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Evaluation of secondhand smoke effects on CFTR function in vivo

Lawrence W Rasmussen1,2, Denise Stanford1,3, Krina Patel1

  • 1Departments of Medicine, The University of Alabama at Birmingham, Birmingham, AL, USA.

Respiratory Research
|March 21, 2020
PubMed
Summary

No abstract available in PubMed .

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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
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Cystic fibrosis (CF) is an autosomal recessive disorder that predominantly affects individuals of Northern European descent, occurring at a rate of 1 in 3500. It is caused by a genetic mutation in a gene on chromosome 7, most commonly the ΔF508 mutation, that codes for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. This results in thicker mucus secretions and obstruction pathologies in multiple organs, including the lungs and sinuses.
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