(Q71698854)

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20 October 2019

title

Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens (English)

1 reference

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20 October 2019

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3

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20 October 2019

David J. Porteous

8

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20 October 2019

author name string

Davidson DJ

1

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20 October 2019

Dorin JR

2

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20 October 2019

Ranaldi V

4

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20 October 2019

Lamb D

5

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20 October 2019

Doherty C

6

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20 October 2019

Govan J

7

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20 October 2019

publication date

1 April 1995

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20 October 2019

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20 October 2019

volume

9

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20 October 2019

page(s)

351-357

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20 October 2019

issue

4

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https://scigraph.springernature.com/pub.10.1038/ng0495-351

20 October 2019

exact match

0 references

cites work

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA

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7 January 2021

Identification of the cystic fibrosis gene: genetic analysis

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7 January 2021

Correlation between genotype and phenotype in patients with cystic fibrosis

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7 January 2021

Microbiology of airway disease in patients with cystic fibrosis

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7 January 2021

Cystic fibrosis in the mouse by targeted insertional mutagenesis

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7 January 2021

Long-term survival of the exon 10 insertional cystic fibrosis mutant mouse is a consequence of low level residual wild-type Cftr gene expression.

1 reference

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7 January 2021

A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations

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7 January 2021

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

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7 January 2021

An animal model for cystic fibrosis made by gene targeting

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7 January 2021

Production of a severe cystic fibrosis mutation in mice by gene targeting

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7 January 2021

A severe phenotype in mice with a duplication of exon 3 in the cystic fibrosis locus.

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7 January 2021

Pseudomonas cepacia infection in cystic fibrosis: an emerging problem

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7 January 2021

Colonization of the respiratory tract with Pseudomonas cepacia in cystic fibrosis. Risk factors and outcomes

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7 January 2021

Evidence for transmission of Pseudomonas cepacia by social contact in cystic fibrosis

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7 January 2021

Microbiology of lung infection in cystic fibrosis

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7 January 2021

Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis

1 reference

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7 January 2021

Mucociliary transport in trachea of patients with cystic fibrosis

1 reference

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7 January 2021

Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0495-351

7 January 2021

Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis

1 reference

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7 January 2021

Bioelectric properties of cystic fibrosis airways obtained at heart-lung transplantation

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Identifiers

DOI

10.1038/NG0495-351

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7540910%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference