(Q45869605)

17 December 2017

title

Expression of CFTR from a ciliated cell-specific promoter is ineffective at correcting nasal potential difference in CF mice (English)

1 reference

17 December 2017

author name string

Ostrowski LE

1

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17 December 2017

Yin W

2

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17 December 2017

Diggs PS

3

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17 December 2017

Rogers TD

4

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17 December 2017

O'Neal WK

5

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17 December 2017

Grubb BR

6

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17 December 2017

publication date

19 July 2007

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17 December 2017

published in

Gene Therapy

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17 December 2017

volume

14

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17 December 2017

issue

20

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17 December 2017

page(s)

1492-1501

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17 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.gt.3302994

exact match

0 references

cites work

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Abnormal apical cell membrane in cystic fibrosis respiratory epithelium. An in vitro electrophysiologic analysis

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Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia

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Differential localization of the cystic fibrosis transmembrane conductance regulator in normal and cystic fibrosis airway epithelium

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7 January 2021

Submucosal glands are the predominant site of CFTR expression in the human bronchus

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7 January 2021

Expression of the human cystic fibrosis transmembrane conductance regulator gene in the mouse lung after in vivo intratracheal plasmid-mediated gene transfer

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Enhancing rAAV vector expression in the lung

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Increased persistence of lung gene expression using plasmids containing the ubiquitin C or elongation factor 1alpha promoter.

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7 January 2021

Targeting expression of a transgene to the airway surface epithelium using a ciliated cell-specific promoter

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7 January 2021

An animal model for cystic fibrosis made by gene targeting

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7 January 2021

Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer

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7 January 2021

The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon

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7 January 2021

Anomalies in ion transport in CF mouse tracheal epithelium

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7 January 2021

Mouse models of cystic fibrosis

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7 January 2021

Pathophysiology of gene-targeted mouse models for cystic fibrosis

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7 January 2021

Distribution of ion transport mRNAs throughout murine nose and lung

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Yes-associated protein 65 localizes p62(c-Yes) to the apical compartment of airway epithelia by association with EBP50

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7 January 2021

The human hepatocyte nuclear factor 3/fork head gene FKHL13: genomic structure and pattern of expression

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7 January 2021

Real-time analysis of cAMP-mediated regulation of ciliary motility in single primary human airway epithelial cells

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7 January 2021

Lung development and repair: contribution of the ciliated lineage

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7 January 2021

Cystic fibrosis in the mouse by targeted insertional mutagenesis

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7 January 2021

Functional evidence of CFTR gene transfer in nasal epithelium of cystic fibrosis mice in vivo following luminal application of DNA complexes targeted to the serpin-enzyme complex receptor

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7 January 2021

Recovery of airway cystic fibrosis transmembrane conductance regulator function in mice with cystic fibrosis after single-dose lentivirus-mediated gene transfer

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7 January 2021

Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans

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7 January 2021

Enhanced in vivo airway gene transfer via transient modification of host barrier properties with a surface-active agent

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7 January 2021

Molecular cloning and sequence analysis of the murine cDNA for the cystic fibrosis transmembrane conductance regulator

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7 January 2021

Comparison of the gating behaviour of human and murine cystic fibrosis transmembrane conductance regulator Cl- channels expressed in mammalian cells

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7 January 2021

Cystic fibrosis transmembrane conductance regulator differentially regulates human and mouse epithelial sodium channels in Xenopus oocytes

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7 January 2021

Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA.

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7 January 2021

Correction of lethal intestinal defect in a mouse model of cystic fibrosis by human CFTR

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7 January 2021

A delta F508 mutation in mouse cystic fibrosis transmembrane conductance regulator results in a temperature-sensitive processing defect in vivo

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7 January 2021

Development of substituted Benzo[c]quinolizinium compounds as novel activators of the cystic fibrosis chloride channel.

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7 January 2021

Olfactory epithelia exhibit progressive functional and morphological defects in CF mice

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7 January 2021

Airway gene transfer in mouse nasal-airways: importance of identification of epithelial type for assessment of gene transfer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302994

7 January 2021

Increased contact time improves adenovirus-mediated CFTR gene transfer to nasal epithelium of CF mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302994

7 January 2021

In vivo expression of adenovirus-mediated lacZ gene in murine nasal mucosa.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GT.3302994

7 January 2021

Identifiers

DOI

10.1038/SJ.GT.3302994

1 reference

17 December 2017

Dimensions Publication ID

1038980990

0 references

1 reference

17 December 2017