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Keywords: Cystic fibrosis
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Journal Articles

Cystic Fibrosis Transmembrane Conductance Regulator Can Export Hyaluronan

Open Access
Subject Area:
Further Areas , Oncology , Pathology and Cell Biology
Tobias Schulz, Udo Schumacher, Christian Prante, Wolfgang Sextro, Peter Prehm
Journal: Pathobiology
Pathobiology (2010) 77 (4): 200–209.
https://doi.org/10.1159/000295859
Published Online: 07 July 2010
... synthesis is vital for embryogenesis, MRP5-deficient mice are without phenotype, suggesting that another transporter had substituted for the MRP5 protein. Thus, we searched for a compensatory exporter in fibroblasts from MRP5 deficient mice and found that cystic fibrosis transmembrane conductance regulator...
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Journal Articles

Lung Pathology in Response to Repeated Exposure to Staphylococcus aureus in Congenic Residual Function Cystic Fibrosis Mice Does Not Increase in Response to Decreased CFTR Levels or Increased Bacterial Load

Available to Purchase
Subject Area:
Further Areas , Oncology , Pathology and Cell Biology
Donald J. Davidson, Sheila Webb, Peter Teague, John R. W. Govan, Julia R. Dorin
Journal: Pathobiology
Pathobiology (2004) 71 (3): 152–158.
https://doi.org/10.1159/000076470
Published Online: 02 April 2004
...Donald J. Davidson; Sheila Webb; Peter Teague; John R. W. Govan; Julia R. Dorin Objective: To establish the role of defects in murine Cftr in the susceptibility to Staphylococcus aureus lung disease using mouse models of cystic fibrosis (CF), congenic or inbred strains. Methods: We describe...
View article titled, Lung Pathology in Response to Repeated Exposure to Staphylococcus aureus in Congenic Residual Function Cystic Fibrosis Mice Does Not Increase in Response to Decreased CFTR Levels or Increased Bacterial Load
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Journal Articles

Residual cftr Expression Varies with Age in cftr tm1Hgu Cystic Fibrosis Mice: Impact on Morphology and Physiology

Available to Purchase
Subject Area:
Further Areas , Oncology , Pathology and Cell Biology
M. Larbig, S. Jansen, M. Dorsch, W. Bernhard, B. Bellmann, J.R. Dorin, D.J. Porteous, H. von der Hardt, I. Steinmetz, H.-J. Hedrich, B. Tuemmler, T. Tschernig
Journal: Pathobiology
Pathobiology (2002) 70 (2): 89–97.
https://doi.org/10.1159/000067308
Published Online: 20 December 2002
...M. Larbig; S. Jansen; M. Dorsch; W. Bernhard; B. Bellmann; J.R. Dorin; D.J. Porteous; H. von der Hardt; I. Steinmetz; H.-J. Hedrich; B. Tuemmler; T. Tschernig Mouse models for cystic fibrosis (CF) mimic intestinal manifestations of the human disease, but the lung disease phenotypes are lacking...
View article titled, Residual cftr Expression Varies with Age in cftr tm1Hgu Cystic Fibrosis Mice: Impact on Morphology and Physiology
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