(Q40379256)

20 September 2017

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title

Development of mouse models for cystic fibrosis (English)

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20 September 2017

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J R Dorin

1

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20 September 2017

publication date

1 January 1995

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Journal of Inherited Metabolic Disease

20 September 2017

published in

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20 September 2017

volume

18

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20 September 2017

issue

4

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20 September 2017

page(s)

495-500

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

20 September 2017

cites work

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12 December 2020

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive

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12 December 2020

Cystic fibrosis mouse with intestinal obstruction

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12 December 2020

Ion transport characteristics of the murine trachea and caecum

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12 December 2020

Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis

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12 December 2020

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

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12 December 2020

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

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12 December 2020

In vivo cell-specific expression of the cystic fibrosis transmembrane conductance regulator

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens

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12 December 2020

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

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12 December 2020

An animal model for cystic fibrosis made by gene targeting

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12 December 2020

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

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12 December 2020

Bioelectric characteristics of exon 10 insertional cystic fibrosis mouse: comparison with humans

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12 December 2020

The new mouse genetics: altering the genome by gene targeting

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Disruption of the proto-oncogene int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes

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12 December 2020

CFTR and calcium-activated chloride currents in pancreatic duct cells of a transgenic CF mouse

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12 December 2020

Identifiers

DOI

10.1007/BF00710060

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Dimensions Publication ID

20 September 2017

1009571164

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