-mediated transfer of the human endothelial nitric oxide synthase gene reduces acute hypoxic pulmonary vasoconstriction in rats.Augmentation of lung liquid clearance via adenovirus-mediated transfer of a Na,K-ATPase beta1 subunit gene.Incorporation of adenovirus in calcium phosphate precipitates enhances gene transfer to airway epithelia in vitro and in vivo.Therapeutics: Gene Therapy for Alpha-1 Antitrypsin Deficiency.Genetic delivery of bevacizumab to suppress vascular endothelial growth factor-induced high-permeability pulmonary edema.Elimination of both E1 and E2 from adenovirus vectors further improves prospects for in vivo human gene therapy.Cl transport in complemented CF bronchial epithelial cells correlates with CFTR mRNA expression levels.St. John's Wort protein, p27SJ, regulates the MCP-1 promoter.Gene therapy for the respiratory manifestations of cystic fibrosis.New strategies for treatment of pulmonary fibrosis.Restoration of cyclic adenosine monophosphate-stimulated chloride channel activity in human cystic fibrosis tracheobronchial submucosal gland cells by adenovirus-mediated and cationic lipid-mediated gene transfer.Novel flow cytometry approach to identify bronchial epithelial cells from healthy human airways.Transduction of non-small cell lung cancer cells by adenoviral and retroviral vectors.Gene transfer of the vascular endothelial growth factor receptor flt-1 suppresses pulmonary metastasis associated with lung growth.Pulmonary inflammation associated with repeated, prenatal exposure to an E1, E3-deleted adenoviral vector in sheep.An integrin-targeted non-viral vector for pulmonary gene therapy.Effect of Pseudomonas-induced chronic lung inflammation on specific cytotoxic T-cell responses to adenoviral vectors in mice.Surfactant protein A-producing cells in human fetal lung are good targets for recombinant adenovirus-mediated gene transfer.Infection of replication-deficient adenoviral vector enhances interleukin-8 production in small airway epithelial cells more than in large airway epithelial cells.Towards a gene therapy for cystic fibrosis lung disease.TGF-beta1 gene transfer to the mouse colon leads to intestinal fibrosis.
P2860
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P2860
Diversity of airway epithelial cell targets for in vivo recombinant adenovirus-mediated gene transfer.
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
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@ast
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@en
type
label
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@ast
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@en
prefLabel
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@ast
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@en
P2093
P2860
P356
P1476
Diversity of airway epithelial ...... ovirus-mediated gene transfer.
@en
P2093
Crystal RG
Mastrangeli A
Pavirani A
Rosenfeld MA
Stratford-Perricaudet L
P2860
P304
P356
10.1172/JCI116175
P407
P577
1993-01-01T00:00:00Z