(Q42476540)

1 November 2017

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

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1 November 2017

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B R Grubb

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1 November 2017

R J Pickles

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1 November 2017

H Ye

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1 November 2017

J R Yankaskas

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R N Vick

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1 November 2017

J F Engelhardt

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1 November 2017

J M Wilson

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L G Johnson

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1 November 2017

R C Boucher

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1 November 2017

language of work or name

English

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publication date

1 October 1994

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1 November 2017

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1 November 2017

371

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1 November 2017

802-806

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1 November 2017

6500

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https://scigraph.springernature.com/pub.10.1038/371802a0

1 November 2017

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cites work

Correction of cAMP-stimulated fluid secretion in cystic fibrosis airway epithelia: efficiency of adenovirus-mediated gene transfer in vitro

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7 January 2021

An animal model for cystic fibrosis made by gene targeting

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7 January 2021

Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis

1 reference

7 January 2021

Relative ion permeability of normal and cystic fibrosis nasal epithelium

1 reference

7 January 2021

Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis.

1 reference

7 January 2021

Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill.

1 reference

7 January 2021

Gene therapy of cystic fibrosis lung disease using E1 deleted adenoviruses: a phase I trial

1 reference

7 January 2021

Hyperabsorption of Na+ and raised Ca(2+)-mediated Cl- secretion in nasal epithelia of CF mice.

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7 January 2021

Direct gene transfer of human CFTR into human bronchial epithelia of xenografts with E1-deleted adenoviruses.

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7 January 2021

Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis

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7 January 2021

Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice

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7 January 2021

Two steps closer to gene therapy for cystic fibrosis

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7 January 2021

Expression of "cell-type-specific" markers during rat tracheal epithelial regeneration

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7 January 2021

Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis.

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7 January 2021

Diversity of airway epithelial cell targets for in vivo recombinant adenovirus-mediated gene transfer

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7 January 2021

Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: biological efficacy study.

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7 January 2021

Lung gene therapy: in vivo adenovirus-mediated gene transfer to rhesus monkey airway epithelium

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7 January 2021

Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: toxicity study

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7 January 2021

Safety and efficacy of repetitive adenovirus-mediated transfer of CFTR cDNA to airway epithelia of primates and cotton rats.

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7 January 2021

Correction of the ion transport defect in cystic fibrosis transgenic mice by gene therapy

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7 January 2021

Defective epithelial chloride transport in a gene-targeted mouse model of cystic fibrosis

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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

Identifiers

DOI

10.1038/371802A0

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Dimensions Publication ID

1 November 2017

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