Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.
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Chromatin Dynamics in the Regulation of CFTR ExpressionProduction of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transferEfficient gene transfer into human normal and cystic fibrosis tracheal gland serous cells with synthetic vectors.Improved oxygenation promotes CFTR maturation and trafficking in MDCK monolayers.Laser fluorescence bronchoscopy for detection of fluorescent reporter genes in airway epithelia.Large-scale gene discovery in human airway epithelia reveals novel transcripts.In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot studyAssessing the residual CFTR gene expression in human nasal epithelium cells bearing CFTR splicing mutations causing cystic fibrosis.Gene therapy for cystic fibrosis.A shortened adeno-associated virus expression cassette for CFTR gene transfer to cystic fibrosis airway epithelia.Airway epithelial CFTR mRNA expression in cystic fibrosis patients after repetitive administration of a recombinant adenovirus.Gene 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.Persistent gene expression in mouse nasal epithelia following feline immunodeficiency virus-based vector gene transfer.Expression of the cystic fibrosis gene in adult human lungRNA-Seq quantification of the human small airway epithelium transcriptomeSevere deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator.Cystic fibrosis transmembrane conductance regulator is involved in airway epithelial wound repairMiR-101 and miR-144 regulate the expression of the CFTR chloride channel in the lungCFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR.Effects of C-terminal deletions on cystic fibrosis transmembrane conductance regulator function in cystic fibrosis airway epitheliaIn vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glandsCurrent status of gene therapy for inherited lung diseasesExpression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer.CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium.A mouse model for the delta F508 allele of cystic fibrosis.Gene therapy for cystic fibrosis: challenges and future directionsExpression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin.Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifDiversity of airway epithelial cell targets for in vivo recombinant adenovirus-mediated gene transfer.Targeted Integration of a Super-Exon into the CFTR Locus Leads to Functional Correction of a Cystic Fibrosis Cell Line Model.Transcriptional targeting in the airway using novel gene regulatory elements.CFTR, mucins, and mucus obstruction in cystic fibrosis.Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epitheliaMaximizing morphologic data from lung biopsies from normal and asthmatic humans.Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapiesDown-regulation of cystic fibrosis transmembrane conductance regulator gene expression by agents that modulate intracellular divalent cations.Guanylyl cyclase C is a selective marker for metastatic colorectal tumors in human extraintestinal tissuesPost-transcriptional regulation of cystic fibrosis transmembrane conductance regulator expression and function by microRNAs.
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P2860
Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on August 1991
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@en
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@nl
type
label
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@en
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@nl
prefLabel
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@en
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@nl
P2093
P2860
P356
P1476
Expression of the cystic fibro ...... ividuals with cystic fibrosis.
@en
P2093
Chernick MS
Crystal RG
Ferrans VJ
Trapnell BC
Yoshimura K
P2860
P304
P356
10.1073/PNAS.88.15.6565
P407
P577
1991-08-01T00:00:00Z