Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
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Packaging capacity of adeno-associated virus serotypes: impact of larger genomes on infectivity and postentry steps.Defective regulation of gap junctional coupling in cystic fibrosis pancreatic duct cellsTransgenic hCFTR expression fails to correct β-ENaC mouse lung diseaseTaking stock of gene therapy for cystic fibrosisMechanisms of lipid malabsorption in Cystic Fibrosis: the impact of essential fatty acids deficiencyBinding of protegrin-1 to Pseudomonas aeruginosa and Burkholderia cepacia.Pathophysiology of gene-targeted mouse models for cystic fibrosisCystic fibrosis epithelial cells have a receptor for pathogenic bacteria on their apical surfaceExpression and regulation of the cystic fibrosis gene during rat liver regenerationMicrobial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepaciaFUNCTIONAL NANOPARTICLES FOR MOLECULAR IMAGING GUIDED GENE DELIVERYCystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation.Gene therapy for cystic fibrosis.Cystic fibrosis: exploiting its genetic basis in the hunt for new therapiesGene transfer into hepatoma cell lines via the serpin enzyme complex receptorEffect of host modification and age on airway epithelial gene transfer mediated by a murine leukemia virus-derived vectorGene transfer into respiratory epithelial cells by targeting the polymeric immunoglobulin receptor.Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue.Regulation of CFTR expression and function during differentiation of intestinal epithelial cells.Physiological adaptation of the bacterium Lactococcus lactis in response to the production of human CFTR.Slow conversions among subconductance states of cystic fibrosis transmembrane conductance regulator chloride channelRectification of cystic fibrosis transmembrane conductance regulator chloride channel mediated by extracellular divalent cations.Interaction between permeation and gating in a putative pore domain mutant in the cystic fibrosis transmembrane conductance regulator.Cystic fibrosis in adults. From researcher to practitioner.Localization of the cystic fibrosis transmembrane conductance regulator in pancreas.Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channelProteomic identification of calumenin as a G551D-CFTR associated protein.Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channelsCystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice.Towards the pharmacogenomics of cystic fibrosis.Transfer of a constitutive viral promoter-cystic fibrosis transmembrane conductance regulator cDNA to human epithelial cells conveys resistance to down-regulation of cAMP-regulated Cl- secretion in the presence of inflammatory stimuli.Prevalence of neutralizing antibodies against adeno-associated virus (AAV) types 2, 5, and 6 in cystic fibrosis and normal populations: Implications for gene therapy using AAV vectors.Retrovirus-mediated gene transfer to cystic fibrosis airway epithelial cells: effect of selectable marker sequences on long-term expressionAdeno-associated virus serotype 9 vectors transduce murine alveolar and nasal epithelia and can be readministered.Identification of an ion channel-forming motif in the primary structure of CFTR, the cystic fibrosis chloride channelExpression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer.Identification of a nonframeshift 84-bp deletion in exon 13 of the cystic fibrosis gene.Altered protein folding may be the molecular basis of most cases of cystic fibrosis.Rapid endocytosis of the cystic fibrosis transmembrane conductance regulator chloride channel.Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.
P2860
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P2860
Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
@en
type
label
Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
@en
prefLabel
Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
@en
P2093
P1433
P1476
Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
@en
P2093
Collins FS
Frizzell RA
Rommens JM
P304
P356
10.1016/0092-8674(90)90398-X
P407
P577
1990-09-01T00:00:00Z