Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model (Q35097413)

6 August 2017

title

Characteristic multiorgan pathology of cystic fibrosis in a long-living cystic fibrosis transmembrane regulator knockout murine model (English)

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6 August 2017

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transmembrane protein

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Peter R Durie

1

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6 August 2017

Geraldine Kent

series ordinal

2

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6 August 2017

M James Phillips

series ordinal

3

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6 August 2017

Cameron A Ackerley

series ordinal

4

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6 August 2017

language of work or name

English

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publication date

1 April 2004

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The American Journal of Pathology

6 August 2017

published in

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6 August 2017

volume

164

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6 August 2017

issue

4

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6 August 2017

page(s)

1481-1493

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Enhanced susceptibility to pulmonary infection with Burkholderia cepacia in Cftr(-/-) mice

6 August 2017

cites work

1 reference

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9 July 2018

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Early alterations in airway mucociliary clearance and inflammation of the lamina propria in CF mice

9 July 2018

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Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.

9 July 2018

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9 July 2018

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A mouse model for the delta F508 allele of cystic fibrosis.

9 July 2018

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9 July 2018

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9 July 2018

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Generation of cAMP-Activated Chloride Currents by Expression of CFTR

9 July 2018

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9 July 2018

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9 July 2018

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9 July 2018

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Parotid Gland Function in Children with Cystic Fibrosis and Child Control Subjects

9 July 2018

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The lung in cystic fibrosis. A quantitative study including prevalence of pathologic findings among different age groups

9 July 2018

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Pathology of cystic fibrosis review of the literature and comparison with 146 autopsied cases

9 July 2018

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Quantitative evaluation of the development of the exocrine pancreas in cystic fibrosis and control infants

9 July 2018

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Generation and characterization of a delta F508 cystic fibrosis mouse model

9 July 2018

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27 September 2018

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7 January 2021

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Studies on parotid saliva in cystic fibrosis

7 January 2021

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Recommendations for management of liver and biliary tract disease in cystic fibrosis. Cystic Fibrosis Foundation Hepatobiliary Disease Consensus Group

7 January 2021

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7 January 2021

The Visibly Fatty Liver

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Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus

7 January 2021

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Phenotypic abnormalities in long-term surviving cystic fibrosis mice

7 January 2021

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

7 January 2021

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Submucosal gland distribution in the mouse has a genetic determination localized on chromosome 9

7 January 2021

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The distribution and structure of cells in the tracheal epithelium of the mouse

7 January 2021

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Lung disease in the cystic fibrosis mouse exposed to bacterial pathogens

7 January 2021

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G551D Cystic Fibrosis Mice Exhibit Abnormal Regulation of Inflammation in Lungs and Macrophages

7 January 2021

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

7 January 2021

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The pathological changes in the liver in cystic fibrosis of the pancreas

7 January 2021

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15039235

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Early detection of pulmonary function abnormalities in cystic fibrosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15039235

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A distinctive type of biliary cirrhosis of the liver associated with cystic fibrosis of the pancreas; recognition through signs of portal hypertension

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15039235

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/S0002-9440(10)63234-8

1 reference

6 August 2017

1 reference

6 August 2017

1 reference